| geneid | 55125 |
|---|---|
| ensemblid | ENSG00000101639.19 |
| hgncid | 25515 |
| symbol | CEP192 |
| name | centrosomal protein 192 |
| refseq_nuc | NM_032142.4 |
| refseq_prot | NP_115518.3 |
| ensembl_nuc | ENST00000506447.5 |
| ensembl_prot | ENSP00000427550.1 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 12991362 |
| end | 13125036 |
| strand | + |
| ver | v1.2 |
| region | chr18:12991362-13125036 |
| region5000 | chr18:12986362-13130036 |
| regionname0 | CEP192_chr18_12991362_13125036 |
| regionname5000 | CEP192_chr18_12986362_13130036 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000 | 0/0 | 0 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0001 | 0/0 | 2537 | 73 | 6 | 6 | 50 | 1 | 10 | 38 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0002 | 0/0 | 2537 | 71 | 10 | 17 | 32 | 5 | 7 | 22 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0003 | 1/1 | 2537 | 63 | 3 | 17 | 23 | 4 | 14 | 17 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0004 | 0/0 | 2537 | 50 | 0 | 2 | 44 | 0 | 4 | 36 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0005 | 0/0 | 2537 | 47 | 21 | 4 | 15 | 2 | 5 | 12 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0006 | 0/0 | 2537 | 12 | 10 | 0 | 0 | 1 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0007 | 0/0 | 2536 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0008 | 0/0 | 2537 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0009 | 0/0 | 2537 | 7 | 1 | 0 | 6 | 0 | 0 | 5 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0010 | 0/0 | 2537 | 7 | 0 | 7 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0011 | 0/0 | 2537 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0012 | 0/0 | 2537 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0013 | 0/0 | 2537 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0014 | 0/0 | 2537 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0015 | 0/0 | 2537 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0016 | 0/0 | 2537 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0017 | 0/0 | 2537 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0018 | 0/0 | 2537 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0019 | 0/0 | 2537 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0020 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0021 | 0/0 | 2537 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0022 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0023 | 0/0 | 2537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0024 | 0/0 | 2537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0025 | 0/0 | 2537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0026 | 0/0 | 2537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0027 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0028 | 0/0 | 2537 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0029 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0030 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0031 | 0/0 | 2537 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0032 | 0/0 | 2537 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0033 | 0/0 | 2537 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0034 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0035 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0036 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 7614 | 69 | 10 | 16 | 31 | 5 | 7 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0002 | 0/0 | 7614 | 68 | 5 | 6 | 47 | 1 | 9 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0003 | 1/1 | 7614 | 63 | 3 | 17 | 23 | 4 | 14 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0004 | 0/0 | 7614 | 50 | 0 | 2 | 44 | 0 | 4 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0005 | 0/0 | 7614 | 47 | 21 | 4 | 15 | 2 | 5 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0006 | 0/0 | 7614 | 12 | 10 | 0 | 0 | 1 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0007 | 0/0 | 7611 | 10 | 9 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0008 | 0/0 | 7614 | 8 | 8 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0009 | 0/0 | 7614 | 7 | 1 | 0 | 6 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0010 | 0/0 | 7614 | 7 | 0 | 7 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0011 | 0/0 | 7614 | 5 | 3 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0012 | 0/0 | 7614 | 3 | 3 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0013 | 0/0 | 7614 | 3 | 3 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0014 | 0/0 | 7614 | 3 | 0 | 0 | 3 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0015 | 0/0 | 7614 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0016 | 0/0 | 7614 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0017 | 0/0 | 7614 | 2 | 1 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0018 | 0/0 | 7614 | 2 | 0 | 0 | 0 | 2 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0019 | 0/0 | 7614 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0020 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0021 | 0/0 | 7614 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0022 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0023 | 0/0 | 7614 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0024 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0025 | 0/0 | 7614 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0026 | 0/0 | 7614 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0027 | 0/0 | 7614 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0028 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0029 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0030 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0031 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0032 | 0/0 | 7614 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0033 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0034 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0035 | 0/0 | 7614 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0036 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0037 | 0/0 | 7614 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0038 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0039 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0040 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0041 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0042 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0043 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0044 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0045 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| c0046 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 347 | 286 | 62 | 35 | 151 | 10 | 28 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| t0002 | 1/1 | 347 | 101 | 29 | 25 | 25 | 6 | 14 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| t0003 | 0/0 | 347 | 3 | 3 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| t0004 | 0/0 | 347 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| t0005 | 0/0 | 347 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| 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 | 5 | 0 | 0 | 5 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0009 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0019 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0035 | 0/0 | 7614 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0001c0002 | 0/0 | 7614 | 68 | 5 | 6 | 47 | 1 | 9 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0001c0033 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0001c0034 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0001c0037 | 0/0 | 7614 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0001c0041 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0001c0045 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0002c0001 | 0/0 | 7614 | 69 | 10 | 16 | 31 | 5 | 7 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0002c0022 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0002c0023 | 0/0 | 7614 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0003c0003 | 1/1 | 7614 | 63 | 3 | 17 | 23 | 4 | 14 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0004c0004 | 0/0 | 7614 | 50 | 0 | 2 | 44 | 0 | 4 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0005c0005 | 0/0 | 7614 | 47 | 21 | 4 | 15 | 2 | 5 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0006c0006 | 0/0 | 7614 | 12 | 10 | 0 | 0 | 1 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0007c0007 | 0/0 | 7611 | 10 | 9 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0008c0008 | 0/0 | 7614 | 8 | 8 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0009c0009 | 0/0 | 7614 | 7 | 1 | 0 | 6 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0010c0010 | 0/0 | 7614 | 7 | 0 | 7 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0011c0011 | 0/0 | 7614 | 5 | 3 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0012c0013 | 0/0 | 7614 | 3 | 3 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0012c0040 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0013c0016 | 0/0 | 7614 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0013c0029 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0014c0014 | 0/0 | 7614 | 3 | 0 | 0 | 3 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0015c0012 | 0/0 | 7614 | 3 | 3 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0016c0015 | 0/0 | 7614 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0017c0018 | 0/0 | 7614 | 2 | 0 | 0 | 0 | 2 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0018c0017 | 0/0 | 7614 | 2 | 1 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0019c0019 | 0/0 | 7614 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0020c0046 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0021c0030 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0022c0028 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0023c0027 | 0/0 | 7614 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0024c0026 | 0/0 | 7614 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0025c0021 | 0/0 | 7614 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0026c0025 | 0/0 | 7614 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0027c0024 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0028c0042 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0029c0036 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0030c0039 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0031c0038 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0032c0032 | 0/0 | 7614 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0033c0043 | 0/0 | 7614 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0034c0031 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0035c0044 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0036c0020 | 0/0 | 7614 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0035t0001 | 0/0 | 7960 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0001c0002t0001 | 0/0 | 7960 | 68 | 5 | 6 | 47 | 1 | 9 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0001c0033t0001 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0001c0034t0001 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0001c0037t0001 | 0/0 | 7960 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0001c0041t0001 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0001c0045t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0002c0001t0001 | 0/0 | 7960 | 69 | 10 | 16 | 31 | 5 | 7 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0002c0022t0001 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0002c0023t0001 | 0/0 | 7960 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0003c0003t0002 | 1/1 | 7960 | 62 | 3 | 17 | 22 | 4 | 14 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0003c0003t0005 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0004c0004t0001 | 0/0 | 7960 | 49 | 0 | 2 | 43 | 0 | 4 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0004c0004t0004 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0005c0005t0001 | 0/0 | 7960 | 47 | 21 | 4 | 15 | 2 | 5 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0006c0006t0001 | 0/0 | 7960 | 2 | 0 | 0 | 0 | 1 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0006c0006t0002 | 0/0 | 7960 | 10 | 10 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0007c0007t0002 | 0/0 | 7957 | 10 | 9 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0008c0008t0001 | 0/0 | 7960 | 8 | 8 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0009c0009t0001 | 0/0 | 7960 | 7 | 1 | 0 | 6 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0010c0010t0002 | 0/0 | 7960 | 7 | 0 | 7 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0011c0011t0001 | 0/0 | 7960 | 5 | 3 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0012c0013t0002 | 0/0 | 7960 | 3 | 3 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0012c0040t0002 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0013c0016t0003 | 0/0 | 7960 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0013c0029t0003 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0014c0014t0001 | 0/0 | 7960 | 3 | 0 | 0 | 3 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0015c0012t0001 | 0/0 | 7960 | 3 | 3 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0016c0015t0002 | 0/0 | 7960 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0017c0018t0002 | 0/0 | 7960 | 2 | 0 | 0 | 0 | 2 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0018c0017t0002 | 0/0 | 7960 | 2 | 1 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0019c0019t0001 | 0/0 | 7960 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0020c0046t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0021c0030t0001 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0022c0028t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0023c0027t0001 | 0/0 | 7960 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0024c0026t0001 | 0/0 | 7960 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0025c0021t0001 | 0/0 | 7960 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0026c0025t0001 | 0/0 | 7960 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0027c0024t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0028c0042t0002 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0029c0036t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0030c0039t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0031c0038t0002 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0032c0032t0001 | 0/0 | 7960 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0033c0043t0001 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0034c0031t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0035c0044t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| a0036c0020t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | copy fasta | chr18 | 12986362 | 13130036 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0035t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0033t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0034t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0037t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0041t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0001c0045t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0019 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0022t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0002c0023t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0003c0003t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0004c0004t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0005c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0006c0006t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0006c0006t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0006c0006t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0006c0006t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0006c0006t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0006c0006t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0006c0006t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0006c0006t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0006c0006t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0006c0006t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0006c0006t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0006c0006t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0007c0007t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0007c0007t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0007c0007t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0007c0007t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0007c0007t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0007c0007t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0007c0007t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0007c0007t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0007c0007t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0008c0008t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0008c0008t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0008c0008t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0008c0008t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0008c0008t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0008c0008t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0008c0008t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0008c0008t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0009c0009t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0009c0009t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0009c0009t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0009c0009t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0010c0010t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0010c0010t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0010c0010t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0010c0010t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0010c0010t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0010c0010t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0010c0010t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0011c0011t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0011c0011t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0011c0011t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0011c0011t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0011c0011t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0012c0013t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0012c0013t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0012c0013t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0012c0040t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0013c0016t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0013c0016t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0013c0029t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0014c0014t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0014c0014t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0015c0012t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0015c0012t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0015c0012t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0016c0015t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0016c0015t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0017c0018t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0017c0018t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0018c0017t0002g0009 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0019c0019t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0019c0019t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0020c0046t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0021c0030t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0022c0028t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0023c0027t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0024c0026t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0025c0021t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0026c0025t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0027c0024t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0028c0042t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0029c0036t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0030c0039t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0031c0038t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0032c0032t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0033c0043t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0034c0031t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0035c0044t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| a0036c0020t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0002 | g0090 | EUR | GBR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00099 | hp2 | a0005 | c0005 | t0001 | g0137 | EUR | GBR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00140 | hp1 | a0002 | c0001 | t0001 | g0301 | EUR | GBR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00140 | hp2 | a0003 | c0003 | t0002 | g0103 | EUR | GBR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0282 | EUR | FIN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00280 | hp2 | a0003 | c0003 | t0002 | g0058 | EUR | FIN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00323 | hp1 | a0003 | c0003 | t0002 | g0057 | EUR | FIN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00323 | hp2 | a0002 | c0001 | t0001 | g0345 | EUR | FIN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00408 | hp2 | a0004 | c0004 | t0001 | g0118 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00423 | hp1 | a0004 | c0004 | t0001 | g0204 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0335 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00438 | hp1 | a0004 | c0004 | t0001 | g0120 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00438 | hp2 | a0002 | c0001 | t0001 | g0349 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0304 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00558 | hp1 | a0003 | c0003 | t0002 | g0075 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00558 | hp2 | a0004 | c0004 | t0004 | g0177 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00597 | hp1 | a0005 | c0005 | t0001 | g0285 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00597 | hp2 | a0003 | c0003 | t0002 | g0074 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00609 | hp1 | a0004 | c0004 | t0001 | g0186 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0305 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00621 | hp1 | a0004 | c0004 | t0001 | g0200 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00621 | hp2 | a0009 | c0009 | t0001 | g0003 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00639 | hp1 | a0002 | c0023 | t0001 | g0296 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00639 | hp2 | a0003 | c0003 | t0002 | g0060 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00642 | hp1 | a0002 | c0001 | t0001 | g0021 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00642 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0327 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00735 | hp1 | a0002 | c0001 | t0001 | g0286 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00735 | hp2 | a0003 | c0003 | t0002 | g0054 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00738 | hp1 | a0026 | c0025 | t0001 | g0300 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00738 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0298 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG00741 | hp2 | a0003 | c0003 | t0002 | g0111 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01069 | hp1 | a0002 | c0001 | t0001 | g0293 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01069 | hp2 | a0003 | c0003 | t0002 | g0007 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01071 | hp1 | a0003 | c0003 | t0002 | g0007 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01071 | hp2 | a0005 | c0005 | t0001 | g0116 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01074 | hp1 | a0002 | c0001 | t0001 | g0021 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01074 | hp2 | a0003 | c0003 | t0002 | g0066 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0291 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01081 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0354 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01099 | hp2 | a0005 | c0005 | t0001 | g0135 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01109 | hp1 | a0024 | c0026 | t0001 | g0299 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01109 | hp2 | a0025 | c0021 | t0001 | g0348 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01167 | hp1 | a0005 | c0005 | t0001 | g0125 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01167 | hp2 | a0011 | c0011 | t0001 | g0284 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01168 | hp1 | a0010 | c0010 | t0002 | g0112 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01169 | hp1 | a0011 | c0011 | t0001 | g0283 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01169 | hp2 | a0010 | c0010 | t0002 | g0113 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01192 | hp1 | a0023 | c0027 | t0001 | g0344 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0267 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01255 | hp1 | a0005 | c0005 | t0001 | g0128 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01255 | hp2 | a0003 | c0003 | t0002 | g0101 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01256 | hp1 | a0003 | c0003 | t0002 | g0010 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01256 | hp2 | a0002 | c0001 | t0001 | g0309 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01258 | hp1 | a0003 | c0003 | t0002 | g0010 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01258 | hp2 | a0010 | c0010 | t0002 | g0104 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01261 | hp1 | a0002 | c0001 | t0001 | g0022 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01261 | hp2 | a0003 | c0003 | t0002 | g0061 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01361 | hp1 | a0002 | c0001 | t0001 | g0310 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01361 | hp2 | a0004 | c0004 | t0001 | g0181 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01496 | hp1 | a0003 | c0003 | t0002 | g0073 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01496 | hp2 | a0002 | c0001 | t0001 | g0295 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01515 | hp1 | a0006 | c0006 | t0001 | g0358 | EUR | IBS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01515 | hp2 | a0017 | c0018 | t0002 | g0092 | EUR | IBS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01516 | hp1 | a0005 | c0005 | t0001 | g0148 | EUR | IBS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01516 | hp2 | a0002 | c0001 | t0001 | g0020 | EUR | IBS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01517 | hp1 | a0017 | c0018 | t0002 | g0062 | EUR | IBS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01517 | hp2 | a0002 | c0001 | t0001 | g0020 | EUR | IBS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01884 | hp1 | a0005 | c0005 | t0001 | g0163 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01884 | hp2 | a0005 | c0005 | t0001 | g0159 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01891 | hp1 | a0008 | c0008 | t0001 | g0133 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01891 | hp2 | a0006 | c0006 | t0002 | g0042 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01928 | hp1 | a0002 | c0001 | t0001 | g0316 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01928 | hp2 | a0010 | c0010 | t0002 | g0079 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01952 | hp1 | a0003 | c0003 | t0002 | g0072 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01952 | hp2 | a0007 | c0007 | t0002 | g0026 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0056 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0318 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01981 | hp1 | a0010 | c0010 | t0002 | g0081 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01981 | hp2 | a0004 | c0004 | t0001 | g0175 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0328 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG01993 | hp2 | a0010 | c0010 | t0002 | g0080 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02004 | hp2 | a0010 | c0010 | t0002 | g0048 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02015 | hp1 | a0005 | c0005 | t0001 | g0127 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0347 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02056 | hp2 | a0002 | c0001 | t0001 | g0329 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02071 | hp1 | a0005 | c0005 | t0001 | g0015 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02071 | hp2 | a0002 | c0001 | t0001 | g0303 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02074 | hp1 | a0003 | c0003 | t0002 | g0050 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02074 | hp2 | a0002 | c0001 | t0001 | g0314 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02080 | hp1 | a0018 | c0017 | t0002 | g0009 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02083 | hp2 | a0003 | c0003 | t0002 | g0065 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02129 | hp1 | a0003 | c0003 | t0002 | g0045 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02132 | hp1 | a0033 | c0043 | t0001 | g0141 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02145 | hp1 | a0012 | c0040 | t0002 | g0105 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02145 | hp2 | a0008 | c0008 | t0001 | g0169 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02257 | hp1 | a0018 | c0017 | t0002 | g0009 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02257 | hp2 | a0006 | c0006 | t0002 | g0025 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02258 | hp1 | a0006 | c0006 | t0002 | g0037 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02258 | hp2 | a0013 | c0029 | t0003 | g0215 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0274 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02273 | hp2 | a0002 | c0001 | t0001 | g0022 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02280 | hp1 | a0006 | c0006 | t0002 | g0044 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02280 | hp2 | a0003 | c0003 | t0002 | g0086 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0276 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02293 | hp2 | a0002 | c0001 | t0001 | g0323 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02300 | hp1 | a0003 | c0003 | t0002 | g0099 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02451 | hp1 | a0005 | c0005 | t0001 | g0134 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0330 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02572 | hp1 | a0001 | c0045 | t0001 | g0269 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02572 | hp2 | a0008 | c0008 | t0001 | g0130 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02615 | hp1 | a0015 | c0012 | t0001 | g0011 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02615 | hp2 | a0007 | c0007 | t0002 | g0029 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02622 | hp1 | a0034 | c0031 | t0001 | g0011 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02622 | hp2 | a0007 | c0007 | t0002 | g0024 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02630 | hp1 | a0008 | c0008 | t0001 | g0129 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02630 | hp2 | a0005 | c0005 | t0001 | g0123 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02647 | hp1 | a0006 | c0006 | t0002 | g0038 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02647 | hp2 | a0005 | c0005 | t0001 | g0146 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0236 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02683 | hp2 | a0003 | c0003 | t0002 | g0059 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02698 | hp1 | a0002 | c0001 | t0001 | g0297 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02698 | hp2 | a0003 | c0003 | t0002 | g0083 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02717 | hp1 | a0030 | c0039 | t0001 | g0152 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02717 | hp2 | a0008 | c0008 | t0001 | g0132 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02723 | hp1 | a0006 | c0006 | t0002 | g0036 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02723 | hp2 | a0011 | c0011 | t0001 | g0289 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0336 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02735 | hp2 | a0003 | c0003 | t0002 | g0087 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0280 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02738 | hp2 | a0003 | c0003 | t0002 | g0106 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02818 | hp1 | a0007 | c0007 | t0002 | g0006 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02818 | hp2 | a0005 | c0005 | t0001 | g0164 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02886 | hp1 | a0005 | c0005 | t0001 | g0158 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02886 | hp2 | a0008 | c0008 | t0001 | g0147 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02895 | hp1 | a0016 | c0015 | t0002 | g0041 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02896 | hp1 | a0015 | c0012 | t0001 | g0115 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02896 | hp2 | a0007 | c0007 | t0002 | g0031 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02897 | hp1 | a0015 | c0012 | t0001 | g0114 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02897 | hp2 | a0016 | c0015 | t0002 | g0040 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02922 | hp1 | a0007 | c0007 | t0002 | g0028 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02922 | hp2 | a0020 | c0046 | t0001 | g0287 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02965 | hp1 | a0012 | c0013 | t0002 | g0084 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02965 | hp2 | a0006 | c0006 | t0002 | g0034 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02976 | hp1 | a0002 | c0001 | t0001 | g0342 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02976 | hp2 | a0019 | c0019 | t0001 | g0166 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03041 | hp1 | a0002 | c0001 | t0001 | g0339 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03041 | hp2 | a0013 | c0016 | t0003 | g0216 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03098 | hp1 | a0005 | c0005 | t0001 | g0154 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03098 | hp2 | a0012 | c0013 | t0002 | g0109 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03130 | hp1 | a0005 | c0005 | t0001 | g0162 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03130 | hp2 | a0007 | c0007 | t0002 | g0023 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03139 | hp1 | a0035 | c0044 | t0001 | g0165 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03139 | hp2 | a0006 | c0006 | t0002 | g0035 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03195 | hp1 | a0005 | c0005 | t0001 | g0153 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03195 | hp2 | a0002 | c0001 | t0001 | g0338 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03209 | hp1 | a0008 | c0008 | t0001 | g0131 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03209 | hp2 | a0002 | c0001 | t0001 | g0361 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03225 | hp1 | a0007 | c0007 | t0002 | g0030 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03225 | hp2 | a0002 | c0001 | t0001 | g0340 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03239 | hp1 | a0005 | c0005 | t0001 | g0139 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03239 | hp2 | a0006 | c0006 | t0001 | g0356 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03453 | hp1 | a0013 | c0016 | t0003 | g0217 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03453 | hp2 | a0011 | c0011 | t0001 | g0290 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03486 | hp1 | a0006 | c0006 | t0002 | g0039 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03486 | hp2 | a0005 | c0005 | t0001 | g0151 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03491 | hp1 | a0002 | c0001 | t0001 | g0292 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03491 | hp2 | a0001 | c0037 | t0001 | g0223 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03492 | hp1 | a0003 | c0003 | t0002 | g0052 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03492 | hp2 | a0002 | c0001 | t0001 | g0294 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03516 | hp1 | a0002 | c0001 | t0001 | g0360 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03516 | hp2 | a0008 | c0008 | t0001 | g0168 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03540 | hp1 | a0005 | c0005 | t0001 | g0160 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03540 | hp2 | a0005 | c0005 | t0001 | g0124 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03579 | hp1 | a0002 | c0001 | t0001 | g0019 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0341 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03654 | hp1 | a0005 | c0005 | t0001 | g0117 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03654 | hp2 | a0000 | c0035 | t0001 | g0264 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03669 | hp1 | a0005 | c0005 | t0001 | g0142 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03669 | hp2 | a0003 | c0003 | t0002 | g0088 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03688 | hp1 | a0003 | c0003 | t0002 | g0076 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0249 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03704 | hp1 | a0004 | c0004 | t0001 | g0206 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03704 | hp2 | a0005 | c0005 | t0001 | g0161 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0346 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03710 | hp2 | a0004 | c0004 | t0001 | g0180 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03831 | hp1 | a0003 | c0003 | t0002 | g0098 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03834 | hp1 | a0005 | c0005 | t0001 | g0136 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0254 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03927 | hp2 | a0003 | c0003 | t0002 | g0077 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03942 | hp1 | a0003 | c0003 | t0002 | g0055 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0281 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG04184 | hp1 | a0003 | c0003 | t0002 | g0096 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0261 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG04199 | hp1 | a0004 | c0004 | t0001 | g0174 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG04199 | hp2 | a0003 | c0003 | t0002 | g0053 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG04204 | hp1 | a0003 | c0003 | t0002 | g0063 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG04204 | hp2 | a0002 | c0001 | t0001 | g0313 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0302 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG04228 | hp2 | a0003 | c0003 | t0002 | g0082 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18522 | hp1 | a0009 | c0009 | t0001 | g0220 | AFR | YRI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | YRI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18612 | hp1 | a0003 | c0003 | t0002 | g0094 | EAS | CHB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18612 | hp2 | a0004 | c0004 | t0001 | g0190 | EAS | CHB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | CHB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18747 | hp2 | a0004 | c0004 | t0001 | g0209 | EAS | CHB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18906 | hp1 | a0012 | c0013 | t0002 | g0097 | AFR | YRI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18906 | hp2 | a0007 | c0007 | t0002 | g0006 | AFR | YRI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18940 | hp2 | a0002 | c0001 | t0001 | g0351 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18941 | hp1 | a0005 | c0005 | t0001 | g0140 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18941 | hp2 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18942 | hp1 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18944 | hp1 | a0014 | c0014 | t0001 | g0012 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18944 | hp2 | a0003 | c0003 | t0002 | g0069 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18945 | hp2 | a0002 | c0001 | t0001 | g0312 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18946 | hp2 | a0003 | c0003 | t0002 | g0047 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18947 | hp1 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18947 | hp2 | a0028 | c0042 | t0002 | g0107 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18949 | hp1 | a0004 | c0004 | t0001 | g0205 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18949 | hp2 | a0002 | c0022 | t0001 | g0307 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18950 | hp1 | a0001 | c0041 | t0001 | g0240 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18950 | hp2 | a0002 | c0001 | t0001 | g0311 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18954 | hp1 | a0009 | c0009 | t0001 | g0218 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0334 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18956 | hp2 | a0005 | c0005 | t0001 | g0171 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18959 | hp2 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18961 | hp1 | a0004 | c0004 | t0001 | g0203 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18962 | hp1 | a0003 | c0003 | t0002 | g0078 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18963 | hp1 | a0004 | c0004 | t0001 | g0192 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18964 | hp1 | a0004 | c0004 | t0001 | g0183 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18964 | hp2 | a0003 | c0003 | t0002 | g0064 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18965 | hp1 | a0004 | c0004 | t0001 | g0188 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18965 | hp2 | a0002 | c0001 | t0001 | g0333 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18966 | hp1 | a0005 | c0005 | t0001 | g0013 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18966 | hp2 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18967 | hp1 | a0003 | c0003 | t0002 | g0091 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18968 | hp1 | a0004 | c0004 | t0001 | g0202 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18968 | hp2 | a0003 | c0003 | t0005 | g0100 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18969 | hp1 | a0003 | c0003 | t0002 | g0067 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18969 | hp2 | a0002 | c0001 | t0001 | g0326 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18970 | hp1 | a0009 | c0009 | t0001 | g0003 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18971 | hp1 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18974 | hp1 | a0004 | c0004 | t0001 | g0178 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18975 | hp1 | a0004 | c0004 | t0001 | g0197 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18977 | hp1 | a0021 | c0030 | t0001 | g0176 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18977 | hp2 | a0005 | c0005 | t0001 | g0170 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18979 | hp1 | a0002 | c0001 | t0001 | g0350 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18979 | hp2 | a0031 | c0038 | t0002 | g0070 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18980 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18981 | hp1 | a0001 | c0033 | t0001 | g0211 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18981 | hp2 | a0004 | c0004 | t0001 | g0182 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18982 | hp1 | a0005 | c0005 | t0001 | g0145 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18982 | hp2 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18983 | hp1 | a0014 | c0014 | t0001 | g0013 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18983 | hp2 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18984 | hp2 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18985 | hp2 | a0014 | c0014 | t0001 | g0012 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18986 | hp1 | a0002 | c0001 | t0001 | g0319 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18989 | hp1 | a0004 | c0004 | t0001 | g0185 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18990 | hp1 | a0003 | c0003 | t0002 | g0102 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0331 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18992 | hp1 | a0002 | c0001 | t0001 | g0322 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18993 | hp2 | a0004 | c0004 | t0001 | g0194 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0325 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18998 | hp2 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19000 | hp1 | a0004 | c0004 | t0001 | g0198 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19001 | hp2 | a0004 | c0004 | t0001 | g0191 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19002 | hp1 | a0002 | c0001 | t0001 | g0315 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19002 | hp2 | a0009 | c0009 | t0001 | g0003 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19003 | hp1 | a0003 | c0003 | t0002 | g0046 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19004 | hp1 | a0002 | c0001 | t0001 | g0324 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19004 | hp2 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19005 | hp1 | a0004 | c0004 | t0001 | g0193 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19005 | hp2 | a0005 | c0005 | t0001 | g0126 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19006 | hp1 | a0003 | c0003 | t0002 | g0108 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19006 | hp2 | a0004 | c0004 | t0001 | g0184 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19007 | hp1 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0306 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19009 | hp1 | a0004 | c0004 | t0001 | g0187 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19009 | hp2 | a0001 | c0034 | t0001 | g0246 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19010 | hp2 | a0002 | c0001 | t0001 | g0353 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19030 | hp1 | a0005 | c0005 | t0001 | g0172 | AFR | LWK | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19030 | hp2 | a0027 | c0024 | t0001 | g0359 | AFR | LWK | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19043 | hp1 | a0005 | c0005 | t0001 | g0157 | AFR | LWK | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19043 | hp2 | a0002 | c0001 | t0001 | g0343 | AFR | LWK | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19055 | hp1 | a0005 | c0005 | t0001 | g0143 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19056 | hp2 | a0004 | c0004 | t0001 | g0199 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19057 | hp1 | a0003 | c0003 | t0002 | g0071 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19057 | hp2 | a0004 | c0004 | t0001 | g0196 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19058 | hp1 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19058 | hp2 | a0002 | c0001 | t0001 | g0308 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19060 | hp1 | a0002 | c0001 | t0001 | g0320 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19060 | hp2 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19064 | hp1 | a0005 | c0005 | t0001 | g0121 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19064 | hp2 | a0003 | c0003 | t0002 | g0093 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19065 | hp1 | a0004 | c0004 | t0001 | g0179 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19065 | hp2 | a0005 | c0005 | t0001 | g0015 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19067 | hp2 | a0005 | c0005 | t0001 | g0208 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19074 | hp1 | a0003 | c0003 | t0002 | g0068 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19076 | hp2 | a0002 | c0001 | t0001 | g0332 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19078 | hp2 | a0004 | c0004 | t0001 | g0201 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19079 | hp1 | a0002 | c0001 | t0001 | g0352 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19082 | hp1 | a0004 | c0004 | t0001 | g0195 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19084 | hp1 | a0005 | c0005 | t0001 | g0144 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19084 | hp2 | a0003 | c0003 | t0002 | g0095 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19085 | hp2 | a0005 | c0005 | t0001 | g0138 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19087 | hp1 | a0002 | c0001 | t0001 | g0321 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19087 | hp2 | a0003 | c0003 | t0002 | g0110 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19088 | hp1 | a0004 | c0004 | t0001 | g0189 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19088 | hp2 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19090 | hp1 | a0009 | c0009 | t0001 | g0003 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0337 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19240 | hp1 | a0005 | c0005 | t0001 | g0155 | AFR | YRI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA19240 | hp2 | a0011 | c0011 | t0001 | g0288 | AFR | YRI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA20129 | hp1 | a0005 | c0005 | t0001 | g0156 | AFR | ASW | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA20129 | hp2 | a0003 | c0003 | t0002 | g0049 | AFR | ASW | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA20805 | hp1 | a0032 | c0032 | t0001 | g0119 | EUR | TSI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0019 | EUR | TSI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA20905 | hp1 | a0004 | c0004 | t0001 | g0207 | SAS | GIH | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0245 | SAS | GIH | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02109 | hp1 | a0005 | c0005 | t0001 | g0149 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02109 | hp2 | a0002 | c0001 | t0001 | g0317 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02486 | hp2 | a0007 | c0007 | t0002 | g0027 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0263 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG02559 | hp2 | a0019 | c0019 | t0001 | g0167 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03471 | hp1 | a0036 | c0020 | t0001 | g0355 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG03471 | hp2 | a0005 | c0005 | t0001 | g0122 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG06807 | hp1 | a0005 | c0005 | t0001 | g0150 | AFR | USA | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| HG06807 | hp2 | a0006 | c0006 | t0002 | g0043 | AFR | USA | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18955 | hp1 | a0009 | c0009 | t0001 | g0219 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA20300 | hp1 | a0005 | c0005 | t0001 | g0173 | AFR | USA | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA20300 | hp2 | a0003 | c0003 | t0002 | g0089 | AFR | USA | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA21309 | hp1 | a0022 | c0028 | t0001 | g0357 | AFR | LWK | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| NA21309 | hp2 | a0029 | c0036 | t0001 | g0214 | AFR | LWK | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0002 | g0085 | REF | REF | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0002 | g0051 | REF | REF | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:13001459
|
A | G | 1 | a0020 | 1 | HG02922.hp2 | missense_variant&splice_region_variant | MODERATE | c.167A>G | p.Tyr56Cys | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/45 | 247/7960 | 167/7614 | 56/2537 | chr18 | 13001459 | ||
| chr18:13001491
|
G | A | 1 | a0036 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.199G>A | p.Gly67Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/45 | 279/7960 | 199/7614 | 67/2537 | chr18 | 13001491 | ||
| chr18:13001513
|
G | C | 17 | a0002a0004a0006others(14): Show | 169 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
missense_variant | MODERATE | c.221G>C | p.Gly74Ala | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/45 | 301/7960 | 221/7614 | 74/2537 | chr18 | 13001513 | ||
| chr18:13001524
|
G | A | 9 | a0002a0011a0020others(6): Show | 83 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
missense_variant | MODERATE | c.232G>A | p.Gly78Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/45 | 312/7960 | 232/7614 | 78/2537 | chr18 | 13001524 | ||
| chr18:13008498
|
G | C | 1 | a0010 | 7 | HG01168.hp1 HG01169.hp2 HG01258.hp2 others(4): Show |
missense_variant | MODERATE | c.333G>C | p.Leu111Phe | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/45 | 413/7960 | 333/7614 | 111/2537 | chr18 | 13008498 | ||
| chr18:13008578
|
C | G | 1 | a0009 | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
missense_variant | MODERATE | c.413C>G | p.Ser138Cys | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/45 | 493/7960 | 413/7614 | 138/2537 | chr18 | 13008578 | ||
| chr18:13015328
|
A | C | 2 | a0019a0035 | 3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
missense_variant&splice_region_variant | MODERATE | c.520A>C | p.Ile174Leu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/45 | 600/7960 | 520/7614 | 174/2537 | chr18 | 13015328 | ||
| chr18:13015367
|
A | G | 1 | a0023 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.559A>G | p.Thr187Ala | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/45 | 639/7960 | 559/7614 | 187/2537 | chr18 | 13015367 | ||
| chr18:13018510
|
T | C | 2 | a0015a0034 | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.820T>C | p.Phe274Leu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/45 | 900/7960 | 820/7614 | 274/2537 | chr18 | 13018510 | ||
| chr18:13042248
|
A | G | 2 | a0014a0033 | 4 | HG02132.hp1 NA18944.hp1 NA18983.hp1 others(1): Show |
missense_variant | MODERATE | c.1981A>G | p.Ile661Val | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/45 | 2061/7960 | 1981/7614 | 661/2537 | chr18 | 13042248 | ||
| chr18:13049151
|
A | G | 1 | a0032 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.2360A>G | p.Lys787Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 16/45 | 2440/7960 | 2360/7614 | 787/2537 | chr18 | 13049151 | ||
| chr18:13049280
|
C | T | 1 | a0032 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.2489C>T | p.Thr830Ile | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 16/45 | 2569/7960 | 2489/7614 | 830/2537 | chr18 | 13049280 | ||
| chr18:13049812
|
GAGC | G | 1 | a0007 | 10 | HG01952.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
conservative_inframe_deletion | MODERATE | c.2941_2943delCAG | p.Gln981del | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/45 | 3021/7960 | 2941/7614 | 981/2537 | INFO_REALIGN_3_PRIME | chr18 | 13049812 | |
| chr18:13049816
|
A | G | 1 | a0007 | 10 | HG01952.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
missense_variant | MODERATE | c.2942A>G | p.Gln981Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/45 | 3022/7960 | 2942/7614 | 981/2537 | chr18 | 13049816 | ||
| chr18:13053032
|
C | T | 1 | a0028 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.3131C>T | p.Ser1044Phe | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/45 | 3211/7960 | 3131/7614 | 1044/2537 | chr18 | 13053032 | ||
| chr18:13053058
|
A | G | 2 | a0011a0020 | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
missense_variant | MODERATE | c.3157A>G | p.Thr1053Ala | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/45 | 3237/7960 | 3157/7614 | 1053/2537 | chr18 | 13053058 | ||
| chr18:13055916
|
A | C | 1 | a0024 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.3326A>C | p.Gln1109Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3406/7960 | 3326/7614 | 1109/2537 | chr18 | 13055916 | ||
| chr18:13056066
|
C | G | 1 | a0013 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.3476C>G | p.Pro1159Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3556/7960 | 3476/7614 | 1159/2537 | chr18 | 13056066 | ||
| chr18:13056231
|
A | G | 1 | a0016 | 2 | HG02895.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.3641A>G | p.Gln1214Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3721/7960 | 3641/7614 | 1214/2537 | chr18 | 13056231 | ||
| chr18:13056362
|
G | A | 1 | a0034 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.3772G>A | p.Ala1258Thr | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3852/7960 | 3772/7614 | 1258/2537 | chr18 | 13056362 | ||
| chr18:13056561
|
G | C | 1 | a0019 | 2 | HG02559.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.3971G>C | p.Gly1324Ala | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 4051/7960 | 3971/7614 | 1324/2537 | chr18 | 13056561 | ||
| chr18:13056563
|
A | C | 1 | a0017 | 2 | HG01515.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.3973A>C | p.Thr1325Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 4053/7960 | 3973/7614 | 1325/2537 | chr18 | 13056563 | ||
| chr18:13056683
|
G | A | 4 | a0000a0001a0025others(1): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
missense_variant | MODERATE | c.4093G>A | p.Val1365Met | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 4173/7960 | 4093/7614 | 1365/2537 | chr18 | 13056683 | ||
| chr18:13057656
|
C | T | 1 | a0025 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.4180C>T | p.Leu1394Phe | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/45 | 4260/7960 | 4180/7614 | 1394/2537 | chr18 | 13057656 | ||
| chr18:13057699
|
T | G | 1 | a0033 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.4223T>G | p.Ile1408Ser | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/45 | 4303/7960 | 4223/7614 | 1408/2537 | chr18 | 13057699 | ||
| chr18:13059223
|
T | C | 1 | a0031 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.4399T>C | p.Cys1467Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/45 | 4479/7960 | 4399/7614 | 1467/2537 | chr18 | 13059223 | ||
| chr18:13068110
|
G | A | 3 | a0000a0001a0025 | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
missense_variant | MODERATE | c.4631G>A | p.Arg1544His | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 23/45 | 4711/7960 | 4631/7614 | 1544/2537 | chr18 | 13068110 | ||
| chr18:13068133
|
T | C | 29 | a0000a0001a0002others(26): Show | 304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
missense_variant | MODERATE | c.4654T>C | p.Ser1552Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 23/45 | 4734/7960 | 4654/7614 | 1552/2537 | chr18 | 13068133 | ||
| chr18:13068235
|
C | G | 1 | a0016 | 2 | HG02895.hp1 HG02897.hp2 |
missense_variant&splice_region_variant | MODERATE | c.4756C>G | p.Gln1586Glu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 23/45 | 4836/7960 | 4756/7614 | 1586/2537 | chr18 | 13068235 | ||
| chr18:13069132
|
A | G | 1 | a0018 | 2 | HG02080.hp1 HG02257.hp1 |
missense_variant | MODERATE | c.5006A>G | p.His1669Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 26/45 | 5086/7960 | 5006/7614 | 1669/2537 | chr18 | 13069132 | ||
| chr18:13069783
|
C | T | 30 | a0000a0001a0002others(27): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
missense_variant | MODERATE | c.5101C>T | p.Leu1701Phe | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/45 | 5181/7960 | 5101/7614 | 1701/2537 | chr18 | 13069783 | ||
| chr18:13071110
|
C | T | 1 | a0026 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.5246C>T | p.Ser1749Leu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/45 | 5326/7960 | 5246/7614 | 1749/2537 | chr18 | 13071110 | ||
| chr18:13087048
|
A | G | 1 | a0008 | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
missense_variant | MODERATE | c.5648A>G | p.Asn1883Ser | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 31/45 | 5728/7960 | 5648/7614 | 1883/2537 | chr18 | 13087048 | ||
| chr18:13089457
|
G | T | 1 | a0022 | 1 | NA21309.hp1 | missense_variant&splice_region_variant | MODERATE | c.5995G>T | p.Ala1999Ser | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/45 | 6075/7960 | 5995/7614 | 1999/2537 | chr18 | 13089457 | ||
| chr18:13092425
|
G | A | 2 | a0004a0021 | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
missense_variant | MODERATE | c.6152G>A | p.Ser2051Asn | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/45 | 6232/7960 | 6152/7614 | 2051/2537 | chr18 | 13092425 | ||
| chr18:13095592
|
G | A | 4 | a0000a0001a0025others(1): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
missense_variant | MODERATE | c.6344G>A | p.Arg2115Gln | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/45 | 6424/7960 | 6344/7614 | 2115/2537 | chr18 | 13095592 | ||
| chr18:13095610
|
T | C | 30 | a0000a0001a0002others(27): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
missense_variant | MODERATE | c.6362T>C | p.Leu2121Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/45 | 6442/7960 | 6362/7614 | 2121/2537 | chr18 | 13095610 | ||
| chr18:13095627
|
G | A | 1 | a0021 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.6379G>A | p.Glu2127Lys | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/45 | 6459/7960 | 6379/7614 | 2127/2537 | chr18 | 13095627 | ||
| chr18:13095655
|
A | G | 2 | a0015a0034 | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.6407A>G | p.His2136Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/45 | 6487/7960 | 6407/7614 | 2136/2537 | chr18 | 13095655 | ||
| chr18:13100327
|
G | A | 1 | a0010 | 7 | HG01168.hp1 HG01169.hp2 HG01258.hp2 others(4): Show |
missense_variant | MODERATE | c.6686G>A | p.Arg2229Gln | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/45 | 6766/7960 | 6686/7614 | 2229/2537 | chr18 | 13100327 | ||
| chr18:13100452
|
A | G | 2 | a0004a0021 | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
missense_variant | MODERATE | c.6811A>G | p.Lys2271Glu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/45 | 6891/7960 | 6811/7614 | 2271/2537 | chr18 | 13100452 | ||
| chr18:13105006
|
