Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9267 |
|---|---|
| ensemblid | ENSG00000108669.18 |
| hgncid | 9501 |
| symbol | CYTH1 |
| name | cytohesin 1 |
| refseq_nuc | NM_004762.6 |
| refseq_prot | NP_004753.1 |
| ensembl_nuc | ENST00000446868.8 |
| ensembl_prot | ENSP00000389095.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 78674048 |
| end | 78782273 |
| strand | - |
| ver | v1.2 |
| region | chr17:78674048-78782273 |
| region5000 | chr17:78669048-78787273 |
| regionname0 | CYTH1_chr17_78674048_78782273 |
| regionname5000 | CYTH1_chr17_78669048_78787273 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 398 | 378 | 88 | 60 | 178 | 12 | 38 | 138 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1197 | 373 | 83 | 60 | 178 | 12 | 38 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| c0002 | 0/0 | 1197 | 4 | 4 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| c0003 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2094 | 90 | 30 | 13 | 39 | 2 | 5 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0002 | 0/0 | 2093 | 77 | 2 | 12 | 54 | 1 | 8 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0003 | 0/0 | 2093 | 55 | 22 | 2 | 31 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0004 | 0/0 | 2094 | 44 | 3 | 10 | 19 | 1 | 11 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0005 | 0/0 | 2093 | 28 | 1 | 0 | 20 | 0 | 7 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0006 | 0/0 | 2093 | 23 | 1 | 7 | 7 | 4 | 4 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0007 | 0/1 | 2094 | 11 | 3 | 6 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0008 | 0/0 | 2093 | 9 | 0 | 6 | 0 | 3 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0009 | 0/0 | 2093 | 8 | 8 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0010 | 0/0 | 2093 | 4 | 4 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0011 | 0/0 | 2094 | 3 | 0 | 0 | 3 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0012 | 0/0 | 2093 | 2 | 1 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0013 | 0/0 | 2093 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0014 | 0/0 | 2093 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0015 | 0/0 | 2094 | 2 | 1 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0016 | 0/0 | 2094 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0017 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0018 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0019 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0020 | 0/0 | 2093 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0021 | 0/0 | 2093 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0022 | 0/0 | 2094 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0023 | 0/0 | 2094 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0024 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0025 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0026 | 0/0 | 2094 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0027 | 0/0 | 2094 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0028 | 0/0 | 2094 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0029 | 0/0 | 2094 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0030 | 0/0 | 2094 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0031 | 0/0 | 2093 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| t0032 | 0/0 | 2093 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1197 | 373 | 83 | 60 | 178 | 12 | 38 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0002 | 0/0 | 1197 | 4 | 4 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0003 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3290 | 90 | 30 | 13 | 39 | 2 | 5 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0002 | 0/0 | 3289 | 77 | 2 | 12 | 54 | 1 | 8 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0003 | 0/0 | 3289 | 55 | 22 | 2 | 31 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0004 | 0/0 | 3290 | 44 | 3 | 10 | 19 | 1 | 11 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0005 | 0/0 | 3289 | 28 | 1 | 0 | 20 | 0 | 7 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0006 | 0/0 | 3289 | 23 | 1 | 7 | 7 | 4 | 4 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0007 | 0/1 | 3290 | 11 | 3 | 6 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0008 | 0/0 | 3289 | 9 | 0 | 6 | 0 | 3 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0009 | 0/0 | 3289 | 8 | 8 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0011 | 0/0 | 3290 | 3 | 0 | 0 | 3 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0012 | 0/0 | 3289 | 2 | 1 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0013 | 0/0 | 3289 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0014 | 0/0 | 3289 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0015 | 0/0 | 3290 | 2 | 1 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0016 | 0/0 | 3290 | 2 | 2 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0018 | 0/0 | 3289 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0019 | 0/0 | 3289 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0020 | 0/0 | 3289 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0021 | 0/0 | 3289 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0022 | 0/0 | 3290 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0023 | 0/0 | 3290 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0024 | 0/0 | 3290 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0025 | 0/0 | 3290 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0026 | 0/0 | 3290 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0027 | 0/0 | 3290 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0028 | 0/0 | 3290 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0029 | 0/0 | 3290 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0030 | 0/0 | 3290 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0031 | 0/0 | 3289 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0001t0032 | 0/0 | 3289 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0002t0010 | 0/0 | 3289 | 4 | 4 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| a0001c0003t0017 | 0/0 | 3289 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | copy fasta | chr17 | 78669048 | 78787273 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0003g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0004g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0006g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0008g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0011g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0011g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0011g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0012g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0012g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0013g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0013g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0014g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0014g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0015g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0015g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0016g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0016g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0018g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0019g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0020g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0021g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0022g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0023g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0024g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0025g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0026g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0027g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0028g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0029g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0030g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0031g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0001t0032g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0002t0010g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0002t0010g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0002t0010g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0002t0010g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| a0001c0003t0017g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0251 | EUR | GBR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0328 | EUR | GBR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0330 | EUR | GBR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0131 | EUR | GBR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0291 | EUR | FIN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0333 | EUR | FIN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0335 | EUR | FIN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00423 | hp1 | a0001 | c0001 | t0006 | g0343 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00558 | hp2 | a0001 | c0001 | t0006 | g0339 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0344 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0223 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0270 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | CHS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00733 | hp1 | a0001 | c0001 | t0008 | g0269 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0336 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0216 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0349 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0062 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0303 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0114 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0337 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0134 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01074 | hp1 | a0001 | c0001 | t0031 | g0285 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0215 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0210 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0211 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0327 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01168 | hp2 | a0001 | c0001 | t0023 | g0153 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0213 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0222 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0321 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01243 | hp1 | a0001 | c0001 | t0022 | g0105 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0334 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01257 | hp2 | a0001 | c0001 | t0007 | g0060 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01261 | hp1 | a0001 | c0001 | t0012 | g0120 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0350 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0209 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01346 | hp2 | a0001 | c0001 | t0008 | g0322 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0338 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0267 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0132 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0236 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | IBS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01516 | hp2 | a0001 | c0001 | t0008 | g0268 | EUR | IBS | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0133 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0346 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02055 | hp2 | a0001 | c0001 | t0018 | g0190 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0347 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CDX | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | CDX | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | CDX | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | CDX | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0369 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02258 | hp2 | a0001 | c0001 | t0012 | g0121 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0362 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0372 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02451 | hp2 | a0001 | c0001 | t0013 | g0353 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | KHV | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0374 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0212 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0354 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0370 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0364 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0057 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0180 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0332 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0220 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0052 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0112 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02809 | hp1 | a0001 | c0001 | t0024 | g0376 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0136 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0367 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0368 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0373 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02895 | hp2 | a0001 | c0001 | t0025 | g0050 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0311 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0363 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02897 | hp1 | a0001 | c0001 | t0019 | g0045 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0055 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0056 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0361 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0047 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0375 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0351 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0054 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03130 | hp1 | a0001 | c0001 | t0014 | g0053 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0051 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0348 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03209 | hp2 | a0001 | c0002 | t0010 | g0359 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03225 | hp1 | a0001 | c0002 | t0010 | g0360 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0331 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0038 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0039 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03491 | hp1 | a0001 | c0001 | t0026 | g0099 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0043 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | ESN | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0366 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0204 | AFR | GWD | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03579 | hp1 | a0001 | c0003 | t0017 | g0016 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0371 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0036 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0313 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03669 | hp2 | a0001 | c0001 | t0030 | g0005 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0214 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0031 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03710 | hp1 | a0001 | c0001 | t0032 | g0281 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0030 | SAS | BEB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0342 | SAS | BEB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0042 | SAS | BEB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0230 | SAS | BEB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0232 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0217 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0290 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0218 | SAS | STU | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0365 | AFR | YRI | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0033 | EAS | CHB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | CHB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18747 | hp1 | a0001 | c0001 | t0021 | g0182 | EAS | CHB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0341 | EAS | CHB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18939 | hp2 | a0001 | c0001 | t0011 | g0174 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18943 | hp2 | a0001 | c0001 | t0027 | g0172 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18946 | hp1 | a0001 | c0001 | t0020 | g0231 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18968 | hp2 | a0001 | c0001 | t0006 | g0340 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0345 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18979 | hp2 | a0001 | c0001 | t0015 | g0041 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18983 | hp2 | a0001 | c0001 | t0011 | g0242 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | LWK | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19043 | hp2 | a0001 | c0002 | t0010 | g0358 | AFR | LWK | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19058 | hp2 | a0001 | c0001 | t0028 | g0119 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19084 | hp1 | a0001 | c0001 | t0011 | g0040 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | YRI | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0206 | AFR | ASW | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ASW | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0264 | EUR | TSI | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20752 | hp2 | a0001 | c0001 | t0007 | g0208 | EUR | TSI | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0329 | SAS | GIH | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0241 | SAS | GIH | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0355 | AMR | CLM | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0352 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02109 | hp2 | a0001 | c0002 | t0010 | g0357 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0207 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0377 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0356 | AFR | ACB | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03471 | hp1 | a0001 | c0001 | t0015 | g0326 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | USA | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| HG06807 | hp2 | a0001 | c0001 | t0029 | g0116 | AFR | USA | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20300 | hp1 | a0001 | c0001 | t0014 | g0048 | AFR | USA | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | USA | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0378 | AFR | LWK | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | LWK | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0205 | REF | REF | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0235 | REF | REF | CYTH1_chr17_78669048_78787273 | CYTH1 | chr17 | 78669048 | 78787273 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78701721
|
T | C | 1 | a0001c0003 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.387A>G | p.Ala129Ala | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/14 | 437/3290 | 387/1197 | 129/398 | chr17 | 78701721 | ||
| chr17:78709713
|
T | G | 1 | a0001c0002 | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.42A>C | p.Ala14Ala | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/14 | 92/3290 | 42/1197 | 14/398 | chr17 | 78709713 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78674151
|
C | G | 5 | a0001c0001t0006a0001c0001t0009a0001c0001t0019others(2): Show | 34 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1940G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1940 | chr17 | 78674151 | |||||
| chr17:78674179
|
T | C | 1 | a0001c0001t0026 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1912A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1912 | chr17 | 78674179 | |||||
| chr17:78674625
|
C | T | 1 | a0001c0001t0027 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1466G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1466 | chr17 | 78674625 | |||||
| chr17:78674656
|
C | T | 1 | a0001c0001t0008 | 9 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1435G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1435 | chr17 | 78674656 | |||||
| chr17:78674667
|
A | G | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(15): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1424T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1424 | chr17 | 78674667 | |||||
| chr17:78674684
|
C | T | 1 | a0001c0001t0026 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1407G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1407 | chr17 | 78674684 | |||||
| chr17:78674713
|
G | A | 1 | a0001c0001t0018 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1378C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1378 | chr17 | 78674713 | |||||
| chr17:78674729
|
A | C | 11 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(8): Show | 102 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1362T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1362 | chr17 | 78674729 | |||||
| chr17:78674880
|
A | G | 6 | a0001c0001t0005a0001c0001t0009a0001c0001t0014others(3): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1211T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1211 | chr17 | 78674880 | |||||
| chr17:78675053
|
C | T | 2 | a0001c0001t0009a0001c0003t0017 | 9 | HG02647.hp2 HG02723.hp1 HG02922.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1038G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1038 | chr17 | 78675053 | |||||
| chr17:78675057
|
G | A | 1 | a0001c0001t0028 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1034C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1034 | chr17 | 78675057 | |||||
| chr17:78675060
|
C | T | 1 | a0001c0001t0024 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1031G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 1031 | chr17 | 78675060 | |||||
| chr17:78675279
|
C | T | 1 | a0001c0001t0031 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*812G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 812 | chr17 | 78675279 | |||||
| chr17:78675331
|
G | A | 1 | a0001c0001t0029 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 760 | chr17 | 78675331 | |||||
| chr17:78675341
|
G | A | 1 | a0001c0001t0014 | 2 | HG03130.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*750C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 750 | chr17 | 78675341 | |||||
| chr17:78675387
|
C | T | 1 | a0001c0001t0023 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*704G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 704 | chr17 | 78675387 | |||||
| chr17:78675459
|
C | T | 1 | a0001c0001t0013 | 2 | HG02451.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*632G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 632 | chr17 | 78675459 | |||||
| chr17:78675477
|
G | C | 1 | a0001c0001t0032 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*614C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 614 | chr17 | 78675477 | |||||
| chr17:78675520
|
C | T | 1 | a0001c0001t0011 | 3 | NA18939.hp2 NA18983.hp2 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*571G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 571 | chr17 | 78675520 | |||||
| chr17:78675542
|
T | C | 1 | a0001c0002t0010 | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*549A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 549 | chr17 | 78675542 | |||||
| chr17:78675587
|
C | T | 1 | a0001c0001t0022 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*504G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 504 | chr17 | 78675587 | |||||
| chr17:78675631
|
TA | T | 17 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(14): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*459delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 459 | chr17 | 78675631 | |||||
| chr17:78675633
|
A | T | 2 | a0001c0001t0012a0001c0001t0018 | 3 | HG01261.hp1 HG02055.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*458T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 458 | chr17 | 78675633 | |||||
| chr17:78675751
|
C | T | 1 | a0001c0003t0017 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*340G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 340 | chr17 | 78675751 | |||||
| chr17:78675775
|
T | C | 1 | a0001c0001t0030 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*316A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 316 | chr17 | 78675775 | |||||
| chr17:78675915
|
A | G | 1 | a0001c0001t0007 | 11 | HG00642.hp1 HG01106.hp1 HG01109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*176T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 176 | chr17 | 78675915 | |||||
| chr17:78675920
|
T | C | 4 | a0001c0001t0002a0001c0001t0008a0001c0001t0031others(1): Show | 88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*171A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 14/14 | 171 | chr17 | 78675920 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78676240
|
A | T | 65 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1119-71T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676240 | ||||||
| chr17:78676308
|
C | T | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1119-139G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676308 | ||||||
| chr17:78676364
|
G | C | 3 | a0001c0001t0002g0014a0001c0001t0002g0311a0001c0001t0002g0312 | 3 | HG01175.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1119-195C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676364 | ||||||
| chr17:78676377
|
G | A | 1 | a0001c0001t0003g0072 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1119-208C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676377 | ||||||
| chr17:78676521
|
T | C | 1 | a0001c0001t0002g0287 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1119-352A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676521 | ||||||
| chr17:78676555
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1119-386G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676555 | ||||||
| chr17:78676618
|
T | A | 23 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0329others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1119-449A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676618 | ||||||
| chr17:78676688
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0003g0239 | 2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1119-519G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676688 | ||||||
| chr17:78676741
|
C | T | 5 | a0001c0001t0003g0351a0001c0002t0010g0357a0001c0002t0010g0358others(2): Show | 5 | HG02109.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119-572G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676741 | ||||||
| chr17:78676811
|
G | A | 1 | a0001c0001t0004g0180 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1119-642C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676811 | ||||||
| chr17:78676821
|
G | A | 10 | a0001c0001t0001g0025a0001c0001t0001g0102a0001c0001t0001g0103others(7): Show | 10 | HG01496.hp2 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.1119-652C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676821 | ||||||
| chr17:78676958
|
C | T | 1 | a0001c0001t0004g0219 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1119-789G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78676958 | ||||||
| chr17:78677111
|
A | G | 1 | a0001c0001t0004g0218 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1119-942T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78677111 | ||||||
| chr17:78677152
|
A | G | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1119-983T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78677152 | ||||||
| chr17:78677221
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1119-1052A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78677221 | ||||||
| chr17:78677840
|
T | C | 1 | a0001c0001t0006g0330 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1119-1671A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78677840 | ||||||
| chr17:78677941
|
G | A | 3 | a0001c0001t0006g0333a0001c0001t0006g0335a0001c0001t0006g0336 | 3 | HG00280.hp2 HG00323.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.1119-1772C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78677941 | ||||||
| chr17:78677963
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1119-1794C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78677963 | ||||||
| chr17:78678175
|
T | C | 221 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1119-2006A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678175 | ||||||
| chr17:78678178
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1119-2009A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678178 | ||||||
| chr17:78678245
|
C | A | 43 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(40): Show | 43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.1118+1945G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678245 | ||||||
| chr17:78678336
|
C | T | 377 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(374): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1118+1854G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678336 | ||||||
| chr17:78678358
|
G | A | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1118+1832C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678358 | ||||||
| chr17:78678377
|
G | T | 2 | a0001c0001t0011g0040a0001c0001t0011g0174 | 2 | NA18939.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1118+1813C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678377 | ||||||
| chr17:78678384
|
A | G | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.1118+1806T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678384 | ||||||
| chr17:78678405
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1118+1785C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678405 | ||||||
| chr17:78678453
|
G | A | 30 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(27): Show | 30 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(27): Show |
intron_variant | MODIFIER | c.1118+1737C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678453 | ||||||
| chr17:78678595
|
G | T | 1 | a0001c0001t0004g0216 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1118+1595C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678595 | ||||||
| chr17:78678612
|
AAC | A | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1118+1576_1118+157 others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678612 | ||||||
| chr17:78678685
|
A | G | 355 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0025others(352): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1118+1505T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678685 | ||||||
| chr17:78678800
|
T | A | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1118+1390A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678800 | ||||||
| chr17:78678853
|
G | C | 1 | a0001c0001t0018g0190 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1118+1337C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678853 | ||||||
| chr17:78678951
|
C | T | 1 | a0001c0001t0013g0354 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1118+1239G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678951 | ||||||
| chr17:78678968
|
A | G | 1 | a0001c0001t0006g0334 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1118+1222T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78678968 | ||||||
| chr17:78679023
|
A | G | 1 | a0001c0001t0003g0366 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1118+1167T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679023 | ||||||
| chr17:78679145
|
A | T | 1 | a0001c0001t0004g0220 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1118+1045T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679145 | ||||||
| chr17:78679146
|
C | T | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1118+1044G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679146 | ||||||
| chr17:78679176
|
G | A | 1 | a0001c0001t0020g0231 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1118+1014C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679176 | ||||||
| chr17:78679276
|
T | C | 1 | a0001c0001t0003g0076 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1118+914A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679276 | ||||||
| chr17:78679356
|
GATCACTG others(64): Show |
G | 7 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0001g0156others(4): Show | 7 | HG00733.hp2 HG01099.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1118+763_1118+833d others(73): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679356 | ||||||
| chr17:78679427
|
C | G | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1118+763G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679427 | ||||||
| chr17:78679520
|
C | T | 2 | a0001c0001t0003g0238a0001c0001t0003g0239 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1118+670G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679520 | ||||||
| chr17:78679577
|
A | T | 1 | a0001c0001t0001g0185 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1118+613T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679577 | ||||||
| chr17:78679579
|
G | C | 218 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1118+611C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679579 | ||||||
| chr17:78679711
|
C | T | 1 | a0001c0001t0029g0116 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1118+479G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679711 | ||||||
| chr17:78679721
|
G | A | 140 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.1118+469C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679721 | ||||||
| chr17:78679927
|
G | A | 4 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0027others(1): Show | 4 | NA18940.hp1 NA18947.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1118+263C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679927 | ||||||
| chr17:78679942
|
C | T | 42 | a0001c0001t0001g0118a0001c0001t0005g0001a0001c0001t0005g0002others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.1118+248G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78679942 | ||||||
| chr17:78680044
|
G | A | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1118+146C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78680044 | ||||||
| chr17:78680116
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01074.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1118+74G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 13/13 | chr17 | 78680116 | ||||||
| chr17:78680815
|
C | T | 1 | a0001c0001t0002g0306 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.963+156G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 12/13 | chr17 | 78680815 | ||||||
| chr17:78680907
|
A | T | 33 | a0001c0001t0002g0299a0001c0001t0005g0001a0001c0001t0005g0002others(30): Show | 33 | HG00673.hp1 HG02080.hp2 HG02132.hp2 others(30): Show |
intron_variant | MODIFIER | c.963+64T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 12/13 | chr17 | 78680907 | ||||||
| chr17:78680931
|
C | T | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.963+40G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 12/13 | chr17 | 78680931 | ||||||
| chr17:78681221
|
T | C | 1 | a0001c0001t0005g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.892-179A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681221 | ||||||
| chr17:78681300
|
T | C | 27 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.892-258A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681300 | ||||||
| chr17:78681399
|
A | G | 178 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.892-357T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681399 | ||||||
| chr17:78681428
|
A | C | 1 | a0001c0001t0003g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.892-386T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681428 | ||||||
| chr17:78681484
|
C | G | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.892-442G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681484 | ||||||
| chr17:78681485
|
T | C | 42 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(39): Show | 42 | HG00673.hp1 HG01074.hp2 HG02080.hp2 others(39): Show |
intron_variant | MODIFIER | c.892-443A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681485 | ||||||
| chr17:78681662
|
C | T | 65 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.892-620G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681662 | ||||||
| chr17:78681679
|
A | G | 66 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.892-637T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681679 | ||||||
| chr17:78681687
|
GA | G | 4 | a0001c0001t0002g0254a0001c0001t0002g0274a0001c0001t0002g0275others(1): Show | 4 | HG00673.hp2 HG02165.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.892-646delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681687 | ||||||
| chr17:78681837
|
C | CA | 9 | a0001c0001t0001g0185a0001c0001t0001g0195a0001c0001t0001g0283others(6): Show | 9 | HG02486.hp1 HG02895.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.892-796dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681837 | ||||||
| chr17:78681837
|
C | CAA | 39 | a0001c0001t0003g0065a0001c0001t0003g0072a0001c0001t0003g0237others(36): Show | 39 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(36): Show |
intron_variant | MODIFIER | c.892-797_892-796dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681837 | ||||||
| chr17:78681837
|
C | CAAA | 30 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0066others(27): Show | 30 | HG00558.hp1 HG02027.hp1 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.892-798_892-796dup others(3): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681837 | ||||||
| chr17:78681847
|
A | AC | 138 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.892-806_892-805ins others(1): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681847 | ||||||
| chr17:78681863
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.892-821C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681863 | ||||||
| chr17:78681968
|
C | T | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-926G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78681968 | ||||||
| chr17:78682013
|
G | A | 2 | a0001c0001t0012g0120a0001c0001t0012g0121 | 2 | HG01261.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.892-971C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682013 | ||||||
| chr17:78682014
|
A | C | 2 | a0001c0001t0012g0120a0001c0001t0012g0121 | 2 | HG01261.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.892-972T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682014 | ||||||
| chr17:78682030
|
T | C | 1 | a0001c0001t0027g0172 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.892-988A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682030 | ||||||
| chr17:78682098
|
A | ATT | 31 | a0001c0001t0002g0278a0001c0001t0003g0107a0001c0001t0003g0351others(28): Show | 31 | HG01123.hp2 HG01255.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.892-1057_892-1056i others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682098 | ||||||
| chr17:78682128
|
C | A | 87 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.892-1086G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682128 | ||||||
| chr17:78682209
|
C | A | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.892-1167G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682209 | ||||||
| chr17:78682513
|
G | A | 1 | a0001c0001t0005g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.892-1471C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682513 | ||||||
| chr17:78682547
|
C | T | 1 | a0001c0001t0004g0126 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.892-1505G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682547 | ||||||
| chr17:78682576
|
GGT | G | 7 | a0001c0001t0001g0117a0001c0001t0001g0152a0001c0001t0001g0159others(4): Show | 7 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-1536_892-1535d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682576 | ||||||
| chr17:78682716
|
C | T | 5 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-1674G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682716 | ||||||
| chr17:78682858
|
T | C | 23 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0329others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.892-1816A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78682858 | ||||||
| chr17:78683158
|
G | A | 74 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(71): Show | 74 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.892-2116C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683158 | ||||||
| chr17:78683218
|
G | A | 1 | a0001c0001t0003g0237 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.892-2176C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683218 | ||||||
| chr17:78683222
|
C | G | 1 | a0001c0001t0001g0186 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.892-2180G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683222 | ||||||
| chr17:78683227
|
C | G | 4 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | HG02145.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-2185G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683227 | ||||||
| chr17:78683240
|
A | T | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.892-2198T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683240 | ||||||
| chr17:78683261
|
C | T | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-2219G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683261 | ||||||
| chr17:78683481
|
C | T | 31 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(28): Show | 31 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(28): Show |
intron_variant | MODIFIER | c.892-2439G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683481 | ||||||
| chr17:78683484
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.892-2442C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683484 | ||||||
| chr17:78683490
|
C | T | 1 | a0001c0001t0004g0218 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.892-2448G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683490 | ||||||
| chr17:78683567
|
G | A | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.892-2525C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683567 | ||||||
| chr17:78683655
|
A | C | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.892-2613T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683655 | ||||||
| chr17:78683698
|
T | G | 1 | a0001c0001t0001g0185 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.892-2656A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683698 | ||||||
| chr17:78683877
|
C | A | 2 | a0001c0002t0010g0358a0001c0002t0010g0359 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.892-2835G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683877 | ||||||
| chr17:78683910
|
G | A | 1 | a0001c0001t0014g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.892-2868C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683910 | ||||||
| chr17:78683992
|
C | T | 1 | a0001c0001t0003g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.892-2950G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78683992 | ||||||
| chr17:78684004
|
A | G | 22 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0329others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.892-2962T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684004 | ||||||
| chr17:78684178
|
C | G | 141 | a0001c0001t0001g0162a0001c0001t0002g0011a0001c0001t0002g0012others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.892-3136G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684178 | ||||||
| chr17:78684179
|
C | T | 141 | a0001c0001t0001g0162a0001c0001t0002g0011a0001c0001t0002g0012others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.892-3137G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684179 | ||||||
| chr17:78684249
|
T | A | 1 | a0001c0001t0003g0079 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.892-3207A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684249 | ||||||
| chr17:78684276
|
C | T | 4 | a0001c0002t0010g0357a0001c0002t0010g0358a0001c0002t0010g0359others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.892-3234G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684276 | ||||||
| chr17:78684381
|
C | T | 2 | a0001c0001t0003g0072a0001c0001t0003g0083 | 2 | NA18978.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.892-3339G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684381 | ||||||
| chr17:78684882
|
T | C | 31 | a0001c0001t0004g0009a0001c0001t0004g0062a0001c0001t0004g0112others(28): Show | 31 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.892-3840A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684882 | ||||||
| chr17:78684924
|
G | A | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.892-3882C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684924 | ||||||
| chr17:78684939
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.892-3897C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78684939 | ||||||
| chr17:78685055
|
C | T | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.892-4013G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685055 | ||||||
| chr17:78685202
|
T | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0124a0001c0001t0004g0125others(1): Show | 4 | HG00597.hp2 NA18975.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-4160A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685202 | ||||||
| chr17:78685203
|
C | CA | 73 | a0001c0001t0001g0109a0001c0001t0001g0144a0001c0001t0001g0145others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.892-4162dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685203 | ||||||
| chr17:78685203
|
C | CAA | 16 | a0001c0001t0003g0363a0001c0001t0003g0364a0001c0001t0003g0365others(13): Show | 16 | HG00280.hp2 HG00323.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.892-4163_892-4162d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685203 | ||||||
| chr17:78685203
|
CA | C | 15 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0115others(12): Show | 15 | HG00423.hp2 HG00738.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.892-4162delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685203 | ||||||
| chr17:78685203
|
CAA | C | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0066others(26): Show | 29 | HG00558.hp1 HG02027.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.892-4163_892-4162d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685203 | ||||||
| chr17:78685331
|
T | C | 1 | a0001c0001t0004g0232 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.892-4289A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685331 | ||||||
| chr17:78685351
|
T | TATTG | 97 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.892-4310_892-4309i others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685351 | ||||||
| chr17:78685380
|
T | C | 1 | a0001c0001t0004g0232 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.892-4338A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685380 | ||||||
| chr17:78685424
|
T | C | 1 | a0001c0001t0002g0265 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.892-4382A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685424 | ||||||
| chr17:78685468
|
ATTTAAG | A | 24 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0329others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.892-4432_892-4427d others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685468 | ||||||
| chr17:78685525
|
C | T | 10 | a0001c0001t0004g0061a0001c0001t0004g0198a0001c0001t0004g0202others(7): Show | 10 | HG01081.hp2 HG02155.hp2 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.892-4483G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685525 | ||||||
| chr17:78685700
|
G | A | 1 | a0001c0001t0004g0219 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.892-4658C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685700 | ||||||
| chr17:78685744
|
C | T | 65 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.892-4702G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685744 | ||||||
| chr17:78685768
|
T | C | 1 | a0001c0001t0004g0220 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.892-4726A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685768 | ||||||
| chr17:78685777
|
G | C | 1 | a0001c0001t0002g0262 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.892-4735C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685777 | ||||||
| chr17:78685783
|
G | A | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.892-4741C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685783 | ||||||
| chr17:78685814
|
GGCT | G | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.892-4775_892-4773d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685814 | ||||||
| chr17:78685818
|
G | A | 2 | a0001c0001t0006g0327a0001c0001t0006g0331 | 2 | HG01168.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.892-4776C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685818 | ||||||
| chr17:78685976
|
C | A | 1 | a0001c0001t0005g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.892-4934G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78685976 | ||||||
| chr17:78686096
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.892-5054T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78686096 | ||||||
| chr17:78686378
|
C | T | 1 | a0001c0001t0003g0364 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.892-5336G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78686378 | ||||||
| chr17:78686561
|
G | C | 1 | a0001c0001t0002g0251 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.892-5519C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78686561 | ||||||
| chr17:78686682
|
C | G | 1 | a0001c0001t0002g0299 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.892-5640G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78686682 | ||||||
| chr17:78687067
|
C | T | 2 | a0001c0001t0009g0051a0001c0001t0009g0054 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.891+5350G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687067 | ||||||
| chr17:78687070
|
C | T | 5 | a0001c0001t0005g0049a0001c0001t0014g0048a0001c0001t0014g0053others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+5347G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687070 | ||||||
| chr17:78687071
|
G | A | 1 | a0001c0001t0008g0264 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.891+5346C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687071 | ||||||
| chr17:78687072
|
C | T | 5 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0069others(2): Show | 5 | HG03471.hp1 NA18971.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+5345G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687072 | ||||||
| chr17:78687333
|
G | A | 1 | a0001c0001t0014g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.891+5084C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687333 | ||||||
| chr17:78687394
|
A | G | 1 | a0001c0001t0002g0015 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.891+5023T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687394 | ||||||
| chr17:78687430
|
G | A | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.891+4987C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687430 | ||||||
| chr17:78687433
|
C | T | 23 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0329others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.891+4984G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687433 | ||||||
| chr17:78687490
|
C | A | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.891+4927G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687490 | ||||||
| chr17:78687537
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.891+4880G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687537 | ||||||
| chr17:78687573
|
C | T | 2 | a0001c0001t0009g0047a0001c0001t0009g0052 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.891+4844G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687573 | ||||||
| chr17:78687976
|
C | T | 5 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+4441G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78687976 | ||||||
| chr17:78688087
|
T | C | 1 | a0001c0001t0026g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.891+4330A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688087 | ||||||
| chr17:78688108
|
A | G | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+4309T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688108 | ||||||
| chr17:78688226
|
A | G | 1 | a0001c0001t0004g0009 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.891+4191T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688226 | ||||||
| chr17:78688263
|
G | T | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.891+4154C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688263 | ||||||
| chr17:78688543
|
G | A | 1 | a0001c0001t0003g0369 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.891+3874C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688543 | ||||||
| chr17:78688643
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.891+3774C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688643 | ||||||
| chr17:78688741
|
G | A | 1 | a0001c0001t0003g0369 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.891+3676C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688741 | ||||||
| chr17:78688888
|
G | A | 214 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.891+3529C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78688888 | ||||||
| chr17:78689024
|
A | G | 229 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.891+3393T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689024 | ||||||
| chr17:78689325
|
T | C | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.891+3092A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689325 | ||||||
| chr17:78689435
|
C | T | 1 | a0001c0001t0007g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.891+2982G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689435 | ||||||
| chr17:78689449
|
T | C | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.891+2968A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689449 | ||||||
| chr17:78689477
|
C | T | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.891+2940G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689477 | ||||||
| chr17:78689480
|
C | T | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.891+2937G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689480 | ||||||
| chr17:78689566
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.891+2851G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689566 | ||||||
| chr17:78689571
|
G | A | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.891+2846C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689571 | ||||||
| chr17:78689855
|
C | T | 28 | a0001c0001t0001g0092a0001c0001t0005g0002a0001c0001t0005g0018others(25): Show | 28 | HG01074.hp2 HG02135.hp1 HG03239.hp2 others(25): Show |
intron_variant | MODIFIER | c.891+2562G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689855 | ||||||
| chr17:78689880
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.891+2537C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689880 | ||||||
| chr17:78689911
|
G | A | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.891+2506C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689911 | ||||||
| chr17:78689926
|
T | C | 1 | a0001c0001t0002g0265 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.891+2491A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689926 | ||||||
| chr17:78689959
|
G | A | 87 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.891+2458C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689959 | ||||||
| chr17:78689967
|
C | T | 2 | a0001c0001t0002g0278a0001c0001t0018g0190 | 2 | HG01255.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.891+2450G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689967 | ||||||
| chr17:78689968
|
G | A | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.891+2449C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78689968 | ||||||
| chr17:78690014
|
C | T | 1 | a0001c0001t0003g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.891+2403G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690014 | ||||||
| chr17:78690155
|
G | T | 5 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+2262C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690155 | ||||||
| chr17:78690255
|
C | T | 1 | a0001c0002t0010g0357 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.891+2162G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690255 | ||||||
| chr17:78690266
|
C | T | 1 | a0001c0001t0002g0306 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.891+2151G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690266 | ||||||
| chr17:78690318
|
C | T | 1 | a0001c0001t0004g0377 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.891+2099G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690318 | ||||||
| chr17:78690326
|
G | A | 1 | a0001c0001t0031g0285 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.891+2091C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690326 | ||||||
| chr17:78690380
|
C | T | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.891+2037G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690380 | ||||||
| chr17:78690389
|
ATCTCAAA others(298): Show |
A | 1 | a0001c0001t0016g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.891+1723_891+2027d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690389 | ||||||
| chr17:78690393
|
C | CA | 25 | a0001c0001t0001g0007a0001c0001t0001g0113a0001c0001t0001g0130others(22): Show | 25 | HG00738.hp1 HG01257.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.891+2023dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAA | 15 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0001g0179others(12): Show | 15 | HG00140.hp2 HG00323.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.891+2022_891+2023d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAA | 10 | a0001c0001t0002g0278a0001c0001t0002g0292a0001c0001t0003g0356others(7): Show | 10 | HG00280.hp2 HG01255.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+2021_891+2023d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAA | 14 | a0001c0001t0002g0251a0001c0001t0002g0305a0001c0001t0002g0317others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.891+2020_891+2023d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAA | 24 | a0001c0001t0002g0244a0001c0001t0002g0247a0001c0001t0002g0250others(21): Show | 24 | HG00280.hp1 HG00597.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.891+2019_891+2023d others(7): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAA | 32 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0020others(29): Show | 32 | HG00642.hp2 HG00733.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.891+2018_891+2023d others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA | 11 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0255others(8): Show | 11 | HG01175.hp1 HG01361.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.891+2017_891+2023d others(9): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(1): Show |
8 | a0001c0001t0002g0011a0001c0001t0002g0253a0001c0001t0002g0307others(5): Show | 8 | HG00099.hp2 HG00408.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.891+2016_891+2023d others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(3): Show |
7 | a0001c0001t0002g0256a0001c0001t0002g0315a0001c0001t0003g0361others(4): Show | 7 | HG00423.hp1 HG00621.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+2014_891+2023d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0002g0243a0001c0001t0002g0273a0001c0001t0003g0362 | 3 | HG02280.hp1 HG04199.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.891+2013_891+2023d others(13): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0003g0081 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.891+2012_891+2023d others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(6): Show |
7 | a0001c0001t0002g0265a0001c0001t0003g0068a0001c0001t0003g0069others(4): Show | 7 | HG02572.hp2 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.891+2011_891+2023d others(15): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0003g0071a0001c0001t0006g0347 | 2 | HG02080.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.891+2010_891+2023d others(16): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0003g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.891+2009_891+2023d others(17): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.891+2008_891+2023d others(18): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(11): Show |
5 | a0001c0001t0003g0072a0001c0001t0003g0076a0001c0001t0003g0079others(2): Show | 5 | HG02027.hp1 NA18978.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+2006_891+2023d others(20): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0003g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.891+2005_891+2023d others(21): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0003g0089 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.891+1997_891+2023d others(29): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(21): Show |
1 | a0001c0001t0003g0084 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.891+1996_891+2023d others(30): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0003g0371 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.891+1992_891+2023d others(34): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
C | CAAAAAAA others(28): Show |
1 | a0001c0001t0003g0080 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.891+1989_891+2023d others(37): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CA | C | 14 | a0001c0001t0001g0092a0001c0001t0001g0100a0001c0001t0001g0109others(11): Show | 14 | HG01074.hp2 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.891+2023delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAA | C | 13 | a0001c0001t0001g0106a0001c0001t0001g0189a0001c0001t0004g0114others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.891+2022_891+2023d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAAAAAAA | C | 11 | a0001c0001t0002g0249a0001c0001t0002g0260a0001c0001t0002g0296others(8): Show | 11 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+2017_891+2023d others(9): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0002g0293others(4): Show | 7 | HG00621.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.891+2014_891+2023d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0005g0031 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.891+2013_891+2023d others(13): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0005g0028a0001c0001t0005g0032a0001c0001t0005g0034 | 3 | NA18940.hp1 NA18961.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.891+2012_891+2023d others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAAAAAAA others(6): Show |
C | 24 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(21): Show | 24 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(21): Show |
intron_variant | MODIFIER | c.891+2011_891+2023d others(15): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAAAAAAA others(7): Show |
C | 9 | a0001c0001t0001g0192a0001c0001t0003g0085a0001c0001t0003g0086others(6): Show | 9 | HG03130.hp1 HG03209.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.891+2010_891+2023d others(16): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAAAAAAA others(8): Show |
C | 52 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0025others(49): Show | 52 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.891+2009_891+2023d others(17): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0001g0170a0001c0001t0006g0340a0001c0001t0023g0153 | 3 | HG01168.hp2 HG02683.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.891+2008_891+2023d others(18): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0002g0261 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.891+2006_891+2023d others(20): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAAAAAAA others(12): Show |
C | 9 | a0001c0001t0001g0059a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.891+2005_891+2023d others(21): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAAAAAAA others(13): Show |
C | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.891+2004_891+2023d others(22): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAAAAAAA others(17): Show |
C | 1 | a0001c0001t0006g0329 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.891+2000_891+2023d others(26): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690393
|
CAAAAAAA others(19): Show |
C | 1 | a0001c0001t0004g0221 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.891+1998_891+2023d others(28): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690393 | ||||||
| chr17:78690532
|
G | A | 2 | a0001c0001t0006g0333a0001c0001t0006g0335 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.891+1885C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690532 | ||||||
| chr17:78690546
|
A | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.891+1871T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690546 | ||||||
| chr17:78690564
|
C | T | 5 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+1853G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690564 | ||||||
| chr17:78690620
|
C | T | 1 | a0001c0001t0005g0035 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.891+1797G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690620 | ||||||
| chr17:78690885
|
G | C | 1 | a0001c0001t0004g0215 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.891+1532C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78690885 | ||||||
| chr17:78691099
|
G | A | 1 | a0001c0001t0005g0042 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.891+1318C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691099 | ||||||
| chr17:78691123
|
A | G | 1 | a0001c0001t0005g0030 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.891+1294T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691123 | ||||||
| chr17:78691130
|
C | T | 1 | a0001c0001t0005g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.891+1287G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691130 | ||||||
| chr17:78691149
|
C | A | 1 | a0001c0001t0005g0029 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.891+1268G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691149 | ||||||
| chr17:78691357
|
C | T | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.891+1060G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691357 | ||||||
| chr17:78691412
|
G | C | 77 | a0001c0001t0002g0305a0001c0001t0002g0316a0001c0001t0002g0323others(74): Show | 77 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.891+1005C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691412 | ||||||
| chr17:78691729
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.891+688G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78691729 | ||||||
| chr17:78692071
|
A | G | 355 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0025others(352): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.891+346T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78692071 | ||||||
| chr17:78692211
|
C | T | 1 | a0001c0001t0003g0352 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.891+206G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78692211 | ||||||
| chr17:78692243
|
G | A | 1 | a0001c0001t0003g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.891+174C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78692243 | ||||||
| chr17:78692300
|
C | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0130a0001c0001t0001g0178others(1): Show | 4 | HG02615.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+117G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 11/13 | chr17 | 78692300 | ||||||
| chr17:78692497
|
C | A | 9 | a0001c0001t0003g0107a0001c0001t0003g0363a0001c0001t0003g0364others(6): Show | 9 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.815-4G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692497 | ||||||
| chr17:78692595
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.815-102C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692595 | ||||||
| chr17:78692707
|
G | A | 1 | a0001c0001t0005g0039 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.815-214C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692707 | ||||||
| chr17:78692805
|
GC | G | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.815-313delG | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692805 | ||||||
| chr17:78692811
|
G | C | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.815-318C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692811 | ||||||
| chr17:78692895
|
C | A | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.815-402G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692895 | ||||||
| chr17:78692928
|
A | C | 2 | a0001c0001t0002g0260a0001c0001t0002g0262 | 2 | NA18965.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.815-435T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78692928 | ||||||
| chr17:78693052
|
G | A | 4 | a0001c0001t0004g0114a0001c0001t0004g0124a0001c0001t0004g0125others(1): Show | 4 | HG01070.hp2 HG01071.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.815-559C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693052 | ||||||
| chr17:78693377
|
C | T | 4 | a0001c0001t0007g0208a0001c0001t0007g0209a0001c0001t0007g0210others(1): Show | 4 | HG01106.hp1 HG01109.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.815-884G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693377 | ||||||
| chr17:78693585
|
C | T | 5 | a0001c0001t0003g0351a0001c0002t0010g0357a0001c0002t0010g0358others(2): Show | 5 | HG02109.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.815-1092G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693585 | ||||||
| chr17:78693608
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.815-1115C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693608 | ||||||
| chr17:78693620
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.815-1138_815-1128d others(13): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693620 | ||||||
| chr17:78693692
|
T | A | 2 | a0001c0001t0006g0328a0001c0001t0006g0338 | 2 | HG00099.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.815-1199A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693692 | ||||||
| chr17:78693696
|
G | A | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.815-1203C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693696 | ||||||
| chr17:78693842
|
A | G | 3 | a0001c0001t0006g0339a0001c0001t0006g0340a0001c0001t0006g0341 | 3 | HG00558.hp2 NA18747.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.815-1349T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78693842 | ||||||
| chr17:78694103
|
C | T | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.815-1610G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694103 | ||||||
| chr17:78694354
|
C | T | 1 | a0001c0001t0002g0324 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.814+1653G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694354 | ||||||
| chr17:78694459
|
A | G | 2 | a0001c0001t0004g0131a0001c0001t0004g0180 | 2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.814+1548T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694459 | ||||||
| chr17:78694588
|
C | T | 11 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(8): Show | 11 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.814+1419G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694588 | ||||||
| chr17:78694625
|
G | A | 1 | a0001c0001t0003g0371 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.814+1382C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694625 | ||||||
| chr17:78694702
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.814+1305A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694702 | ||||||
| chr17:78694703
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.814+1304T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694703 | ||||||
| chr17:78694712
|
T | A | 11 | a0001c0001t0001g0113a0001c0001t0001g0130a0001c0001t0001g0135others(8): Show | 11 | HG02145.hp2 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.814+1295A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694712 | ||||||
| chr17:78694772
|
A | G | 1 | a0001c0001t0006g0338 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.814+1235T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694772 | ||||||
| chr17:78694848
|
C | T | 1 | a0001c0001t0005g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.814+1159G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694848 | ||||||
| chr17:78694893
|
G | T | 1 | a0001c0001t0005g0037 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.814+1114C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694893 | ||||||
| chr17:78694922
|
A | C | 1 | a0001c0001t0002g0271 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.814+1085T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694922 | ||||||
| chr17:78694938
|
G | A | 2 | a0001c0001t0004g0131a0001c0001t0004g0180 | 2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.814+1069C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694938 | ||||||
| chr17:78694984
|
C | T | 1 | a0001c0001t0003g0356 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.814+1023G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78694984 | ||||||
| chr17:78695006
|
C | T | 11 | a0001c0001t0001g0113a0001c0001t0001g0130a0001c0001t0001g0135others(8): Show | 11 | HG02145.hp2 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.814+1001G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695006 | ||||||
| chr17:78695176
|
T | C | 228 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.814+831A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695176 | ||||||
| chr17:78695346
|
C | T | 4 | a0001c0001t0002g0254a0001c0001t0002g0274a0001c0001t0002g0275others(1): Show | 4 | HG00673.hp2 HG02165.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.814+661G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695346 | ||||||
| chr17:78695437
|
T | A | 1 | a0001c0001t0004g0212 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.814+570A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695437 | ||||||
| chr17:78695467
|
T | C | 1 | a0001c0001t0004g0180 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.814+540A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695467 | ||||||
| chr17:78695482
|
T | C | 111 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.814+525A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695482 | ||||||
| chr17:78695495
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.814+512A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695495 | ||||||
| chr17:78695688
|
G | A | 3 | a0001c0001t0005g0049a0001c0001t0014g0048a0001c0001t0014g0053 | 3 | HG03130.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.814+319C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695688 | ||||||
| chr17:78695758
|
A | G | 23 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0329others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.814+249T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 10/13 | chr17 | 78695758 | ||||||
| chr17:78696128
|
C | A | 1 | a0001c0001t0004g0201 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.812-119G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696128 | ||||||
| chr17:78696163
|
A | G | 2 | a0001c0001t0002g0260a0001c0001t0002g0262 | 2 | NA18965.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.812-154T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696163 | ||||||
| chr17:78696216
|
G | C | 106 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.812-207C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696216 | ||||||
| chr17:78696216
|
G | T | 4 | a0001c0001t0002g0011a0001c0001t0002g0244a0001c0001t0002g0245others(1): Show | 4 | NA18940.hp2 NA18945.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.812-207C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696216 | ||||||
| chr17:78696316
|
A | G | 2 | a0001c0001t0014g0048a0001c0001t0014g0053 | 2 | HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.812-307T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696316 | ||||||
| chr17:78696529
|
G | A | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.812-520C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696529 | ||||||
| chr17:78696702
|
G | A | 13 | a0001c0001t0003g0107a0001c0001t0003g0355a0001c0001t0003g0356others(10): Show | 13 | HG01123.hp2 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.812-693C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696702 | ||||||
| chr17:78696715
|
A | G | 1 | a0001c0001t0004g0230 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.812-706T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696715 | ||||||
| chr17:78696742
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.812-733G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696742 | ||||||
| chr17:78696824
|
G | A | 6 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0054others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.812-815C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696824 | ||||||
| chr17:78696906
|
T | C | 1 | a0001c0001t0016g0348 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.812-897A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696906 | ||||||
| chr17:78696968
|
T | C | 3 | a0001c0001t0014g0048a0001c0001t0019g0045a0001c0001t0025g0050 | 3 | HG02895.hp2 HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.812-959A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696968 | ||||||
| chr17:78696973
|
G | C | 377 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(374): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.812-964C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696973 | ||||||
| chr17:78696974
|
G | T | 377 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(374): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.812-965C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696974 | ||||||
| chr17:78696988
|
A | G | 1 | a0001c0001t0016g0348 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.812-979T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78696988 | ||||||
| chr17:78697039
|
G | A | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.812-1030C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697039 | ||||||
| chr17:78697082
|
A | C | 3 | a0001c0001t0002g0278a0001c0001t0016g0136a0001c0001t0018g0190 | 3 | HG01255.hp1 HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.812-1073T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697082 | ||||||
| chr17:78697200
|
T | G | 6 | a0001c0001t0003g0361a0001c0001t0003g0362a0001c0002t0010g0357others(3): Show | 6 | HG02109.hp2 HG02280.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.811+1069A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697200 | ||||||