T | G | 1 | a0030 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.6974T>G | p.Val2325Gly | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/45 | 7054/7960 | 6974/7614 | 2325/2537 | chr18 | 13105006 | ||
| chr18:13105034
|
A | T | 1 | a0027 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.7002A>T | p.Arg2334Ser | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/45 | 7082/7960 | 7002/7614 | 2334/2537 | chr18 | 13105034 | ||
| chr18:13116433
|
G | T | 31 | a0000a0001a0002others(28): Show | 316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
missense_variant | MODERATE | c.7346G>T | p.Arg2449Leu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/45 | 7426/7960 | 7346/7614 | 2449/2537 | chr18 | 13116433 | ||
| chr18:13124770
|
A | T | 1 | a0000 | 1 | HG03654.hp2 | stop_lost | HIGH | c.7614A>T | p.Ter2538Tyrext*? | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 45/45 | 7694/7960 | 7614/7614 | 2538/2537 | chr18 | 13124770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:13008564
|
C | T | 1 | a0001c0045 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.399C>T | p.Ala133Ala | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/45 | 479/7960 | 399/7614 | 133/2537 | chr18 | 13008564 | ||
| chr18:13019206
|
T | C | 3 | a0015c0012a0032c0032a0034c0031 | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.1050T>C | p.Ser350Ser | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/45 | 1130/7960 | 1050/7614 | 350/2537 | chr18 | 13019206 | ||
| chr18:13038432
|
A | G | 2 | a0004c0004a0021c0030 | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
synonymous_variant | LOW | c.1662A>G | p.Thr554Thr | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/45 | 1742/7960 | 1662/7614 | 554/2537 | chr18 | 13038432 | ||
| chr18:13040859
|
A | G | 2 | a0013c0016a0013c0029 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.1839A>G | p.Pro613Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/45 | 1919/7960 | 1839/7614 | 613/2537 | chr18 | 13040859 | ||
| chr18:13055830
|
C | T | 1 | a0001c0041 | 1 | NA18950.hp1 | synonymous_variant | LOW | c.3240C>T | p.Ala1080Ala | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3320/7960 | 3240/7614 | 1080/2537 | chr18 | 13055830 | ||
| chr18:13056082
|
G | C | 1 | a0001c0033 | 1 | NA18981.hp1 | synonymous_variant | LOW | c.3492G>C | p.Pro1164Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3572/7960 | 3492/7614 | 1164/2537 | chr18 | 13056082 | ||
| chr18:13056334
|
C | T | 10 | a0002c0001a0002c0022a0002c0023others(7): Show | 82 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
synonymous_variant | LOW | c.3744C>T | p.His1248His | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3824/7960 | 3744/7614 | 1248/2537 | chr18 | 13056334 | ||
| chr18:13059096
|
A | G | 1 | a0001c0037 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.4272A>G | p.Thr1424Thr | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/45 | 4352/7960 | 4272/7614 | 1424/2537 | chr18 | 13059096 | ||
| chr18:13059174
|
A | G | 1 | a0009c0009 | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
synonymous_variant | LOW | c.4350A>G | p.Pro1450Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/45 | 4430/7960 | 4350/7614 | 1450/2537 | chr18 | 13059174 | ||
| chr18:13067906
|
T | C | 2 | a0019c0019a0035c0044 | 3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.4564T>C | p.Leu1522Leu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 22/45 | 4644/7960 | 4564/7614 | 1522/2537 | chr18 | 13067906 | ||
| chr18:13068192
|
C | A | 1 | a0013c0016 | 2 | HG03041.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.4713C>A | p.Gly1571Gly | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 23/45 | 4793/7960 | 4713/7614 | 1571/2537 | chr18 | 13068192 | ||
| chr18:13092480
|
C | T | 1 | a0012c0040 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.6207C>T | p.Ser2069Ser | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/45 | 6287/7960 | 6207/7614 | 2069/2537 | chr18 | 13092480 | ||
| chr18:13099554
|
C | A | 1 | a0002c0022 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.6636C>A | p.Ile2212Ile | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/45 | 6716/7960 | 6636/7614 | 2212/2537 | chr18 | 13099554 | ||
| chr18:13113654
|
T | A | 1 | a0001c0034 | 1 | NA19009.hp2 | synonymous_variant | LOW | c.7116T>A | p.Pro2372Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/45 | 7196/7960 | 7116/7614 | 2372/2537 | chr18 | 13113654 | ||
| chr18:13117641
|
G | A | 1 | a0002c0023 | 1 | HG00639.hp1 | splice_region_variant&synonymous_variant | LOW | c.7473G>A | p.Leu2491Leu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/45 | 7553/7960 | 7473/7614 | 2491/2537 | chr18 | 13117641 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:12991377
|
C | T | 1 | a0003c0003t0005 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-65C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/45 | 8048 | chr18 | 12991377 | |||||
| chr18:12991394
|
T | C | 37 | a0000c0035t0001a0001c0002t0001a0001c0033t0001others(34): Show | 290 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(287): Show |
5_prime_UTR_variant | MODIFIER | c.-48T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/45 | 8031 | chr18 | 12991394 | |||||
| chr18:13124935
|
T | C | 1 | a0004c0004t0004 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*165T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 45/45 | 165 | chr18 | 13124935 | |||||
| chr18:13125021
|
A | G | 2 | a0013c0016t0003a0013c0029t0003 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*251A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 45/45 | 251 | chr18 | 13125021 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:12991522
|
C | T | 83 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(80): Show | 87 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-5+85C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991522 | ||||||
| chr18:12991526
|
G | A | 10 | a0006c0006t0002g0025a0007c0007t0002g0006a0007c0007t0002g0023others(7): Show | 11 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-5+89G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991526 | ||||||
| chr18:12991554
|
G | T | 6 | a0007c0007t0002g0006a0007c0007t0002g0027a0007c0007t0002g0028others(3): Show | 7 | HG02486.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+117G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991554 | ||||||
| chr18:12991578
|
G | A | 2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-5+141G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991578 | ||||||
| chr18:12991618
|
G | T | 67 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(64): Show | 70 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-5+181G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991618 | ||||||
| chr18:12991632
|
C | A | 2 | a0011c0011t0001g0283a0011c0011t0001g0284 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-5+195C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991632 | ||||||
| chr18:12991845
|
T | C | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-5+408T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991845 | ||||||
| chr18:12991920
|
A | ATG | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-5+483_-5+484insTG | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991920 | ||||||
| chr18:12992163
|
C | T | 1 | a0001c0002t0001g0282 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-5+726C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992163 | ||||||
| chr18:12992173
|
T | TA | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+737dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chr18 | 12992173 | |||||
| chr18:12992220
|
A | T | 3 | a0006c0006t0002g0042a0006c0006t0002g0043a0006c0006t0002g0044 | 3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5+783A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992220 | ||||||
| chr18:12992262
|
C | G | 161 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(158): Show | 171 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.-5+825C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992262 | ||||||
| chr18:12992276
|
A | G | 1 | a0002c0001t0001g0361 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-5+839A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992276 | ||||||
| chr18:12992279
|
C | A | 2 | a0005c0005t0001g0116a0005c0005t0001g0117 | 2 | HG01071.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-5+842C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992279 | ||||||
| chr18:12992308
|
C | A | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-5+871C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992308 | ||||||
| chr18:12992314
|
G | A | 1 | a0004c0004t0001g0118 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-5+877G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992314 | ||||||
| chr18:12992403
|
T | C | 1 | a0001c0002t0001g0221 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-5+966T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992403 | ||||||
| chr18:12992524
|
T | C | 1 | a0032c0032t0001g0119 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5+1087T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992524 | ||||||
| chr18:12992551
|
G | T | 1 | a0004c0004t0001g0209 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-5+1114G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992551 | ||||||
| chr18:12992559
|
T | C | 2 | a0002c0001t0001g0019a0002c0001t0001g0286 | 3 | HG00735.hp1 HG03579.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-5+1122T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992559 | ||||||
| chr18:12992630
|
T | C | 1 | a0004c0004t0001g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-5+1193T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992630 | ||||||
| chr18:12992666
|
T | C | 1 | a0005c0005t0001g0121 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-5+1229T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992666 | ||||||
| chr18:12992830
|
T | A | 1 | a0001c0002t0001g0222 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-5+1393T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992830 | ||||||
| chr18:12992853
|
G | C | 4 | a0001c0002t0001g0210a0001c0002t0001g0212a0001c0002t0001g0213others(1): Show | 4 | HG02132.hp2 HG02486.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+1416G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992853 | ||||||
| chr18:12992904
|
A | G | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+1467A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992904 | ||||||
| chr18:12992978
|
A | G | 2 | a0005c0005t0001g0015a0005c0005t0001g0208 | 3 | HG02071.hp1 NA19065.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-5+1541A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992978 | ||||||
| chr18:12993158
|
G | T | 2 | a0004c0004t0001g0206a0004c0004t0001g0207 | 2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-5+1721G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993158 | ||||||
| chr18:12993196
|
A | C | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-5+1759A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993196 | ||||||
| chr18:12993249
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+1812G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993249 | ||||||
| chr18:12993357
|
G | A | 138 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(135): Show | 143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-5+1920G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993357 | ||||||
| chr18:12993382
|
A | G | 1 | a0001c0002t0001g0213 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-5+1945A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993382 | ||||||
| chr18:12993544
|
A | G | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-5+2107A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993544 | ||||||
| chr18:12993598
|
G | T | 30 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(27): Show | 40 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-5+2161G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993598 | ||||||
| chr18:12993606
|
C | T | 1 | a0005c0005t0001g0208 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-5+2169C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993606 | ||||||
| chr18:12993684
|
T | G | 1 | a0004c0004t0001g0183 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-5+2247T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993684 | ||||||
| chr18:12993710
|
C | T | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+2273C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993710 | ||||||
| chr18:12993748
|
CTCTT | C | 6 | a0011c0011t0001g0283a0011c0011t0001g0284a0011c0011t0001g0288others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+2314_-5+2317del others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chr18 | 12993748 | |||||
| chr18:12993760
|
C | T | 2 | a0010c0010t0002g0112a0010c0010t0002g0113 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-5+2323C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993760 | ||||||
| chr18:12993889
|
C | T | 1 | a0003c0003t0002g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-5+2452C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993889 | ||||||
| chr18:12993902
|
C | T | 1 | a0001c0002t0001g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-5+2465C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993902 | ||||||
| chr18:12994247
|
C | T | 1 | a0005c0005t0001g0173 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-5+2810C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994247 | ||||||
| chr18:12994251
|
G | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-5+2814G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994251 | ||||||
| chr18:12994444
|
G | A | 1 | a0005c0005t0001g0121 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-5+3007G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994444 | ||||||
| chr18:12994469
|
G | A | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-5+3032G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994469 | ||||||
| chr18:12994592
|
G | A | 1 | a0002c0001t0001g0291 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-5+3155G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994592 | ||||||
| chr18:12994779
|
C | T | 85 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(82): Show | 89 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-5+3342C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994779 | ||||||
| chr18:12994784
|
G | T | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-5+3347G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994784 | ||||||
| chr18:12994852
|
G | T | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-5+3415G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994852 | ||||||
| chr18:12994966
|
A | C | 1 | a0003c0003t0002g0110 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-5+3529A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994966 | ||||||
| chr18:12995053
|
A | AT | 17 | a0003c0003t0002g0010a0003c0003t0002g0098a0003c0003t0002g0099others(14): Show | 19 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.-5+3642dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chr18 | 12995053 | |||||
| chr18:12995053
|
ATT | A | 43 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0267others(40): Show | 44 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.-5+3641_-5+3642del others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chr18 | 12995053 | |||||
| chr18:12995053
|
ATTT | A | 233 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(230): Show | 252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.-5+3640_-5+3642del others(3): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chr18 | 12995053 | |||||
| chr18:12995053
|
ATTTT | A | 13 | a0002c0001t0001g0292a0002c0001t0001g0293a0004c0004t0001g0174others(10): Show | 16 | HG00621.hp2 HG01069.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5+3639_-5+3642del others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chr18 | 12995053 | |||||
| chr18:12995122
|
C | T | 4 | a0002c0001t0001g0347a0019c0019t0001g0166a0019c0019t0001g0167others(1): Show | 4 | HG02040.hp1 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+3685C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995122 | ||||||
| chr18:12995130
|
C | T | 151 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(148): Show | 169 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.-5+3693C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995130 | ||||||
| chr18:12995186
|
T | C | 288 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(285): Show | 311 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.-5+3749T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995186 | ||||||
| chr18:12995207
|
G | T | 1 | a0002c0001t0001g0346 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-5+3770G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995207 | ||||||
| chr18:12995223
|
G | A | 138 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(135): Show | 143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-5+3786G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995223 | ||||||
| chr18:12995307
|
G | A | 1 | a0025c0021t0001g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-5+3870G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995307 | ||||||
| chr18:12995315
|
C | G | 1 | a0001c0002t0001g0222 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-5+3878C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995315 | ||||||
| chr18:12995342
|
G | A | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-5+3905G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995342 | ||||||
| chr18:12995380
|
A | T | 1 | a0032c0032t0001g0119 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5+3943A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995380 | ||||||
| chr18:12995472
|
G | A | 19 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(16): Show | 20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-4-3949G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995472 | ||||||
| chr18:12995546
|
G | A | 57 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(54): Show | 59 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.-4-3875G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995546 | ||||||
| chr18:12995963
|
C | T | 1 | a0005c0005t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-4-3458C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995963 | ||||||
| chr18:12996047
|
G | A | 1 | a0002c0001t0001g0286 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-4-3374G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996047 | ||||||
| chr18:12996110
|
G | A | 1 | a0006c0006t0002g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-4-3311G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996110 | ||||||
| chr18:12996170
|
G | A | 2 | a0002c0001t0001g0292a0002c0001t0001g0294 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-4-3251G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996170 | ||||||
| chr18:12996262
|
A | G | 66 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(63): Show | 68 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.-4-3159A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996262 | ||||||
| chr18:12996411
|
AT | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-4-3009delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996411 | ||||||
| chr18:12996438
|
A | C | 1 | a0007c0007t0002g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-4-2983A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996438 | ||||||
| chr18:12996445
|
G | A | 1 | a0002c0001t0001g0295 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-4-2976G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996445 | ||||||
| chr18:12996501
|
C | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-4-2920C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996501 | ||||||
| chr18:12996535
|
C | T | 1 | a0003c0003t0002g0096 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-4-2886C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996535 | ||||||
| chr18:12996536
|
G | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-4-2885G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996536 | ||||||
| chr18:12996572
|
C | T | 3 | a0002c0001t0001g0293a0002c0001t0001g0345a0023c0027t0001g0344 | 3 | HG00323.hp2 HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-4-2849C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996572 | ||||||
| chr18:12996577
|
A | T | 1 | a0005c0005t0001g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-4-2844A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996577 | ||||||
| chr18:12996746
|
C | T | 1 | a0001c0002t0001g0266 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-4-2675C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996746 | ||||||
| chr18:12997024
|
C | G | 1 | a0001c0002t0001g0279 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-4-2397C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997024 | ||||||
| chr18:12997144
|
G | T | 4 | a0003c0003t0002g0008a0003c0003t0002g0093a0003c0003t0002g0094others(1): Show | 5 | NA18612.hp1 NA19007.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-2277G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997144 | ||||||
| chr18:12997288
|
A | G | 1 | a0004c0004t0001g0202 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-4-2133A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997288 | ||||||
| chr18:12997544
|
T | C | 1 | a0002c0023t0001g0296 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-4-1877T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997544 | ||||||
| chr18:12997645
|
A | G | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-4-1776A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997645 | ||||||
| chr18:12997774
|
A | G | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-4-1647A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997774 | ||||||
| chr18:12997795
|
G | A | 1 | a0001c0002t0001g0213 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-4-1626G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997795 | ||||||
| chr18:12998006
|
T | G | 1 | a0002c0001t0001g0297 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-4-1415T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12998006 | ||||||
| chr18:12998268
|
G | A | 137 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(134): Show | 142 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-4-1153G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12998268 | ||||||
| chr18:12998356
|
A | C | 10 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(7): Show | 10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4-1065A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12998356 | ||||||
| chr18:12998437
|
A | G | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-4-984A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12998437 | ||||||
| chr18:12998656
|
G | A | 62 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(59): Show | 66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-4-765G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12998656 | ||||||
| chr18:12998930
|
G | T | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-4-491G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12998930 | ||||||
| chr18:12999143
|
T | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-278T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12999143 | ||||||
| chr18:12999620
|
G | C | 1 | a0005c0005t0001g0208 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.164+32G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 12999620 | ||||||
| chr18:12999676
|
G | A | 1 | a0003c0003t0002g0045 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.164+88G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 12999676 | ||||||
| chr18:12999755
|
C | T | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.164+167C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 12999755 | ||||||
| chr18:12999822
|
C | T | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.164+234C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 12999822 | ||||||
| chr18:12999828
|
A | AT | 11 | a0002c0001t0001g0337a0002c0001t0001g0354a0003c0003t0002g0091others(8): Show | 11 | HG01099.hp1 HG01515.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.164+258dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 12999828 | |||||
| chr18:12999828
|
AT | A | 64 | a0001c0002t0001g0210a0001c0002t0001g0212a0001c0002t0001g0213others(61): Show | 75 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.164+258delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 12999828 | |||||
| chr18:12999828
|
ATTTTTTT | A | 61 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(58): Show | 63 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.164+252_164+258del others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 12999828 | |||||
| chr18:12999965
|
A | G | 232 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(229): Show | 253 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.164+377A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 12999965 | ||||||
| chr18:12999987
|
G | A | 4 | a0003c0003t0002g0008a0003c0003t0002g0093a0003c0003t0002g0094others(1): Show | 5 | NA18612.hp1 NA19007.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+399G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 12999987 | ||||||
| chr18:13000085
|
T | TTCTCTC | 13 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(10): Show | 14 | HG01952.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.164+499_164+504dup others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000085 | |||||
| chr18:13000091
|
C | CT | 36 | a0003c0003t0002g0085a0003c0003t0002g0086a0003c0003t0002g0096others(33): Show | 46 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.164+530dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000091
|
C | CTCTCTTT | 27 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(24): Show | 30 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.164+504_164+505ins others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000091
|
C | CTCTCTTT others(1): Show |
13 | a0002c0001t0001g0294a0002c0001t0001g0295a0002c0001t0001g0310others(10): Show | 13 | HG00438.hp2 HG01361.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.164+504_164+505ins others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000091
|
C | CTCTCTTT others(2): Show |
9 | a0002c0001t0001g0319a0002c0001t0001g0320a0002c0001t0001g0321others(6): Show | 9 | HG02040.hp1 HG02976.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.164+504_164+505ins others(9): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000091
|
C | CTCTCTTT others(3): Show |
13 | a0002c0001t0001g0022a0002c0001t0001g0322a0002c0001t0001g0323others(10): Show | 14 | HG00673.hp1 HG01099.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.164+504_164+505ins others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000091
|
C | CTCTCTTT others(4): Show |
6 | a0002c0001t0001g0330a0002c0001t0001g0331a0002c0001t0001g0332others(3): Show | 6 | HG02523.hp2 HG03516.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.164+504_164+505ins others(11): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000091
|
C | CTCTCTTT others(5): Show |
3 | a0002c0001t0001g0333a0002c0001t0001g0334a0002c0001t0001g0335 | 3 | HG00423.hp2 NA18954.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.164+504_164+505ins others(12): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000091
|
C | CTT | 10 | a0003c0003t0002g0087a0003c0003t0002g0088a0003c0003t0002g0089others(7): Show | 10 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.164+529_164+530dup others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000091
|
CT | C | 11 | a0001c0002t0001g0212a0001c0002t0001g0224a0001c0002t0001g0225others(8): Show | 11 | HG02004.hp2 HG02132.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.164+530delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000091
|
CTTTT | C | 6 | a0002c0001t0001g0298a0002c0001t0001g0338a0002c0001t0001g0339others(3): Show | 6 | HG00741.hp1 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.164+527_164+530del others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000091
|
CTTTTTT | C | 6 | a0004c0004t0001g0174a0004c0004t0001g0175a0004c0004t0001g0206others(3): Show | 6 | HG01109.hp2 HG01981.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.164+525_164+530del others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000091
|
CTTTTTTT | C | 9 | a0001c0037t0001g0223a0005c0005t0001g0125a0009c0009t0001g0003others(6): Show | 12 | HG00621.hp2 HG01167.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.164+524_164+530del others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000091
|
CTTTTTTT others(1): Show |
C | 58 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(55): Show | 60 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.164+523_164+530del others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000091
|
CTTTTTTT others(3): Show |
C | 1 | a0005c0005t0001g0161 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.164+521_164+530del others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | |||||
| chr18:13000092
|
T | TC | 4 | a0000c0035t0001g0264a0001c0002t0001g0263a0001c0002t0001g0265others(1): Show | 4 | HG02559.hp1 HG03654.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+504_164+505ins others(1): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000092 | ||||||
| chr18:13000093
|
T | C | 63 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(60): Show | 66 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.164+505T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000093 | ||||||
| chr18:13000094
|
T | C | 12 | a0000c0035t0001g0264a0001c0002t0001g0212a0001c0002t0001g0224others(9): Show | 12 | HG02132.hp2 HG02559.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.164+506T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000094 | ||||||
| chr18:13000095
|
T | C | 62 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(59): Show | 65 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.164+507T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000095 | ||||||
| chr18:13000096
|
T | C | 11 | a0001c0002t0001g0212a0001c0002t0001g0224a0001c0002t0001g0225others(8): Show | 11 | HG01515.hp1 HG02132.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.164+508T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000096 | ||||||
| chr18:13000097
|
T | C | 6 | a0002c0001t0001g0298a0002c0001t0001g0338a0002c0001t0001g0339others(3): Show | 6 | HG00741.hp1 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.164+509T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000097 | ||||||
| chr18:13000098
|
T | C | 3 | a0006c0006t0001g0356a0006c0006t0001g0358a0022c0028t0001g0357 | 3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.164+510T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000098 | ||||||
| chr18:13000099
|
T | C | 7 | a0002c0001t0001g0298a0002c0001t0001g0338a0002c0001t0001g0339others(4): Show | 7 | HG00741.hp1 HG01109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.164+511T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000099 | ||||||
| chr18:13000100
|
T | C | 9 | a0001c0037t0001g0223a0005c0005t0001g0125a0009c0009t0001g0003others(6): Show | 12 | HG00621.hp2 HG01167.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.164+512T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000100 | ||||||
| chr18:13000101
|
T | C | 59 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(56): Show | 61 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.164+513T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000101 | ||||||
| chr18:13000102
|
T | C | 10 | a0001c0037t0001g0223a0005c0005t0001g0125a0005c0005t0001g0162others(7): Show | 13 | HG00621.hp2 HG01167.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.164+514T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000102 | ||||||
| chr18:13000103
|
T | C | 59 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(56): Show | 61 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.164+515T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000103 | ||||||
| chr18:13000104
|
T | C | 1 | a0005c0005t0001g0162 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.164+516T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000104 | ||||||
| chr18:13000167
|
A | G | 85 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(82): Show | 88 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.164+579A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000167 | ||||||
| chr18:13000211
|
A | G | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.164+623A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000211 | ||||||
| chr18:13000231
|
TAC | T | 138 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(135): Show | 143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.164+647_164+648del others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000231 | |||||
| chr18:13000278
|
A | G | 1 | a0001c0002t0001g0280 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.164+690A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000278 | ||||||
| chr18:13000339
|
C | T | 2 | a0012c0013t0002g0084a0012c0040t0002g0105 | 2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.164+751C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000339 | ||||||
| chr18:13000438
|
A | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+850A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000438 | ||||||
| chr18:13000486
|
G | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.164+898G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000486 | ||||||
| chr18:13000547
|
A | G | 40 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(37): Show | 42 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.165-910A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000547 | ||||||
| chr18:13000548
|
T | C | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.165-909T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000548 | ||||||
| chr18:13000737
|
C | T | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.165-720C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000737 | ||||||
| chr18:13000976
|
C | T | 151 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(148): Show | 169 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.165-481C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000976 | ||||||
| chr18:13001343
|
C | T | 2 | a0003c0003t0002g0082a0003c0003t0002g0083 | 2 | HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.165-114C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13001343 | ||||||
| chr18:13001380
|
C | T | 1 | a0002c0001t0001g0318 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.165-77C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13001380 | ||||||
| chr18:13001411
|
T | A | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.165-46T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13001411 | ||||||
| chr18:13001705
|
T | C | 61 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(58): Show | 63 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.290+123T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13001705 | ||||||
| chr18:13001949
|
C | A | 79 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(76): Show | 83 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.290+367C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13001949 | ||||||
| chr18:13002010
|
G | A | 1 | a0001c0002t0001g0229 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.290+428G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002010 | ||||||
| chr18:13002197
|
C | T | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.290+615C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002197 | ||||||
| chr18:13002304
|
G | C | 1 | a0005c0005t0001g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.290+722G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002304 | ||||||
| chr18:13002309
|
AGC | A | 138 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(135): Show | 143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.290+728_290+729del others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002309 | ||||||
| chr18:13002310
|
G | A | 151 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(148): Show | 169 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.290+728G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002310 | ||||||
| chr18:13002312
|
T | A | 138 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(135): Show | 143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.290+730T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002312 | ||||||
| chr18:13002353
|
C | G | 67 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(64): Show | 69 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.290+771C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002353 | ||||||
| chr18:13002497
|
G | T | 7 | a0010c0010t0002g0048a0010c0010t0002g0079a0010c0010t0002g0080others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+915G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002497 | ||||||
| chr18:13002755
|
G | T | 138 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(135): Show | 143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.290+1173G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002755 | ||||||
| chr18:13002798
|
TGTATTTG others(1): Show |
T | 3 | a0019c0019t0001g0166a0019c0019t0001g0167a0035c0044t0001g0165 | 3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.290+1223_290+1230d others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13002798 | |||||
| chr18:13002807
|
G | A | 1 | a0012c0013t0002g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.290+1225G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002807 | ||||||
| chr18:13003192
|
T | A | 62 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(59): Show | 66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.290+1610T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003192 | ||||||
| chr18:13003225
|
G | C | 89 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(86): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.290+1643G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003225 | ||||||
| chr18:13003268
|
G | A | 62 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(59): Show | 66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.290+1686G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003268 | ||||||
| chr18:13003391
|
A | G | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.290+1809A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003391 | ||||||
| chr18:13003436
|
G | A | 3 | a0019c0019t0001g0166a0019c0019t0001g0167a0035c0044t0001g0165 | 3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.290+1854G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003436 | ||||||
| chr18:13003451
|
GA | G | 137 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(134): Show | 155 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.290+1890delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13003451 | |||||
| chr18:13003451
|
GAA | G | 9 | a0002c0001t0001g0292a0002c0001t0001g0295a0002c0001t0001g0309others(6): Show | 9 | HG01167.hp2 HG01256.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.290+1889_290+1890d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13003451 | |||||
| chr18:13003451
|
GAAAAA | G | 135 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(132): Show | 140 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.290+1886_290+1890d others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13003451 | |||||
| chr18:13003480
|
T | C | 1 | a0013c0029t0003g0215 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.290+1898T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003480 | ||||||
| chr18:13003548
|
T | A | 10 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(7): Show | 10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.290+1966T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003548 | ||||||
| chr18:13003579
|
A | T | 138 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(135): Show | 143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.290+1997A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003579 | ||||||
| chr18:13003605
|
C | A | 1 | a0005c0005t0001g0126 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.290+2023C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003605 | ||||||
| chr18:13003630
|
A | G | 66 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(63): Show | 68 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.290+2048A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003630 | ||||||
| chr18:13003873
|
TTGTC | T | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.290+2294_290+2297d others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13003873 | |||||
| chr18:13003912
|
G | T | 1 | a0004c0004t0001g0198 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.290+2330G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003912 | ||||||
| chr18:13004062
|
A | C | 2 | a0005c0005t0001g0149a0005c0005t0001g0150 | 2 | HG02109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.290+2480A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004062 | ||||||
| chr18:13004105
|
T | G | 10 | a0006c0006t0002g0025a0007c0007t0002g0006a0007c0007t0002g0023others(7): Show | 11 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.290+2523T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004105 | ||||||
| chr18:13004193
|
G | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.290+2611G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004193 | ||||||
| chr18:13004201
|
T | C | 1 | a0018c0017t0002g0009 | 2 | HG02080.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.290+2619T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004201 | ||||||
| chr18:13004252
|
C | T | 61 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(58): Show | 63 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.290+2670C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004252 | ||||||
| chr18:13004260
|
T | C | 1 | a0001c0002t0001g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.290+2678T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004260 | ||||||
| chr18:13004273
|
G | T | 10 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(7): Show | 10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.290+2691G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004273 | ||||||
| chr18:13004299
|
C | CT | 139 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(136): Show | 144 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.290+2728dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13004299 | |||||
| chr18:13004421
|
C | T | 138 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(135): Show | 143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.290+2839C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004421 | ||||||
| chr18:13004453
|
C | T | 10 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(7): Show | 10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.290+2871C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004453 | ||||||
| chr18:13004732
|
A | G | 44 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(41): Show | 46 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.290+3150A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004732 | ||||||
| chr18:13004826
|
G | A | 10 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(7): Show | 10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.290+3244G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004826 | ||||||
| chr18:13004998
|
C | T | 3 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219 | 6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+3416C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004998 | ||||||
| chr18:13004999
|
A | C | 1 | a0002c0001t0001g0308 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.290+3417A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004999 | ||||||
| chr18:13005474
|
T | C | 291 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(288): Show | 314 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.291-2982T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13005474 | ||||||
| chr18:13005541
|
C | G | 1 | a0005c0005t0001g0171 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.291-2915C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13005541 | ||||||
| chr18:13005629
|
G | C | 3 | a0006c0006t0002g0042a0006c0006t0002g0043a0006c0006t0002g0044 | 3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.291-2827G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13005629 | ||||||
| chr18:13005668
|
C | A | 4 | a0002c0001t0001g0342a0002c0001t0001g0343a0002c0001t0001g0360others(1): Show | 4 | HG02976.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.291-2788C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13005668 | ||||||
| chr18:13005917
|
G | A | 10 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(7): Show | 10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.291-2539G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13005917 | ||||||
| chr18:13005950
|
A | G | 1 | a0021c0030t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.291-2506A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13005950 | ||||||
| chr18:13006113
|
C | T | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-2343C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006113 | ||||||
| chr18:13006196
|
A | G | 1 | a0001c0002t0001g0212 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.291-2260A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006196 | ||||||
| chr18:13006285
|
A | G | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.291-2171A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006285 | ||||||
| chr18:13006327
|
C | T | 66 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(63): Show | 68 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.291-2129C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006327 | ||||||
| chr18:13006404
|
A | G | 66 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(63): Show | 68 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.291-2052A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006404 | ||||||
| chr18:13006598
|
A | G | 1 | a0006c0006t0002g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.291-1858A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006598 | ||||||
| chr18:13006765
|
TG | T | 61 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(58): Show | 63 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.291-1690delG | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006765 | ||||||
| chr18:13007154
|
T | C | 1 | a0030c0039t0001g0152 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.291-1302T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007154 | ||||||
| chr18:13007195
|
A | G | 1 | a0004c0004t0001g0181 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.291-1261A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007195 | ||||||
| chr18:13007339
|
A | G | 2 | a0003c0003t0002g0077a0003c0003t0002g0103 | 2 | HG00140.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.291-1117A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007339 | ||||||
| chr18:13007347
|
C | A | 138 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(135): Show | 143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.291-1109C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007347 | ||||||
| chr18:13007481
|
T | G | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.291-975T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007481 | ||||||
| chr18:13007516
|
G | T | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.291-940G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007516 | ||||||
| chr18:13007558
|
C | T | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.291-898C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007558 | ||||||
| chr18:13007621
|
A | G | 1 | a0001c0002t0001g0280 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.291-835A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007621 | ||||||
| chr18:13007828
|
C | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.291-628C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007828 | ||||||
| chr18:13007830
|
C | T | 66 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(63): Show | 68 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.291-626C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007830 | ||||||
| chr18:13008124
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.291-332G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13008124 | ||||||
| chr18:13008246
|
C | CTG | 293 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(290): Show | 316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.291-208_291-207dup others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13008246 | |||||
| chr18:13008308
|
T | C | 1 | a0036c0020t0001g0355 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291-148T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13008308 | ||||||
| chr18:13008309
|
A | G | 1 | a0005c0005t0001g0162 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.291-147A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13008309 | ||||||
| chr18:13008370
|
A | G | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.291-86A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13008370 | ||||||
| chr18:13008377
|
A | G | 1 | a0003c0003t0002g0076 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.291-79A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13008377 | ||||||
| chr18:13008393
|
T | C | 1 | a0001c0002t0001g0266 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.291-63T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13008393 | ||||||
| chr18:13008702
|
A | AT | 23 | a0001c0002t0001g0018a0001c0002t0001g0262a0001c0002t0001g0267others(20): Show | 24 | HG00438.hp2 HG01192.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.466+89dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13008702 | |||||
| chr18:13008742
|
C | T | 22 | a0003c0003t0002g0008a0003c0003t0002g0046a0003c0003t0002g0047others(19): Show | 23 | HG00558.hp1 HG00597.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.466+111C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13008742 | ||||||
| chr18:13008895
|
A | G | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+264A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13008895 | ||||||
| chr18:13008969
|
A | G | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.466+338A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13008969 | ||||||
| chr18:13009008
|
C | CT | 11 | a0001c0002t0001g0227a0001c0002t0001g0228a0001c0002t0001g0257others(8): Show | 11 | HG02293.hp1 HG02451.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+382dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13009008 | |||||
| chr18:13009012
|
TTG | T | 53 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(50): Show | 55 | HG00099.hp2 HG01071.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.466+383_466+384del others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13009012 | |||||
| chr18:13009013
|
TG | T | 11 | a0005c0005t0001g0117a0005c0005t0001g0122a0005c0005t0001g0123others(8): Show | 11 | HG01167.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+383delG | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009013 | ||||||
| chr18:13009014
|
G | GT | 8 | a0003c0003t0002g0091a0003c0003t0002g0095a0003c0003t0002g0108others(5): Show | 8 | HG02145.hp1 HG02965.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.466+400dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13009014 | |||||
| chr18:13009014
|
G | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.466+383G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009014 | ||||||
| chr18:13009014
|
GT | G | 42 | a0002c0001t0001g0353a0003c0003t0002g0090a0004c0004t0001g0001others(39): Show | 52 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.466+400delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13009014 | |||||
| chr18:13009014
|
GTT | G | 104 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(101): Show | 109 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.466+399_466+400del others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13009014 | |||||
| chr18:13009289
|
G | A | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+658G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009289 | ||||||
| chr18:13009366
|
T | C | 4 | a0001c0002t0001g0016a0001c0002t0001g0230a0001c0002t0001g0231others(1): Show | 5 | HG02523.hp1 NA18940.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+735T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009366 | ||||||
| chr18:13009409
|
C | T | 61 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(58): Show | 63 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.466+778C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009409 | ||||||
| chr18:13009443
|
T | A | 1 | a0002c0001t0001g0322 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.466+812T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009443 | ||||||
| chr18:13009447
|
A | C | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.466+816A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009447 | ||||||
| chr18:13009482
|
G | A | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.466+851G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009482 | ||||||
| chr18:13009597
|
C | G | 1 | a0002c0001t0001g0350 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.466+966C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009597 | ||||||
| chr18:13009623
|
A | G | 3 | a0011c0011t0001g0289a0011c0011t0001g0290a0020c0046t0001g0287 | 3 | HG02723.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.466+992A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009623 | ||||||
| chr18:13009731
|
G | C | 57 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(54): Show | 59 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.466+1100G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009731 | ||||||
| chr18:13009906
|
T | C | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.466+1275T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009906 | ||||||
| chr18:13009913
|
G | A | 1 | a0005c0005t0001g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.466+1282G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009913 | ||||||
| chr18:13010017
|
G | A | 85 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(82): Show | 89 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.466+1386G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010017 | ||||||
| chr18:13010128
|
C | A | 1 | a0001c0002t0001g0233 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.466+1497C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010128 | ||||||
| chr18:13010182
|
T | A | 2 | a0003c0003t0002g0050a0028c0042t0002g0107 | 2 | HG02074.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.466+1551T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010182 | ||||||
| chr18:13010191
|
C | A | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.466+1560C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010191 | ||||||
| chr18:13010239
|
C | G | 151 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(148): Show | 169 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.466+1608C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010239 | ||||||
| chr18:13010617
|
C | T | 67 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(64): Show | 69 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.466+1986C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010617 | ||||||
| chr18:13010634
|
T | G | 138 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(135): Show | 143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.466+2003T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010634 | ||||||
| chr18:13010702
|
C | T | 1 | a0007c0007t0002g0029 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.466+2071C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010702 | ||||||
| chr18:13010801
|
G | A | 1 | a0005c0005t0001g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.466+2170G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010801 | ||||||
| chr18:13010993
|
G | A | 1 | a0005c0005t0001g0161 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.467-1980G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010993 | ||||||
| chr18:13011001
|
C | T | 57 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(54): Show | 59 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.467-1972C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011001 | ||||||
| chr18:13011079
|
T | C | 2 | a0006c0006t0002g0034a0006c0006t0002g0037 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.467-1894T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011079 | ||||||
| chr18:13011183
|
T | C | 288 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(285): Show | 311 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.467-1790T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011183 | ||||||
| chr18:13011184
|
G | A | 10 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(7): Show | 10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.467-1789G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011184 | ||||||
| chr18:13011226
|
C | CA | 68 | a0003c0003t0002g0090a0003c0003t0002g0106a0005c0005t0001g0013others(65): Show | 70 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.467-1733dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13011226 | |||||
| chr18:13011226
|
CA | C | 221 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(218): Show | 242 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.467-1733delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13011226 | |||||
| chr18:13011432
|
T | C | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.467-1541T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011432 | ||||||
| chr18:13011531
|
GT | G | 293 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(290): Show | 316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.467-1433delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13011531 | |||||
| chr18:13011639
|
C | T | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.467-1334C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011639 | ||||||
| chr18:13011846
|
A | G | 10 | a0001c0002t0001g0250a0001c0002t0001g0251a0001c0002t0001g0252others(7): Show | 10 | HG00673.hp2 HG02040.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.467-1127A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011846 | ||||||
| chr18:13011863
|
C | G | 10 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(7): Show | 10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.467-1110C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011863 | ||||||
| chr18:13011898
|
A | C | 1 | a0003c0003t0002g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.467-1075A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011898 | ||||||
| chr18:13012045
|
A | G | 7 | a0010c0010t0002g0048a0010c0010t0002g0079a0010c0010t0002g0080others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-928A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012045 | ||||||
| chr18:13012153
|
C | G | 1 | a0011c0011t0001g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.467-820C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012153 | ||||||
| chr18:13012295
|
T | A | 151 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(148): Show | 169 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.467-678T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012295 | ||||||
| chr18:13012364
|
A | G | 1 | a0004c0004t0001g0202 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.467-609A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012364 | ||||||
| chr18:13012453
|
C | A | 1 | a0003c0003t0002g0085 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.467-520C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012453 | ||||||
| chr18:13012471
|
C | T | 1 | a0002c0001t0001g0293 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.467-502C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012471 | ||||||
| chr18:13012483
|
C | T | 62 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(59): Show | 66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.467-490C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012483 | ||||||
| chr18:13012548
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-425G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012548 | ||||||
| chr18:13012651
|
T | C | 62 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(59): Show | 64 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.467-322T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012651 | ||||||
| chr18:13012873
|
A | T | 1 | a0008c0008t0001g0147 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.467-100A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012873 | ||||||
| chr18:13013153
|
T | C | 2 | a0001c0002t0001g0258a0001c0002t0001g0268 | 2 | NA18985.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.519+128T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013153 | ||||||
| chr18:13013196
|
G | T | 6 | a0011c0011t0001g0283a0011c0011t0001g0284a0011c0011t0001g0288others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+171G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013196 | ||||||
| chr18:13013203
|
GGGTAGTG others(9): Show |
G | 14 | a0006c0006t0002g0025a0006c0006t0002g0035a0006c0006t0002g0036others(11): Show | 15 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.519+181_519+196del others(16): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chr18 | 13013203 | |||||
| chr18:13013231
|
C | G | 1 | a0021c0030t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.519+206C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013231 | ||||||