| chr17:78697220
|
A | G | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.811+1049T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697220 | ||||||
| chr17:78697256
|
C | G | 1 | a0001c0001t0003g0369 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.811+1013G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697256 | ||||||
| chr17:78697279
|
A | G | 1 | a0001c0001t0015g0041 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.811+990T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697279 | ||||||
| chr17:78697325
|
C | CA | 178 | a0001c0001t0001g0163a0001c0001t0001g0193a0001c0001t0002g0011others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.811+943dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697325 | ||||||
| chr17:78697325
|
C | CAA | 38 | a0001c0001t0002g0012a0001c0001t0002g0258a0001c0001t0002g0289others(35): Show | 38 | HG00673.hp1 HG01106.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.811+942_811+943dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697325 | ||||||
| chr17:78697325
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0004g0180 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.811+934_811+943del others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697325 | ||||||
| chr17:78697341
|
A | C | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.811+928T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697341 | ||||||
| chr17:78697409
|
T | G | 1 | a0001c0001t0002g0280 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.811+860A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697409 | ||||||
| chr17:78697469
|
C | G | 110 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.811+800G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697469 | ||||||
| chr17:78697604
|
A | G | 3 | a0001c0001t0001g0092a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01074.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.811+665T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697604 | ||||||
| chr17:78697613
|
A | AG | 3 | a0001c0001t0002g0259a0001c0001t0002g0324a0001c0001t0008g0269 | 3 | HG00733.hp1 HG03654.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.811+655dupC | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697613 | ||||||
| chr17:78697614
|
G | GA | 11 | a0001c0001t0001g0092a0001c0001t0001g0100a0001c0001t0001g0101others(8): Show | 11 | HG01074.hp2 HG01106.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.811+654dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697614 | ||||||
| chr17:78697615
|
A | G | 108 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.811+654T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697615 | ||||||
| chr17:78697629
|
A | G | 219 | a0001c0001t0001g0111a0001c0001t0001g0167a0001c0001t0001g0168others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.811+640T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697629 | ||||||
| chr17:78697957
|
C | T | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.811+312G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78697957 | ||||||
| chr17:78698018
|
C | T | 2 | a0001c0001t0002g0250a0001c0001t0002g0284 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.811+251G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698018 | ||||||
| chr17:78698019
|
G | A | 9 | a0001c0001t0004g0061a0001c0001t0004g0198a0001c0001t0004g0202others(6): Show | 9 | HG01081.hp2 HG02155.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.811+250C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698019 | ||||||
| chr17:78698024
|
T | C | 10 | a0001c0001t0003g0107a0001c0001t0003g0363a0001c0001t0003g0364others(7): Show | 10 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.811+245A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698024 | ||||||
| chr17:78698098
|
T | C | 2 | a0001c0001t0005g0031a0001c0001t0005g0038 | 2 | HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.811+171A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698098 | ||||||
| chr17:78698128
|
C | T | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.811+141G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698128 | ||||||
| chr17:78698143
|
G | A | 1 | a0001c0001t0007g0204 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.811+126C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698143 | ||||||
| chr17:78698144
|
C | G | 7 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.811+125G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698144 | ||||||
| chr17:78698147
|
G | A | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.811+122C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698147 | ||||||
| chr17:78698149
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.811+120C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698149 | ||||||
| chr17:78698187
|
A | G | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.811+82T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698187 | ||||||
| chr17:78698211
|
A | G | 45 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239others(42): Show | 45 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(42): Show |
intron_variant | MODIFIER | c.811+58T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 9/13 | chr17 | 78698211 | ||||||
| chr17:78698564
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.700-184G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 8/13 | chr17 | 78698564 | ||||||
| chr17:78698700
|
AC | A | 31 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(28): Show | 31 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(28): Show |
intron_variant | MODIFIER | c.699+119delG | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 8/13 | chr17 | 78698700 | ||||||
| chr17:78698712
|
A | C | 1 | a0001c0001t0003g0091 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.699+108T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 8/13 | chr17 | 78698712 | ||||||
| chr17:78699084
|
C | T | 1 | a0001c0001t0005g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.551-116G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78699084 | ||||||
| chr17:78699274
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.551-306C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78699274 | ||||||
| chr17:78699375
|
A | C | 1 | a0001c0001t0016g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.551-407T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78699375 | ||||||
| chr17:78699394
|
G | T | 1 | a0001c0001t0004g0220 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.551-426C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78699394 | ||||||
| chr17:78699416
|
C | A | 1 | a0001c0001t0021g0182 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.551-448G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78699416 | ||||||
| chr17:78699468
|
T | C | 1 | a0001c0001t0002g0272 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.551-500A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78699468 | ||||||
| chr17:78700117
|
T | C | 3 | a0001c0001t0002g0014a0001c0001t0002g0311a0001c0001t0002g0312 | 3 | HG01175.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.550+214A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78700117 | ||||||
| chr17:78700213
|
T | C | 1 | a0001c0001t0006g0334 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.550+118A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78700213 | ||||||
| chr17:78700295
|
C | T | 1 | a0001c0001t0005g0030 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.550+36G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 7/13 | chr17 | 78700295 | ||||||
| chr17:78700484
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.438-41G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700484 | ||||||
| chr17:78700529
|
T | C | 2 | a0001c0001t0006g0329a0001c0001t0006g0330 | 2 | HG00140.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.438-86A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700529 | ||||||
| chr17:78700532
|
T | C | 3 | a0001c0001t0004g0112a0001c0001t0004g0217a0001c0001t0004g0232 | 3 | HG02735.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.438-89A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700532 | ||||||
| chr17:78700788
|
G | T | 1 | a0001c0001t0002g0255 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.438-345C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700788 | ||||||
| chr17:78700904
|
G | A | 122 | a0001c0001t0001g0194a0001c0001t0002g0011a0001c0001t0002g0012others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.438-461C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700904 | ||||||
| chr17:78700947
|
T | C | 1 | a0001c0001t0004g0216 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.438-504A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700947 | ||||||
| chr17:78700970
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.438-527C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78700970 | ||||||
| chr17:78701030
|
C | T | 31 | a0001c0001t0001g0144a0001c0001t0005g0001a0001c0001t0005g0002others(28): Show | 31 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(28): Show |
intron_variant | MODIFIER | c.438-587G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701030 | ||||||
| chr17:78701109
|
T | C | 5 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.437+562A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701109 | ||||||
| chr17:78701134
|
G | A | 11 | a0001c0001t0001g0240a0001c0001t0003g0352a0001c0001t0003g0363others(8): Show | 11 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.437+537C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701134 | ||||||
| chr17:78701170
|
G | GACAGGTT others(1): Show |
4 | a0001c0002t0010g0357a0001c0002t0010g0358a0001c0002t0010g0359others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.437+493_437+500dup others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701170 | ||||||
| chr17:78701441
|
C | T | 2 | a0001c0001t0004g0131a0001c0001t0004g0180 | 2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.437+230G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701441 | ||||||
| chr17:78701495
|
T | G | 1 | a0001c0001t0014g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.437+176A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701495 | ||||||
| chr17:78701497
|
G | A | 4 | a0001c0002t0010g0357a0001c0002t0010g0358a0001c0002t0010g0359others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.437+174C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 6/13 | chr17 | 78701497 | ||||||
| chr17:78701775
|
G | T | 1 | a0001c0001t0003g0363 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.357-24C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 5/13 | chr17 | 78701775 | ||||||
| chr17:78701903
|
G | A | 1 | a0001c0001t0003g0369 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.357-152C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 5/13 | chr17 | 78701903 | ||||||
| chr17:78702064
|
T | C | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.356+58A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 5/13 | chr17 | 78702064 | ||||||
| chr17:78702074
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.356+48C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 5/13 | chr17 | 78702074 | ||||||
| chr17:78702294
|
A | C | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.238-54T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 4/13 | chr17 | 78702294 | ||||||
| chr17:78702310
|
C | G | 2 | a0001c0001t0002g0289a0001c0001t0002g0314 | 2 | HG02056.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.238-70G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 4/13 | chr17 | 78702310 | ||||||
| chr17:78702376
|
G | A | 1 | a0001c0001t0016g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.238-136C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 4/13 | chr17 | 78702376 | ||||||
| chr17:78702793
|
T | C | 1 | a0001c0001t0002g0266 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.171-189A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78702793 | ||||||
| chr17:78702868
|
C | A | 125 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.171-264G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78702868 | ||||||
| chr17:78702892
|
G | C | 4 | a0001c0002t0010g0357a0001c0002t0010g0358a0001c0002t0010g0359others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.171-288C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78702892 | ||||||
| chr17:78703111
|
T | A | 1 | a0001c0001t0002g0284 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.171-507A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703111 | ||||||
| chr17:78703149
|
C | T | 1 | a0001c0001t0002g0315 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.171-545G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703149 | ||||||
| chr17:78703176
|
G | A | 1 | a0001c0001t0005g0042 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.171-572C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703176 | ||||||
| chr17:78703182
|
G | A | 2 | a0001c0001t0006g0337a0001c0001t0006g0349 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.171-578C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703182 | ||||||
| chr17:78703411
|
C | CA | 34 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0096others(31): Show | 34 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.171-808dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703411 | ||||||
| chr17:78703411
|
CA | C | 168 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.171-808delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703411 | ||||||
| chr17:78703498
|
A | G | 1 | a0001c0001t0006g0328 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.171-894T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703498 | ||||||
| chr17:78703505
|
C | T | 32 | a0001c0001t0001g0025a0001c0001t0001g0102a0001c0001t0001g0103others(29): Show | 32 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.171-901G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703505 | ||||||
| chr17:78703514
|
G | A | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.171-910C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703514 | ||||||
| chr17:78703944
|
C | G | 1 | a0001c0001t0014g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.171-1340G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703944 | ||||||
| chr17:78703971
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.171-1367G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703971 | ||||||
| chr17:78703981
|
G | A | 214 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.171-1377C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78703981 | ||||||
| chr17:78704326
|
G | A | 28 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(25): Show | 28 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(25): Show |
intron_variant | MODIFIER | c.171-1722C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78704326 | ||||||
| chr17:78704413
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.171-1809C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78704413 | ||||||
| chr17:78704474
|
T | C | 28 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(25): Show | 28 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(25): Show |
intron_variant | MODIFIER | c.171-1870A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78704474 | ||||||
| chr17:78704735
|
T | G | 1 | a0001c0001t0002g0273 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.171-2131A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78704735 | ||||||
| chr17:78704812
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.171-2208C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78704812 | ||||||
| chr17:78705094
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.171-2490A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78705094 | ||||||
| chr17:78705104
|
T | C | 2 | a0001c0001t0009g0051a0001c0001t0009g0054 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.171-2500A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78705104 | ||||||
| chr17:78705122
|
G | A | 1 | a0001c0001t0002g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.171-2518C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78705122 | ||||||
| chr17:78705462
|
G | A | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.170+2735C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78705462 | ||||||
| chr17:78705556
|
T | C | 3 | a0001c0001t0002g0278a0001c0001t0016g0136a0001c0001t0018g0190 | 3 | HG01255.hp1 HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.170+2641A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78705556 | ||||||
| chr17:78705876
|
C | T | 3 | a0001c0001t0003g0352a0001c0001t0013g0353a0001c0001t0013g0354 | 3 | HG02109.hp1 HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.170+2321G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78705876 | ||||||
| chr17:78706066
|
C | G | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.170+2131G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78706066 | ||||||
| chr17:78706298
|
A | G | 1 | a0001c0001t0002g0300 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.170+1899T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78706298 | ||||||
| chr17:78706408
|
CCA | C | 5 | a0001c0001t0003g0351a0001c0002t0010g0357a0001c0002t0010g0358others(2): Show | 5 | HG02109.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.170+1787_170+1788d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78706408 | ||||||
| chr17:78706710
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0177 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.170+1487C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78706710 | ||||||
| chr17:78706739
|
T | G | 13 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0104others(10): Show | 13 | HG00544.hp2 HG02004.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.170+1458A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78706739 | ||||||
| chr17:78706860
|
T | C | 1 | a0001c0001t0004g0202 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.170+1337A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78706860 | ||||||
| chr17:78707021
|
C | T | 43 | a0001c0001t0001g0147a0001c0001t0005g0001a0001c0001t0005g0002others(40): Show | 43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.170+1176G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707021 | ||||||
| chr17:78707118
|
A | T | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.170+1079T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707118 | ||||||
| chr17:78707434
|
G | T | 22 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0329others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.170+763C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707434 | ||||||
| chr17:78707533
|
C | T | 1 | a0001c0001t0004g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.170+664G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707533 | ||||||
| chr17:78707595
|
C | T | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.170+602G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707595 | ||||||
| chr17:78707615
|
G | A | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.170+582C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707615 | ||||||
| chr17:78707663
|
T | C | 1 | a0001c0001t0016g0348 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.170+534A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707663 | ||||||
| chr17:78707672
|
C | T | 1 | a0001c0001t0004g0180 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.170+525G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707672 | ||||||
| chr17:78707682
|
A | AT | 6 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0255others(3): Show | 6 | HG00408.hp2 HG01168.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.170+514dupA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707682 | ||||||
| chr17:78707682
|
A | ATTT | 29 | a0001c0001t0003g0064a0001c0001t0003g0066a0001c0001t0003g0067others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.170+512_170+514dup others(3): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707682 | ||||||
| chr17:78707682
|
AT | A | 11 | a0001c0001t0001g0187a0001c0001t0002g0250a0001c0001t0002g0279others(8): Show | 11 | HG00140.hp1 HG02280.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.170+514delA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707682 | ||||||
| chr17:78707684
|
T | A | 1 | a0001c0001t0001g0059 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.170+513A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707684 | ||||||
| chr17:78707704
|
C | T | 28 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(25): Show | 28 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(25): Show |
intron_variant | MODIFIER | c.170+493G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707704 | ||||||
| chr17:78707773
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.170+424G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707773 | ||||||
| chr17:78707802
|
T | A | 1 | a0001c0001t0016g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.170+395A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707802 | ||||||
| chr17:78707808
|
G | A | 3 | a0001c0001t0002g0014a0001c0001t0002g0311a0001c0001t0002g0312 | 3 | HG01175.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.170+389C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707808 | ||||||
| chr17:78707968
|
C | T | 43 | a0001c0001t0001g0147a0001c0001t0005g0001a0001c0001t0005g0002others(40): Show | 43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.170+229G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707968 | ||||||
| chr17:78707983
|
G | A | 11 | a0001c0001t0006g0327a0001c0001t0006g0329a0001c0001t0006g0330others(8): Show | 11 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.170+214C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78707983 | ||||||
| chr17:78708058
|
T | C | 4 | a0001c0002t0010g0357a0001c0002t0010g0358a0001c0002t0010g0359others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.170+139A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78708058 | ||||||
| chr17:78708075
|
G | C | 1 | a0001c0001t0026g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.170+122C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 3/13 | chr17 | 78708075 | ||||||
| chr17:78708491
|
C | G | 2 | a0001c0001t0006g0344a0001c0001t0006g0346 | 2 | HG00621.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.106-230G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78708491 | ||||||
| chr17:78708640
|
C | A | 1 | a0001c0001t0005g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.106-379G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78708640 | ||||||
| chr17:78708746
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.106-485C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78708746 | ||||||
| chr17:78708944
|
G | C | 1 | a0001c0001t0006g0344 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.106-683C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78708944 | ||||||
| chr17:78709057
|
T | G | 1 | a0001c0001t0003g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.105+593A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709057 | ||||||
| chr17:78709070
|
G | A | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.105+580C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709070 | ||||||
| chr17:78709201
|
T | A | 1 | a0001c0001t0002g0294 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.105+449A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709201 | ||||||
| chr17:78709274
|
AGAGCCAG others(16): Show |
A | 89 | a0001c0001t0001g0195a0001c0001t0001g0283a0001c0001t0002g0011others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.105+353_105+375del others(23): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709274 | ||||||
| chr17:78709291
|
G | C | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.105+359C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709291 | ||||||
| chr17:78709416
|
C | T | 1 | a0001c0001t0002g0015 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.105+234G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709416 | ||||||
| chr17:78709630
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.105+20G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 2/13 | chr17 | 78709630 | ||||||
| chr17:78709889
|
A | C | 1 | a0001c0001t0001g0059 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.23-157T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78709889 | ||||||
| chr17:78710114
|
A | G | 1 | a0001c0001t0005g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.23-382T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710114 | ||||||
| chr17:78710194
|
C | T | 1 | a0001c0001t0004g0212 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.23-462G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710194 | ||||||
| chr17:78710595
|
A | G | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-863T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710595 | ||||||
| chr17:78710634
|
T | C | 1 | a0001c0001t0004g0006 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.23-902A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710634 | ||||||
| chr17:78710824
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.23-1092A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710824 | ||||||
| chr17:78710931
|
A | G | 5 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-1199T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710931 | ||||||
| chr17:78710979
|
G | A | 1 | a0001c0001t0005g0018 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.23-1247C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710979 | ||||||
| chr17:78710987
|
G | C | 1 | a0001c0001t0005g0001 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.23-1255C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78710987 | ||||||
| chr17:78711122
|
C | T | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-1390G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711122 | ||||||
| chr17:78711153
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.23-1421A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711153 | ||||||
| chr17:78711206
|
G | A | 1 | a0001c0001t0009g0055 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.23-1474C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711206 | ||||||
| chr17:78711226
|
C | T | 1 | a0001c0001t0002g0271 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.23-1494G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711226 | ||||||
| chr17:78711261
|
C | CAAAT | 27 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(24): Show | 27 | HG01069.hp2 HG01175.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.23-1533_23-1530dup others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711261 | ||||||
| chr17:78711261
|
CAAAT | C | 6 | a0001c0001t0001g0147a0001c0001t0003g0237a0001c0001t0003g0238others(3): Show | 6 | HG01106.hp2 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-1533_23-1530del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711261 | ||||||
| chr17:78711261
|
CAAATAAA others(1): Show |
C | 4 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0069others(1): Show | 4 | NA18971.hp1 NA18981.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-1537_23-1530del others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711261 | ||||||
| chr17:78711261
|
CAAATAAA others(5): Show |
C | 27 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(24): Show | 27 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.23-1541_23-1530del others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711261 | ||||||
| chr17:78711290
|
AAATAAAT others(7): Show |
A | 4 | a0001c0001t0006g0329a0001c0001t0006g0330a0001c0001t0006g0332others(1): Show | 4 | HG00140.hp1 HG01257.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-1572_23-1559del others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711290 | ||||||
| chr17:78711291
|
AATAAATA others(3): Show |
A | 1 | a0001c0001t0003g0063 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.23-1569_23-1560del others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711291 | ||||||
| chr17:78711298
|
AAATAAT | A | 3 | a0001c0001t0006g0336a0001c0001t0006g0338a0001c0001t0013g0353 | 3 | HG00735.hp2 HG01361.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.23-1572_23-1567del others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711298 | ||||||
| chr17:78711302
|
A | AAATAAT | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0004g0009 | 3 | HG00639.hp1 HG01074.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.23-1571_23-1570ins others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711302 | ||||||
| chr17:78711302
|
A | T | 1 | a0001c0001t0003g0063 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.23-1570T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711302 | ||||||
| chr17:78711302
|
AAT | A | 104 | a0001c0001t0001g0283a0001c0001t0002g0012a0001c0001t0002g0013others(101): Show | 104 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.23-1572_23-1571del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711302 | ||||||
| chr17:78711303
|
A | AAT | 15 | a0001c0001t0002g0011a0001c0001t0002g0244a0001c0001t0002g0250others(12): Show | 15 | HG00099.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.23-1572_23-1571ins others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711303 | ||||||
| chr17:78711304
|
T | A | 39 | a0001c0001t0002g0011a0001c0001t0002g0244a0001c0001t0002g0250others(36): Show | 39 | HG00099.hp1 HG00673.hp1 HG02080.hp2 others(36): Show |
intron_variant | MODIFIER | c.23-1572A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711304 | ||||||
| chr17:78711305
|
A | T | 22 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(19): Show | 22 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.23-1573T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711305 | ||||||
| chr17:78711306
|
T | A | 22 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(19): Show | 22 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.23-1574A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711306 | ||||||
| chr17:78711310
|
T | C | 2 | a0001c0001t0003g0063a0001c0003t0017g0016 | 2 | HG03579.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.23-1578A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711310 | ||||||
| chr17:78711312
|
T | C | 48 | a0001c0001t0001g0092a0001c0001t0002g0260a0001c0001t0002g0262others(45): Show | 48 | HG00423.hp2 HG00558.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.23-1580A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711312 | ||||||
| chr17:78711312
|
T | TAC | 6 | a0001c0001t0001g0113a0001c0001t0001g0135a0001c0001t0001g0141others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.23-1581_23-1580ins others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711312 | ||||||
| chr17:78711312
|
TATAC | T | 4 | a0001c0001t0005g0026a0001c0001t0005g0029a0001c0001t0005g0039others(1): Show | 4 | HG03490.hp1 HG03927.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-1584_23-1581del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711312 | ||||||
| chr17:78711312
|
TATACAC | T | 13 | a0001c0001t0005g0049a0001c0001t0009g0003a0001c0001t0009g0047others(10): Show | 13 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.23-1586_23-1581del others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711312 | ||||||
| chr17:78711314
|
T | C | 177 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.23-1582A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711314 | ||||||
| chr17:78711314
|
T | TAC | 4 | a0001c0001t0001g0163a0001c0001t0001g0240a0001c0001t0004g0131others(1): Show | 4 | HG00140.hp2 HG01255.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-1584_23-1583dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711314 | ||||||
| chr17:78711314
|
TAC | T | 4 | a0001c0001t0001g0123a0001c0001t0001g0139a0001c0001t0001g0146others(1): Show | 4 | HG00408.hp1 NA18984.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-1584_23-1583del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711314 | ||||||
| chr17:78711316
|
C | T | 25 | a0001c0001t0001g0183a0001c0001t0001g0189a0001c0001t0005g0001others(22): Show | 25 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.23-1584G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711316 | ||||||
| chr17:78711318
|
C | T | 1 | a0001c0001t0014g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.23-1586G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711318 | ||||||
| chr17:78711706
|
CT | C | 11 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0155others(8): Show | 11 | HG01099.hp1 HG02109.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.23-1975delA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711706 | ||||||
| chr17:78711872
|
T | C | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG00544.hp2 HG02083.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-2140A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711872 | ||||||
| chr17:78711906
|
T | A | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.23-2174A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78711906 | ||||||
| chr17:78712076
|
A | AGAAAGAA others(1): Show |
30 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0067others(27): Show | 30 | HG00423.hp2 HG00558.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.23-2352_23-2345dup others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712076 | ||||||
| chr17:78712076
|
AGAAAGAA others(1): Show |
A | 27 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(24): Show | 27 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(24): Show |
intron_variant | MODIFIER | c.23-2352_23-2345del others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712076 | ||||||
| chr17:78712096
|
A | G | 1 | a0001c0001t0005g0039 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.23-2364T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712096 | ||||||
| chr17:78712104
|
G | A | 3 | a0001c0001t0003g0063a0001c0001t0003g0066a0001c0001t0003g0074 | 3 | NA18946.hp2 NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.23-2372C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712104 | ||||||
| chr17:78712106
|
AAGGAAGG others(1): Show |
A | 3 | a0001c0001t0003g0063a0001c0001t0003g0066a0001c0001t0003g0074 | 3 | NA18946.hp2 NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.23-2382_23-2375del others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712106 | ||||||
| chr17:78712126
|
G | A | 3 | a0001c0001t0003g0063a0001c0001t0003g0066a0001c0001t0003g0074 | 3 | NA18946.hp2 NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.23-2394C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712126 | ||||||
| chr17:78712128
|
G | A | 1 | a0001c0001t0015g0326 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.23-2396C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712128 | ||||||
| chr17:78712129
|
G | C | 1 | a0001c0001t0003g0081 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.23-2397C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712129 | ||||||
| chr17:78712134
|
A | G | 5 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 5 | HG02145.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.23-2402T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712134 | ||||||
| chr17:78712138
|
AAGGGAAG others(13): Show |
A | 1 | a0001c0001t0015g0326 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.23-2426_23-2407del others(20): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712138 | ||||||
| chr17:78712154
|
AAGGG | A | 194 | a0001c0001t0001g0163a0001c0001t0001g0283a0001c0001t0002g0011others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.23-2426_23-2423del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712154 | ||||||
| chr17:78712163
|
A | G | 1 | a0001c0001t0003g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.23-2431T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712163 | ||||||
| chr17:78712178
|
GAGGT | G | 12 | a0001c0001t0006g0327a0001c0001t0006g0329a0001c0001t0006g0330others(9): Show | 12 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.23-2450_23-2447del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712178 | ||||||
| chr17:78712466
|
A | C | 1 | a0001c0001t0001g0173 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.23-2734T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712466 | ||||||
| chr17:78712558
|
A | T | 1 | a0001c0001t0002g0286 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.23-2826T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712558 | ||||||
| chr17:78712684
|
A | C | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.23-2952T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712684 | ||||||
| chr17:78712684
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.23-2952T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78712684 | ||||||
| chr17:78713026
|
C | T | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-3294G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713026 | ||||||
| chr17:78713081
|
T | TAA | 10 | a0001c0001t0005g0017a0001c0001t0005g0019a0001c0001t0005g0021others(7): Show | 10 | HG02080.hp2 HG02135.hp1 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.23-3351_23-3350dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713081 | ||||||
| chr17:78713086
|
A | AAT | 37 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239others(34): Show | 37 | HG00673.hp1 HG01106.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.23-3356_23-3355dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713086 | ||||||
| chr17:78713086
|
AAT | A | 8 | a0001c0001t0002g0020a0001c0001t0002g0247a0001c0001t0002g0252others(5): Show | 8 | HG02004.hp1 HG02280.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.23-3356_23-3355del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713086 | ||||||
| chr17:78713088
|
T | A | 22 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0329others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-3356A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713088 | ||||||
| chr17:78713128
|
C | T | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-3396G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713128 | ||||||
| chr17:78713183
|
A | G | 1 | a0001c0001t0003g0369 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.23-3451T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713183 | ||||||
| chr17:78713196
|
G | A | 1 | a0001c0001t0015g0041 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.23-3464C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713196 | ||||||
| chr17:78713233
|
C | T | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-3501G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713233 | ||||||
| chr17:78713285
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.23-3553T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713285 | ||||||
| chr17:78713392
|
C | A | 1 | a0001c0001t0003g0364 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.23-3660G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713392 | ||||||
| chr17:78713480
|
G | A | 2 | a0001c0001t0002g0313a0001c0001t0032g0281 | 2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.23-3748C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713480 | ||||||
| chr17:78713546
|
T | C | 1 | a0001c0001t0002g0307 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.23-3814A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713546 | ||||||