| chr18:13013242
|
TGATGTCA others(3): Show |
T | 1 | a0010c0010t0002g0079 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.519+218_519+227del others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013242 | ||||||
| chr18:13013275
|
C | T | 1 | a0010c0010t0002g0104 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.519+250C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013275 | ||||||
| chr18:13013310
|
T | A | 3 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219 | 6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+285T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013310 | ||||||
| chr18:13013391
|
C | T | 1 | a0003c0003t0002g0066 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.519+366C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013391 | ||||||
| chr18:13013558
|
A | G | 1 | a0021c0030t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.519+533A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013558 | ||||||
| chr18:13013661
|
C | T | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.519+636C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013661 | ||||||
| chr18:13013763
|
A | C | 2 | a0006c0006t0002g0043a0006c0006t0002g0044 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.519+738A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013763 | ||||||
| chr18:13014138
|
T | C | 4 | a0004c0004t0001g0174a0004c0004t0001g0175a0004c0004t0001g0206others(1): Show | 4 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+1113T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014138 | ||||||
| chr18:13014384
|
T | TCTCAC | 6 | a0001c0002t0001g0016a0001c0002t0001g0230a0001c0002t0001g0231others(3): Show | 7 | HG00544.hp2 HG02523.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-940_520-939ins others(5): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chr18 | 13014384 | |||||
| chr18:13014528
|
A | G | 6 | a0002c0001t0001g0303a0002c0001t0001g0304a0002c0001t0001g0305others(3): Show | 6 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-800A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014528 | ||||||
| chr18:13014792
|
C | CATATATA others(4): Show |
3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.520-526_520-516dup others(11): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chr18 | 13014792 | |||||
| chr18:13014864
|
G | A | 1 | a0002c0001t0001g0319 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.520-464G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014864 | ||||||
| chr18:13014874
|
A | G | 1 | a0002c0001t0001g0328 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.520-454A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014874 | ||||||
| chr18:13014882
|
G | A | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.520-446G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014882 | ||||||
| chr18:13014882
|
G | C | 85 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(82): Show | 89 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.520-446G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014882 | ||||||
| chr18:13014904
|
C | T | 1 | a0002c0023t0001g0296 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.520-424C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014904 | ||||||
| chr18:13014927
|
T | G | 1 | a0001c0002t0001g0262 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.520-401T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014927 | ||||||
| chr18:13015028
|
G | A | 1 | a0001c0002t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.520-300G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13015028 | ||||||
| chr18:13015147
|
G | A | 1 | a0003c0003t0002g0066 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.520-181G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13015147 | ||||||
| chr18:13015247
|
T | C | 67 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(64): Show | 69 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.520-81T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13015247 | ||||||
| chr18:13015292
|
A | G | 6 | a0006c0006t0001g0356a0006c0006t0001g0358a0013c0016t0003g0216others(3): Show | 6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-36A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13015292 | ||||||
| chr18:13015491
|
A | C | 1 | a0036c0020t0001g0355 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.640+43A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13015491 | ||||||
| chr18:13015510
|
T | G | 1 | a0001c0002t0001g0236 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.640+62T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13015510 | ||||||
| chr18:13015626
|
A | G | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.640+178A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13015626 | ||||||
| chr18:13015814
|
C | T | 4 | a0001c0002t0001g0249a0013c0016t0003g0216a0013c0016t0003g0217others(1): Show | 4 | HG02258.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+366C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13015814 | ||||||
| chr18:13015843
|
T | C | 6 | a0011c0011t0001g0283a0011c0011t0001g0284a0011c0011t0001g0288others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+395T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13015843 | ||||||
| chr18:13015859
|
C | T | 71 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(68): Show | 74 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.640+411C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13015859 | ||||||
| chr18:13016036
|
G | A | 1 | a0006c0006t0002g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.640+588G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016036 | ||||||
| chr18:13016274
|
C | T | 1 | a0002c0001t0001g0308 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.640+826C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016274 | ||||||
| chr18:13016475
|
T | C | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.641-713T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016475 | ||||||
| chr18:13016514
|
T | C | 1 | a0005c0005t0001g0127 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.641-674T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016514 | ||||||
| chr18:13016737
|
C | G | 1 | a0009c0009t0001g0218 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.641-451C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016737 | ||||||
| chr18:13016813
|
T | C | 1 | a0002c0001t0001g0351 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.641-375T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016813 | ||||||
| chr18:13016863
|
A | G | 1 | a0005c0005t0001g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.641-325A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016863 | ||||||
| chr18:13017123
|
A | G | 2 | a0001c0002t0001g0234a0001c0002t0001g0235 | 2 | HG00544.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.641-65A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13017123 | ||||||
| chr18:13017416
|
T | C | 19 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(16): Show | 20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.789+80T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13017416 | ||||||
| chr18:13017463
|
G | A | 70 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(67): Show | 73 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.789+127G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13017463 | ||||||
| chr18:13017673
|
A | G | 36 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(33): Show | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.789+337A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13017673 | ||||||
| chr18:13017724
|
T | A | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.789+388T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13017724 | ||||||
| chr18:13017857
|
A | G | 1 | a0001c0002t0001g0257 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.789+521A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13017857 | ||||||
| chr18:13017888
|
T | C | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+552T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13017888 | ||||||
| chr18:13018072
|
A | G | 292 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(289): Show | 315 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.790-408A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13018072 | ||||||
| chr18:13018080
|
A | G | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.790-400A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13018080 | ||||||
| chr18:13018430
|
A | G | 1 | a0001c0002t0001g0229 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.790-50A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13018430 | ||||||
| chr18:13018460
|
C | T | 1 | a0004c0004t0001g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.790-20C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13018460 | ||||||
| chr18:13018667
|
CT | C | 56 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0018others(53): Show | 58 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.925+59delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | INFO_REALIGN_3_PRIME | chr18 | 13018667 | |||||
| chr18:13018674
|
T | A | 7 | a0001c0002t0001g0250a0001c0002t0001g0251a0001c0002t0001g0259others(4): Show | 7 | HG02080.hp2 HG02083.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+59T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | chr18 | 13018674 | ||||||
| chr18:13018674
|
TA | T | 7 | a0001c0002t0001g0017a0001c0002t0001g0221a0001c0002t0001g0233others(4): Show | 8 | HG02015.hp2 HG02129.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+69delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | INFO_REALIGN_3_PRIME | chr18 | 13018674 | |||||
| chr18:13018675
|
A | T | 5 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(2): Show | 5 | HG01891.hp2 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+60A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | chr18 | 13018675 | ||||||
| chr18:13018807
|
G | A | 1 | a0005c0005t0001g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.925+192G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | chr18 | 13018807 | ||||||
| chr18:13018808
|
T | C | 1 | a0029c0036t0001g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.925+193T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | chr18 | 13018808 | ||||||
| chr18:13018966
|
A | G | 2 | a0003c0003t0002g0082a0003c0003t0002g0083 | 2 | HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.926-116A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | chr18 | 13018966 | ||||||
| chr18:13019264
|
G | C | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1050+58G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019264 | ||||||
| chr18:13019337
|
T | C | 89 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(86): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1050+131T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019337 | ||||||
| chr18:13019494
|
G | A | 1 | a0001c0002t0001g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1050+288G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019494 | ||||||
| chr18:13019697
|
A | G | 1 | a0022c0028t0001g0357 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1050+491A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019697 | ||||||
| chr18:13019873
|
C | T | 89 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(86): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1050+667C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019873 | ||||||
| chr18:13019893
|
A | G | 1 | a0002c0001t0001g0316 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1050+687A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019893 | ||||||
| chr18:13019951
|
T | G | 4 | a0001c0002t0001g0210a0001c0002t0001g0213a0006c0006t0002g0035others(1): Show | 4 | HG02486.hp1 HG02647.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1050+745T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019951 | ||||||
| chr18:13020102
|
C | T | 1 | a0032c0032t0001g0119 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1050+896C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13020102 | ||||||
| chr18:13020167
|
T | G | 89 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(86): Show | 96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1050+961T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13020167 | ||||||
| chr18:13020250
|
A | G | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1050+1044A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13020250 | ||||||
| chr18:13020312
|
T | C | 2 | a0006c0006t0002g0043a0006c0006t0002g0044 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1050+1106T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13020312 | ||||||
| chr18:13020651
|
A | G | 1 | a0001c0002t0001g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1050+1445A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13020651 | ||||||
| chr18:13020882
|
T | A | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1050+1676T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13020882 | ||||||
| chr18:13021020
|
T | C | 6 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050+1814T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021020 | ||||||
| chr18:13021078
|
G | T | 1 | a0001c0002t0001g0267 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1050+1872G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021078 | ||||||
| chr18:13021211
|
A | G | 1 | a0002c0001t0001g0021 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1050+2005A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021211 | ||||||
| chr18:13021274
|
G | A | 9 | a0007c0007t0002g0006a0007c0007t0002g0023a0007c0007t0002g0024others(6): Show | 10 | HG01952.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1050+2068G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021274 | ||||||
| chr18:13021305
|
G | A | 11 | a0005c0005t0001g0134a0005c0005t0001g0149a0005c0005t0001g0150others(8): Show | 11 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1050+2099G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021305 | ||||||
| chr18:13021631
|
G | A | 244 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(241): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1050+2425G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021631 | ||||||
| chr18:13021992
|
T | C | 1 | a0006c0006t0002g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1050+2786T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021992 | ||||||
| chr18:13022432
|
G | C | 2 | a0006c0006t0001g0356a0006c0006t0001g0358 | 2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1050+3226G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13022432 | ||||||
| chr18:13022484
|
G | A | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1050+3278G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13022484 | ||||||
| chr18:13022593
|
C | T | 3 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124 | 3 | HG02630.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1050+3387C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13022593 | ||||||
| chr18:13022607
|
C | A | 1 | a0004c0004t0001g0187 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1050+3401C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13022607 | ||||||
| chr18:13023026
|
A | G | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1050+3820A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023026 | ||||||
| chr18:13023104
|
C | T | 6 | a0011c0011t0001g0283a0011c0011t0001g0284a0011c0011t0001g0288others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050+3898C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023104 | ||||||
| chr18:13023150
|
A | G | 62 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(59): Show | 64 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.1050+3944A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023150 | ||||||
| chr18:13023266
|
A | G | 1 | a0001c0045t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1050+4060A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023266 | ||||||
| chr18:13023476
|
A | AT | 7 | a0001c0002t0001g0228a0001c0002t0001g0265a0009c0009t0001g0003others(4): Show | 10 | HG00621.hp2 HG01928.hp2 NA18522.hp1 others(7): Show |
intron_variant | MODIFIER | c.1050+4284dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chr18 | 13023476 | |||||
| chr18:13023476
|
AT | A | 63 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(60): Show | 67 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1050+4284delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chr18 | 13023476 | |||||
| chr18:13023569
|
A | T | 2 | a0001c0002t0001g0259a0001c0002t0001g0260 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1050+4363A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023569 | ||||||
| chr18:13023761
|
C | A | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1050+4555C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023761 | ||||||
| chr18:13023974
|
T | C | 1 | a0013c0029t0003g0215 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1050+4768T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023974 | ||||||
| chr18:13024187
|
G | A | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1050+4981G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024187 | ||||||
| chr18:13024236
|
T | C | 1 | a0014c0014t0001g0012 | 2 | NA18944.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1050+5030T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024236 | ||||||
| chr18:13024372
|
A | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1050+5166A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024372 | ||||||
| chr18:13024459
|
GTTTA | G | 3 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219 | 6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051-5188_1051-518 others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chr18 | 13024459 | |||||
| chr18:13024562
|
A | G | 2 | a0004c0004t0001g0002a0004c0004t0001g0196 | 5 | NA18942.hp1 NA18983.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051-5101A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024562 | ||||||
| chr18:13024596
|
A | G | 6 | a0011c0011t0001g0283a0011c0011t0001g0284a0011c0011t0001g0288others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1051-5067A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024596 | ||||||
| chr18:13024767
|
T | A | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1051-4896T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024767 | ||||||
| chr18:13024780
|
A | AT | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1051-4876dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chr18 | 13024780 | |||||
| chr18:13024793
|
C | T | 79 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(76): Show | 83 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1051-4870C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024793 | ||||||
| chr18:13024848
|
C | T | 3 | a0004c0004t0001g0005a0004c0004t0001g0201a0004c0004t0001g0203 | 5 | NA18961.hp1 NA18980.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051-4815C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024848 | ||||||
| chr18:13024849
|
G | A | 1 | a0001c0002t0001g0249 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1051-4814G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024849 | ||||||
| chr18:13024918
|
C | T | 20 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(17): Show | 20 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1051-4745C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024918 | ||||||
| chr18:13024921
|
C | T | 20 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(17): Show | 20 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1051-4742C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024921 | ||||||
| chr18:13024926
|
C | A | 85 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(82): Show | 89 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1051-4737C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024926 | ||||||
| chr18:13025051
|
C | T | 20 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(17): Show | 20 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1051-4612C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13025051 | ||||||
| chr18:13025065
|
C | A | 36 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(33): Show | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1051-4598C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13025065 | ||||||
| chr18:13025118
|
A | G | 1 | a0008c0008t0001g0168 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1051-4545A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13025118 | ||||||
| chr18:13025417
|
A | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051-4246A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13025417 | ||||||
| chr18:13025672
|
C | T | 351 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(348): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.1051-3991C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13025672 | ||||||
| chr18:13026037
|
A | G | 2 | a0005c0005t0001g0144a0005c0005t0001g0145 | 2 | NA18982.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1051-3626A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026037 | ||||||
| chr18:13026051
|
G | A | 3 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219 | 6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051-3612G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026051 | ||||||
| chr18:13026055
|
A | G | 1 | a0005c0005t0001g0134 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1051-3608A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026055 | ||||||
| chr18:13026070
|
T | A | 1 | a0001c0002t0001g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1051-3593T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026070 | ||||||
| chr18:13026106
|
T | C | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051-3557T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026106 | ||||||
| chr18:13026121
|
T | C | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1051-3542T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026121 | ||||||
| chr18:13026367
|
G | T | 3 | a0003c0003t0002g0064a0003c0003t0002g0065a0018c0017t0002g0009 | 4 | HG02080.hp1 HG02083.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051-3296G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026367 | ||||||
| chr18:13026383
|
G | T | 2 | a0001c0002t0001g0212a0001c0033t0001g0211 | 2 | HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1051-3280G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026383 | ||||||
| chr18:13026408
|
C | G | 1 | a0002c0001t0001g0318 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1051-3255C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026408 | ||||||
| chr18:13026587
|
T | A | 1 | a0001c0002t0001g0224 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1051-3076T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026587 | ||||||
| chr18:13026604
|
G | C | 1 | a0001c0002t0001g0268 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1051-3059G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026604 | ||||||
| chr18:13026796
|
G | C | 1 | a0012c0013t0002g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1051-2867G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026796 | ||||||
| chr18:13026917
|
G | GT | 5 | a0001c0002t0001g0265a0001c0033t0001g0211a0003c0003t0002g0091others(2): Show | 5 | HG02895.hp1 HG02897.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051-2738dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chr18 | 13026917 | |||||
| chr18:13026939
|
C | A | 1 | a0008c0008t0001g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1051-2724C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026939 | ||||||
| chr18:13027085
|
G | A | 1 | a0011c0011t0001g0288 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1051-2578G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027085 | ||||||
| chr18:13027223
|
T | C | 3 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124 | 3 | HG02630.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1051-2440T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027223 | ||||||
| chr18:13027542
|
G | T | 79 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(76): Show | 83 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1051-2121G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027542 | ||||||
| chr18:13027555
|
C | T | 14 | a0006c0006t0002g0025a0006c0006t0002g0035a0006c0006t0002g0036others(11): Show | 15 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1051-2108C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027555 | ||||||
| chr18:13027656
|
G | A | 2 | a0002c0001t0001g0292a0002c0001t0001g0294 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1051-2007G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027656 | ||||||
| chr18:13027663
|
T | C | 62 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(59): Show | 64 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.1051-2000T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027663 | ||||||
| chr18:13027800
|
G | A | 1 | a0004c0004t0001g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1051-1863G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027800 | ||||||
| chr18:13027906
|
T | C | 1 | a0030c0039t0001g0152 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1051-1757T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027906 | ||||||
| chr18:13028102
|
C | T | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1051-1561C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028102 | ||||||
| chr18:13028204
|
T | G | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1051-1459T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028204 | ||||||
| chr18:13028369
|
T | C | 1 | a0028c0042t0002g0107 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1051-1294T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028369 | ||||||
| chr18:13028597
|
G | A | 1 | a0022c0028t0001g0357 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1051-1066G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028597 | ||||||
| chr18:13028634
|
CT | C | 3 | a0006c0006t0001g0356a0006c0006t0001g0358a0022c0028t0001g0357 | 3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1051-1028delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028634 | ||||||
| chr18:13028644
|
C | G | 1 | a0004c0004t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1051-1019C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028644 | ||||||
| chr18:13028645
|
G | A | 92 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(89): Show | 96 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1051-1018G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028645 | ||||||
| chr18:13028676
|
C | T | 1 | a0001c0002t0001g0247 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1051-987C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028676 | ||||||
| chr18:13028767
|
G | A | 1 | a0004c0004t0004g0177 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1051-896G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028767 | ||||||
| chr18:13028966
|
G | A | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1051-697G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028966 | ||||||
| chr18:13029069
|
T | G | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1051-594T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13029069 | ||||||
| chr18:13029118
|
G | A | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1051-545G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13029118 | ||||||
| chr18:13029148
|
G | GT | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051-511dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chr18 | 13029148 | |||||
| chr18:13029158
|
G | A | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1051-505G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13029158 | ||||||
| chr18:13029201
|
A | C | 1 | a0002c0001t0001g0337 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1051-462A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13029201 | ||||||
| chr18:13029447
|
A | G | 2 | a0003c0003t0002g0077a0003c0003t0002g0103 | 2 | HG00140.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1051-216A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13029447 | ||||||
| chr18:13029576
|
A | G | 67 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(64): Show | 69 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.1051-87A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13029576 | ||||||
| chr18:13030084
|
G | A | 10 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(7): Show | 10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1390+82G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 10/44 | chr18 | 13030084 | ||||||
| chr18:13030213
|
C | G | 1 | a0021c0030t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1390+211C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 10/44 | chr18 | 13030213 | ||||||
| chr18:13030384
|
G | A | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1391-81G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 10/44 | chr18 | 13030384 | ||||||
| chr18:13030437
|
T | A | 1 | a0003c0003t0002g0093 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1391-28T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 10/44 | chr18 | 13030437 | ||||||
| chr18:13030618
|
T | C | 19 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(16): Show | 20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1534+10T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030618 | ||||||
| chr18:13030734
|
T | G | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1534+126T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030734 | ||||||
| chr18:13030835
|
A | G | 1 | a0004c0004t0001g0179 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1534+227A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030835 | ||||||
| chr18:13030838
|
T | C | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1534+230T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030838 | ||||||
| chr18:13030887
|
T | C | 1 | a0004c0004t0001g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1534+279T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030887 | ||||||
| chr18:13030955
|
C | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534+347C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030955 | ||||||
| chr18:13030981
|
AGT | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1534+377_1534+378d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13030981 | |||||
| chr18:13030984
|
G | A | 1 | a0002c0001t0001g0339 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1534+376G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030984 | ||||||
| chr18:13031031
|
CA | C | 11 | a0005c0005t0001g0151a0005c0005t0001g0153a0005c0005t0001g0154others(8): Show | 11 | HG01884.hp2 HG02818.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1534+425delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13031031 | |||||
| chr18:13031072
|
A | T | 2 | a0004c0004t0001g0206a0004c0004t0001g0207 | 2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1534+464A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031072 | ||||||
| chr18:13031157
|
C | T | 2 | a0002c0001t0001g0297a0002c0001t0001g0302 | 2 | HG02698.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1534+549C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031157 | ||||||
| chr18:13031243
|
G | GT | 85 | a0001c0002t0001g0226a0001c0002t0001g0232a0001c0002t0001g0272others(82): Show | 87 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1534+657dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13031243 | |||||
| chr18:13031243
|
G | GTT | 26 | a0001c0002t0001g0261a0002c0001t0001g0301a0002c0001t0001g0327others(23): Show | 27 | HG00140.hp1 HG00673.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1534+656_1534+657d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13031243 | |||||
| chr18:13031243
|
GT | G | 48 | a0001c0002t0001g0210a0002c0001t0001g0303a0004c0004t0001g0001others(45): Show | 58 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1534+657delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13031243 | |||||
| chr18:13031278
|
C | T | 88 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(85): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1534+670C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031278 | ||||||
| chr18:13031287
|
G | A | 1 | a0009c0009t0001g0003 | 4 | HG00621.hp2 NA18970.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+679G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031287 | ||||||
| chr18:13031489
|
T | C | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534+881T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031489 | ||||||
| chr18:13031490
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534+882G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031490 | ||||||
| chr18:13031500
|
G | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1534+892G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031500 | ||||||
| chr18:13031526
|
C | T | 3 | a0006c0006t0001g0356a0006c0006t0001g0358a0022c0028t0001g0357 | 3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1534+918C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031526 | ||||||
| chr18:13031539
|
G | A | 1 | a0006c0006t0002g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1534+931G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031539 | ||||||
| chr18:13031660
|
G | A | 1 | a0009c0009t0001g0218 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1534+1052G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031660 | ||||||
| chr18:13031991
|
C | T | 1 | a0001c0002t0001g0212 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1534+1383C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031991 | ||||||
| chr18:13032277
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534+1669G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032277 | ||||||
| chr18:13032484
|
C | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1534+1876C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032484 | ||||||
| chr18:13032537
|
G | T | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1534+1929G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032537 | ||||||
| chr18:13032541
|
G | A | 9 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(6): Show | 9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.1534+1933G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032541 | ||||||
| chr18:13032623
|
A | G | 1 | a0022c0028t0001g0357 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1534+2015A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032623 | ||||||
| chr18:13032667
|
G | A | 2 | a0001c0002t0001g0258a0001c0002t0001g0268 | 2 | NA18985.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1534+2059G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032667 | ||||||
| chr18:13032929
|
C | T | 1 | a0035c0044t0001g0165 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1534+2321C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032929 | ||||||
| chr18:13032930
|
ACT | A | 3 | a0006c0006t0001g0356a0006c0006t0001g0358a0022c0028t0001g0357 | 3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1534+2325_1534+232 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13032930 | |||||
| chr18:13032962
|
A | G | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1534+2354A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032962 | ||||||
| chr18:13033054
|
G | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1534+2446G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033054 | ||||||
| chr18:13033148
|
A | T | 2 | a0003c0003t0002g0053a0003c0003t0002g0054 | 2 | HG00735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1534+2540A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033148 | ||||||
| chr18:13033308
|
C | T | 58 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(55): Show | 60 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1534+2700C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033308 | ||||||
| chr18:13033471
|
A | G | 1 | a0002c0001t0001g0298 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1534+2863A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033471 | ||||||
| chr18:13033970
|
T | A | 1 | a0003c0003t0002g0055 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1535-3267T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033970 | ||||||
| chr18:13033975
|
G | A | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1535-3262G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033975 | ||||||
| chr18:13033976
|
T | C | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535-3261T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033976 | ||||||
| chr18:13034409
|
T | C | 1 | a0002c0001t0001g0304 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1535-2828T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034409 | ||||||
| chr18:13034423
|
G | A | 1 | a0025c0021t0001g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1535-2814G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034423 | ||||||
| chr18:13034527
|
G | A | 4 | a0005c0005t0001g0135a0005c0005t0001g0136a0005c0005t0001g0137others(1): Show | 4 | HG00099.hp2 HG01099.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535-2710G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034527 | ||||||
| chr18:13034603
|
C | T | 1 | a0001c0002t0001g0245 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1535-2634C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034603 | ||||||
| chr18:13034604
|
G | A | 1 | a0000c0035t0001g0264 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1535-2633G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034604 | ||||||
| chr18:13034814
|
G | A | 1 | a0007c0007t0002g0024 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1535-2423G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034814 | ||||||
| chr18:13034820
|
T | TA | 117 | a0001c0002t0001g0252a0001c0002t0001g0273a0001c0002t0001g0275others(114): Show | 125 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1535-2399dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13034820 | |||||
| chr18:13034922
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535-2315G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034922 | ||||||
| chr18:13035202
|
T | C | 1 | a0005c0005t0001g0208 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1535-2035T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13035202 | ||||||
| chr18:13035282
|
T | C | 1 | a0006c0006t0002g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1535-1955T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13035282 | ||||||
| chr18:13035394
|
G | C | 1 | a0027c0024t0001g0359 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1535-1843G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13035394 | ||||||
| chr18:13035832
|
G | A | 244 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(241): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1535-1405G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13035832 | ||||||
| chr18:13036035
|
T | G | 285 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(282): Show | 305 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.1535-1202T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036035 | ||||||
| chr18:13036145
|
C | CA | 47 | a0001c0002t0001g0259a0001c0002t0001g0260a0001c0045t0001g0269others(44): Show | 49 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.1535-1079dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13036145 | |||||
| chr18:13036151
|
A | C | 1 | a0005c0005t0001g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1535-1086A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036151 | ||||||
| chr18:13036162
|
TTTTG | T | 19 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(16): Show | 20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1535-1067_1535-106 others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13036162 | |||||
| chr18:13036178
|
T | A | 9 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(6): Show | 9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.1535-1059T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036178 | ||||||
| chr18:13036182
|
A | T | 1 | a0001c0002t0001g0266 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1535-1055A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036182 | ||||||
| chr18:13036255
|
C | G | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1535-982C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036255 | ||||||
| chr18:13036425
|
C | T | 67 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(64): Show | 70 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1535-812C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036425 | ||||||
| chr18:13036639
|
C | CCT | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1535-595_1535-594d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13036639 | |||||
| chr18:13036681
|
A | G | 1 | a0029c0036t0001g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1535-556A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036681 | ||||||
| chr18:13036748
|
C | T | 1 | a0003c0003t0002g0057 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1535-489C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036748 | ||||||
| chr18:13036781
|
T | A | 20 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(17): Show | 20 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1535-456T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036781 | ||||||
| chr18:13036782
|
C | T | 20 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(17): Show | 20 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1535-455C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036782 | ||||||
| chr18:13036875
|
C | CTT | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1535-361_1535-360d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13036875 | |||||
| chr18:13036900
|
A | C | 3 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219 | 6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1535-337A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036900 | ||||||
| chr18:13036917
|
A | G | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1535-320A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036917 | ||||||
| chr18:13036947
|
A | C | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535-290A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036947 | ||||||
| chr18:13037019
|
C | A | 288 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(285): Show | 311 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1535-218C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13037019 | ||||||
| chr18:13037117
|
G | A | 2 | a0003c0003t0002g0004a0003c0003t0002g0066 | 4 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1535-120G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13037117 | ||||||
| chr18:13037433
|
A | G | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1599+132A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13037433 | ||||||
| chr18:13037596
|
C | G | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1599+295C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13037596 | ||||||
| chr18:13037696
|
C | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1599+395C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13037696 | ||||||
| chr18:13037698
|
G | A | 1 | a0001c0033t0001g0211 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1599+397G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13037698 | ||||||
| chr18:13037830
|
C | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1599+529C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13037830 | ||||||
| chr18:13038014
|
A | C | 1 | a0036c0020t0001g0355 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1600-356A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13038014 | ||||||
| chr18:13038195
|
A | G | 1 | a0002c0001t0001g0322 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1600-175A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13038195 | ||||||
| chr18:13038202
|
T | C | 1 | a0003c0003t0002g0058 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1600-168T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13038202 | ||||||
| chr18:13038306
|
A | G | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1600-64A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13038306 | ||||||
| chr18:13038635
|
A | G | 1 | a0004c0004t0001g0202 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1809+56A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13038635 | ||||||
| chr18:13038786
|
C | T | 3 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219 | 6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1809+207C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13038786 | ||||||
| chr18:13038825
|
T | A | 1 | a0002c0001t0001g0332 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1809+246T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13038825 | ||||||
| chr18:13039054
|
A | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1809+475A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039054 | ||||||
| chr18:13039181
|
G | T | 36 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(33): Show | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1809+602G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039181 | ||||||
| chr18:13039230
|
G | A | 1 | a0003c0003t0002g0007 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1809+651G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039230 | ||||||
| chr18:13039262
|
C | T | 66 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(63): Show | 68 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.1809+683C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039262 | ||||||
| chr18:13039263
|
G | A | 1 | a0005c0005t0001g0148 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1809+684G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039263 | ||||||
| chr18:13039310
|
C | T | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1809+731C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039310 | ||||||
| chr18:13039326
|
G | A | 5 | a0001c0002t0001g0210a0001c0002t0001g0212a0001c0002t0001g0213others(2): Show | 5 | HG01109.hp2 HG02132.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1809+747G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039326 | ||||||
| chr18:13039424
|
C | G | 67 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(64): Show | 69 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.1809+845C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039424 | ||||||
| chr18:13039455
|
CA | C | 350 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(347): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1809+892delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | INFO_REALIGN_3_PRIME | chr18 | 13039455 | |||||
| chr18:13039455
|
CAA | C | 6 | a0004c0004t0001g0174a0004c0004t0001g0175a0004c0004t0001g0206others(3): Show | 6 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.1809+891_1809+892d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | INFO_REALIGN_3_PRIME | chr18 | 13039455 | |||||
| chr18:13039753
|
G | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1810-1077G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039753 | ||||||
| chr18:13039779
|
C | T | 8 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(5): Show | 8 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1810-1051C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039779 | ||||||
| chr18:13039828
|
G | A | 1 | a0001c0002t0001g0237 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1810-1002G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039828 | ||||||
| chr18:13040085
|
A | C | 109 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(106): Show | 117 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1810-745A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13040085 | ||||||
| chr18:13040114
|
T | C | 5 | a0001c0002t0001g0210a0001c0002t0001g0212a0001c0002t0001g0213others(2): Show | 5 | HG01109.hp2 HG02132.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1810-716T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13040114 | ||||||
| chr18:13041033
|
G | A | 2 | a0006c0006t0001g0356a0006c0006t0001g0358 | 2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1936+77G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041033 | ||||||
| chr18:13041050
|
A | T | 1 | a0004c0004t0001g0192 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1936+94A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041050 | ||||||
| chr18:13041231
|
G | T | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936+275G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041231 | ||||||
| chr18:13041303
|
GATA | G | 4 | a0001c0002t0001g0244a0001c0002t0001g0270a0001c0002t0001g0273others(1): Show | 4 | NA19001.hp1 NA19056.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936+350_1936+352d others(5): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chr18 | 13041303 | |||||
| chr18:13041476
|
G | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1936+520G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041476 | ||||||
| chr18:13041519
|
A | G | 1 | a0002c0001t0001g0317 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1936+563A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041519 | ||||||
| chr18:13041547
|
C | G | 1 | a0005c0005t0001g0160 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1936+591C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041547 | ||||||
| chr18:13041580
|
T | C | 1 | a0001c0002t0001g0238 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1936+624T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041580 | ||||||
| chr18:13041581
|
C | CT | 7 | a0001c0002t0001g0256a0001c0002t0001g0257a0002c0001t0001g0322others(4): Show | 7 | HG02040.hp2 HG02056.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.1937-609dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chr18 | 13041581 | |||||
| chr18:13041581
|
C | T | 1 | a0001c0002t0001g0238 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1937-623C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041581 | ||||||
| chr18:13041581
|
CT | C | 6 | a0001c0002t0001g0210a0003c0003t0002g0046a0015c0012t0001g0011others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1937-609delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chr18 | 13041581 | |||||
| chr18:13041787
|
A | C | 5 | a0005c0005t0001g0013a0005c0005t0001g0126a0014c0014t0001g0012others(2): Show | 6 | HG02132.hp1 NA18944.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.1937-417A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041787 | ||||||
| chr18:13041831
|
G | C | 41 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(38): Show | 43 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.1937-373G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041831 | ||||||
| chr18:13041856
|
G | A | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1937-348G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041856 | ||||||
| chr18:13041860
|
C | A | 1 | a0002c0001t0001g0305 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1937-344C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041860 | ||||||
| chr18:13042143
|
C | T | 1 | a0014c0014t0001g0012 | 2 | NA18944.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1937-61C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13042143 | ||||||
| chr18:13042549
|
A | G | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2067+215A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13042549 | ||||||
| chr18:13042638
|
C | T | 1 | a0036c0020t0001g0355 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2067+304C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13042638 | ||||||
| chr18:13042639
|
G | A | 9 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(6): Show | 9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.2067+305G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13042639 | ||||||
| chr18:13042931
|
C | T | 1 | a0001c0002t0001g0260 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2067+597C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13042931 | ||||||
| chr18:13043059
|
G | A | 1 | a0007c0007t0002g0023 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2067+725G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13043059 | ||||||
| chr18:13043608
|
G | C | 1 | a0003c0003t0002g0085 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2067+1274G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13043608 | ||||||
| chr18:13043729
|
T | C | 1 | a0002c0001t0001g0324 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2067+1395T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13043729 | ||||||
| chr18:13043910
|
T | C | 1 | a0002c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2067+1576T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13043910 | ||||||
| chr18:13043974
|
C | T | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2067+1640C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13043974 | ||||||
| chr18:13044015
|
T | A | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.2067+1681T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13044015 | ||||||
| chr18:13044093
|
G | C | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.2067+1759G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13044093 | ||||||
| chr18:13044262
|
A | G | 6 | a0001c0002t0001g0221a0001c0002t0001g0233a0001c0002t0001g0247others(3): Show | 6 | HG02129.hp2 NA18942.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.2067+1928A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13044262 | ||||||
| chr18:13044420
|
T | TTTTTG | 114 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(111): Show | 119 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2067+2101_2067+210 others(9): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13044420 | |||||
| chr18:13044683
|
T | C | 1 | a0002c0023t0001g0296 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2067+2349T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13044683 | ||||||
| chr18:13045032
|
T | C | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.2067+2698T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13045032 | ||||||
| chr18:13045217
|
C | T | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.2067+2883C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13045217 | ||||||
| chr18:13045321
|
T | C | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2067+2987T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13045321 | ||||||
| chr18:13045563
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2067+3229G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13045563 | ||||||
| chr18:13045768
|
G | A | 1 | a0001c0002t0001g0272 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2068-3091G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13045768 | ||||||
| chr18:13046069
|
G | A | 1 | a0001c0002t0001g0276 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2068-2790G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046069 | ||||||
| chr18:13046078
|
G | T | 1 | a0001c0002t0001g0280 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2068-2781G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046078 | ||||||
| chr18:13046081
|
C | G | 3 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219 | 6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.2068-2778C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046081 | ||||||
| chr18:13046127
|
G | T | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.2068-2732G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046127 | ||||||
| chr18:13046133
|
G | A | 3 | a0005c0005t0001g0135a0005c0005t0001g0136a0005c0005t0001g0137 | 3 | HG00099.hp2 HG01099.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2068-2726G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046133 | ||||||
| chr18:13046146
|
T | C | 114 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(111): Show | 119 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2068-2713T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046146 | ||||||
| chr18:13046147
|
G | A | 1 | a0005c0005t0001g0127 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2068-2712G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046147 | ||||||
| chr18:13046178
|
G | A | 78 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(75): Show | 82 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.2068-2681G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046178 | ||||||
| chr18:13046260
|
G | A | 3 | a0006c0006t0001g0356a0006c0006t0001g0358a0022c0028t0001g0357 | 3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2068-2599G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046260 | ||||||
| chr18:13046565
|
A | G | 1 | a0006c0006t0002g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2068-2294A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046565 | ||||||
| chr18:13046669
|
A | G | 2 | a0015c0012t0001g0114a0015c0012t0001g0115 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2068-2190A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046669 | ||||||
| chr18:13046751
|
A | T | 1 | a0001c0002t0001g0243 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2068-2108A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046751 | ||||||
| chr18:13046788
|
C | G | 6 | a0003c0003t0002g0046a0003c0003t0002g0072a0003c0003t0002g0073others(3): Show | 6 | HG00558.hp1 HG00597.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.2068-2071C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046788 | ||||||
| chr18:13046829
|
C | CT | 74 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(71): Show | 80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.2068-2012dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13046829 | |||||
| chr18:13046829
|
C | CTT | 42 | a0001c0002t0001g0228a0001c0002t0001g0261a0001c0002t0001g0273others(39): Show | 44 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.2068-2013_2068-201 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13046829 | |||||
| chr18:13046829
|
CTTTTTTT | C | 6 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2068-2018_2068-201 others(11): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13046829 | |||||
| chr18:13046847
|
T | G | 1 | a0002c0001t0001g0291 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2068-2012T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046847 | ||||||
| chr18:13046920
|
A | G | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2068-1939A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046920 | ||||||
| chr18:13047209
|
C | T | 1 | a0001c0002t0001g0237 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2068-1650C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047209 | ||||||
| chr18:13047222
|
T | C | 3 | a0006c0006t0001g0356a0006c0006t0001g0358a0022c0028t0001g0357 | 3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2068-1637T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047222 | ||||||
| chr18:13047234
|
A | G | 67 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(64): Show | 70 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.2068-1625A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047234 | ||||||
| chr18:13047269
|
C | T | 1 | a0003c0003t0002g0110 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2068-1590C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047269 | ||||||
| chr18:13047271
|
G | A | 2 | a0015c0012t0001g0011a0034c0031t0001g0011 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2068-1588G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047271 | ||||||
| chr18:13047295
|
A | G | 2 | a0006c0006t0002g0043a0006c0006t0002g0044 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2068-1564A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047295 | ||||||
| chr18:13047360
|
T | TAC | 30 | a0002c0001t0001g0021a0004c0004t0001g0002a0004c0004t0001g0196others(27): Show | 35 | HG00642.hp1 HG01074.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.2068-1482_2068-148 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13047360 | |||||
| chr18:13047360
|
T | TACAC | 4 | a0001c0002t0001g0273a0013c0016t0003g0216a0013c0016t0003g0217others(1): Show | 4 | HG02258.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068-1484_2068-148 others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13047360 | |||||
| chr18:13047552
|
C | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.2068-1307C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047552 | ||||||
| chr18:13047785
|
T | G | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.2068-1074T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047785 | ||||||
| chr18:13047786
|
C | T | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068-1073C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047786 | ||||||
| chr18:13047806
|
T | C | 42 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(39): Show | 44 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.2068-1053T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047806 | ||||||
| chr18:13047819
|
C | A | 4 | a0001c0002t0001g0239a0001c0002t0001g0258a0001c0002t0001g0268others(1): Show | 4 | NA18950.hp1 NA18985.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068-1040C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047819 | ||||||
| chr18:13047835
|
C | G | 3 | a0005c0005t0001g0146a0005c0005t0001g0162a0005c0005t0001g0163 | 3 | HG01884.hp1 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2068-1024C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047835 | ||||||
| chr18:13047984
|
T | C | 114 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(111): Show | 119 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2068-875T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047984 | ||||||