| chr17:78713546
|
T | TCCTATCT others(223): Show |
1 | a0001c0001t0018g0190 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.23-4044_23-3815dup others(230): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713546 | ||||||
| chr17:78713546
|
TCCTATCT others(223): Show |
T | 10 | a0001c0001t0003g0352a0001c0001t0003g0363a0001c0001t0003g0364others(7): Show | 10 | HG02109.hp1 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.23-4044_23-3815del | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713546 | ||||||
| chr17:78713624
|
T | G | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-3892A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713624 | ||||||
| chr17:78713805
|
G | A | 1 | a0001c0001t0003g0237 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.23-4073C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713805 | ||||||
| chr17:78713956
|
C | T | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-4224G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78713956 | ||||||
| chr17:78714027
|
C | T | 1 | a0001c0001t0003g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.23-4295G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714027 | ||||||
| chr17:78714095
|
G | A | 43 | a0001c0001t0002g0306a0001c0001t0005g0001a0001c0001t0005g0002others(40): Show | 43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.23-4363C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714095 | ||||||
| chr17:78714118
|
C | G | 1 | a0001c0001t0016g0348 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.23-4386G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714118 | ||||||
| chr17:78714155
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.23-4423G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714155 | ||||||
| chr17:78714163
|
AC | A | 123 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.23-4432delG | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714163 | ||||||
| chr17:78714249
|
C | T | 1 | a0001c0001t0004g0201 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.23-4517G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714249 | ||||||
| chr17:78714345
|
T | G | 1 | a0001c0001t0002g0290 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.23-4613A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714345 | ||||||
| chr17:78714428
|
C | T | 1 | a0001c0001t0003g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.23-4696G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714428 | ||||||
| chr17:78714691
|
G | A | 13 | a0001c0001t0005g0049a0001c0001t0009g0003a0001c0001t0009g0047others(10): Show | 13 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.23-4959C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714691 | ||||||
| chr17:78714859
|
G | A | 1 | a0001c0001t0026g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.23-5127C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714859 | ||||||
| chr17:78714872
|
G | GA | 39 | a0001c0001t0001g0160a0001c0001t0002g0318a0001c0001t0003g0063others(36): Show | 39 | HG00423.hp2 HG00558.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.23-5141dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714872 | ||||||
| chr17:78714875
|
A | G | 1 | a0001c0001t0003g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.23-5143T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714875 | ||||||
| chr17:78714919
|
T | C | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.23-5187A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78714919 | ||||||
| chr17:78715108
|
G | C | 1 | a0001c0001t0002g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.23-5376C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715108 | ||||||
| chr17:78715119
|
A | G | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-5387T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715119 | ||||||
| chr17:78715120
|
T | C | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-5388A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715120 | ||||||
| chr17:78715230
|
A | G | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-5498T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715230 | ||||||
| chr17:78715252
|
T | C | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-5520A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715252 | ||||||
| chr17:78715536
|
A | G | 1 | a0001c0001t0002g0287 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.23-5804T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715536 | ||||||
| chr17:78715552
|
C | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0124a0001c0001t0004g0125others(1): Show | 4 | HG00597.hp2 NA18975.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-5820G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715552 | ||||||
| chr17:78715605
|
G | A | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-5873C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715605 | ||||||
| chr17:78715739
|
G | GCT | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.23-6009_23-6008dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78715739 | ||||||
| chr17:78716099
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.23-6367T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716099 | ||||||
| chr17:78716200
|
G | C | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.23-6468C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716200 | ||||||
| chr17:78716435
|
C | T | 3 | a0001c0001t0007g0205a0001c0001t0007g0206a0001c0001t0007g0207 | 3 | HG02486.hp1 NA20129.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.23-6703G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716435 | ||||||
| chr17:78716486
|
A | T | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-6754T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716486 | ||||||
| chr17:78716750
|
G | C | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-7018C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716750 | ||||||
| chr17:78716831
|
G | T | 4 | a0001c0002t0010g0357a0001c0002t0010g0358a0001c0002t0010g0359others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-7099C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716831 | ||||||
| chr17:78716963
|
C | T | 1 | a0001c0001t0004g0112 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.23-7231G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78716963 | ||||||
| chr17:78717061
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.23-7329G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717061 | ||||||
| chr17:78717117
|
A | G | 1 | a0001c0001t0002g0316 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.23-7385T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717117 | ||||||
| chr17:78717217
|
A | G | 43 | a0001c0001t0001g0240a0001c0001t0003g0365a0001c0001t0005g0001others(40): Show | 43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.23-7485T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717217 | ||||||
| chr17:78717234
|
G | T | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-7502C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717234 | ||||||
| chr17:78717263
|
G | A | 1 | a0001c0001t0004g0201 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.23-7531C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717263 | ||||||
| chr17:78717440
|
T | C | 2 | a0001c0001t0003g0363a0001c0001t0003g0366 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.23-7708A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717440 | ||||||
| chr17:78717483
|
C | T | 1 | a0001c0001t0004g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.23-7751G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717483 | ||||||
| chr17:78717620
|
C | T | 3 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0020g0231 | 3 | HG02523.hp2 NA18946.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.23-7888G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717620 | ||||||
| chr17:78717667
|
C | T | 2 | a0001c0001t0002g0305a0001c0001t0002g0316 | 2 | NA19056.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.23-7935G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717667 | ||||||
| chr17:78717668
|
G | A | 44 | a0001c0001t0004g0009a0001c0001t0004g0061a0001c0001t0004g0112others(41): Show | 44 | HG00642.hp1 HG00738.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.23-7936C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717668 | ||||||
| chr17:78717841
|
G | A | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-8109C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717841 | ||||||
| chr17:78717904
|
C | T | 5 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 5 | HG02145.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.23-8172G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78717904 | ||||||
| chr17:78718140
|
G | A | 1 | a0001c0001t0008g0322 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.23-8408C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718140 | ||||||
| chr17:78718153
|
C | T | 1 | a0001c0001t0004g0221 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.23-8421G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718153 | ||||||
| chr17:78718218
|
T | TAC | 31 | a0001c0001t0001g0092a0001c0001t0001g0100a0001c0001t0001g0101others(28): Show | 31 | HG01074.hp2 HG02040.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.23-8488_23-8487dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
T | TACAC | 16 | a0001c0001t0001g0137a0001c0001t0003g0063a0001c0001t0003g0066others(13): Show | 16 | HG00099.hp2 HG02135.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.23-8490_23-8487dup others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
T | TACACAC | 15 | a0001c0001t0003g0064a0001c0001t0003g0067a0001c0001t0003g0071others(12): Show | 15 | HG00558.hp1 HG01106.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.23-8492_23-8487dup others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
T | TACACACA others(1): Show |
8 | a0001c0001t0003g0065a0001c0001t0003g0077a0001c0001t0003g0079others(5): Show | 8 | HG00423.hp2 HG02165.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-8494_23-8487dup others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
T | TACACACA others(3): Show |
11 | a0001c0001t0001g0178a0001c0001t0003g0069a0001c0001t0003g0072others(8): Show | 11 | HG01081.hp2 HG02071.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.23-8496_23-8487dup others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
T | TACACACA others(5): Show |
3 | a0001c0001t0001g0166a0001c0001t0003g0068a0001c0001t0003g0083 | 3 | NA18978.hp1 NA18980.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.23-8498_23-8487dup others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
T | TACACACA others(7): Show |
3 | a0001c0001t0003g0070a0001c0001t0003g0356a0001c0001t0026g0099 | 3 | HG02559.hp2 HG03491.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.23-8500_23-8487dup others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
T | TACACACA others(9): Show |
3 | a0001c0001t0003g0088a0001c0001t0003g0355a0001c0001t0003g0369 | 3 | HG01123.hp2 HG02257.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.23-8502_23-8487dup others(16): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
T | TACACACA others(13): Show |
1 | a0001c0001t0003g0087 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.23-8506_23-8487dup others(20): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
T | TACACACA others(17): Show |
1 | a0001c0001t0003g0085 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.23-8510_23-8487dup others(24): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
T | TCACACAC others(12): Show |
1 | a0001c0001t0003g0086 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.23-8487_23-8486ins others(19): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
TAC | T | 58 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(55): Show | 58 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.23-8488_23-8487del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
TACAC | T | 49 | a0001c0001t0001g0010a0001c0001t0001g0093a0001c0001t0001g0094others(46): Show | 49 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.23-8490_23-8487del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
TACACAC | T | 68 | a0001c0001t0001g0157a0001c0001t0001g0195a0001c0001t0001g0283others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.23-8492_23-8487del others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
TACACACA others(1): Show |
T | 6 | a0001c0001t0004g0375a0001c0001t0006g0327a0001c0001t0008g0269others(3): Show | 6 | HG00733.hp1 HG01168.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-8494_23-8487del others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
TACACACA others(3): Show |
T | 19 | a0001c0001t0001g0025a0001c0001t0002g0245a0001c0001t0002g0246others(16): Show | 19 | HG00597.hp2 HG00735.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.23-8496_23-8487del others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
TACACACA others(5): Show |
T | 5 | a0001c0001t0002g0248a0001c0001t0002g0306a0001c0001t0002g0308others(2): Show | 5 | HG00408.hp2 NA18969.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-8498_23-8487del others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
TACACACA others(9): Show |
T | 2 | a0001c0001t0002g0015a0001c0001t0004g0180 | 2 | HG02683.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.23-8502_23-8487del others(16): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718218
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0008g0268 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.23-8508_23-8487del others(22): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718218 | ||||||
| chr17:78718220
|
C | T | 14 | a0001c0001t0005g0001a0001c0001t0005g0017a0001c0001t0005g0049others(11): Show | 14 | HG00673.hp1 HG02080.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.23-8488G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718220 | ||||||
| chr17:78718222
|
C | T | 1 | a0001c0001t0005g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.23-8490G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718222 | ||||||
| chr17:78718224
|
C | T | 19 | a0001c0001t0005g0002a0001c0001t0005g0018a0001c0001t0005g0019others(16): Show | 19 | HG02135.hp1 HG03239.hp2 HG03490.hp1 others(16): Show |
intron_variant | MODIFIER | c.23-8492G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718224 | ||||||
| chr17:78718226
|
C | T | 4 | a0001c0001t0005g0021a0001c0001t0005g0033a0001c0001t0005g0034others(1): Show | 4 | NA18612.hp1 NA18961.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-8494G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718226 | ||||||
| chr17:78718344
|
C | T | 1 | a0001c0001t0005g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.23-8612G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718344 | ||||||
| chr17:78718391
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.23-8659A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718391 | ||||||
| chr17:78718403
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.23-8671C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718403 | ||||||
| chr17:78718421
|
C | T | 2 | a0001c0001t0004g0218a0001c0001t0004g0220 | 2 | HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.23-8689G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718421 | ||||||
| chr17:78718522
|
T | C | 2 | a0001c0001t0003g0355a0001c0001t0003g0356 | 2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.23-8790A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718522 | ||||||
| chr17:78718900
|
T | C | 1 | a0001c0001t0006g0328 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.23-9168A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718900 | ||||||
| chr17:78718922
|
T | C | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-9190A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718922 | ||||||
| chr17:78718935
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.23-9203A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78718935 | ||||||
| chr17:78719184
|
G | C | 3 | a0001c0001t0003g0072a0001c0001t0003g0083a0001c0001t0003g0089 | 3 | NA18978.hp1 NA19085.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.23-9452C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719184 | ||||||
| chr17:78719479
|
T | C | 43 | a0001c0001t0001g0200a0001c0001t0005g0001a0001c0001t0005g0002others(40): Show | 43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.23-9747A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719479 | ||||||
| chr17:78719588
|
A | G | 1 | a0001c0001t0005g0042 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.23-9856T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719588 | ||||||
| chr17:78719602
|
G | A | 5 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-9870C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719602 | ||||||
| chr17:78719650
|
G | A | 4 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0027others(1): Show | 4 | NA18940.hp1 NA18947.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-9918C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719650 | ||||||
| chr17:78719726
|
A | C | 1 | a0001c0001t0008g0268 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.23-9994T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719726 | ||||||
| chr17:78719747
|
G | A | 1 | a0001c0001t0004g0180 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.23-10015C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719747 | ||||||
| chr17:78719765
|
G | A | 1 | a0001c0001t0027g0172 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.23-10033C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719765 | ||||||
| chr17:78719963
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.23-10231G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719963 | ||||||
| chr17:78719982
|
T | C | 1 | a0001c0001t0004g0230 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.23-10250A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78719982 | ||||||
| chr17:78720248
|
T | C | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-10516A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720248 | ||||||
| chr17:78720447
|
T | C | 1 | a0001c0001t0013g0353 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.23-10715A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720447 | ||||||
| chr17:78720468
|
G | A | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-10736C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720468 | ||||||
| chr17:78720517
|
C | T | 5 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-10785G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720517 | ||||||
| chr17:78720593
|
A | G | 4 | a0001c0001t0002g0254a0001c0001t0002g0274a0001c0001t0002g0275others(1): Show | 4 | HG00673.hp2 HG02165.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-10861T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720593 | ||||||
| chr17:78720832
|
C | T | 2 | a0001c0001t0002g0012a0001c0001t0002g0013 | 2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.23-11100G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720832 | ||||||
| chr17:78720854
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.23-11122C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720854 | ||||||
| chr17:78720949
|
T | C | 1 | a0001c0001t0002g0278 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.23-11217A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720949 | ||||||
| chr17:78720982
|
G | C | 1 | a0001c0001t0004g0224 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.23-11250C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78720982 | ||||||
| chr17:78721109
|
C | T | 7 | a0001c0001t0003g0351a0001c0001t0003g0361a0001c0001t0003g0362others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-11377G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721109 | ||||||
| chr17:78721164
|
T | C | 1 | a0001c0001t0005g0017 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.23-11432A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721164 | ||||||
| chr17:78721216
|
G | C | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-11484C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721216 | ||||||
| chr17:78721265
|
G | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 5 | HG02145.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.23-11533C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721265 | ||||||
| chr17:78721437
|
C | T | 12 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(9): Show | 12 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.23-11705G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721437 | ||||||
| chr17:78721461
|
T | C | 2 | a0001c0001t0004g0214a0001c0001t0004g0215 | 2 | HG01081.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.23-11729A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721461 | ||||||
| chr17:78721604
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.23-11872G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721604 | ||||||
| chr17:78721775
|
G | A | 73 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(70): Show | 73 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.23-12043C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721775 | ||||||
| chr17:78721990
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.23-12258G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78721990 | ||||||
| chr17:78722472
|
A | T | 74 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(71): Show | 74 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.23-12740T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722472 | ||||||
| chr17:78722583
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.23-12851C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722583 | ||||||
| chr17:78722708
|
A | G | 1 | a0001c0001t0002g0324 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.23-12976T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722708 | ||||||
| chr17:78722760
|
C | T | 189 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.23-13028G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722760 | ||||||
| chr17:78722762
|
C | T | 1 | a0001c0001t0003g0369 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.23-13030G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722762 | ||||||
| chr17:78722763
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.23-13031C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722763 | ||||||
| chr17:78722766
|
G | A | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-13034C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722766 | ||||||
| chr17:78722865
|
C | T | 1 | a0001c0001t0002g0325 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.23-13133G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722865 | ||||||
| chr17:78722911
|
T | C | 50 | a0001c0001t0003g0361a0001c0001t0003g0362a0001c0001t0003g0363others(47): Show | 50 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(47): Show |
intron_variant | MODIFIER | c.23-13179A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722911 | ||||||
| chr17:78722954
|
G | A | 4 | a0001c0001t0009g0003a0001c0001t0009g0055a0001c0001t0009g0056others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-13222C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722954 | ||||||
| chr17:78722958
|
T | C | 4 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0373others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-13226A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78722958 | ||||||
| chr17:78723009
|
T | A | 2 | a0001c0001t0008g0270a0001c0001t0008g0303 | 2 | HG00642.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.23-13277A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723009 | ||||||
| chr17:78723186
|
T | C | 1 | a0001c0001t0002g0287 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.23-13454A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723186 | ||||||
| chr17:78723258
|
C | A | 1 | a0001c0001t0003g0083 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.23-13526G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723258 | ||||||
| chr17:78723261
|
G | T | 4 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0373others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-13529C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723261 | ||||||
| chr17:78723275
|
A | G | 2 | a0001c0001t0008g0267a0001c0001t0008g0322 | 2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.23-13543T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723275 | ||||||
| chr17:78723434
|
G | A | 1 | a0001c0001t0005g0042 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.23-13702C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723434 | ||||||
| chr17:78723517
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.23-13785C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723517 | ||||||
| chr17:78723649
|
G | A | 1 | a0001c0001t0003g0081 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.23-13917C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723649 | ||||||
| chr17:78723840
|
G | A | 2 | a0001c0001t0003g0355a0001c0001t0003g0356 | 2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.23-14108C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78723840 | ||||||
| chr17:78724242
|
G | A | 1 | a0001c0001t0008g0291 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.23-14510C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724242 | ||||||
| chr17:78724289
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.23-14557C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724289 | ||||||
| chr17:78724385
|
A | G | 1 | a0001c0001t0003g0369 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.23-14653T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724385 | ||||||
| chr17:78724413
|
G | C | 4 | a0001c0001t0001g0154a0001c0001t0001g0165a0001c0001t0001g0194others(1): Show | 4 | HG02257.hp2 HG03669.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-14681C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724413 | ||||||
| chr17:78724451
|
A | C | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.23-14719T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724451 | ||||||
| chr17:78724512
|
C | A | 1 | a0001c0001t0004g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.23-14780G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724512 | ||||||
| chr17:78724512
|
C | T | 6 | a0001c0001t0003g0363a0001c0001t0003g0364a0001c0001t0003g0365others(3): Show | 6 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-14780G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724512 | ||||||
| chr17:78724631
|
T | C | 215 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.23-14899A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724631 | ||||||
| chr17:78724686
|
A | G | 1 | a0001c0001t0009g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.23-14954T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724686 | ||||||
| chr17:78724727
|
G | T | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-14995C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724727 | ||||||
| chr17:78724754
|
C | T | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-15022G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724754 | ||||||
| chr17:78724945
|
C | T | 2 | a0001c0001t0003g0355a0001c0001t0003g0356 | 2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.23-15213G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78724945 | ||||||
| chr17:78725031
|
A | AAC | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.23-15301_23-15300d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725031 | ||||||
| chr17:78725174
|
G | C | 1 | a0001c0001t0016g0348 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.23-15442C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725174 | ||||||
| chr17:78725187
|
A | G | 73 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(70): Show | 73 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.23-15455T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725187 | ||||||
| chr17:78725269
|
A | G | 7 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-15537T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725269 | ||||||
| chr17:78725275
|
C | T | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.23-15543G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725275 | ||||||
| chr17:78725482
|
G | T | 4 | a0001c0002t0010g0357a0001c0002t0010g0358a0001c0002t0010g0359others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-15750C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725482 | ||||||
| chr17:78725499
|
T | A | 2 | a0001c0001t0002g0243a0001c0001t0002g0315 | 2 | NA18952.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.23-15767A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725499 | ||||||
| chr17:78725535
|
C | T | 1 | a0001c0001t0009g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.23-15803G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725535 | ||||||
| chr17:78725666
|
G | T | 1 | a0001c0001t0002g0250 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.23-15934C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725666 | ||||||
| chr17:78725668
|
C | T | 4 | a0001c0002t0010g0357a0001c0002t0010g0358a0001c0002t0010g0359others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-15936G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725668 | ||||||
| chr17:78725856
|
A | G | 212 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.23-16124T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725856 | ||||||
| chr17:78725963
|
C | T | 1 | a0001c0001t0005g0038 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.23-16231G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78725963 | ||||||
| chr17:78726042
|
C | CT | 56 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(53): Show | 56 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.23-16311dupA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726042 | ||||||
| chr17:78726105
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.23-16373C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726105 | ||||||
| chr17:78726178
|
G | A | 1 | a0001c0001t0002g0315 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.23-16446C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726178 | ||||||
| chr17:78726195
|
T | C | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-16463A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726195 | ||||||
| chr17:78726376
|
CGAGGCCC others(19): Show |
C | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-16670_23-16645d others(28): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726376 | ||||||
| chr17:78726380
|
G | A | 112 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.23-16648C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726380 | ||||||
| chr17:78726408
|
C | T | 1 | a0001c0001t0006g0342 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.23-16676G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726408 | ||||||
| chr17:78726443
|
A | G | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-16711T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726443 | ||||||
| chr17:78726662
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.23-16930C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726662 | ||||||
| chr17:78726751
|
G | A | 1 | a0001c0001t0003g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.23-17019C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78726751 | ||||||
| chr17:78727104
|
T | C | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-17372A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78727104 | ||||||
| chr17:78727312
|
G | T | 8 | a0001c0001t0006g0339a0001c0001t0006g0340a0001c0001t0006g0341others(5): Show | 8 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.23-17580C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78727312 | ||||||
| chr17:78727479
|
T | C | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-17747A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78727479 | ||||||
| chr17:78727511
|
C | T | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-17779G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78727511 | ||||||
| chr17:78727618
|
G | A | 1 | a0001c0001t0004g0061 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.23-17886C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78727618 | ||||||
| chr17:78727620
|
G | A | 4 | a0001c0001t0002g0299a0001c0001t0003g0237a0001c0001t0003g0238others(1): Show | 4 | HG01106.hp2 HG02132.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-17888C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78727620 | ||||||
| chr17:78728026
|
G | A | 1 | a0001c0001t0003g0128 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.23-18294C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728026 | ||||||
| chr17:78728095
|
A | G | 1 | a0001c0001t0005g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.23-18363T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728095 | ||||||
| chr17:78728130
|
C | T | 1 | a0001c0001t0002g0011 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.23-18398G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728130 | ||||||
| chr17:78728220
|
C | G | 1 | a0001c0001t0003g0089 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.23-18488G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728220 | ||||||
| chr17:78728230
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.23-18498C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728230 | ||||||
| chr17:78728312
|
G | A | 1 | a0001c0001t0031g0285 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.23-18580C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728312 | ||||||
| chr17:78728450
|
T | A | 1 | a0001c0001t0002g0011 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.23-18718A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728450 | ||||||
| chr17:78728661
|
A | G | 12 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(9): Show | 12 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.23-18929T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728661 | ||||||
| chr17:78728804
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.23-19072T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728804 | ||||||
| chr17:78728830
|
G | C | 1 | a0001c0001t0003g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.23-19098C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78728830 | ||||||
| chr17:78729102
|
T | A | 1 | a0001c0001t0003g0366 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.23-19370A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729102 | ||||||
| chr17:78729165
|
T | C | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-19433A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729165 | ||||||
| chr17:78729169
|
G | A | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-19437C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729169 | ||||||
| chr17:78729227
|
C | A | 11 | a0001c0001t0006g0327a0001c0001t0006g0329a0001c0001t0006g0330others(8): Show | 11 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.23-19495G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729227 | ||||||
| chr17:78729236
|
T | C | 1 | a0001c0001t0004g0132 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.23-19504A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729236 | ||||||
| chr17:78729665
|
C | T | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-19933G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729665 | ||||||
| chr17:78729858
|
T | C | 10 | a0001c0001t0009g0003a0001c0001t0009g0047a0001c0001t0009g0051others(7): Show | 10 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.23-20126A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78729858 | ||||||
| chr17:78730236
|
A | T | 1 | a0001c0001t0004g0198 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.23-20504T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730236 | ||||||
| chr17:78730248
|
G | A | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-20516C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730248 | ||||||
| chr17:78730254
|
G | A | 13 | a0001c0001t0003g0352a0001c0001t0003g0355a0001c0001t0003g0356others(10): Show | 13 | HG01123.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.23-20522C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730254 | ||||||
| chr17:78730268
|
T | G | 290 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0092others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.23-20536A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730268 | ||||||
| chr17:78730341
|
C | T | 17 | a0001c0001t0001g0025a0001c0001t0003g0127a0001c0001t0003g0128others(14): Show | 17 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.23-20609G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730341 | ||||||
| chr17:78730369
|
C | CA | 149 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.23-20638dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730369 | ||||||
| chr17:78730369
|
C | CAA | 64 | a0001c0001t0001g0098a0001c0001t0001g0135a0001c0001t0001g0144others(61): Show | 64 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.23-20639_23-20638d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730369 | ||||||
| chr17:78730369
|
C | CAAA | 17 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(14): Show | 17 | HG00408.hp2 HG02027.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.23-20640_23-20638d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730369 | ||||||
| chr17:78730433
|
G | A | 137 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.23-20701C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730433 | ||||||
| chr17:78730468
|
G | A | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-20736C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730468 | ||||||
| chr17:78730532
|
G | A | 1 | a0001c0001t0005g0022 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.23-20800C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730532 | ||||||
| chr17:78730654
|
G | A | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-20922C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730654 | ||||||
| chr17:78730814
|
G | A | 3 | a0001c0001t0004g0375a0001c0001t0004g0377a0001c0001t0024g0376 | 3 | HG02559.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.23-21082C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730814 | ||||||
| chr17:78730910
|
T | C | 12 | a0001c0001t0006g0327a0001c0001t0006g0329a0001c0001t0006g0330others(9): Show | 12 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.23-21178A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730910 | ||||||
| chr17:78730943
|
T | C | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-21211A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730943 | ||||||
| chr17:78730995
|
T | G | 1 | a0001c0001t0005g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.23-21263A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78730995 | ||||||
| chr17:78731373
|
C | T | 22 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0251others(19): Show | 22 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-21641G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731373 | ||||||
| chr17:78731547
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.23-21815G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731547 | ||||||
| chr17:78731566
|
T | G | 4 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-21834A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731566 | ||||||
| chr17:78731755
|
C | CA | 76 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0102others(73): Show | 76 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.23-22024dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731755 | ||||||
| chr17:78731755
|
C | CAA | 6 | a0001c0001t0001g0111a0001c0001t0001g0166a0001c0001t0005g0027others(3): Show | 6 | HG00642.hp1 HG03927.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.23-22025_23-22024d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731755 | ||||||
| chr17:78731755
|
CA | C | 6 | a0001c0001t0002g0011a0001c0001t0002g0246a0001c0001t0002g0272others(3): Show | 6 | HG03209.hp1 NA18940.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-22024delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731755 | ||||||
| chr17:78731766
|
A | C | 1 | a0001c0001t0008g0291 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.23-22034T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731766 | ||||||
| chr17:78731767
|
A | C | 1 | a0001c0001t0004g0224 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.23-22035T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731767 | ||||||
| chr17:78731772
|
C | A | 43 | a0001c0001t0001g0130a0001c0001t0003g0367a0001c0001t0005g0001others(40): Show | 43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.23-22040G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731772 | ||||||
| chr17:78731841
|
C | A | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-22109G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78731841 | ||||||
| chr17:78732033
|
G | A | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-22301C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732033 | ||||||
| chr17:78732147
|
G | C | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.23-22415C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732147 | ||||||
| chr17:78732586
|
C | T | 111 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.23-22854G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732586 | ||||||
| chr17:78732638
|
C | T | 373 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(370): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.23-22906G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732638 | ||||||
| chr17:78732842
|
A | T | 1 | a0001c0001t0004g0213 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.23-23110T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732842 | ||||||
| chr17:78732943
|
C | T | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-23211G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732943 | ||||||
| chr17:78732979
|
C | A | 7 | a0001c0001t0004g0061a0001c0001t0004g0198a0001c0001t0004g0202others(4): Show | 7 | HG02155.hp2 NA18954.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.23-23247G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78732979 | ||||||
| chr17:78733011
|
C | T | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-23279G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733011 | ||||||
| chr17:78733012
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0059a0001c0001t0001g0186others(2): Show | 5 | HG02056.hp1 NA18955.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-23280C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733012 | ||||||
| chr17:78733070
|
C | T | 1 | a0001c0001t0003g0369 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.23-23338G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733070 | ||||||
| chr17:78733076
|
C | CAAAAAA | 14 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(11): Show | 14 | HG00558.hp1 HG02027.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.23-23350_23-23345d others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733076 | ||||||
| chr17:78733076
|
C | CAAAAAAA | 10 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070others(7): Show | 10 | HG02135.hp2 NA18945.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.23-23351_23-23345d others(9): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733076 | ||||||
| chr17:78733076
|
CA | C | 201 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(198): Show | 201 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.23-23345delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733076 | ||||||
| chr17:78733076
|
CAA | C | 35 | a0001c0001t0001g0092a0001c0001t0001g0101a0001c0001t0001g0117others(32): Show | 35 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.23-23346_23-23345d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733076 | ||||||
| chr17:78733076
|
CAAA | C | 34 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(31): Show | 34 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(31): Show |
intron_variant | MODIFIER | c.23-23347_23-23345d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733076 | ||||||
| chr17:78733076
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0378 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.23-23355_23-23345d others(13): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733076 | ||||||
| chr17:78733132
|
G | A | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-23400C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733132 | ||||||
| chr17:78733632
|
G | A | 1 | a0001c0001t0003g0078 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.23-23900C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733632 | ||||||
| chr17:78733675
|
C | A | 112 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.23-23943G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733675 | ||||||
| chr17:78733702
|
A | G | 211 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.23-23970T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733702 | ||||||
| chr17:78733957
|
A | T | 111 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.23-24225T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78733957 | ||||||
| chr17:78734199
|
A | T | 1 | a0001c0001t0001g0183 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.23-24467T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734199 | ||||||
| chr17:78734241
|
C | CA | 33 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(30): Show | 33 | HG00423.hp2 HG00558.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.23-24510dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734241 | ||||||
| chr17:78734241
|
CA | C | 40 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(37): Show | 40 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(37): Show |
intron_variant | MODIFIER | c.23-24510delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734241 | ||||||
| chr17:78734395
|
TATGTACC others(1): Show |
T | 345 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(342): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.23-24671_23-24664d others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734395 | ||||||
| chr17:78734423
|
A | T | 1 | a0001c0001t0005g0031 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.23-24691T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734423 | ||||||
| chr17:78734432
|
C | CT | 30 | a0001c0001t0001g0007a0001c0001t0001g0144a0001c0001t0001g0145others(27): Show | 30 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.23-24701dupA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734432 | ||||||
| chr17:78734432
|
CTT | C | 33 | a0001c0001t0001g0100a0001c0001t0001g0106a0001c0001t0001g0109others(30): Show | 33 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.23-24702_23-24701d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734432 | ||||||
| chr17:78734432
|
CTTT | C | 183 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0092others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.23-24703_23-24701d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734432 | ||||||
| chr17:78734432
|
CTTTT | C | 62 | a0001c0001t0001g0117a0001c0001t0001g0171a0001c0001t0002g0316others(59): Show | 62 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.23-24704_23-24701d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734432 | ||||||
| chr17:78734432
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0005g0017 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.23-24716_23-24701d others(18): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734432 | ||||||
| chr17:78734435
|
T | G | 2 | a0001c0001t0003g0355a0001c0001t0003g0356 | 2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.23-24703A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734435 | ||||||
| chr17:78734477
|
G | A | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-24745C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734477 | ||||||
| chr17:78734482
|
C | A | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-24750G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734482 | ||||||
| chr17:78734676
|
G | A | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-24944C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734676 | ||||||
| chr17:78734717
|
A | G | 211 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.23-24985T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734717 | ||||||
| chr17:78734907
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0157 | 2 | HG02004.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.23-25175G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734907 | ||||||
| chr17:78734959
|
T | A | 1 | a0001c0001t0002g0015 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.23-25227A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78734959 | ||||||
| chr17:78735237
|
C | T | 211 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.23-25505G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78735237 | ||||||
| chr17:78735803
|
C | G | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-26071G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78735803 | ||||||
| chr17:78735838
|
C | T | 223 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.23-26106G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78735838 | ||||||
| chr17:78735858
|
A | G | 1 | a0001c0001t0003g0065 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.23-26126T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78735858 | ||||||
| chr17:78735867
|
T | C | 1 | a0001c0001t0002g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.23-26135A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78735867 | ||||||
| chr17:78736166
|
C | A | 1 | a0001c0001t0006g0346 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.23-26434G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736166 | ||||||
| chr17:78736166
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.23-26434G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736166 | ||||||
| chr17:78736175
|
C | T | 5 | a0001c0001t0003g0351a0001c0002t0010g0357a0001c0002t0010g0358others(2): Show | 5 | HG02109.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-26443G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736175 | ||||||
| chr17:78736256
|
T | C | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-26524A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736256 | ||||||
| chr17:78736332
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.23-26600G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736332 | ||||||
| chr17:78736410
|
TTC | T | 4 | a0001c0002t0010g0357a0001c0002t0010g0358a0001c0002t0010g0359others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-26680_23-26679d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736410 | ||||||
| chr17:78736598
|
G | A | 2 | a0001c0001t0003g0367a0001c0001t0003g0368 | 2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.23-26866C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736598 | ||||||
| chr17:78736976
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.23-27244G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78736976 | ||||||
| chr17:78737079
|
A | G | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-27347T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737079 | ||||||
| chr17:78737099
|
C | T | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-27367G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737099 | ||||||
| chr17:78737380
|
C | T | 1 | a0001c0001t0003g0369 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.23-27648G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737380 | ||||||
| chr17:78737602
|
C | CA | 34 | a0001c0001t0001g0185a0001c0001t0001g0193a0001c0001t0002g0324others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.23-27871dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737602 | ||||||
| chr17:78737602
|
CA | C | 41 | a0001c0001t0001g0115a0001c0001t0005g0001a0001c0001t0005g0002others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-27871delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737602 | ||||||
| chr17:78737678
|
C | A | 8 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(5): Show | 8 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.23-27946G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737678 | ||||||
| chr17:78737844
|
A | G | 1 | a0001c0001t0002g0257 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.23-28112T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737844 | ||||||
| chr17:78737870
|
T | C | 1 | a0001c0001t0015g0041 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.23-28138A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737870 | ||||||
| chr17:78737874
|
T | TAC | 177 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(174): Show | 177 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.23-28144_23-28143d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737874 | ||||||
| chr17:78737874
|
T | TACAC | 11 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(8): Show | 11 | HG00544.hp2 HG00639.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.23-28146_23-28143d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737874 | ||||||
| chr17:78737874
|
TAC | T | 46 | a0001c0001t0003g0351a0001c0001t0003g0352a0001c0001t0003g0361others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.23-28144_23-28143d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737874 | ||||||
| chr17:78737874
|
TACACACA others(1): Show |
T | 28 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(25): Show | 28 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.23-28150_23-28143d others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737874 | ||||||
| chr17:78737874
|
TACACACA others(3): Show |
T | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-28152_23-28143d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737874 | ||||||
| chr17:78737874
|
TACACACA others(5): Show |
T | 90 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.23-28154_23-28143d others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737874 | ||||||
| chr17:78737891
|
A | T | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-28159T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78737891 | ||||||
| chr17:78738081
|
A | G | 1 | a0001c0001t0004g0377 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.23-28349T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738081 | ||||||
| chr17:78738089
|
C | T | 1 | a0001c0001t0016g0348 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.23-28357G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738089 | ||||||
| chr17:78738386
|
C | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0147a0001c0001t0001g0151others(1): Show | 4 | HG02922.hp1 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-28654G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738386 | ||||||
| chr17:78738415
|
A | G | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-28683T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738415 | ||||||
| chr17:78738480
|
T | C | 4 | a0001c0001t0004g0061a0001c0001t0004g0198a0001c0001t0004g0202others(1): Show | 4 | NA18954.hp1 NA18960.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-28748A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738480 | ||||||
| chr17:78738501
|
C | A | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-28769G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738501 | ||||||
| chr17:78738547
|
A | G | 73 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(70): Show | 73 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.23-28815T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738547 | ||||||
| chr17:78738626
|
T | TA | 6 | a0001c0001t0001g0147a0001c0001t0002g0271a0001c0001t0002g0278others(3): Show | 6 | HG01106.hp2 HG01255.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-28895dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738626 | ||||||
| chr17:78738626
|
TA | T | 19 | a0001c0001t0002g0014a0001c0001t0002g0308a0001c0001t0002g0309others(16): Show | 19 | HG00408.hp2 HG01123.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.23-28895delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738626 | ||||||
| chr17:78738626
|
TAA | T | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-28896_23-28895d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738626 | ||||||
| chr17:78738935
|
A | G | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-29203T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78738935 | ||||||
| chr17:78739096
|
A | G | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-29364T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739096 | ||||||
| chr17:78739276
|
T | G | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-29544A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739276 | ||||||
| chr17:78739598
|
C | T | 1 | a0001c0001t0004g0224 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.23-29866G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739598 | ||||||
| chr17:78739639
|
G | A | 1 | a0001c0001t0026g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.23-29907C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739639 | ||||||
| chr17:78739730
|
G | A | 17 | a0001c0001t0001g0025a0001c0001t0003g0127a0001c0001t0003g0128others(14): Show | 17 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.23-29998C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739730 | ||||||
| chr17:78739759
|
T | A | 2 | a0001c0001t0002g0289a0001c0001t0002g0314 | 2 | HG02056.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.23-30027A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739759 | ||||||
| chr17:78739934
|
A | ATCT | 374 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(371): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.23-30205_23-30203d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78739934 | ||||||
| chr17:78740414
|
T | C | 4 | a0001c0001t0006g0329a0001c0001t0006g0330a0001c0001t0006g0332others(1): Show | 4 | HG00140.hp1 HG01257.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-30682A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740414 | ||||||
| chr17:78740457
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.23-30725C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740457 | ||||||
| chr17:78740478
|
T | C | 1 | a0001c0001t0004g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.23-30746A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740478 | ||||||
| chr17:78740552
|
CCTGGCTC others(9): Show |
C | 1 | a0001c0001t0006g0350 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.23-30836_23-30821d others(18): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740552 | ||||||
| chr17:78740651
|
C | T | 1 | a0001c0001t0005g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.23-30919G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740651 | ||||||
| chr17:78740772
|
C | T | 1 | a0001c0001t0003g0065 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.23-31040G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740772 | ||||||
| chr17:78740815
|
T | C | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-31083A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78740815 | ||||||
| chr17:78741036
|
A | G | 23 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0329others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.23-31304T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741036 | ||||||
| chr17:78741108
|
C | G | 212 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.23-31376G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741108 | ||||||
| chr17:78741390
|
A | G | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-31658T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741390 | ||||||
| chr17:78741462
|
A | G | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.23-31730T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741462 | ||||||
| chr17:78741623
|
A | T | 5 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-31891T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741623 | ||||||
| chr17:78741765
|
T | C | 211 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.23-32033A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741765 | ||||||
| chr17:78741811
|
C | G | 1 | a0001c0001t0004g0122 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.23-32079G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741811 | ||||||
| chr17:78741840
|
G | C | 1 | a0001c0001t0006g0336 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.23-32108C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741840 | ||||||
| chr17:78741978
|
T | C | 1 | a0001c0001t0008g0291 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.23-32246A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78741978 | ||||||
| chr17:78742304
|
A | G | 211 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.23-32572T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742304 | ||||||
| chr17:78742525
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.23-32793C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742525 | ||||||
| chr17:78742574
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.23-32842G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742574 | ||||||
| chr17:78742577
|
G | C | 1 | a0001c0001t0002g0263 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.23-32845C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742577 | ||||||
| chr17:78742708
|
C | G | 1 | a0001c0001t0002g0015 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.23-32976G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742708 | ||||||
| chr17:78742726
|
G | A | 2 | a0001c0001t0004g0218a0001c0001t0004g0220 | 2 | HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.23-32994C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742726 | ||||||
| chr17:78742828
|
C | T | 40 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(37): Show | 40 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(37): Show |
intron_variant | MODIFIER | c.23-33096G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742828 | ||||||
| chr17:78742847
|
T | A | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-33115A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742847 | ||||||
| chr17:78742848
|
C | A | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-33116G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742848 | ||||||
| chr17:78742885
|
T | C | 13 | a0001c0001t0005g0049a0001c0001t0009g0003a0001c0001t0009g0047others(10): Show | 13 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.23-33153A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742885 | ||||||
| chr17:78742988
|
G | T | 1 | a0001c0001t0002g0015 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.23-33256C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78742988 | ||||||
| chr17:78743053
|
T | A | 1 | a0001c0001t0001g0185 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.23-33321A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78743053 | ||||||
| chr17:78743059
|
G | A | 111 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.23-33327C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78743059 | ||||||
| chr17:78743282
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.23-33550G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78743282 | ||||||
| chr17:78743373
|
C | T | 2 | a0001c0001t0019g0045a0001c0001t0025g0050 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.23-33641G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78743373 | ||||||
| chr17:78743505
|
T | C | 25 | a0001c0001t0003g0351a0001c0001t0003g0352a0001c0001t0003g0355others(22): Show | 25 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.23-33773A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78743505 | ||||||
| chr17:78743768
|
C | T | 137 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.23-34036G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78743768 | ||||||
| chr17:78744504
|
C | T | 1 | a0001c0001t0005g0046 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.23-34772G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744504 | ||||||
| chr17:78744508
|
C | G | 22 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0006g0329others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-34776G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744508 | ||||||
| chr17:78744535
|
G | A | 1 | a0001c0001t0006g0338 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.23-34803C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744535 | ||||||
| chr17:78744575
|
G | A | 13 | a0001c0001t0003g0352a0001c0001t0003g0355a0001c0001t0003g0356others(10): Show | 13 | HG01123.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.23-34843C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744575 | ||||||
| chr17:78744677
|
T | C | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-34945A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744677 | ||||||
| chr17:78744686
|
A | T | 1 | a0001c0001t0002g0274 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.23-34954T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744686 | ||||||
| chr17:78744785
|
A | G | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-35053T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744785 | ||||||
| chr17:78744845
|
C | CA | 55 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0093others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.23-35114dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744845 | ||||||
| chr17:78744845
|
CA | C | 12 | a0001c0001t0002g0011a0001c0001t0002g0244a0001c0001t0003g0067others(9): Show | 12 | HG01106.hp2 HG02165.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.23-35114delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744845 | ||||||
| chr17:78744845
|
CAAA | C | 41 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-35116_23-35114d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78744845 | ||||||
| chr17:78745095
|
G | A | 1 | a0001c0001t0003g0080 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.23-35363C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745095 | ||||||
| chr17:78745211
|
T | C | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.23-35479A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745211 | ||||||
| chr17:78745499
|
T | C | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-35767A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745499 | ||||||
| chr17:78745565
|
T | C | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.23-35833A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745565 | ||||||
| chr17:78745576
|
T | C | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-35844A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745576 | ||||||
| chr17:78745899
|
G | GA | 44 | a0001c0001t0002g0265a0001c0001t0003g0083a0001c0001t0005g0001others(41): Show | 44 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(41): Show |
intron_variant | MODIFIER | c.23-36168dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745899 | ||||||
| chr17:78745926
|
C | T | 1 | a0001c0001t0003g0078 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.23-36194G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745926 | ||||||
| chr17:78745940
|
G | A | 1 | a0001c0001t0007g0208 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.23-36208C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745940 | ||||||
| chr17:78745982
|
T | C | 42 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.22+36220A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78745982 | ||||||
| chr17:78746098
|
T | A | 1 | a0001c0001t0016g0348 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.22+36104A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746098 | ||||||
| chr17:78746102
|
C | T | 4 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+36100G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746102 | ||||||
| chr17:78746176
|
G | A | 1 | a0001c0001t0003g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.22+36026C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746176 | ||||||
| chr17:78746211
|
G | T | 1 | a0001c0001t0001g0007 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.22+35991C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746211 | ||||||
| chr17:78746299
|
C | CA | 71 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(68): Show | 71 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.22+35902dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746299 | ||||||
| chr17:78746523
|
TA | T | 70 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(67): Show | 70 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.22+35678delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746523 | ||||||
| chr17:78746661
|
G | T | 1 | a0001c0001t0006g0335 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.22+35541C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746661 | ||||||
| chr17:78746723
|
C | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0139a0001c0001t0001g0146 | 3 | HG00408.hp1 NA18984.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.22+35479G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746723 | ||||||
| chr17:78746923
|
GAC | G | 3 | a0001c0001t0001g0092a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01074.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22+35277_22+35278d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746923 | ||||||
| chr17:78746967
|
A | G | 1 | a0001c0001t0003g0369 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.22+35235T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78746967 | ||||||
| chr17:78747145
|
C | CA | 147 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0094others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.22+35056dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747145 | ||||||
| chr17:78747145
|
C | CAA | 21 | a0001c0001t0002g0252a0001c0001t0002g0259a0001c0001t0002g0266others(18): Show | 21 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.22+35055_22+35056d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747145 | ||||||
| chr17:78747145
|
CA | C | 7 | a0001c0001t0001g0118a0001c0001t0001g0200a0001c0001t0003g0064others(4): Show | 7 | HG00558.hp1 HG03098.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+35056delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747145 | ||||||
| chr17:78747145
|
CAA | C | 37 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(34): Show | 37 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(34): Show |
intron_variant | MODIFIER | c.22+35055_22+35056d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747145 | ||||||
| chr17:78747145
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+35046_22+35056d others(13): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747145 | ||||||
| chr17:78747164
|
A | G | 27 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0017others(24): Show | 27 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(24): Show |
intron_variant | MODIFIER | c.22+35038T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747164 | ||||||
| chr17:78747179
|
T | G | 1 | a0001c0001t0008g0267 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.22+35023A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747179 | ||||||
| chr17:78747212
|
C | A | 1 | a0001c0001t0003g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.22+34990G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747212 | ||||||
| chr17:78747383
|
G | A | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+34819C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747383 | ||||||
| chr17:78747762
|
G | T | 7 | a0001c0001t0003g0127a0001c0001t0003g0128a0001c0001t0003g0129others(4): Show | 7 | HG00597.hp2 NA18941.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+34440C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747762 | ||||||
| chr17:78747865
|
T | C | 4 | a0001c0002t0010g0357a0001c0002t0010g0358a0001c0002t0010g0359others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+34337A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78747865 | ||||||
| chr17:78748044
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.22+34158A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748044 | ||||||
| chr17:78748291
|
G | A | 11 | a0001c0001t0003g0352a0001c0001t0003g0363a0001c0001t0003g0364others(8): Show | 11 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.22+33911C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748291 | ||||||
| chr17:78748473
|
C | A | 223 | a0001c0001t0001g0025a0001c0001t0001g0092a0001c0001t0001g0093others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.22+33729G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748473 | ||||||
| chr17:78748576
|
G | C | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+33626C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748576 | ||||||
| chr17:78748764
|
G | A | 5 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0069others(2): Show | 5 | HG02165.hp2 NA18971.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+33438C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748764 | ||||||
| chr17:78748949
|
C | T | 1 | a0001c0001t0003g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.22+33253G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748949 | ||||||
| chr17:78748999
|
G | T | 10 | a0001c0001t0003g0352a0001c0001t0003g0363a0001c0001t0003g0364others(7): Show | 10 | HG02109.hp1 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.22+33203C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78748999 | ||||||
| chr17:78749278
|
G | T | 1 | a0001c0001t0006g0328 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.22+32924C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749278 | ||||||
| chr17:78749287
|
C | T | 1 | a0001c0001t0006g0328 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.22+32915G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749287 | ||||||
| chr17:78749289
|
G | A | 1 | a0001c0001t0007g0208 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.22+32913C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749289 | ||||||
| chr17:78749305
|
T | C | 1 | a0001c0001t0006g0338 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.22+32897A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749305 | ||||||
| chr17:78749353
|
G | A | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.22+32849C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749353 | ||||||
| chr17:78749457
|
C | T | 20 | a0001c0001t0003g0351a0001c0001t0003g0352a0001c0001t0003g0355others(17): Show | 20 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.22+32745G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749457 | ||||||
| chr17:78749537
|
G | A | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+32665C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749537 | ||||||
| chr17:78749587
|
GCCATTAT others(3): Show |
G | 1 | a0001c0001t0005g0019 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.22+32605_22+32614d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749587 | ||||||
| chr17:78749665
|
T | A | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+32537A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749665 | ||||||
| chr17:78749665
|
T | TA | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+32536dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749665 | ||||||
| chr17:78749694
|
T | C | 1 | a0001c0001t0002g0296 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.22+32508A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78749694 | ||||||
| chr17:78750052
|
G | T | 1 | a0001c0001t0003g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.22+32150C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750052 | ||||||
| chr17:78750130
|
G | A | 12 | a0001c0001t0003g0351a0001c0001t0003g0361a0001c0001t0003g0362others(9): Show | 12 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.22+32072C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750130 | ||||||
| chr17:78750243
|
G | A | 213 | a0001c0001t0001g0025a0001c0001t0001g0283a0001c0001t0002g0011others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.22+31959C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750243 | ||||||
| chr17:78750442
|
C | A | 1 | a0001c0001t0005g0021 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.22+31760G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750442 | ||||||
| chr17:78750450
|
T | C | 1 | a0001c0001t0006g0334 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.22+31752A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750450 | ||||||
| chr17:78750538
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.22+31664C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750538 | ||||||
| chr17:78750590
|
C | T | 1 | a0001c0001t0003g0081 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.22+31612G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750590 | ||||||
| chr17:78750669
|
G | C | 1 | a0001c0001t0002g0266 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.22+31533C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750669 | ||||||
| chr17:78750672
|
G | C | 4 | a0001c0001t0002g0317a0001c0001t0002g0318a0001c0001t0002g0319others(1): Show | 4 | NA18948.hp2 NA18993.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+31530C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750672 | ||||||
| chr17:78750727
|
G | A | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.22+31475C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750727 | ||||||
| chr17:78750763
|
A | C | 377 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(374): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.22+31439T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750763 | ||||||
| chr17:78750780
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.22+31422G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750780 | ||||||
| chr17:78750791
|
G | C | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+31411C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750791 | ||||||
| chr17:78750801
|
C | CA | 15 | a0001c0001t0003g0127a0001c0001t0003g0128a0001c0001t0003g0129others(12): Show | 15 | HG00597.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.22+31400dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750801 | ||||||
| chr17:78750801
|
CA | C | 187 | a0001c0001t0001g0025a0001c0001t0001g0283a0001c0001t0002g0011others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.22+31400delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750801 | ||||||
| chr17:78750813
|
A | C | 2 | a0001c0001t0006g0337a0001c0001t0006g0349 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.22+31389T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750813 | ||||||
| chr17:78750814
|
A | C | 1 | a0001c0001t0005g0023 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.22+31388T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750814 | ||||||
| chr17:78750859
|