| chr18:13048497
|
C | T | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2068-362C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13048497 | ||||||
| chr18:13048534
|
C | T | 1 | a0004c0004t0001g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2068-325C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13048534 | ||||||
| chr18:13048571
|
AT | A | 11 | a0005c0005t0001g0151a0005c0005t0001g0153a0005c0005t0001g0154others(8): Show | 11 | HG01884.hp2 HG02818.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.2068-286delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13048571 | |||||
| chr18:13048575
|
C | A | 11 | a0005c0005t0001g0151a0005c0005t0001g0153a0005c0005t0001g0154others(8): Show | 11 | HG01884.hp2 HG02818.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.2068-284C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13048575 | ||||||
| chr18:13048785
|
A | G | 2 | a0005c0005t0001g0162a0005c0005t0001g0163 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2068-74A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13048785 | ||||||
| chr18:13048797
|
G | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.2068-62G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13048797 | ||||||
| chr18:13049949
|
G | A | 1 | a0001c0002t0001g0270 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3017+58G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13049949 | ||||||
| chr18:13049949
|
G | GA | 288 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(285): Show | 311 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.3017+65dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chr18 | 13049949 | |||||
| chr18:13050048
|
C | G | 6 | a0006c0006t0001g0356a0006c0006t0001g0358a0013c0016t0003g0216others(3): Show | 6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3017+157C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050048 | ||||||
| chr18:13050061
|
C | CT | 19 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(16): Show | 20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.3017+180dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chr18 | 13050061 | |||||
| chr18:13050147
|
G | T | 3 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0265 | 3 | HG02040.hp2 NA18974.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.3017+256G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050147 | ||||||
| chr18:13050170
|
G | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3017+279G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050170 | ||||||
| chr18:13050390
|
C | G | 82 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(79): Show | 89 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.3017+499C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050390 | ||||||
| chr18:13050452
|
C | T | 2 | a0001c0002t0001g0212a0001c0033t0001g0211 | 2 | HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.3017+561C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050452 | ||||||
| chr18:13050533
|
C | T | 2 | a0001c0002t0001g0212a0001c0033t0001g0211 | 2 | HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.3017+642C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050533 | ||||||
| chr18:13050568
|
T | G | 6 | a0006c0006t0001g0356a0006c0006t0001g0358a0013c0016t0003g0216others(3): Show | 6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3017+677T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050568 | ||||||
| chr18:13050575
|
CT | C | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.3017+696delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chr18 | 13050575 | |||||
| chr18:13050611
|
G | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3017+720G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050611 | ||||||
| chr18:13050752
|
G | A | 1 | a0032c0032t0001g0119 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3017+861G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050752 | ||||||
| chr18:13050883
|
A | G | 1 | a0003c0003t0002g0065 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3017+992A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050883 | ||||||
| chr18:13050929
|
G | A | 6 | a0006c0006t0001g0356a0006c0006t0001g0358a0013c0016t0003g0216others(3): Show | 6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3017+1038G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050929 | ||||||
| chr18:13050982
|
C | T | 1 | a0001c0002t0001g0254 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3017+1091C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050982 | ||||||
| chr18:13050996
|
T | C | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.3017+1105T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050996 | ||||||
| chr18:13051138
|
A | G | 1 | a0004c0004t0001g0196 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3017+1247A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051138 | ||||||
| chr18:13051250
|
A | G | 2 | a0017c0018t0002g0062a0017c0018t0002g0092 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3017+1359A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051250 | ||||||
| chr18:13051365
|
T | TTG | 20 | a0005c0005t0001g0124a0006c0006t0002g0025a0006c0006t0002g0034others(17): Show | 21 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.3017+1489_3017+149 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chr18 | 13051365 | |||||
| chr18:13051506
|
T | C | 1 | a0005c0005t0001g0139 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3018-1413T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051506 | ||||||
| chr18:13051612
|
C | T | 2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3018-1307C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051612 | ||||||
| chr18:13051703
|
C | G | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3018-1216C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051703 | ||||||
| chr18:13051771
|
C | T | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.3018-1148C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051771 | ||||||
| chr18:13051893
|
C | T | 1 | a0003c0003t0002g0010 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3018-1026C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051893 | ||||||
| chr18:13052039
|
C | T | 1 | a0001c0002t0001g0282 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3018-880C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052039 | ||||||
| chr18:13052070
|
G | A | 1 | a0001c0002t0001g0248 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3018-849G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052070 | ||||||
| chr18:13052229
|
A | G | 1 | a0002c0001t0001g0309 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3018-690A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052229 | ||||||
| chr18:13052431
|
T | C | 18 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(15): Show | 18 | HG01167.hp1 HG01884.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.3018-488T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052431 | ||||||
| chr18:13052474
|
C | A | 78 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(75): Show | 82 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.3018-445C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052474 | ||||||
| chr18:13052664
|
C | T | 62 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(59): Show | 64 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.3018-255C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052664 | ||||||
| chr18:13052689
|
G | A | 1 | a0004c0004t0001g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3018-230G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052689 | ||||||
| chr18:13052829
|
A | C | 19 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(16): Show | 20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.3018-90A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052829 | ||||||
| chr18:13052864
|
T | C | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3018-55T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052864 | ||||||
| chr18:13052868
|
G | T | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3018-51G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052868 | ||||||
| chr18:13052895
|
G | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3018-24G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052895 | ||||||
| chr18:13052896
|
T | C | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3018-23T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052896 | ||||||
| chr18:13052897
|
G | C | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3018-22G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052897 | ||||||
| chr18:13052898
|
TGA | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3018-19_3018-18del others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chr18 | 13052898 | |||||
| chr18:13052901
|
G | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3018-18G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052901 | ||||||
| chr18:13052903
|
T | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3018-16T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052903 | ||||||
| chr18:13053150
|
A | G | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3189+60A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13053150 | ||||||
| chr18:13053512
|
G | A | 1 | a0005c0005t0001g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3189+422G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13053512 | ||||||
| chr18:13053752
|
C | T | 1 | a0005c0005t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3189+662C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13053752 | ||||||
| chr18:13054104
|
A | G | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.3189+1014A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054104 | ||||||
| chr18:13054276
|
A | G | 2 | a0004c0004t0001g0206a0004c0004t0001g0207 | 2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3189+1186A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054276 | ||||||
| chr18:13054383
|
G | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3189+1293G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054383 | ||||||
| chr18:13054455
|
T | C | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.3190-1325T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054455 | ||||||
| chr18:13054529
|
T | G | 3 | a0001c0002t0001g0259a0001c0002t0001g0260a0001c0045t0001g0269 | 3 | HG02451.hp2 HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3190-1251T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054529 | ||||||
| chr18:13054534
|
A | G | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3190-1246A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054534 | ||||||
| chr18:13054975
|
C | T | 2 | a0002c0001t0001g0336a0026c0025t0001g0300 | 2 | HG00738.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3190-805C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054975 | ||||||
| chr18:13055183
|
G | T | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3190-597G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13055183 | ||||||
| chr18:13055279
|
C | CA | 9 | a0001c0002t0001g0228a0001c0002t0001g0273a0002c0001t0001g0360others(6): Show | 9 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.3190-484dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | INFO_REALIGN_3_PRIME | chr18 | 13055279 | |||||
| chr18:13055279
|
CA | C | 16 | a0001c0002t0001g0238a0004c0004t0001g0191a0005c0005t0001g0151others(13): Show | 16 | HG01515.hp1 HG01884.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.3190-484delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | INFO_REALIGN_3_PRIME | chr18 | 13055279 | |||||
| chr18:13055302
|
C | T | 57 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(54): Show | 59 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.3190-478C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13055302 | ||||||
| chr18:13055400
|
G | A | 1 | a0003c0003t0002g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3190-380G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13055400 | ||||||
| chr18:13055402
|
T | C | 1 | a0028c0042t0002g0107 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3190-378T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13055402 | ||||||
| chr18:13055513
|
C | T | 1 | a0003c0003t0002g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3190-267C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13055513 | ||||||
| chr18:13055766
|
T | G | 2 | a0006c0006t0002g0034a0006c0006t0002g0037 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3190-14T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13055766 | ||||||
| chr18:13056852
|
G | A | 1 | a0001c0002t0001g0257 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4108+154G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13056852 | ||||||
| chr18:13056908
|
A | G | 2 | a0003c0003t0002g0058a0003c0003t0002g0111 | 2 | HG00280.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.4108+210A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13056908 | ||||||
| chr18:13057031
|
C | G | 1 | a0006c0006t0002g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4108+333C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13057031 | ||||||
| chr18:13057046
|
G | A | 7 | a0002c0001t0001g0310a0002c0001t0001g0311a0002c0001t0001g0316others(4): Show | 7 | HG01361.hp1 HG01928.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.4108+348G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13057046 | ||||||
| chr18:13057065
|
C | T | 3 | a0006c0006t0002g0042a0006c0006t0002g0043a0006c0006t0002g0044 | 3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4108+367C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13057065 | ||||||
| chr18:13057253
|
G | GT | 40 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(37): Show | 42 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.4109-329dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | INFO_REALIGN_3_PRIME | chr18 | 13057253 | |||||
| chr18:13057253
|
G | T | 6 | a0004c0004t0001g0014a0004c0004t0001g0184a0004c0004t0001g0188others(3): Show | 7 | HG00621.hp1 NA18612.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.4109-332G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13057253 | ||||||
| chr18:13057257
|
G | GT | 318 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(315): Show | 345 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.4109-317dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | INFO_REALIGN_3_PRIME | chr18 | 13057257 | |||||
| chr18:13057257
|
G | T | 40 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(37): Show | 42 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.4109-328G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13057257 | ||||||
| chr18:13057799
|
C | T | 1 | a0036c0020t0001g0355 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4257+66C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13057799 | ||||||
| chr18:13057856
|
T | C | 1 | a0002c0001t0001g0306 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.4257+123T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13057856 | ||||||
| chr18:13058020
|
T | G | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4257+287T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058020 | ||||||
| chr18:13058319
|
A | G | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.4257+586A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058319 | ||||||
| chr18:13058407
|
C | T | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4257+674C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058407 | ||||||
| chr18:13058460
|
C | T | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4258-622C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058460 | ||||||
| chr18:13058495
|
T | C | 240 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(237): Show | 253 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.4258-587T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058495 | ||||||
| chr18:13058503
|
A | G | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4258-579A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058503 | ||||||
| chr18:13058616
|
G | A | 2 | a0002c0001t0001g0312a0002c0001t0001g0315 | 2 | NA18945.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.4258-466G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058616 | ||||||
| chr18:13058837
|
A | G | 3 | a0001c0002t0001g0259a0001c0002t0001g0260a0001c0045t0001g0269 | 3 | HG02451.hp2 HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4258-245A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058837 | ||||||
| chr18:13058864
|
A | T | 1 | a0025c0021t0001g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4258-218A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058864 | ||||||
| chr18:13058870
|
C | G | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4258-212C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058870 | ||||||
| chr18:13058922
|
C | T | 68 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(65): Show | 71 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.4258-160C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058922 | ||||||
| chr18:13059034
|
T | C | 3 | a0019c0019t0001g0166a0019c0019t0001g0167a0035c0044t0001g0165 | 3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4258-48T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13059034 | ||||||
| chr18:13059327
|
A | G | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4488+15A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059327 | ||||||
| chr18:13059373
|
T | C | 34 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(31): Show | 36 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.4488+61T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059373 | ||||||
| chr18:13059377
|
A | C | 1 | a0001c0002t0001g0282 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4488+65A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059377 | ||||||
| chr18:13059408
|
G | A | 1 | a0006c0006t0002g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4488+96G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059408 | ||||||
| chr18:13059495
|
T | A | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.4488+183T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059495 | ||||||
| chr18:13059537
|
A | G | 2 | a0005c0005t0001g0123a0005c0005t0001g0124 | 2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4488+225A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059537 | ||||||
| chr18:13059539
|
G | A | 1 | a0005c0005t0001g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4488+227G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059539 | ||||||
| chr18:13059876
|
C | T | 13 | a0005c0005t0001g0151a0005c0005t0001g0153a0005c0005t0001g0154others(10): Show | 13 | HG01884.hp2 HG02717.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.4488+564C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059876 | ||||||
| chr18:13060023
|
G | A | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4488+711G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060023 | ||||||
| chr18:13060080
|
A | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4488+768A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060080 | ||||||
| chr18:13060144
|
G | A | 1 | a0006c0006t0001g0356 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4488+832G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060144 | ||||||
| chr18:13060181
|
G | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.4488+869G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060181 | ||||||
| chr18:13060486
|
G | C | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4488+1174G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060486 | ||||||
| chr18:13060638
|
ATT | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4488+1328_4488+132 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13060638 | |||||
| chr18:13060763
|
A | T | 9 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(6): Show | 9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.4488+1451A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060763 | ||||||
| chr18:13060799
|
T | C | 1 | a0005c0005t0001g0285 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4488+1487T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060799 | ||||||
| chr18:13060911
|
G | A | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4488+1599G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060911 | ||||||
| chr18:13060929
|
GA | G | 278 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(275): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.4488+1629delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13060929 | |||||
| chr18:13061003
|
T | C | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4488+1691T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061003 | ||||||
| chr18:13061013
|
T | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4488+1701T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061013 | ||||||
| chr18:13061089
|
G | A | 1 | a0002c0001t0001g0293 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4488+1777G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061089 | ||||||
| chr18:13061319
|
C | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4488+2007C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061319 | ||||||
| chr18:13061322
|
GA | G | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.4488+2018delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13061322 | |||||
| chr18:13061340
|
T | C | 1 | a0001c0002t0001g0250 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4488+2028T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061340 | ||||||
| chr18:13061542
|
A | G | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4488+2230A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061542 | ||||||
| chr18:13061668
|
G | A | 1 | a0002c0001t0001g0328 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4488+2356G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061668 | ||||||
| chr18:13061781
|
A | G | 40 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(37): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.4488+2469A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061781 | ||||||
| chr18:13061859
|
G | A | 1 | a0002c0001t0001g0295 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4488+2547G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061859 | ||||||
| chr18:13061995
|
T | C | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4488+2683T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061995 | ||||||
| chr18:13062074
|
A | C | 1 | a0001c0002t0001g0277 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.4488+2762A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062074 | ||||||
| chr18:13062087
|
C | T | 2 | a0008c0008t0001g0133a0008c0008t0001g0169 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.4488+2775C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062087 | ||||||
| chr18:13062102
|
T | A | 6 | a0011c0011t0001g0283a0011c0011t0001g0284a0011c0011t0001g0288others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4488+2790T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062102 | ||||||
| chr18:13062135
|
A | T | 2 | a0003c0003t0002g0050a0028c0042t0002g0107 | 2 | HG02074.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.4488+2823A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062135 | ||||||
| chr18:13062228
|
CT | C | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4488+2918delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13062228 | |||||
| chr18:13062251
|
G | A | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4488+2939G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062251 | ||||||
| chr18:13062414
|
T | A | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4488+3102T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062414 | ||||||
| chr18:13062486
|
T | C | 2 | a0001c0002t0001g0259a0001c0002t0001g0260 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4488+3174T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062486 | ||||||
| chr18:13062526
|
A | AT | 158 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(155): Show | 165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.4488+3228dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13062526 | |||||
| chr18:13062526
|
AT | A | 43 | a0001c0002t0001g0244a0003c0003t0002g0110a0004c0004t0001g0001others(40): Show | 53 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.4488+3228delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13062526 | |||||
| chr18:13062540
|
T | A | 1 | a0001c0002t0001g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4488+3228T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062540 | ||||||
| chr18:13062572
|
A | G | 1 | a0001c0002t0001g0237 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4488+3260A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062572 | ||||||
| chr18:13062920
|
T | A | 1 | a0005c0005t0001g0015 | 2 | HG02071.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.4488+3608T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062920 | ||||||
| chr18:13062946
|
T | A | 1 | a0005c0005t0001g0015 | 2 | HG02071.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.4488+3634T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062946 | ||||||
| chr18:13062952
|
G | A | 1 | a0005c0005t0001g0015 | 2 | HG02071.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.4488+3640G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062952 | ||||||
| chr18:13063085
|
T | C | 1 | a0036c0020t0001g0355 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4488+3773T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063085 | ||||||
| chr18:13063096
|
T | C | 1 | a0004c0004t0001g0182 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4488+3784T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063096 | ||||||
| chr18:13063127
|
C | G | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4488+3815C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063127 | ||||||
| chr18:13063203
|
C | G | 1 | a0010c0010t0002g0081 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4488+3891C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063203 | ||||||
| chr18:13063341
|
C | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4488+4029C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063341 | ||||||
| chr18:13063475
|
G | A | 11 | a0001c0002t0001g0016a0001c0002t0001g0224a0001c0002t0001g0225others(8): Show | 12 | HG00544.hp2 HG02523.hp1 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.4488+4163G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063475 | ||||||
| chr18:13063772
|
T | A | 1 | a0005c0005t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4489-4059T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063772 | ||||||
| chr18:13063820
|
A | AT | 52 | a0001c0002t0001g0249a0005c0005t0001g0013a0005c0005t0001g0116others(49): Show | 53 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.4489-3993dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13063820 | |||||
| chr18:13063890
|
G | A | 17 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(14): Show | 17 | HG01167.hp1 HG01884.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.4489-3941G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063890 | ||||||
| chr18:13063892
|
C | T | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.4489-3939C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063892 | ||||||
| chr18:13063897
|
T | G | 6 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.4489-3934T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063897 | ||||||
| chr18:13063995
|
A | AT | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4489-3831dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13063995 | |||||
| chr18:13064089
|
G | A | 1 | a0001c0002t0001g0245 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4489-3742G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064089 | ||||||
| chr18:13064127
|
T | G | 1 | a0004c0004t0001g0181 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4489-3704T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064127 | ||||||
| chr18:13064440
|
G | A | 2 | a0011c0011t0001g0283a0011c0011t0001g0284 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4489-3391G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064440 | ||||||
| chr18:13064480
|
C | T | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4489-3351C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064480 | ||||||
| chr18:13064611
|
C | CA | 57 | a0001c0002t0001g0226a0001c0002t0001g0228a0001c0002t0001g0245others(54): Show | 70 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.4489-3201dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13064611 | |||||
| chr18:13064611
|
CA | C | 22 | a0002c0001t0001g0292a0003c0003t0002g0071a0003c0003t0002g0075others(19): Show | 22 | HG00558.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.4489-3201delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13064611 | |||||
| chr18:13064671
|
A | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4489-3160A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064671 | ||||||
| chr18:13064861
|
C | T | 1 | a0002c0001t0001g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4489-2970C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064861 | ||||||
| chr18:13064879
|
G | A | 77 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(74): Show | 80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.4489-2952G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064879 | ||||||
| chr18:13064879
|
G | T | 1 | a0004c0004t0001g0181 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4489-2952G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064879 | ||||||
| chr18:13065096
|
T | C | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4489-2735T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065096 | ||||||
| chr18:13065175
|
G | GT | 63 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(60): Show | 67 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.4489-2644dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13065175 | |||||
| chr18:13065175
|
G | T | 1 | a0002c0001t0001g0354 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4489-2656G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065175 | ||||||
| chr18:13065178
|
T | G | 2 | a0001c0002t0001g0259a0001c0002t0001g0260 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4489-2653T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065178 | ||||||
| chr18:13065290
|
G | T | 1 | a0004c0004t0001g0190 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4489-2541G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065290 | ||||||
| chr18:13065352
|
G | A | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4489-2479G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065352 | ||||||
| chr18:13065361
|