G | A | 6 | a0001c0001t0003g0363a0001c0001t0003g0364a0001c0001t0003g0365others(3): Show | 6 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+31343C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78750859 | ||||||
| chr17:78751064
|
A | ACCTCTAC others(3): Show |
6 | a0001c0001t0004g0114a0001c0001t0004g0122a0001c0001t0004g0132others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+31128_22+31137d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751064 | ||||||
| chr17:78751126
|
G | T | 7 | a0001c0001t0001g0117a0001c0001t0001g0152a0001c0001t0001g0159others(4): Show | 7 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+31076C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751126 | ||||||
| chr17:78751263
|
G | A | 44 | a0001c0001t0001g0025a0001c0001t0005g0001a0001c0001t0005g0002others(41): Show | 44 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(41): Show |
intron_variant | MODIFIER | c.22+30939C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751263 | ||||||
| chr17:78751264
|
C | A | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+30938G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751264 | ||||||
| chr17:78751265
|
C | A | 30 | a0001c0001t0001g0025a0001c0001t0005g0001a0001c0001t0005g0002others(27): Show | 30 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(27): Show |
intron_variant | MODIFIER | c.22+30937G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751265 | ||||||
| chr17:78751315
|
A | G | 1 | a0001c0001t0006g0330 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.22+30887T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751315 | ||||||
| chr17:78751441
|
A | G | 1 | a0001c0001t0003g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.22+30761T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751441 | ||||||
| chr17:78751474
|
C | CA | 143 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0109others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.22+30727dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751474 | ||||||
| chr17:78751474
|
C | CAA | 20 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0003g0064others(17): Show | 20 | HG00558.hp1 HG02027.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.22+30726_22+30727d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751474 | ||||||
| chr17:78751474
|
C | CAAA | 12 | a0001c0001t0002g0278a0001c0001t0003g0063a0001c0001t0003g0066others(9): Show | 12 | HG00423.hp2 HG01255.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.22+30725_22+30727d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751474 | ||||||
| chr17:78751474
|
C | CAAAA | 42 | a0001c0001t0001g0025a0001c0001t0003g0065a0001c0001t0003g0078others(39): Show | 42 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(39): Show |
intron_variant | MODIFIER | c.22+30724_22+30727d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751474 | ||||||
| chr17:78751514
|
G | A | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+30688C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751514 | ||||||
| chr17:78751569
|
G | A | 1 | a0001c0001t0021g0182 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.22+30633C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751569 | ||||||
| chr17:78751664
|
C | T | 30 | a0001c0001t0001g0025a0001c0001t0005g0001a0001c0001t0005g0002others(27): Show | 30 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(27): Show |
intron_variant | MODIFIER | c.22+30538G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751664 | ||||||
| chr17:78751895
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+30307C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78751895 | ||||||
| chr17:78752168
|
C | T | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+30034G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752168 | ||||||
| chr17:78752203
|
T | C | 3 | a0001c0001t0005g0031a0001c0001t0005g0038a0001c0001t0005g0039 | 3 | HG03239.hp2 HG03490.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.22+29999A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752203 | ||||||
| chr17:78752456
|
A | G | 214 | a0001c0001t0001g0025a0001c0001t0001g0283a0001c0001t0002g0011others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.22+29746T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752456 | ||||||
| chr17:78752506
|
C | T | 1 | a0001c0001t0016g0348 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.22+29696G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752506 | ||||||
| chr17:78752519
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.22+29683C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752519 | ||||||
| chr17:78752542
|
T | C | 214 | a0001c0001t0001g0025a0001c0001t0001g0283a0001c0001t0002g0011others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.22+29660A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752542 | ||||||
| chr17:78752623
|
G | A | 43 | a0001c0001t0001g0025a0001c0001t0005g0001a0001c0001t0005g0002others(40): Show | 43 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.22+29579C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752623 | ||||||
| chr17:78752724
|
T | C | 318 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.22+29478A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752724 | ||||||
| chr17:78752883
|
A | G | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+29319T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78752883 | ||||||
| chr17:78753143
|
C | G | 1 | a0001c0001t0003g0071 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.22+29059G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753143 | ||||||
| chr17:78753186
|
G | A | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+29016C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753186 | ||||||
| chr17:78753225
|
T | G | 1 | a0001c0001t0001g0010 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.22+28977A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753225 | ||||||
| chr17:78753239
|
T | C | 1 | a0001c0001t0002g0278 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.22+28963A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753239 | ||||||
| chr17:78753302
|
T | A | 6 | a0001c0001t0003g0363a0001c0001t0003g0364a0001c0001t0003g0365others(3): Show | 6 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+28900A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753302 | ||||||
| chr17:78753499
|
T | TAATA | 76 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.22+28699_22+28702d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753499 | ||||||
| chr17:78753499
|
TAATA | T | 8 | a0001c0001t0001g0148a0001c0001t0001g0157a0001c0001t0001g0158others(5): Show | 8 | HG00544.hp2 HG02004.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+28699_22+28702d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753499 | ||||||
| chr17:78753499
|
TAATAAAT others(1): Show |
T | 118 | a0001c0001t0001g0104a0001c0001t0001g0149a0001c0001t0001g0150others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.22+28695_22+28702d others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753499 | ||||||
| chr17:78753529
|
A | ATAAATAA others(9): Show |
1 | a0001c0001t0005g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.22+28672_22+28673i others(18): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753529 | ||||||
| chr17:78753529
|
A | ATAAATAA others(5): Show |
38 | a0001c0001t0001g0025a0001c0001t0005g0001a0001c0001t0005g0002others(35): Show | 38 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+28672_22+28673i others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753529 | ||||||
| chr17:78753529
|
A | ATAAATAA others(1): Show |
3 | a0001c0001t0005g0030a0001c0001t0005g0042a0001c0001t0009g0047 | 3 | HG02976.hp1 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.22+28672_22+28673i others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753529 | ||||||
| chr17:78753616
|
A | G | 4 | a0001c0001t0004g0061a0001c0001t0004g0198a0001c0001t0004g0202others(1): Show | 4 | NA18954.hp1 NA18960.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+28586T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753616 | ||||||
| chr17:78753707
|
C | T | 1 | a0001c0001t0005g0017 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.22+28495G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753707 | ||||||
| chr17:78753991
|
C | T | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+28211G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78753991 | ||||||
| chr17:78754015
|
G | A | 225 | a0001c0001t0001g0025a0001c0001t0001g0092a0001c0001t0001g0093others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.22+28187C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754015 | ||||||
| chr17:78754245
|
C | T | 2 | a0001c0001t0004g0131a0001c0001t0004g0180 | 2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.22+27957G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754245 | ||||||
| chr17:78754343
|
T | C | 12 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(9): Show | 12 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.22+27859A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754343 | ||||||
| chr17:78754458
|
C | T | 1 | a0001c0001t0002g0299 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.22+27744G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754458 | ||||||
| chr17:78754739
|
A | AGTTT | 44 | a0001c0001t0001g0025a0001c0001t0005g0001a0001c0001t0005g0002others(41): Show | 44 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(41): Show |
intron_variant | MODIFIER | c.22+27462_22+27463i others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754739 | ||||||
| chr17:78754834
|
T | C | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.22+27368A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754834 | ||||||
| chr17:78754906
|
C | T | 29 | a0001c0001t0001g0025a0001c0001t0005g0001a0001c0001t0005g0002others(26): Show | 29 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+27296G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78754906 | ||||||
| chr17:78755044
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.22+27158A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755044 | ||||||
| chr17:78755152
|
A | G | 15 | a0001c0001t0003g0127a0001c0001t0003g0128a0001c0001t0003g0129others(12): Show | 15 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.22+27050T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755152 | ||||||
| chr17:78755413
|
G | A | 38 | a0001c0001t0001g0025a0001c0001t0005g0001a0001c0001t0005g0002others(35): Show | 38 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+26789C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755413 | ||||||
| chr17:78755424
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.22+26778G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755424 | ||||||
| chr17:78755491
|
T | TAAAAA | 12 | a0001c0001t0002g0275a0001c0001t0002g0292a0001c0001t0002g0297others(9): Show | 12 | HG01070.hp1 HG02109.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.22+26706_22+26710d others(7): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755491 | ||||||
| chr17:78755491
|
T | TAAAAAA | 161 | a0001c0001t0001g0008a0001c0001t0001g0059a0001c0001t0001g0096others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.22+26705_22+26710d others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755491 | ||||||
| chr17:78755491
|
T | TAAAAAAA | 193 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0025others(190): Show | 193 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(190): Show |
intron_variant | MODIFIER | c.22+26704_22+26710d others(9): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755491 | ||||||
| chr17:78755491
|
T | TAAAAAAA others(1): Show |
7 | a0001c0001t0001g0181a0001c0001t0001g0189a0001c0001t0003g0370others(4): Show | 7 | HG00544.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+26703_22+26710d others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755491 | ||||||
| chr17:78755596
|
CA | C | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | NA18948.hp1 NA18965.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+26605delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755596 | ||||||
| chr17:78755805
|
G | A | 1 | a0001c0001t0004g0241 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.22+26397C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755805 | ||||||
| chr17:78755910
|
C | CA | 36 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0199others(33): Show | 36 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.22+26291dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755910 | ||||||
| chr17:78755936
|
A | G | 1 | a0001c0001t0005g0002 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.22+26266T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78755936 | ||||||
| chr17:78756029
|
C | T | 210 | a0001c0001t0001g0025a0001c0001t0001g0283a0001c0001t0002g0011others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.22+26173G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756029 | ||||||
| chr17:78756070
|
TTTA | T | 3 | a0001c0001t0002g0305a0001c0001t0002g0316a0001c0001t0002g0323 | 3 | HG00597.hp1 NA19056.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.22+26129_22+26131d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756070 | ||||||
| chr17:78756073
|
A | T | 2 | a0001c0001t0012g0120a0001c0001t0012g0121 | 2 | HG01261.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.22+26129T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756073 | ||||||
| chr17:78756075
|
T | A | 1 | a0001c0001t0003g0369 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.22+26127A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756075 | ||||||
| chr17:78756077
|
T | A | 1 | a0001c0001t0004g0221 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.22+26125A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756077 | ||||||
| chr17:78756078
|
T | A | 3 | a0001c0001t0002g0305a0001c0001t0002g0316a0001c0001t0002g0323 | 3 | HG00597.hp1 NA19056.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.22+26124A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756078 | ||||||
| chr17:78756079
|
A | AT | 161 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0283others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.22+26122dupA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756079 | ||||||
| chr17:78756079
|
A | ATT | 8 | a0001c0001t0002g0259a0001c0001t0002g0278a0001c0001t0005g0031others(5): Show | 8 | HG01255.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.22+26121_22+26122d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756079 | ||||||
| chr17:78756079
|
A | T | 4 | a0001c0001t0002g0305a0001c0001t0002g0316a0001c0001t0002g0323others(1): Show | 4 | HG00597.hp1 HG02155.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+26123T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756079 | ||||||
| chr17:78756080
|
T | A | 1 | a0001c0001t0015g0326 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.22+26122A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756080 | ||||||
| chr17:78756082
|
T | TA | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.22+26119_22+26120i others(3): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756082 | ||||||
| chr17:78756170
|
G | T | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+26032C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756170 | ||||||
| chr17:78756278
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.22+25924C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756278 | ||||||
| chr17:78756322
|
C | A | 1 | a0001c0001t0002g0304 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.22+25880G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756322 | ||||||
| chr17:78756467
|
G | A | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+25735C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756467 | ||||||
| chr17:78756632
|
C | A | 1 | a0001c0001t0026g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.22+25570G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756632 | ||||||
| chr17:78756716
|
G | C | 1 | a0001c0001t0003g0352 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.22+25486C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756716 | ||||||
| chr17:78756876
|
G | A | 1 | a0001c0001t0003g0065 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.22+25326C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756876 | ||||||
| chr17:78756903
|
C | T | 1 | a0001c0001t0026g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.22+25299G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756903 | ||||||
| chr17:78756919
|
C | T | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25283G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756919 | ||||||
| chr17:78756921
|
T | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25281A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756921 | ||||||
| chr17:78756923
|
G | C | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25279C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756923 | ||||||
| chr17:78756926
|
A | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25276T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756926 | ||||||
| chr17:78756927
|
A | T | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25275T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756927 | ||||||
| chr17:78756928
|
A | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25274T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756928 | ||||||
| chr17:78756929
|
A | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25273T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756929 | ||||||
| chr17:78756932
|
A | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25270T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756932 | ||||||
| chr17:78756933
|
G | A | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25269C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756933 | ||||||
| chr17:78756937
|
A | T | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25265T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756937 | ||||||
| chr17:78756938
|
A | T | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25264T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756938 | ||||||
| chr17:78756940
|
A | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25262T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756940 | ||||||
| chr17:78756943
|
A | C | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25259T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756943 | ||||||
| chr17:78756944
|
T | C | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25258A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756944 | ||||||
| chr17:78756946
|
C | A | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25256G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756946 | ||||||
| chr17:78756949
|
A | C | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25253T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756949 | ||||||
| chr17:78756950
|
A | T | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25252T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756950 | ||||||
| chr17:78756951
|
G | C | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25251C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756951 | ||||||
| chr17:78756952
|
G | T | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25250C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756952 | ||||||
| chr17:78756954
|
G | A | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25248C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756954 | ||||||
| chr17:78756956
|
A | C | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25246T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756956 | ||||||
| chr17:78756961
|
C | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25241G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756961 | ||||||
| chr17:78756962
|
A | T | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25240T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756962 | ||||||
| chr17:78756967
|
T | C | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25235A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756967 | ||||||
| chr17:78756969
|
G | C | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25233C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756969 | ||||||
| chr17:78756971
|
A | T | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25231T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756971 | ||||||
| chr17:78756972
|
T | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25230A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756972 | ||||||
| chr17:78756973
|
T | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25229A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756973 | ||||||
| chr17:78756975
|
T | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25227A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756975 | ||||||
| chr17:78756976
|
T | A | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25226A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756976 | ||||||
| chr17:78756977
|
TTC | T | 6 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0069others(3): Show | 6 | HG02165.hp2 NA18945.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+25223_22+25224d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756977 | ||||||
| chr17:78756978
|
TC | T | 21 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0066others(18): Show | 21 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.22+25223delG | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756978 | ||||||
| chr17:78756979
|
C | T | 1 | a0001c0001t0003g0065 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.22+25223G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756979 | ||||||
| chr17:78756980
|
T | A | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25222A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756980 | ||||||
| chr17:78756983
|
T | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25219A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756983 | ||||||
| chr17:78756984
|
T | A | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25218A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756984 | ||||||
| chr17:78756985
|
T | A | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25217A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756985 | ||||||
| chr17:78756986
|
T | C | 1 | a0001c0001t0003g0065 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.22+25216A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756986 | ||||||
| chr17:78756986
|
T | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25216A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756986 | ||||||
| chr17:78756987
|
T | C | 26 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0066others(23): Show | 26 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.22+25215A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756987 | ||||||
| chr17:78756987
|
T | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25215A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756987 | ||||||
| chr17:78756988
|
C | CT | 11 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0003g0237others(8): Show | 11 | HG00597.hp2 HG01106.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+25213dupA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756988 | ||||||
| chr17:78756988
|
C | T | 27 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(24): Show | 27 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.22+25214G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756988 | ||||||
| chr17:78756991
|
T | A | 1 | a0001c0001t0002g0284 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.22+25211A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756991 | ||||||
| chr17:78756992
|
T | C | 1 | a0001c0001t0004g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+25210A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78756992 | ||||||
| chr17:78757009
|
G | A | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25193C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757009 | ||||||
| chr17:78757013
|
G | C | 1 | a0001c0001t0004g0214 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.22+25189C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757013 | ||||||
| chr17:78757020
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.22+25182C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757020 | ||||||
| chr17:78757028
|
G | C | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25174C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757028 | ||||||
| chr17:78757031
|
C | G | 1 | a0001c0001t0003g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.22+25171G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757031 | ||||||
| chr17:78757049
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.22+25153C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757049 | ||||||
| chr17:78757062
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.22+25140G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757062 | ||||||
| chr17:78757092
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.22+25110G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757092 | ||||||
| chr17:78757216
|
G | A | 1 | a0001c0001t0004g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+24986C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757216 | ||||||
| chr17:78757222
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.22+24980T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757222 | ||||||
| chr17:78757500
|
G | C | 1 | a0001c0001t0004g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+24702C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757500 | ||||||
| chr17:78757702
|
G | A | 4 | a0001c0001t0002g0011a0001c0001t0002g0244a0001c0001t0002g0245others(1): Show | 4 | NA18940.hp2 NA18945.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+24500C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757702 | ||||||
| chr17:78757718
|
G | A | 1 | a0001c0001t0015g0326 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.22+24484C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757718 | ||||||
| chr17:78757793
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.22+24409C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757793 | ||||||
| chr17:78757816
|
G | A | 4 | a0001c0001t0002g0254a0001c0001t0002g0274a0001c0001t0002g0275others(1): Show | 4 | HG00673.hp2 HG02165.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+24386C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757816 | ||||||
| chr17:78757985
|
T | G | 4 | a0001c0002t0010g0357a0001c0002t0010g0358a0001c0002t0010g0359others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+24217A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78757985 | ||||||
| chr17:78758027
|
A | G | 1 | a0001c0001t0005g0039 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.22+24175T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758027 | ||||||
| chr17:78758186
|
A | C | 17 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(14): Show | 17 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.22+24016T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758186 | ||||||
| chr17:78758254
|
G | A | 1 | a0001c0001t0004g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+23948C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758254 | ||||||
| chr17:78758324
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0029g0116 | 2 | HG01255.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.22+23878G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758324 | ||||||
| chr17:78758462
|
T | C | 1 | a0001c0001t0002g0305 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.22+23740A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758462 | ||||||
| chr17:78758493
|
T | A | 1 | a0001c0001t0004g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+23709A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758493 | ||||||
| chr17:78758542
|
T | C | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+23660A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758542 | ||||||
| chr17:78758568
|
G | A | 1 | a0001c0001t0004g0377 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.22+23634C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758568 | ||||||
| chr17:78758635
|
C | T | 1 | a0001c0001t0004g0241 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.22+23567G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758635 | ||||||
| chr17:78758655
|
C | T | 1 | a0001c0001t0002g0304 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.22+23547G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78758655 | ||||||
| chr17:78759303
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.22+22899G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78759303 | ||||||
| chr17:78759371
|
A | G | 1 | a0001c0001t0002g0277 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.22+22831T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78759371 | ||||||
| chr17:78759664
|
G | A | 1 | a0001c0001t0008g0269 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.22+22538C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78759664 | ||||||
| chr17:78759908
|
C | A | 1 | a0001c0001t0002g0290 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.22+22294G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78759908 | ||||||
| chr17:78759987
|
T | G | 1 | a0001c0001t0006g0335 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.22+22215A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78759987 | ||||||
| chr17:78760022
|
C | T | 2 | a0001c0001t0003g0238a0001c0001t0003g0239 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+22180G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760022 | ||||||
| chr17:78760090
|
C | T | 38 | a0001c0001t0001g0025a0001c0001t0005g0001a0001c0001t0005g0002others(35): Show | 38 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+22112G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760090 | ||||||
| chr17:78760187
|
C | A | 1 | a0001c0001t0021g0182 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.22+22015G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760187 | ||||||
| chr17:78760269
|
C | T | 1 | a0001c0001t0007g0060 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.22+21933G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760269 | ||||||
| chr17:78760305
|
C | G | 2 | a0001c0001t0007g0222a0001c0001t0007g0223 | 2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.22+21897G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760305 | ||||||
| chr17:78760353
|
GT | G | 4 | a0001c0001t0002g0011a0001c0001t0002g0266a0001c0001t0003g0378others(1): Show | 4 | HG02738.hp2 NA18940.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+21848delA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760353 | ||||||
| chr17:78760355
|
TTATATA | T | 11 | a0001c0001t0003g0237a0001c0001t0006g0327a0001c0001t0006g0329others(8): Show | 11 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+21841_22+21846d others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760355 | ||||||
| chr17:78760361
|
ATATATAT others(117): Show |
A | 2 | a0001c0001t0003g0078a0001c0001t0003g0082 | 2 | NA18989.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.22+21717_22+21840d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760361 | ||||||
| chr17:78760363
|
ATATATAT others(187): Show |
A | 1 | a0001c0001t0002g0257 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.22+21645_22+21838d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760363 | ||||||
| chr17:78760372
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22+21830A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760372 | ||||||
| chr17:78760372
|
TATATATA others(11): Show |
T | 24 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(21): Show | 24 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.22+21812_22+21829d others(20): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760372 | ||||||
| chr17:78760374
|
TATATATA others(9): Show |
T | 3 | a0001c0001t0003g0085a0001c0001t0003g0086a0001c0001t0003g0087 | 3 | NA19003.hp2 NA19057.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.22+21812_22+21827d others(18): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760374 | ||||||
| chr17:78760375
|
ATATATAT others(103): Show |
A | 1 | a0001c0001t0002g0310 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.22+21717_22+21826d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760375 | ||||||
| chr17:78760376
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.22+21826A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760376 | ||||||
| chr17:78760376
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0006g0342 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.22+21816_22+21825d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760376 | ||||||
| chr17:78760376
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0002g0260 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.22+21814_22+21825d others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760376 | ||||||
| chr17:78760377
|
ATATATAT others(123): Show |
A | 21 | a0001c0001t0001g0177a0001c0001t0002g0012a0001c0001t0002g0013others(18): Show | 21 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.22+21695_22+21824d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760377 | ||||||
| chr17:78760378
|
T | C | 11 | a0001c0001t0005g0049a0001c0001t0009g0003a0001c0001t0009g0052others(8): Show | 11 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.22+21824A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760378 | ||||||
| chr17:78760378
|
TATATATA others(1): Show |
T | 3 | a0001c0001t0009g0047a0001c0001t0009g0051a0001c0001t0014g0053 | 3 | HG02976.hp1 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.22+21816_22+21823d others(10): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760378 | ||||||
| chr17:78760378
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0016g0348 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.22+21814_22+21823d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760378 | ||||||
| chr17:78760378
|
TATATATA others(47): Show |
T | 1 | a0001c0001t0005g0019 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.22+21770_22+21823d others(56): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760378 | ||||||
| chr17:78760378
|
TATATATA others(113): Show |
T | 1 | a0001c0001t0031g0285 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.22+21704_22+21823d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760378 | ||||||
| chr17:78760379
|
ATATATAC others(121): Show |
A | 18 | a0001c0001t0002g0020a0001c0001t0002g0245a0001c0001t0002g0246others(15): Show | 18 | HG00280.hp1 HG00408.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.22+21695_22+21822d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760379 | ||||||
| chr17:78760379
|
ATATATAC others(159): Show |
A | 1 | a0001c0001t0005g0031 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.22+21657_22+21822d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760379 | ||||||
| chr17:78760380
|
TATATACA others(45): Show |
T | 1 | a0001c0001t0011g0040 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.22+21770_22+21821d others(54): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760380 | ||||||
| chr17:78760380
|
TATATACA others(149): Show |
T | 2 | a0001c0001t0005g0037a0001c0001t0005g0042 | 2 | HG03927.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.22+21666_22+21821d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760380 | ||||||
| chr17:78760381
|
ATATACAC others(119): Show |
A | 18 | a0001c0001t0001g0283a0001c0001t0002g0261a0001c0001t0002g0273others(15): Show | 18 | HG00423.hp1 HG00642.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.22+21695_22+21820d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760381 | ||||||
| chr17:78760381
|
ATATACAC others(129): Show |
A | 5 | a0001c0001t0002g0254a0001c0001t0002g0275a0001c0001t0002g0276others(2): Show | 5 | HG02109.hp1 HG02165.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+21685_22+21820d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760381 | ||||||
| chr17:78760382
|
T | C | 13 | a0001c0001t0001g0181a0001c0001t0001g0193a0001c0001t0005g0049others(10): Show | 13 | HG00544.hp1 HG01243.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.22+21820A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760382 | ||||||
| chr17:78760382
|
TATACACA others(7): Show |
T | 1 | a0001c0001t0003g0239 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.22+21806_22+21819d others(16): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760382 | ||||||
| chr17:78760382
|
TATACACA others(43): Show |
T | 2 | a0001c0001t0001g0025a0001c0001t0005g0032 | 2 | NA18939.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.22+21770_22+21819d others(52): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760382 | ||||||
| chr17:78760382
|
TATACACA others(147): Show |
T | 1 | a0001c0001t0005g0034 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.22+21666_22+21819d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760382 | ||||||
| chr17:78760383
|
ATACACAC others(19): Show |
A | 2 | a0001c0001t0003g0367a0001c0001t0003g0368 | 2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.22+21793_22+21818d others(28): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760383 | ||||||
| chr17:78760383
|
ATACACAC others(117): Show |
A | 12 | a0001c0001t0002g0015a0001c0001t0002g0271a0001c0001t0002g0298others(9): Show | 12 | HG00099.hp2 HG00597.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.22+21695_22+21818d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760383 | ||||||
| chr17:78760383
|
ATACACAC others(127): Show |
A | 8 | a0001c0001t0002g0274a0001c0001t0002g0311a0001c0001t0002g0312others(5): Show | 8 | HG00673.hp2 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.22+21685_22+21818d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760383 | ||||||
| chr17:78760383
|
ATACACAC others(155): Show |
A | 2 | a0001c0001t0005g0022a0001c0001t0005g0033 | 2 | HG02135.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.22+21657_22+21818d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760383 | ||||||
| chr17:78760384
|
T | C | 84 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0058others(81): Show | 84 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.22+21818A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | ||||||
| chr17:78760384
|
T | TAC | 49 | a0001c0001t0001g0008a0001c0001t0001g0102a0001c0001t0001g0103others(46): Show | 49 | HG00738.hp1 HG01081.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.22+21816_22+21817d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | ||||||
| chr17:78760384
|
T | TATAC | 4 | a0001c0001t0001g0169a0001c0001t0004g0004a0001c0001t0004g0009others(1): Show | 4 | HG00597.hp2 HG01123.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+21817_22+21818i others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | ||||||
| chr17:78760384
|
T | TATATATA others(3): Show |
6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | HG00639.hp1 HG01243.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+21817_22+21818i others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | ||||||
| chr17:78760384
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.22+21817_22+21818i others(14): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | ||||||
| chr17:78760384
|
TACAC | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0003g0361others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+21814_22+21817d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | ||||||
| chr17:78760384
|
TACACACA others(37): Show |
T | 2 | a0001c0001t0005g0029a0001c0001t0005g0046 | 2 | NA18988.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.22+21774_22+21817d others(46): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | ||||||
| chr17:78760384
|
TACACACA others(41): Show |
T | 2 | a0001c0001t0005g0002a0001c0001t0005g0044 | 2 | NA18942.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.22+21770_22+21817d others(50): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | ||||||
| chr17:78760384
|
TACACACA others(107): Show |
T | 1 | a0001c0001t0002g0251 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.22+21704_22+21817d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | ||||||
| chr17:78760384
|
TACACACA others(145): Show |
T | 1 | a0001c0001t0005g0039 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.22+21666_22+21817d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | ||||||
| chr17:78760384
|
TACACACA others(179): Show |
T | 11 | a0001c0001t0005g0049a0001c0001t0009g0003a0001c0001t0009g0052others(8): Show | 11 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.22+21632_22+21817d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760384 | ||||||
| chr17:78760385
|
ACACACAC others(17): Show |
A | 2 | a0001c0001t0002g0304a0001c0003t0017g0016 | 2 | HG03579.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.22+21793_22+21816d others(26): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760385 | ||||||
| chr17:78760385
|
ACACACAC others(51): Show |
A | 1 | a0001c0001t0005g0017 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.22+21759_22+21816d others(60): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760385 | ||||||
| chr17:78760385
|
ACACACAC others(115): Show |
A | 6 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0290others(3): Show | 6 | HG02738.hp2 HG04204.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+21695_22+21816d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760385 | ||||||
| chr17:78760385
|
ACACACAC others(125): Show |
A | 34 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0243others(31): Show | 34 | HG00621.hp1 HG01081.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.22+21685_22+21816d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760385 | ||||||
| chr17:78760385
|
ACACACAC others(153): Show |
A | 9 | a0001c0001t0005g0001a0001c0001t0005g0021a0001c0001t0005g0023others(6): Show | 9 | HG00673.hp1 HG03239.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+21657_22+21816d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760385 | ||||||
| chr17:78760386
|
C | T | 1 | a0001c0001t0005g0030 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.22+21816G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760386 | ||||||
| chr17:78760388
|
C | CACACATA others(29): Show |
1 | a0001c0001t0001g0007 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.22+21813_22+21814i others(38): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760388 | ||||||
| chr17:78760388
|
C | T | 4 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0369others(1): Show | 4 | HG01106.hp2 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+21814G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760388 | ||||||
| chr17:78760390
|
C | T | 7 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0005g0030others(4): Show | 7 | HG02976.hp1 HG03130.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+21812G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760390 | ||||||
| chr17:78760394
|
T | C | 2 | a0001c0001t0007g0222a0001c0001t0007g0223 | 2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.22+21808A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760394 | ||||||
| chr17:78760396
|
CAT | C | 15 | a0001c0001t0002g0260a0001c0001t0005g0043a0001c0001t0006g0327others(12): Show | 15 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.22+21804_22+21805d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760396 | ||||||
| chr17:78760405
|
ATG | A | 23 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0067others(20): Show | 23 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.22+21795_22+21796d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760405 | ||||||
| chr17:78760407
|
G | A | 8 | a0001c0001t0003g0239a0001c0001t0005g0030a0001c0001t0005g0036others(5): Show | 8 | HG00642.hp1 HG01192.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+21795C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760407 | ||||||
| chr17:78760409
|
G | A | 5 | a0001c0001t0003g0063a0001c0001t0003g0066a0001c0001t0003g0074others(2): Show | 5 | HG02965.hp1 NA18946.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+21793C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760409 | ||||||
| chr17:78760409
|
G | GTA | 3 | a0001c0001t0001g0108a0001c0001t0001g0191a0001c0001t0001g0240 | 3 | HG03041.hp2 HG03486.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.22+21791_22+21792d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760409 | ||||||
| chr17:78760409
|
GTA | G | 6 | a0001c0001t0001g0092a0001c0001t0001g0152a0001c0001t0001g0159others(3): Show | 6 | HG00639.hp2 HG01074.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+21791_22+21792d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760409 | ||||||
| chr17:78760411
|
A | G | 12 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(9): Show | 12 | HG00639.hp1 HG00642.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.22+21791T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760411 | ||||||
| chr17:78760411
|
ATATATAT others(167): Show |
A | 5 | a0001c0001t0005g0030a0001c0001t0005g0036a0001c0001t0009g0047others(2): Show | 5 | HG02976.hp1 HG03130.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+21617_22+21790d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760411 | ||||||
| chr17:78760422
|
T | C | 3 | a0001c0001t0003g0239a0001c0001t0003g0367a0001c0001t0003g0368 | 3 | HG02818.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.22+21780A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760422 | ||||||
| chr17:78760426
|
C | T | 29 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0003g0063others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+21776G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760426 | ||||||
| chr17:78760432
|
C | T | 2 | a0001c0001t0005g0029a0001c0001t0005g0046 | 2 | NA18988.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.22+21770G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760432 | ||||||
| chr17:78760432
|
CAT | C | 24 | a0001c0001t0002g0260a0001c0001t0003g0237a0001c0001t0003g0238others(21): Show | 24 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.22+21768_22+21769d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760432 | ||||||
| chr17:78760439
|
A | G | 2 | a0001c0001t0004g0131a0001c0003t0017g0016 | 2 | HG00140.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.22+21763T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760439 | ||||||
| chr17:78760441
|
A | G | 1 | a0001c0001t0002g0304 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.22+21761T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760441 | ||||||
| chr17:78760443
|
G | A | 8 | a0001c0001t0001g0025a0001c0001t0005g0002a0001c0001t0005g0019others(5): Show | 8 | NA18939.hp1 NA18942.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.22+21759C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760443 | ||||||
| chr17:78760445
|
A | G | 6 | a0001c0001t0003g0239a0001c0001t0003g0367a0001c0001t0003g0368others(3): Show | 6 | HG01261.hp1 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+21757T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760445 | ||||||
| chr17:78760445
|
ATATATAT others(65): Show |
A | 1 | a0001c0001t0002g0304 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.22+21685_22+21756d others(74): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760445 | ||||||
| chr17:78760445
|
ATATATAT others(133): Show |
A | 23 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0260others(20): Show | 23 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.22+21617_22+21756d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760445 | ||||||
| chr17:78760447
|
ATATATAT others(131): Show |
A | 26 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(23): Show | 26 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.22+21617_22+21754d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760447 | ||||||
| chr17:78760449
|
ATATATAC others(101): Show |
A | 3 | a0001c0001t0003g0239a0001c0001t0003g0367a0001c0001t0003g0368 | 3 | HG02818.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.22+21645_22+21752d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760449 | ||||||
| chr17:78760453
|
ATACATAC others(57): Show |
A | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+21685_22+21748d others(66): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760453 | ||||||
| chr17:78760453
|
ATACATAC others(97): Show |
A | 1 | a0001c0001t0003g0079 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.22+21645_22+21748d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760453 | ||||||
| chr17:78760454
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0157 | 2 | HG02004.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.22+21748A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760454 | ||||||
| chr17:78760454
|
T | TAC | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+21746_22+21747d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760454 | ||||||
| chr17:78760456
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+21746G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760456 | ||||||
| chr17:78760458
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+21744A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760458 | ||||||
| chr17:78760460
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+21742G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760460 | ||||||
| chr17:78760460
|
CAT | C | 5 | a0001c0001t0001g0140a0001c0001t0001g0191a0001c0001t0003g0127others(2): Show | 5 | HG03225.hp2 NA18747.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+21740_22+21741d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760460 | ||||||
| chr17:78760462
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0003g0129 | 2 | HG03486.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.22+21740A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760462 | ||||||
| chr17:78760464
|
T | C | 9 | a0001c0001t0001g0025a0001c0001t0005g0002a0001c0001t0005g0017others(6): Show | 9 | HG02080.hp2 NA18939.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+21738A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760464 | ||||||
| chr17:78760468
|
T | C | 9 | a0001c0001t0001g0025a0001c0001t0005g0002a0001c0001t0005g0017others(6): Show | 9 | HG02080.hp2 NA18939.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+21734A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760468 | ||||||
| chr17:78760471
|
G | A | 9 | a0001c0001t0001g0025a0001c0001t0005g0002a0001c0001t0005g0017others(6): Show | 9 | HG02080.hp2 NA18939.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+21731C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760471 | ||||||
| chr17:78760485
|
GTATATAT others(95): Show |
G | 9 | a0001c0001t0001g0025a0001c0001t0005g0002a0001c0001t0005g0017others(6): Show | 9 | HG02080.hp2 NA18939.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+21615_22+21716d others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760485 | ||||||
| chr17:78760494
|
T | C | 4 | a0001c0001t0001g0148a0001c0001t0001g0158a0001c0001t0001g0175others(1): Show | 4 | HG00544.hp2 NA18969.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+21708A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760494 | ||||||
| chr17:78760494
|
T | TAC | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+21707_22+21708i others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760494 | ||||||
| chr17:78760498
|
C | T | 1 | a0001c0001t0002g0310 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.22+21704G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760498 | ||||||
| chr17:78760502
|
T | C | 2 | a0001c0001t0003g0078a0001c0001t0003g0082 | 2 | NA18989.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.22+21700A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760502 | ||||||
| chr17:78760507
|
G | A | 5 | a0001c0001t0002g0251a0001c0001t0002g0310a0001c0001t0003g0078others(2): Show | 5 | HG00099.hp1 HG01074.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+21695C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760507 | ||||||
| chr17:78760507
|
GTA | G | 7 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+21693_22+21694d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760507 | ||||||
| chr17:78760508
|
T | TATATATG others(19): Show |
2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.22+21693_22+21694i others(28): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760508 | ||||||
| chr17:78760510
|
T | TATATGTA others(17): Show |
2 | a0001c0001t0001g0113a0001c0001t0001g0130 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.22+21691_22+21692i others(26): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760510 | ||||||
| chr17:78760513
|
A | G | 2 | a0001c0001t0003g0078a0001c0001t0003g0082 | 2 | NA18989.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.22+21689T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760513 | ||||||
| chr17:78760517
|
G | A | 91 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.22+21685C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760517 | ||||||
| chr17:78760517
|
G | GTA | 16 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0059others(13): Show | 16 | HG00408.hp1 NA18747.hp1 NA18948.hp1 others(13): Show |
intron_variant | MODIFIER | c.22+21683_22+21684d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760517 | ||||||
| chr17:78760517
|
GTA | G | 10 | a0001c0001t0001g0008a0001c0001t0001g0108a0001c0001t0001g0147others(7): Show | 10 | HG02572.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.22+21683_22+21684d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760517 | ||||||
| chr17:78760519
|
A | G | 13 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(10): Show | 13 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.22+21683T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760519 | ||||||
| chr17:78760526
|
T | C | 7 | a0001c0001t0003g0351a0001c0001t0003g0363a0001c0001t0003g0364others(4): Show | 7 | HG02647.hp1 HG02896.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.22+21676A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760526 | ||||||
| chr17:78760527
|
A | G | 1 | a0001c0001t0002g0274 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.22+21675T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760527 | ||||||
| chr17:78760528
|
T | C | 8 | a0001c0001t0006g0328a0001c0001t0006g0338a0001c0001t0006g0343others(5): Show | 8 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+21674A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760528 | ||||||
| chr17:78760530
|
T | C | 118 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0152others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.22+21672A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760530 | ||||||
| chr17:78760532
|
C | T | 4 | a0001c0001t0001g0166a0001c0001t0003g0371a0001c0001t0003g0372others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+21670G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760532 | ||||||
| chr17:78760534
|
TAC | T | 4 | a0001c0001t0001g0111a0001c0001t0001g0167a0001c0001t0001g0168others(1): Show | 4 | NA18964.hp2 NA18968.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+21666_22+21667d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760534 | ||||||
| chr17:78760536
|
C | CATATATA others(15): Show |
1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.22+21644_22+21665d others(24): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760536 | ||||||
| chr17:78760538
|
T | C | 10 | a0001c0001t0001g0177a0001c0001t0003g0352a0001c0001t0003g0355others(7): Show | 10 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.22+21664A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760538 | ||||||
| chr17:78760540
|
T | C | 6 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0373others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+21662A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760540 | ||||||
| chr17:78760541
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.22+21661T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760541 | ||||||
| chr17:78760541
|
ATATG | A | 7 | a0001c0001t0003g0351a0001c0001t0003g0363a0001c0001t0003g0364others(4): Show | 7 | HG02647.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+21657_22+21660d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760541 | ||||||
| chr17:78760542
|
T | C | 10 | a0001c0001t0001g0177a0001c0001t0003g0352a0001c0001t0003g0355others(7): Show | 10 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.22+21660A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760542 | ||||||
| chr17:78760544
|
T | C | 5 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0374others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+21658A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760544 | ||||||
| chr17:78760545
|
G | A | 21 | a0001c0001t0001g0177a0001c0001t0003g0078a0001c0001t0003g0082others(18): Show | 21 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.22+21657C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760545 | ||||||
| chr17:78760545
|
GTA | G | 4 | a0001c0001t0001g0092a0001c0001t0001g0166a0001c0001t0026g0099others(1): Show | 4 | HG01074.hp2 HG03491.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+21655_22+21656d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760545 | ||||||
| chr17:78760546
|
T | C | 1 | a0001c0001t0003g0370 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.22+21656A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760546 | ||||||
| chr17:78760547
|
A | G | 105 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.22+21655T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760547 | ||||||
| chr17:78760549
|
A | G | 2 | a0001c0001t0002g0015a0001c0003t0017g0016 | 2 | HG03579.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.22+21653T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760549 | ||||||
| chr17:78760551
|
A | G | 10 | a0001c0001t0003g0351a0001c0001t0003g0352a0001c0001t0003g0363others(7): Show | 10 | HG02109.hp1 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.22+21651T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760551 | ||||||
| chr17:78760551
|
ATATATG | A | 103 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.22+21645_22+21650d others(8): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760551 | ||||||
| chr17:78760553
|
A | G | 16 | a0001c0001t0001g0177a0001c0001t0003g0351a0001c0001t0003g0352others(13): Show | 16 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.22+21649T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760553 | ||||||
| chr17:78760555
|
A | G | 11 | a0001c0001t0001g0177a0001c0001t0003g0355a0001c0001t0003g0356others(8): Show | 11 | HG01123.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+21647T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760555 | ||||||
| chr17:78760557
|
G | A | 34 | a0001c0001t0001g0177a0001c0001t0003g0078a0001c0001t0003g0082others(31): Show | 34 | HG00673.hp1 HG01123.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.22+21645C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760557 | ||||||
| chr17:78760559
|
A | G | 1 | a0001c0001t0003g0370 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.22+21643T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760559 | ||||||
| chr17:78760559
|
ATATATAT others(19): Show |
A | 2 | a0001c0001t0005g0018a0001c0001t0005g0035 | 2 | NA19080.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.22+21617_22+21642d others(28): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760559 | ||||||
| chr17:78760564
|
T | C | 13 | a0001c0001t0005g0001a0001c0001t0005g0021a0001c0001t0005g0022others(10): Show | 13 | HG00673.hp1 HG02135.hp1 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.22+21638A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760564 | ||||||
| chr17:78760566
|
T | C | 4 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0003g0082others(1): Show | 4 | NA18973.hp1 NA18989.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+21636A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760566 | ||||||
| chr17:78760568
|
T | C | 16 | a0001c0001t0004g0221a0001c0001t0005g0001a0001c0001t0005g0021others(13): Show | 16 | HG00673.hp1 HG02135.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.22+21634A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760568 | ||||||
| chr17:78760568
|
TAC | T | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+21632_22+21633d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760568 | ||||||
| chr17:78760570
|
C | T | 20 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(17): Show | 20 | HG00673.hp1 HG02135.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.22+21632G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760570 | ||||||
| chr17:78760572
|
C | T | 3 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0003g0082 | 3 | NA18989.hp2 NA18999.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.22+21630G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760572 | ||||||
| chr17:78760576
|
C | T | 30 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0003g0082others(27): Show | 30 | HG00673.hp1 HG02135.hp1 HG02647.hp2 others(27): Show |
intron_variant | MODIFIER | c.22+21626G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760576 | ||||||
| chr17:78760576
|
CATATATA others(3): Show |
C | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG01255.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.22+21616_22+21625d others(12): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760576 | ||||||
| chr17:78760581
|
A | G | 3 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0003g0082 | 3 | NA18989.hp2 NA18999.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.22+21621T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760581 | ||||||
| chr17:78760585
|
G | A | 3 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0003g0082 | 3 | NA18989.hp2 NA18999.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.22+21617C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760585 | ||||||
| chr17:78760585
|
G | GTA | 190 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0092others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.22+21615_22+21616d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760585 | ||||||
| chr17:78760587
|
A | ATG | 27 | a0001c0001t0005g0001a0001c0001t0005g0021a0001c0001t0005g0022others(24): Show | 27 | HG00673.hp1 HG02135.hp1 HG02647.hp2 others(24): Show |
intron_variant | MODIFIER | c.22+21614_22+21615i others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760587 | ||||||
| chr17:78760587
|
A | G | 7 | a0001c0001t0005g0018a0001c0001t0005g0030a0001c0001t0005g0035others(4): Show | 7 | HG02976.hp1 HG03130.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+21615T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760587 | ||||||
| chr17:78760591
|
A | G | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+21611T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760591 | ||||||
| chr17:78760593
|
A | G | 1 | a0001c0001t0003g0237 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.22+21609T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760593 | ||||||
| chr17:78760658
|
A | G | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+21544T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760658 | ||||||
| chr17:78760997
|
G | A | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+21205C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78760997 | ||||||
| chr17:78761045
|
A | T | 31 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0003g0063others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.22+21157T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761045 | ||||||
| chr17:78761065
|
AC | A | 11 | a0001c0001t0007g0060a0001c0001t0007g0204a0001c0001t0007g0205others(8): Show | 11 | HG00642.hp1 HG01106.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+21136delG | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761065 | ||||||
| chr17:78761134
|
C | T | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+21068G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761134 | ||||||
| chr17:78761214
|
C | A | 130 | a0001c0001t0001g0177a0001c0001t0001g0283a0001c0001t0002g0011others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.22+20988G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761214 | ||||||
| chr17:78761395
|
G | T | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+20807C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761395 | ||||||
| chr17:78761523
|
G | C | 3 | a0001c0001t0003g0063a0001c0001t0003g0066a0001c0001t0003g0074 | 3 | NA18946.hp2 NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.22+20679C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761523 | ||||||
| chr17:78761542
|
G | T | 2 | a0001c0001t0003g0355a0001c0001t0003g0356 | 2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.22+20660C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761542 | ||||||
| chr17:78761566
|
G | A | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+20636C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761566 | ||||||
| chr17:78761580
|
C | T | 377 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(374): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.22+20622G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761580 | ||||||
| chr17:78761607
|
G | A | 2 | a0001c0001t0003g0355a0001c0001t0003g0356 | 2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.22+20595C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761607 | ||||||
| chr17:78761616
|
T | G | 1 | a0001c0001t0013g0354 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.22+20586A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761616 | ||||||
| chr17:78761630
|
T | C | 377 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(374): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.22+20572A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761630 | ||||||
| chr17:78761663
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.22+20539C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761663 | ||||||
| chr17:78761685
|
A | C | 218 | a0001c0001t0001g0025a0001c0001t0001g0100a0001c0001t0001g0101others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.22+20517T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761685 | ||||||
| chr17:78761716
|
G | C | 1 | a0001c0001t0002g0299 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.22+20486C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761716 | ||||||
| chr17:78761810
|
C | G | 5 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+20392G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78761810 | ||||||
| chr17:78762021
|
G | A | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | NA18940.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.22+20181C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762021 | ||||||
| chr17:78762149
|
G | A | 1 | a0001c0001t0005g0042 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.22+20053C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762149 | ||||||
| chr17:78762160
|
T | C | 1 | a0001c0001t0002g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.22+20042A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762160 | ||||||
| chr17:78762169
|
A | G | 96 | a0001c0001t0001g0152a0001c0001t0001g0283a0001c0001t0002g0011others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.22+20033T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762169 | ||||||
| chr17:78762181
|
C | T | 4 | a0001c0002t0010g0357a0001c0002t0010g0358a0001c0002t0010g0359others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+20021G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762181 | ||||||
| chr17:78762226
|
T | C | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+19976A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762226 | ||||||
| chr17:78762240
|
G | C | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+19962C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762240 | ||||||
| chr17:78762293
|
C | T | 1 | a0001c0001t0007g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.22+19909G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762293 | ||||||
| chr17:78762334
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.22+19868C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762334 | ||||||
| chr17:78762363
|
G | A | 20 | a0001c0001t0002g0313a0001c0001t0002g0315a0001c0001t0003g0063others(17): Show | 20 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.22+19839C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762363 | ||||||
| chr17:78762509
|
G | C | 7 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+19693C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762509 | ||||||
| chr17:78762509
|
G | T | 1 | a0001c0001t0029g0116 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.22+19693C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762509 | ||||||
| chr17:78762662
|
A | G | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+19540T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762662 | ||||||
| chr17:78762674
|
G | A | 1 | a0001c0001t0006g0329 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.22+19528C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762674 | ||||||
| chr17:78762928
|
G | A | 69 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0003g0063others(66): Show | 69 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.22+19274C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78762928 | ||||||
| chr17:78763163
|
G | A | 11 | a0001c0001t0001g0025a0001c0001t0005g0017a0001c0001t0005g0019others(8): Show | 11 | HG02080.hp2 HG02135.hp1 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+19039C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763163 | ||||||
| chr17:78763257
|
C | T | 28 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(25): Show | 28 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.22+18945G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763257 | ||||||
| chr17:78763302
|
C | CA | 6 | a0001c0001t0001g0145a0001c0001t0001g0179a0001c0001t0003g0362others(3): Show | 6 | HG02145.hp2 HG02280.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+18899dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763302 | ||||||
| chr17:78763473
|
C | T | 1 | a0001c0001t0014g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.22+18729G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763473 | ||||||
| chr17:78763481
|
C | A | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+18721G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763481 | ||||||
| chr17:78763601
|
TAATA | T | 31 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0005g0001others(28): Show | 31 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(28): Show |
intron_variant | MODIFIER | c.22+18597_22+18600d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763601 | ||||||
| chr17:78763999
|
T | G | 14 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0005g0017others(11): Show | 14 | HG02080.hp2 HG02135.hp1 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.22+18203A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78763999 | ||||||
| chr17:78764198
|
C | CT | 46 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0145others(43): Show | 46 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(43): Show |
intron_variant | MODIFIER | c.22+18003dupA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764198 | ||||||
| chr17:78764198
|
CT | C | 31 | a0001c0001t0001g0195a0001c0001t0003g0063a0001c0001t0003g0064others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.22+18003delA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764198 | ||||||
| chr17:78764283
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0194 | 2 | HG02257.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.22+17919C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764283 | ||||||
| chr17:78764328
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.22+17874G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764328 | ||||||
| chr17:78764342
|
G | A | 1 | a0001c0001t0002g0286 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.22+17860C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764342 | ||||||
| chr17:78764422
|
G | A | 3 | a0001c0001t0007g0209a0001c0001t0007g0210a0001c0001t0007g0211 | 3 | HG01106.hp1 HG01109.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.22+17780C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764422 | ||||||
| chr17:78764453
|
G | A | 1 | a0001c0001t0026g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.22+17749C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764453 | ||||||
| chr17:78764689
|
G | A | 1 | a0001c0001t0014g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.22+17513C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764689 | ||||||
| chr17:78764837
|
G | T | 1 | a0001c0001t0001g0195 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.22+17365C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764837 | ||||||
| chr17:78764859
|
G | A | 41 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0005g0001others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.22+17343C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764859 | ||||||
| chr17:78764920
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.22+17282G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78764920 | ||||||
| chr17:78765009
|
T | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22+17193A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765009 | ||||||
| chr17:78765042
|
G | A | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+17160C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765042 | ||||||
| chr17:78765160
|
G | A | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+17042C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765160 | ||||||
| chr17:78765230
|
G | A | 1 | a0001c0002t0010g0360 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.22+16972C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765230 | ||||||
| chr17:78765428
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.22+16774A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765428 | ||||||
| chr17:78765456
|
T | C | 32 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.22+16746A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765456 | ||||||
| chr17:78765574
|
A | G | 1 | a0001c0001t0006g0328 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.22+16628T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765574 | ||||||
| chr17:78765634
|
G | T | 1 | a0001c0001t0004g0061 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.22+16568C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765634 | ||||||
| chr17:78765711
|
G | T | 1 | a0001c0001t0001g0195 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.22+16491C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765711 | ||||||
| chr17:78765957
|
G | A | 113 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.22+16245C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78765957 | ||||||
| chr17:78766015
|
G | C | 21 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0059others(18): Show | 21 | HG00408.hp1 HG00544.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.22+16187C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766015 | ||||||
| chr17:78766024
|
G | A | 1 | a0001c0001t0002g0287 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.22+16178C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766024 | ||||||
| chr17:78766087
|
G | GA | 95 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0098others(92): Show | 95 | HG00558.hp1 HG00673.hp1 HG01106.hp2 others(92): Show |
intron_variant | MODIFIER | c.22+16114dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766087 | ||||||
| chr17:78766087
|
G | GAA | 34 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0003g0076others(31): Show | 34 | HG00423.hp2 HG01070.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.22+16113_22+16114d others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766087 | ||||||
| chr17:78766087
|
G | GAAA | 102 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.22+16112_22+16114d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766087 | ||||||
| chr17:78766087
|
G | GAAAA | 14 | a0001c0001t0002g0014a0001c0001t0002g0245a0001c0001t0002g0252others(11): Show | 14 | HG00735.hp2 HG01175.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.22+16111_22+16114d others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766087 | ||||||
| chr17:78766299
|
T | A | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+15903A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766299 | ||||||
| chr17:78766559
|
T | A | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.22+15643A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766559 | ||||||
| chr17:78766679
|
C | T | 1 | a0001c0001t0016g0348 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.22+15523G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766679 | ||||||
| chr17:78766761
|
A | C | 1 | a0001c0001t0002g0314 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.22+15441T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766761 | ||||||
| chr17:78766779
|
A | C | 13 | a0001c0001t0005g0049a0001c0001t0009g0003a0001c0001t0009g0047others(10): Show | 13 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.22+15423T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766779 | ||||||
| chr17:78766867
|
G | C | 1 | a0001c0001t0002g0290 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.22+15335C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766867 | ||||||
| chr17:78766985
|
A | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0147a0001c0001t0001g0151 | 3 | HG02922.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.22+15217T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78766985 | ||||||
| chr17:78767231
|
T | C | 46 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0003g0237others(43): Show | 46 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(43): Show |
intron_variant | MODIFIER | c.22+14971A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767231 | ||||||
| chr17:78767283
|
C | T | 1 | a0001c0001t0004g0180 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.22+14919G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767283 | ||||||
| chr17:78767458
|
A | G | 1 | a0001c0001t0005g0021 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.22+14744T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767458 | ||||||
| chr17:78767532
|
CGGATGAA others(13): Show |
C | 6 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0004g0227others(3): Show | 6 | HG02523.hp2 NA18612.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+14650_22+14669d others(22): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767532 | ||||||
| chr17:78767596
|
C | T | 2 | a0001c0001t0002g0265a0001c0001t0002g0266 | 2 | HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.22+14606G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767596 | ||||||
| chr17:78767736
|
G | A | 1 | a0001c0001t0005g0038 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.22+14466C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767736 | ||||||
| chr17:78767738
|
G | T | 1 | a0001c0001t0002g0271 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.22+14464C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78767738 | ||||||
| chr17:78768023
|
C | T | 2 | a0001c0001t0013g0353a0001c0001t0013g0354 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.22+14179G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78768023 | ||||||
| chr17:78768028
|
C | T | 1 | a0001c0001t0002g0316 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.22+14174G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78768028 | ||||||
| chr17:78768063
|
T | C | 219 | a0001c0001t0001g0025a0001c0001t0001g0092a0001c0001t0001g0100others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.22+14139A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78768063 | ||||||
| chr17:78768472
|
C | T | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+13730G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78768472 | ||||||
| chr17:78768687
|
C | T | 1 | a0001c0001t0006g0338 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.22+13515G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78768687 | ||||||
| chr17:78769007
|
G | A | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+13195C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769007 | ||||||
| chr17:78769053
|
C | G | 1 | a0001c0001t0026g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.22+13149G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769053 | ||||||
| chr17:78769145
|
CA | C | 184 | a0001c0001t0001g0025a0001c0001t0001g0100a0001c0001t0001g0101others(181): Show | 184 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.22+13056delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769145 | ||||||
| chr17:78769589
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22+12613G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769589 | ||||||
| chr17:78769738
|
C | T | 13 | a0001c0001t0002g0263a0001c0001t0002g0265a0001c0001t0002g0266others(10): Show | 13 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.22+12464G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769738 | ||||||
| chr17:78769836
|
G | C | 2 | a0001c0001t0003g0355a0001c0001t0003g0356 | 2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.22+12366C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769836 | ||||||
| chr17:78769889
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22+12313A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769889 | ||||||
| chr17:78769901
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+12301G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769901 | ||||||
| chr17:78769994
|
A | G | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+12208T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78769994 | ||||||
| chr17:78770197
|
G | T | 1 | a0001c0001t0008g0264 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.22+12005C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770197 | ||||||
| chr17:78770248
|
G | A | 1 | a0001c0001t0003g0091 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.22+11954C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770248 | ||||||
| chr17:78770272
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0139a0001c0001t0001g0146 | 3 | HG00408.hp1 NA18984.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.22+11930C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770272 | ||||||
| chr17:78770287
|
C | T | 10 | a0001c0001t0003g0352a0001c0001t0003g0363a0001c0001t0003g0364others(7): Show | 10 | HG02109.hp1 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.22+11915G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770287 | ||||||
| chr17:78770301
|
C | A | 1 | a0001c0002t0010g0357 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.22+11901G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770301 | ||||||
| chr17:78770325
|
C | CA | 70 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0058others(67): Show | 70 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.22+11876dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770325 | ||||||
| chr17:78770355
|
GA | G | 179 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0100others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.22+11846delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770355 | ||||||
| chr17:78770361
|
A | G | 1 | a0001c0001t0016g0348 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.22+11841T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770361 | ||||||
| chr17:78770372
|
A | G | 1 | a0001c0001t0005g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.22+11830T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770372 | ||||||
| chr17:78770405
|
T | G | 3 | a0001c0001t0005g0017a0001c0001t0006g0337a0001c0001t0006g0349 | 3 | HG01069.hp1 HG01071.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.22+11797A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770405 | ||||||
| chr17:78770541
|
C | T | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+11661G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770541 | ||||||
| chr17:78770546
|
G | A | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+11656C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770546 | ||||||
| chr17:78770547
|
T | G | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+11655A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770547 | ||||||
| chr17:78770660
|
G | A | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.22+11542C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770660 | ||||||
| chr17:78770691
|
C | T | 4 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0069others(1): Show | 4 | NA18971.hp1 NA18981.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+11511G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770691 | ||||||
| chr17:78770800
|
C | T | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.22+11402G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770800 | ||||||
| chr17:78770817
|
C | G | 1 | a0001c0001t0002g0306 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.22+11385G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770817 | ||||||
| chr17:78770930
|
C | A | 9 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(6): Show | 9 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+11272G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770930 | ||||||
| chr17:78770931
|
C | A | 9 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(6): Show | 9 | HG00639.hp1 HG01243.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+11271G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78770931 | ||||||
| chr17:78771069
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02083.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.22+11133G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771069 | ||||||
| chr17:78771080
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+11122A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771080 | ||||||
| chr17:78771089
|
C | T | 1 | a0001c0001t0004g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+11113G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771089 | ||||||
| chr17:78771161
|
G | C | 31 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0005g0001others(28): Show | 31 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(28): Show |
intron_variant | MODIFIER | c.22+11041C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771161 | ||||||
| chr17:78771162
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.22+11040G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771162 | ||||||
| chr17:78771499
|
G | A | 5 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+10703C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771499 | ||||||
| chr17:78771506
|
G | A | 1 | a0001c0001t0008g0291 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.22+10696C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771506 | ||||||
| chr17:78771662
|
T | G | 2 | a0001c0001t0012g0120a0001c0001t0012g0121 | 2 | HG01261.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.22+10540A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771662 | ||||||
| chr17:78771698
|
T | C | 1 | a0001c0001t0003g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.22+10504A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771698 | ||||||
| chr17:78771721
|
T | C | 215 | a0001c0001t0001g0025a0001c0001t0001g0283a0001c0001t0002g0011others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.22+10481A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771721 | ||||||
| chr17:78771729
|
TA | T | 13 | a0001c0001t0001g0117a0001c0001t0001g0148a0001c0001t0002g0247others(10): Show | 13 | HG00323.hp2 HG01099.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.22+10472delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771729 | ||||||
| chr17:78771909
|
T | C | 91 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.22+10293A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78771909 | ||||||
| chr17:78772187
|
AGAG | A | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+10012_22+10014d others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772187 | ||||||
| chr17:78772248
|
G | A | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+9954C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772248 | ||||||
| chr17:78772496
|
G | A | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | NA18984.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.22+9706C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772496 | ||||||
| chr17:78772519
|
A | G | 1 | a0001c0001t0002g0262 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.22+9683T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772519 | ||||||
| chr17:78772601
|
G | A | 9 | a0001c0001t0005g0049a0001c0001t0009g0047a0001c0001t0009g0051others(6): Show | 9 | HG02723.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+9601C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772601 | ||||||
| chr17:78772607
|
G | A | 30 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0005g0001others(27): Show | 30 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(27): Show |
intron_variant | MODIFIER | c.22+9595C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772607 | ||||||
| chr17:78772741
|
T | G | 1 | a0001c0001t0005g0039 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.22+9461A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772741 | ||||||
| chr17:78772751
|
T | A | 2 | a0001c0001t0006g0337a0001c0001t0006g0349 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.22+9451A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772751 | ||||||
| chr17:78772758
|
G | A | 1 | a0001c0001t0014g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.22+9444C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772758 | ||||||
| chr17:78772760
|
T | A | 4 | a0001c0001t0004g0061a0001c0001t0004g0198a0001c0001t0004g0202others(1): Show | 4 | NA18954.hp1 NA18960.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+9442A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772760 | ||||||
| chr17:78772806
|
G | T | 1 | a0001c0001t0002g0261 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.22+9396C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772806 | ||||||
| chr17:78772933
|
G | A | 1 | a0001c0001t0015g0326 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.22+9269C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772933 | ||||||
| chr17:78772991
|
G | A | 1 | a0001c0001t0018g0190 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.22+9211C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78772991 | ||||||
| chr17:78773045
|
C | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.22+9157G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773045 | ||||||
| chr17:78773053
|
G | A | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+9149C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773053 | ||||||
| chr17:78773098
|
G | C | 1 | a0001c0001t0001g0146 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.22+9104C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773098 | ||||||
| chr17:78773143
|
C | T | 11 | a0001c0001t0001g0025a0001c0001t0005g0017a0001c0001t0005g0019others(8): Show | 11 | HG02080.hp2 HG02135.hp1 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+9059G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773143 | ||||||
| chr17:78773167
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.22+9035T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773167 | ||||||
| chr17:78773194
|
G | T | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+9008C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773194 | ||||||
| chr17:78773352
|
A | G | 225 | a0001c0001t0001g0025a0001c0001t0001g0100a0001c0001t0001g0101others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.22+8850T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773352 | ||||||
| chr17:78773405
|
G | A | 11 | a0001c0001t0006g0328a0001c0001t0006g0338a0001c0001t0006g0339others(8): Show | 11 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(8): Show |
intron_variant | MODIFIER | c.22+8797C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773405 | ||||||
| chr17:78773419
|
C | T | 1 | a0001c0001t0004g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.22+8783G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773419 | ||||||
| chr17:78773488
|
G | C | 52 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0102others(49): Show | 52 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.22+8714C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773488 | ||||||
| chr17:78773514
|
C | CA | 44 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0005g0001others(41): Show | 44 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(41): Show |
intron_variant | MODIFIER | c.22+8687_22+8688ins others(1): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773514 | ||||||
| chr17:78773523
|
G | A | 216 | a0001c0001t0001g0025a0001c0001t0001g0100a0001c0001t0001g0101others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.22+8679C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773523 | ||||||
| chr17:78773535
|
A | C | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.22+8667T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773535 | ||||||
| chr17:78773578
|
G | A | 1 | a0001c0001t0002g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.22+8624C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773578 | ||||||
| chr17:78773628
|
C | CA | 47 | a0001c0001t0001g0025a0001c0001t0001g0178a0001c0001t0001g0179others(44): Show | 47 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(44): Show |
intron_variant | MODIFIER | c.22+8573dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773628 | ||||||
| chr17:78773628
|
CA | C | 15 | a0001c0001t0001g0059a0001c0001t0002g0301a0001c0001t0003g0085others(12): Show | 15 | HG00099.hp2 HG00597.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.22+8573delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773628 | ||||||
| chr17:78773702
|
A | C | 31 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0005g0001others(28): Show | 31 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(28): Show |
intron_variant | MODIFIER | c.22+8500T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773702 | ||||||
| chr17:78773784
|
C | T | 1 | a0001c0001t0003g0083 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.22+8418G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773784 | ||||||
| chr17:78773979
|
T | G | 9 | a0001c0001t0002g0249a0001c0001t0002g0253a0001c0001t0002g0292others(6): Show | 9 | HG00621.hp1 NA18944.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+8223A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773979 | ||||||
| chr17:78773981
|
T | G | 1 | a0001c0001t0003g0081 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.22+8221A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78773981 | ||||||
| chr17:78774063
|
T | TA | 47 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0003g0237others(44): Show | 47 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(44): Show |
intron_variant | MODIFIER | c.22+8138dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774063 | ||||||
| chr17:78774065
|
A | T | 1 | a0001c0001t0002g0324 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.22+8137T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774065 | ||||||
| chr17:78774084
|
T | C | 1 | a0001c0001t0026g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.22+8118A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774084 | ||||||
| chr17:78774133
|
T | C | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+8069A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774133 | ||||||
| chr17:78774156
|
T | C | 1 | a0001c0001t0004g0180 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.22+8046A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774156 | ||||||
| chr17:78774213
|
T | C | 1 | a0001c0001t0002g0325 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.22+7989A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774213 | ||||||
| chr17:78774327
|
T | C | 1 | a0001c0001t0002g0299 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.22+7875A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774327 | ||||||
| chr17:78774334
|
C | A | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.22+7868G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774334 | ||||||
| chr17:78774466
|
T | C | 1 | a0001c0001t0002g0300 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.22+7736A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774466 | ||||||
| chr17:78774593
|
T | C | 6 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+7609A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774593 | ||||||
| chr17:78774599
|
T | C | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+7603A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774599 | ||||||
| chr17:78774640
|
G | T | 1 | a0001c0001t0004g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22+7562C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774640 | ||||||
| chr17:78774664
|
G | A | 40 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0002g0249others(37): Show | 40 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(37): Show |
intron_variant | MODIFIER | c.22+7538C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774664 | ||||||
| chr17:78774708
|
G | A | 1 | a0001c0001t0004g0009 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.22+7494C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774708 | ||||||
| chr17:78774713
|
A | T | 1 | a0001c0001t0002g0324 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.22+7489T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774713 | ||||||
| chr17:78774727
|
C | G | 1 | a0001c0001t0003g0091 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.22+7475G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774727 | ||||||
| chr17:78774892
|
A | G | 1 | a0001c0001t0005g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.22+7310T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774892 | ||||||
| chr17:78774927
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.22+7275G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774927 | ||||||
| chr17:78774938
|
A | C | 1 | a0001c0001t0002g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.22+7264T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774938 | ||||||
| chr17:78774999
|
C | T | 1 | a0001c0001t0004g0122 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.22+7203G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78774999 | ||||||
| chr17:78775136
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.22+7066A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775136 | ||||||
| chr17:78775231
|
T | C | 1 | a0001c0001t0003g0082 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.22+6971A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775231 | ||||||
| chr17:78775234
|
G | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0003t0017g0016 | 3 | HG03486.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.22+6968C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775234 | ||||||
| chr17:78775435
|
T | C | 1 | a0001c0001t0014g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.22+6767A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775435 | ||||||
| chr17:78775798
|
A | G | 1 | a0001c0001t0002g0315 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.22+6404T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775798 | ||||||
| chr17:78775841
|
T | C | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+6361A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775841 | ||||||
| chr17:78775957
|
T | C | 217 | a0001c0001t0001g0025a0001c0001t0001g0100a0001c0001t0001g0101others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.22+6245A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78775957 | ||||||
| chr17:78776091
|
G | A | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01106.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.22+6111C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776091 | ||||||
| chr17:78776206
|
C | T | 138 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.22+5996G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776206 | ||||||
| chr17:78776427
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+5775G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776427 | ||||||
| chr17:78776428
|
G | A | 4 | a0001c0001t0009g0047a0001c0001t0009g0052a0001c0001t0009g0054others(1): Show | 4 | HG02723.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+5774C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776428 | ||||||
| chr17:78776433
|
G | C | 2 | a0001c0001t0002g0258a0001c0001t0002g0301 | 2 | NA18994.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.22+5769C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776433 | ||||||
| chr17:78776483
|
C | A | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+5719G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776483 | ||||||
| chr17:78776658
|
C | CA | 7 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0189others(4): Show | 7 | HG02965.hp1 HG03098.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.22+5543dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776658 | ||||||
| chr17:78776658
|
C | CAAAA | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+5540_22+5543dup others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776658 | ||||||
| chr17:78776658
|
CA | C | 118 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0109others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.22+5543delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776658 | ||||||
| chr17:78776781
|
TTGTC | T | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+5417_22+5420del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776781 | ||||||
| chr17:78776813
|
GT | G | 7 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0195others(4): Show | 7 | HG00323.hp2 HG01069.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.22+5388delA | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776813 | ||||||
| chr17:78776826
|
T | A | 2 | a0001c0001t0002g0305a0001c0001t0003g0351 | 2 | HG03098.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.22+5376A>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776826 | ||||||
| chr17:78776827
|
A | T | 50 | a0001c0001t0001g0025a0001c0001t0001g0100a0001c0001t0001g0101others(47): Show | 50 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(47): Show |
intron_variant | MODIFIER | c.22+5375T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776827 | ||||||
| chr17:78776828
|
A | T | 40 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0005g0001others(37): Show | 40 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(37): Show |
intron_variant | MODIFIER | c.22+5374T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776828 | ||||||
| chr17:78776829
|
A | T | 1 | a0001c0001t0014g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.22+5373T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776829 | ||||||
| chr17:78776962
|
G | A | 25 | a0001c0001t0003g0351a0001c0001t0003g0352a0001c0001t0003g0355others(22): Show | 25 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.22+5240C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776962 | ||||||
| chr17:78776984
|
G | A | 6 | a0001c0001t0002g0248a0001c0001t0002g0306a0001c0001t0002g0307others(3): Show | 6 | HG00408.hp2 HG02027.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+5218C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78776984 | ||||||
| chr17:78777109
|
G | C | 41 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0005g0001others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.22+5093C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777109 | ||||||
| chr17:78777186
|
G | GAGGCCA | 46 | a0001c0001t0001g0025a0001c0001t0001g0100a0001c0001t0001g0101others(43): Show | 46 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(43): Show |
intron_variant | MODIFIER | c.22+5015_22+5016ins others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777186 | ||||||
| chr17:78777379
|
C | T | 2 | a0001c0001t0012g0120a0001c0001t0012g0121 | 2 | HG01261.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.22+4823G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777379 | ||||||
| chr17:78777556
|
T | C | 139 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.22+4646A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777556 | ||||||
| chr17:78777609
|
T | C | 1 | a0001c0001t0015g0041 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.22+4593A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777609 | ||||||
| chr17:78777827
|
A | G | 1 | a0001c0001t0002g0324 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.22+4375T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777827 | ||||||
| chr17:78777830
|
C | CA | 21 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0109others(18): Show | 21 | HG01175.hp1 HG02056.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.22+4371dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777830 | ||||||
| chr17:78777830
|
C | CAA | 13 | a0001c0001t0003g0352a0001c0001t0003g0355a0001c0001t0003g0356others(10): Show | 13 | HG01123.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.22+4370_22+4371dup others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777830 | ||||||
| chr17:78777845
|
A | G | 1 | a0001c0001t0009g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.22+4357T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777845 | ||||||
| chr17:78777894
|
C | T | 1 | a0001c0001t0005g0046 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.22+4308G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777894 | ||||||
| chr17:78777935
|
G | A | 5 | a0001c0001t0001g0092a0001c0001t0009g0003a0001c0001t0009g0055others(2): Show | 5 | HG01074.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+4267C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78777935 | ||||||
| chr17:78778221
|
A | G | 1 | a0001c0002t0010g0357 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.22+3981T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778221 | ||||||
| chr17:78778297
|
C | CA | 14 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0191others(11): Show | 14 | HG01069.hp2 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.22+3904dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778297 | ||||||
| chr17:78778317
|
AAAAG | A | 83 | a0001c0001t0001g0283a0001c0001t0002g0012a0001c0001t0002g0013others(80): Show | 83 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.22+3881_22+3884del others(4): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778317 | ||||||
| chr17:78778318
|
AAAG | A | 54 | a0001c0001t0002g0011a0001c0001t0002g0313a0001c0001t0003g0064others(51): Show | 54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.22+3881_22+3883del others(3): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778318 | ||||||
| chr17:78778319
|
AAG | A | 64 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0003g0063others(61): Show | 64 | HG00423.hp2 HG00673.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.22+3881_22+3882del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778319 | ||||||
| chr17:78778320
|
AG | A | 23 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(20): Show | 23 | HG00323.hp2 HG00639.hp1 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.22+3881delC | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778320 | ||||||
| chr17:78778321
|
G | A | 148 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(145): Show | 148 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.22+3881C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778321 | ||||||
| chr17:78778323
|
G | A | 1 | a0001c0001t0003g0085 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.22+3879C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778323 | ||||||
| chr17:78778347
|
T | G | 1 | a0001c0001t0003g0085 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.22+3855A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778347 | ||||||
| chr17:78778363
|
C | T | 29 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0065others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+3839G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778363 | ||||||
| chr17:78778431
|
A | G | 1 | a0001c0001t0015g0326 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.22+3771T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778431 | ||||||
| chr17:78778494
|
C | A | 5 | a0001c0001t0003g0351a0001c0002t0010g0357a0001c0002t0010g0358others(2): Show | 5 | HG02109.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+3708G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778494 | ||||||
| chr17:78778545
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.22+3657C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778545 | ||||||
| chr17:78778637
|
C | CA | 43 | a0001c0001t0001g0025a0001c0001t0001g0199a0001c0001t0001g0200others(40): Show | 43 | HG02135.hp1 HG02723.hp1 HG02895.hp2 others(40): Show |
intron_variant | MODIFIER | c.22+3564dupT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778637 | ||||||
| chr17:78778637
|
CA | C | 128 | a0001c0001t0001g0093a0001c0001t0001g0106a0001c0001t0001g0111others(125): Show | 128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.22+3564delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778637 | ||||||
| chr17:78778637
|
CAA | C | 9 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0251others(6): Show | 9 | HG00099.hp1 HG01943.hp2 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+3563_22+3564del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778637 | ||||||
| chr17:78778676
|
A | C | 5 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 5 | HG02145.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+3526T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778676 | ||||||
| chr17:78778772
|
A | T | 43 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0003g0237others(40): Show | 43 | HG00673.hp1 HG01106.hp2 HG02080.hp2 others(40): Show |
intron_variant | MODIFIER | c.22+3430T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778772 | ||||||
| chr17:78778904
|
C | G | 1 | a0001c0001t0005g0042 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.22+3298G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78778904 | ||||||
| chr17:78779110
|
A | G | 1 | a0001c0001t0002g0255 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.22+3092T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78779110 | ||||||
| chr17:78779400
|
CA | C | 111 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0058others(108): Show | 111 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.22+2801delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78779400 | ||||||
| chr17:78779400
|
CAA | C | 109 | a0001c0001t0001g0059a0001c0001t0001g0093a0001c0001t0001g0094others(106): Show | 109 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.22+2800_22+2801del others(2): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78779400 | ||||||
| chr17:78779400
|
CAAA | C | 112 | a0001c0001t0001g0025a0001c0001t0001g0092a0001c0001t0002g0020others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.22+2799_22+2801del others(3): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78779400 | ||||||
| chr17:78779495
|
A | T | 375 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(372): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.22+2707T>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78779495 | ||||||
| chr17:78779591
|
G | T | 210 | a0001c0001t0001g0025a0001c0001t0001g0283a0001c0001t0002g0011others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.22+2611C>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78779591 | ||||||
| chr17:78780326
|
A | C | 1 | a0001c0001t0002g0249 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.22+1876T>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780326 | ||||||
| chr17:78780587
|
T | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | NA18945.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.22+1615A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780587 | ||||||
| chr17:78780793
|
G | C | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+1409C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780793 | ||||||
| chr17:78780835
|
T | C | 215 | a0001c0001t0001g0025a0001c0001t0001g0283a0001c0001t0002g0011others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.22+1367A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780835 | ||||||
| chr17:78780858
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.22+1344A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780858 | ||||||
| chr17:78780931
|
A | G | 74 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0003g0063others(71): Show | 74 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.22+1271T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780931 | ||||||
| chr17:78780941
|
C | G | 1 | a0001c0001t0001g0058 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.22+1261G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78780941 | ||||||
| chr17:78781061
|
T | G | 1 | a0001c0001t0004g0241 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.22+1141A>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781061 | ||||||
| chr17:78781112
|
T | C | 1 | a0001c0001t0011g0242 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.22+1090A>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781112 | ||||||
| chr17:78781170
|
TA | T | 9 | a0001c0001t0001g0059a0001c0001t0002g0247a0001c0001t0002g0248others(6): Show | 9 | HG00099.hp2 HG01069.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+1031delT | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781170 | ||||||
| chr17:78781181
|
A | AAAAAAG | 15 | a0001c0001t0005g0046a0001c0001t0005g0049a0001c0001t0009g0003others(12): Show | 15 | HG02647.hp2 HG02723.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.22+1015_22+1020dup others(6): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781181 | ||||||
| chr17:78781181
|
A | AAAAAG | 30 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0005g0001others(27): Show | 30 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(27): Show |
intron_variant | MODIFIER | c.22+1020_22+1021ins others(5): Show |
CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781181 | ||||||
| chr17:78781405
|
C | T | 89 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.22+797G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781405 | ||||||
| chr17:78781420
|
C | G | 5 | a0001c0001t0002g0011a0001c0001t0002g0243a0001c0001t0002g0244others(2): Show | 5 | NA18940.hp2 NA18945.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+782G>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781420 | ||||||
| chr17:78781433
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.22+769G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781433 | ||||||
| chr17:78781448
|
C | T | 45 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0005g0001others(42): Show | 45 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(42): Show |
intron_variant | MODIFIER | c.22+754G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781448 | ||||||
| chr17:78781492
|
C | T | 89 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.22+710G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781492 | ||||||
| chr17:78781505
|
G | A | 41 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0005g0001others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.22+697C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781505 | ||||||
| chr17:78781507
|
G | A | 1 | a0001c0001t0003g0369 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.22+695C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781507 | ||||||
| chr17:78781511
|
C | T | 5 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+691G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781511 | ||||||
| chr17:78781530
|
G | C | 5 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+672C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781530 | ||||||
| chr17:78781609
|
C | T | 1 | a0001c0003t0017g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.22+593G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781609 | ||||||
| chr17:78781612
|
C | A | 113 | a0001c0001t0001g0283a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.22+590G>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781612 | ||||||
| chr17:78781614
|
C | T | 1 | a0001c0001t0003g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.22+588G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781614 | ||||||
| chr17:78781693
|
G | A | 1 | a0001c0001t0002g0015 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.22+509C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781693 | ||||||
| chr17:78781756
|
G | A | 25 | a0001c0001t0003g0351a0001c0001t0003g0352a0001c0001t0003g0355others(22): Show | 25 | HG01123.hp2 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.22+446C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781756 | ||||||
| chr17:78781957
|
A | G | 41 | a0001c0001t0001g0025a0001c0001t0002g0020a0001c0001t0005g0001others(38): Show | 41 | HG00673.hp1 HG02080.hp2 HG02135.hp1 others(38): Show |
intron_variant | MODIFIER | c.22+245T>C | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781957 | ||||||
| chr17:78781995
|
C | T | 1 | a0001c0001t0002g0015 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.22+207G>A | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78781995 | ||||||
| chr17:78782028
|
A | AC | 14 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(11): Show | 14 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.22+173dupG | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78782028 | ||||||
| chr17:78782057
|
G | C | 3 | a0001c0001t0004g0375a0001c0001t0004g0377a0001c0001t0024g0376 | 3 | HG02559.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.22+145C>G | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78782057 | ||||||
| chr17:78782186
|
G | A | 1 | a0001c0001t0003g0378 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.22+16C>T | CYTH1 | ENSG00000108669.18 | transcript | ENST00000446868.8 | protein_coding | 1/13 | chr17 | 78782186 |