A | G | 1 | a0022c0028t0001g0357 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4489-2470A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065361 | ||||||
| chr18:13065364
|
G | A | 1 | a0001c0002t0001g0222 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.4489-2467G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065364 | ||||||
| chr18:13065485
|
C | A | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.4489-2346C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065485 | ||||||
| chr18:13065549
|
A | C | 9 | a0007c0007t0002g0006a0007c0007t0002g0023a0007c0007t0002g0024others(6): Show | 10 | HG01952.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.4489-2282A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065549 | ||||||
| chr18:13065549
|
A | G | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4489-2282A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065549 | ||||||
| chr18:13065712
|
A | G | 9 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(6): Show | 9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.4489-2119A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065712 | ||||||
| chr18:13065729
|
C | G | 13 | a0005c0005t0001g0151a0005c0005t0001g0153a0005c0005t0001g0154others(10): Show | 13 | HG01884.hp2 HG02717.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.4489-2102C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065729 | ||||||
| chr18:13065807
|
A | C | 1 | a0001c0045t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4489-2024A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065807 | ||||||
| chr18:13065934
|
G | A | 1 | a0001c0002t0001g0274 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4489-1897G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065934 | ||||||
| chr18:13065987
|
G | T | 1 | a0005c0005t0001g0173 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4489-1844G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065987 | ||||||
| chr18:13066017
|
A | G | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4489-1814A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066017 | ||||||
| chr18:13066039
|
G | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4489-1792G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066039 | ||||||
| chr18:13066110
|
C | G | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4489-1721C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066110 | ||||||
| chr18:13066124
|
T | C | 281 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(278): Show | 304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.4489-1707T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066124 | ||||||
| chr18:13066365
|
T | C | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4489-1466T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066365 | ||||||
| chr18:13066511
|
C | A | 1 | a0002c0001t0001g0351 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4489-1320C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066511 | ||||||
| chr18:13066706
|
G | C | 1 | a0005c0005t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4489-1125G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066706 | ||||||
| chr18:13066790
|
C | G | 36 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(33): Show | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.4489-1041C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066790 | ||||||
| chr18:13066954
|
T | G | 1 | a0002c0001t0001g0321 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4489-877T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066954 | ||||||
| chr18:13066963
|
C | CTG | 85 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(82): Show | 96 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.4489-833_4489-832d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | |||||
| chr18:13066963
|
C | CTGTG | 49 | a0002c0001t0001g0295a0002c0001t0001g0310a0002c0001t0001g0311others(46): Show | 53 | HG00423.hp2 HG00621.hp1 HG01361.hp1 others(50): Show |
intron_variant | MODIFIER | c.4489-835_4489-832d others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | |||||
| chr18:13066963
|
C | CTGTGTG | 15 | a0002c0001t0001g0022a0002c0001t0001g0321a0002c0001t0001g0323others(12): Show | 16 | HG01099.hp1 HG01261.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.4489-837_4489-832d others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | |||||
| chr18:13066963
|
C | CTGTGTGT others(1): Show |
22 | a0002c0001t0001g0320a0002c0001t0001g0327a0005c0005t0001g0015others(19): Show | 23 | HG00597.hp1 HG00673.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.4489-839_4489-832d others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | |||||
| chr18:13066963
|
C | CTGTGTGT others(3): Show |
10 | a0005c0005t0001g0116a0005c0005t0001g0125a0005c0005t0001g0127others(7): Show | 10 | HG00099.hp2 HG01071.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.4489-841_4489-832d others(12): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | |||||
| chr18:13066963
|
C | CTGTGTGT others(5): Show |
20 | a0005c0005t0001g0013a0005c0005t0001g0117a0005c0005t0001g0126others(17): Show | 24 | HG00621.hp2 HG02717.hp1 HG02818.hp2 others(21): Show |
intron_variant | MODIFIER | c.4489-843_4489-832d others(14): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | |||||
| chr18:13066963
|
C | CTGTGTGT others(7): Show |
5 | a0005c0005t0001g0153a0005c0005t0001g0159a0005c0005t0001g0172others(2): Show | 5 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.4489-845_4489-832d others(16): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | |||||
| chr18:13066963
|
C | CTGTGTGT others(11): Show |
1 | a0027c0024t0001g0359 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4489-849_4489-832d others(20): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | |||||
| chr18:13066963
|
CTG | C | 71 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(68): Show | 74 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.4489-833_4489-832d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | |||||
| chr18:13066969
|
G | GTGTGTGT others(5): Show |
8 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(5): Show | 8 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.4489-851_4489-850i others(14): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066969 | |||||
| chr18:13067057
|
A | C | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4489-774A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067057 | ||||||
| chr18:13067124
|
AT | A | 6 | a0011c0011t0001g0283a0011c0011t0001g0284a0011c0011t0001g0288others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4489-700delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13067124 | |||||
| chr18:13067127
|
T | A | 6 | a0011c0011t0001g0283a0011c0011t0001g0284a0011c0011t0001g0288others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4489-704T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067127 | ||||||
| chr18:13067139
|
T | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4489-692T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067139 | ||||||
| chr18:13067271
|
G | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4489-560G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067271 | ||||||
| chr18:13067297
|
G | A | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4489-534G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067297 | ||||||
| chr18:13067369
|
G | A | 1 | a0025c0021t0001g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4489-462G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067369 | ||||||
| chr18:13067462
|
A | T | 1 | a0010c0010t0002g0104 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.4489-369A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067462 | ||||||
| chr18:13067535
|
T | C | 1 | a0001c0002t0001g0224 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4489-296T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067535 | ||||||
| chr18:13067544
|
G | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4489-287G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067544 | ||||||
| chr18:13067652
|
G | T | 1 | a0001c0002t0001g0212 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4489-179G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067652 | ||||||
| chr18:13067728
|
G | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4489-103G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067728 | ||||||
| chr18:13067774
|
A | G | 1 | a0003c0003t0002g0055 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4489-57A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067774 | ||||||
| chr18:13067802
|
A | G | 2 | a0001c0002t0001g0259a0001c0002t0001g0260 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4489-29A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067802 | ||||||
| chr18:13068324
|
T | G | 5 | a0003c0003t0002g0077a0003c0003t0002g0099a0003c0003t0002g0103others(2): Show | 5 | HG00140.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.4759-35T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 23/44 | chr18 | 13068324 | ||||||
| chr18:13068340
|
T | A | 5 | a0003c0003t0002g0077a0003c0003t0002g0099a0003c0003t0002g0103others(2): Show | 5 | HG00140.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.4759-19T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 23/44 | chr18 | 13068340 | ||||||
| chr18:13068429
|
T | C | 1 | a0005c0005t0001g0121 | 1 | NA19064.hp1 | splice_region_variant&intron_variant | LOW | c.4822+7T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068429 | ||||||
| chr18:13068577
|
G | C | 1 | a0020c0046t0001g0287 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4822+155G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068577 | ||||||
| chr18:13068612
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4822+190G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068612 | ||||||
| chr18:13068694
|
A | C | 2 | a0006c0006t0001g0356a0006c0006t0001g0358 | 2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.4823-158A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068694 | ||||||
| chr18:13068715
|
T | A | 3 | a0001c0002t0001g0210a0001c0002t0001g0213a0025c0021t0001g0348 | 3 | HG01109.hp2 HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.4823-137T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068715 | ||||||
| chr18:13068726
|
C | T | 3 | a0006c0006t0002g0042a0006c0006t0002g0043a0006c0006t0002g0044 | 3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4823-126C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068726 | ||||||
| chr18:13068819
|
G | A | 1 | a0013c0029t0003g0215 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4823-33G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068819 | ||||||
| chr18:13069006
|
C | T | 1 | a0004c0004t0001g0179 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.4962+15C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 25/44 | chr18 | 13069006 | ||||||
| chr18:13069057
|
C | T | 4 | a0012c0013t0002g0084a0012c0013t0002g0097a0012c0013t0002g0109others(1): Show | 4 | HG02145.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4963-32C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 25/44 | chr18 | 13069057 | ||||||
| chr18:13069222
|
C | T | 46 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(43): Show | 56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.5055+41C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 26/44 | chr18 | 13069222 | ||||||
| chr18:13069329
|
G | A | 1 | a0005c0005t0001g0121 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.5055+148G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 26/44 | chr18 | 13069329 | ||||||
| chr18:13069468
|
C | T | 3 | a0019c0019t0001g0166a0019c0019t0001g0167a0035c0044t0001g0165 | 3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5056-270C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 26/44 | chr18 | 13069468 | ||||||
| chr18:13069709
|
T | C | 1 | a0005c0005t0001g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5056-29T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 26/44 | chr18 | 13069709 | ||||||
| chr18:13070120
|
C | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.5174+264C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070120 | ||||||
| chr18:13070156
|
C | CA | 4 | a0002c0001t0001g0337a0009c0009t0001g0003a0009c0009t0001g0218others(1): Show | 7 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.5174+312dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | INFO_REALIGN_3_PRIME | chr18 | 13070156 | |||||
| chr18:13070156
|
CA | C | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.5174+312delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | INFO_REALIGN_3_PRIME | chr18 | 13070156 | |||||
| chr18:13070528
|
T | C | 1 | a0012c0013t0002g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5175-511T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070528 | ||||||
| chr18:13070567
|
C | T | 3 | a0001c0002t0001g0210a0001c0002t0001g0213a0025c0021t0001g0348 | 3 | HG01109.hp2 HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.5175-472C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070567 | ||||||
| chr18:13070712
|
G | A | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.5175-327G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070712 | ||||||
| chr18:13070713
|
C | T | 3 | a0003c0003t0002g0010a0003c0003t0002g0061a0003c0003t0002g0086 | 4 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.5175-326C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070713 | ||||||
| chr18:13070724
|
G | A | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5175-315G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070724 | ||||||
| chr18:13070754
|
C | T | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.5175-285C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070754 | ||||||
| chr18:13070852
|
C | G | 1 | a0001c0002t0001g0210 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5175-187C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070852 | ||||||
| chr18:13070931
|
T | C | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.5175-108T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070931 | ||||||
| chr18:13071237
|
G | A | 1 | a0003c0003t0002g0082 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5348+25G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071237 | ||||||
| chr18:13071321
|
A | T | 1 | a0001c0002t0001g0280 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5348+109A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071321 | ||||||
| chr18:13071353
|
A | T | 6 | a0006c0006t0001g0356a0006c0006t0001g0358a0013c0016t0003g0216others(3): Show | 6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.5348+141A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071353 | ||||||
| chr18:13071385
|
A | G | 1 | a0011c0011t0001g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5348+173A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071385 | ||||||
| chr18:13071396
|
G | A | 1 | a0002c0001t0001g0346 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5348+184G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071396 | ||||||
| chr18:13071441
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5348+229G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071441 | ||||||
| chr18:13071654
|
T | C | 1 | a0011c0011t0001g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5348+442T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071654 | ||||||
| chr18:13071724
|
G | GT | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5348+521dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chr18 | 13071724 | |||||
| chr18:13071752
|
C | T | 5 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.5348+540C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071752 | ||||||
| chr18:13071828
|
A | G | 5 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.5348+616A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071828 | ||||||
| chr18:13071975
|
A | G | 1 | a0002c0001t0001g0349 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5348+763A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071975 | ||||||
| chr18:13072042
|
G | A | 5 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.5349-713G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072042 | ||||||
| chr18:13072110
|
C | T | 5 | a0004c0004t0001g0174a0004c0004t0001g0175a0004c0004t0001g0206others(2): Show | 5 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.5349-645C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072110 | ||||||
| chr18:13072380
|
G | A | 1 | a0007c0007t0002g0029 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5349-375G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072380 | ||||||
| chr18:13072444
|
A | T | 63 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(60): Show | 67 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.5349-311A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072444 | ||||||
| chr18:13072479
|
G | T | 1 | a0006c0006t0002g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5349-276G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072479 | ||||||
| chr18:13072560
|
A | G | 1 | a0005c0005t0001g0135 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.5349-195A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072560 | ||||||
| chr18:13072583
|
A | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5349-172A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072583 | ||||||
| chr18:13072703
|
G | A | 76 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(73): Show | 79 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.5349-52G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072703 | ||||||
| chr18:13072959
|
T | C | 1 | a0002c0001t0001g0309 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.5440-50T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 29/44 | chr18 | 13072959 | ||||||
| chr18:13072964
|
G | T | 2 | a0004c0004t0001g0178a0004c0004t0001g0179 | 2 | NA18974.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.5440-45G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 29/44 | chr18 | 13072964 | ||||||
| chr18:13072980
|
T | C | 138 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(135): Show | 147 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.5440-29T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 29/44 | chr18 | 13072980 | ||||||
| chr18:13073265
|
C | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.5616+80C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073265 | ||||||
| chr18:13073288
|
C | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.5616+103C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073288 | ||||||
| chr18:13073386
|
G | C | 1 | a0001c0002t0001g0249 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5616+201G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073386 | ||||||
| chr18:13073533
|
C | G | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5616+348C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073533 | ||||||
| chr18:13073619
|
C | G | 1 | a0001c0002t0001g0242 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.5616+434C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073619 | ||||||
| chr18:13073642
|
C | T | 127 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(124): Show | 133 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.5616+457C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073642 | ||||||
| chr18:13073703
|
C | G | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+518C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073703 | ||||||
| chr18:13073723
|
G | A | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5616+538G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073723 | ||||||
| chr18:13073776
|
T | C | 1 | a0001c0002t0001g0249 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5616+591T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073776 | ||||||
| chr18:13073809
|
G | A | 1 | a0005c0005t0001g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5616+624G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073809 | ||||||
| chr18:13073864
|
G | A | 1 | a0001c0002t0001g0239 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.5616+679G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073864 | ||||||
| chr18:13073866
|
G | T | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+681G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073866 | ||||||
| chr18:13073878
|
G | A | 1 | a0005c0005t0001g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5616+693G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073878 | ||||||
| chr18:13074014
|
TAA | T | 19 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(16): Show | 20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.5616+832_5616+833d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13074014 | |||||
| chr18:13074142
|
TCTATATC | T | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5616+961_5616+967d others(9): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13074142 | |||||
| chr18:13074143
|
C | G | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+958C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074143 | ||||||
| chr18:13074164
|
G | A | 1 | a0007c0007t0002g0026 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5616+979G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074164 | ||||||
| chr18:13074240
|
C | T | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5616+1055C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074240 | ||||||
| chr18:13074241
|
G | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+1056G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074241 | ||||||
| chr18:13074352
|
A | G | 1 | a0032c0032t0001g0119 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5616+1167A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074352 | ||||||
| chr18:13074395
|
C | T | 3 | a0003c0003t0002g0064a0003c0003t0002g0065a0018c0017t0002g0009 | 4 | HG02080.hp1 HG02083.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.5616+1210C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074395 | ||||||
| chr18:13074396
|
G | A | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5616+1211G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074396 | ||||||
| chr18:13074418
|
A | G | 2 | a0008c0008t0001g0133a0008c0008t0001g0169 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.5616+1233A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074418 | ||||||
| chr18:13074477
|
C | G | 33 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(30): Show | 35 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.5616+1292C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074477 | ||||||
| chr18:13074665
|
A | G | 2 | a0003c0003t0002g0077a0003c0003t0002g0103 | 2 | HG00140.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.5616+1480A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074665 | ||||||
| chr18:13074798
|
G | A | 5 | a0004c0004t0001g0002a0004c0004t0001g0185a0004c0004t0001g0187others(2): Show | 8 | NA18942.hp1 NA18983.hp2 NA18984.hp2 others(5): Show |
intron_variant | MODIFIER | c.5616+1613G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074798 | ||||||
| chr18:13074837
|
C | T | 2 | a0006c0006t0001g0356a0006c0006t0001g0358 | 2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.5616+1652C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074837 | ||||||
| chr18:13074851
|
T | G | 1 | a0007c0007t0002g0027 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5616+1666T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074851 | ||||||
| chr18:13075302
|
CT | C | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+2118delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075302 | ||||||
| chr18:13075458
|
C | T | 1 | a0004c0004t0001g0183 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5616+2273C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075458 | ||||||
| chr18:13075552
|
G | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+2367G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075552 | ||||||
| chr18:13075607
|
C | T | 1 | a0001c0045t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5616+2422C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075607 | ||||||
| chr18:13075712
|
A | T | 1 | a0036c0020t0001g0355 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5616+2527A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075712 | ||||||
| chr18:13075877
|
A | T | 1 | a0004c0004t0001g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5616+2692A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075877 | ||||||
| chr18:13075999
|
G | C | 68 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(65): Show | 71 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.5616+2814G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075999 | ||||||
| chr18:13076133
|
G | C | 1 | a0004c0004t0001g0193 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5616+2948G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076133 | ||||||
| chr18:13076213
|
T | C | 10 | a0006c0006t0002g0025a0007c0007t0002g0006a0007c0007t0002g0023others(7): Show | 11 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.5616+3028T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076213 | ||||||
| chr18:13076251
|
T | C | 78 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(75): Show | 81 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.5616+3066T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076251 | ||||||
| chr18:13076297
|
T | C | 2 | a0015c0012t0001g0011a0034c0031t0001g0011 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.5616+3112T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076297 | ||||||
| chr18:13076344
|
C | T | 137 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(134): Show | 146 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.5616+3159C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076344 | ||||||
| chr18:13076350
|
G | A | 1 | a0001c0002t0001g0267 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5616+3165G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076350 | ||||||
| chr18:13076395
|
TTG | T | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+3214_5616+321 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13076395 | |||||
| chr18:13076616
|
C | G | 1 | a0003c0003t0002g0066 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5616+3431C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076616 | ||||||
| chr18:13076627
|
G | C | 1 | a0001c0045t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5616+3442G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076627 | ||||||
| chr18:13076646
|
C | T | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5616+3461C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076646 | ||||||
| chr18:13076663
|
C | T | 1 | a0001c0002t0001g0257 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.5616+3478C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076663 | ||||||
| chr18:13076664
|
G | A | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5616+3479G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076664 | ||||||
| chr18:13076664
|
G | C | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5616+3479G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076664 | ||||||
| chr18:13076795
|
T | C | 1 | a0002c0001t0001g0350 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.5616+3610T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076795 | ||||||
| chr18:13076932
|
C | T | 19 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(16): Show | 20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.5616+3747C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076932 | ||||||
| chr18:13076941
|
A | G | 281 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(278): Show | 304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.5616+3756A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076941 | ||||||
| chr18:13077185
|
C | T | 1 | a0005c0005t0001g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5616+4000C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077185 | ||||||
| chr18:13077198
|
G | A | 1 | a0001c0002t0001g0237 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.5616+4013G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077198 | ||||||
| chr18:13077213
|
G | A | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5616+4028G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077213 | ||||||
| chr18:13077316
|
A | G | 131 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(128): Show | 137 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.5616+4131A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077316 | ||||||
| chr18:13077729
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5616+4544G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077729 | ||||||
| chr18:13077954
|
CT | C | 236 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(233): Show | 249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.5616+4773delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13077954 | |||||
| chr18:13077966
|
G | T | 62 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(59): Show | 66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.5616+4781G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077966 | ||||||
| chr18:13077978
|
C | A | 3 | a0019c0019t0001g0166a0019c0019t0001g0167a0035c0044t0001g0165 | 3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5616+4793C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077978 | ||||||
| chr18:13078103
|
A | G | 5 | a0003c0003t0002g0007a0003c0003t0002g0058a0003c0003t0002g0059others(2): Show | 6 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.5616+4918A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078103 | ||||||
| chr18:13078307
|
C | T | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5616+5122C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078307 | ||||||
| chr18:13078540
|
C | T | 1 | a0004c0004t0001g0201 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.5616+5355C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078540 | ||||||
| chr18:13078597
|
G | T | 1 | a0001c0002t0001g0244 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.5616+5412G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078597 | ||||||
| chr18:13078619
|
G | A | 1 | a0026c0025t0001g0300 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.5616+5434G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078619 | ||||||
| chr18:13078633
|
G | T | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+5448G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078633 | ||||||
| chr18:13078682
|
C | T | 25 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(22): Show | 26 | HG01167.hp1 HG01891.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.5616+5497C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078682 | ||||||
| chr18:13078742
|
G | A | 1 | a0004c0004t0001g0197 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.5616+5557G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078742 | ||||||
| chr18:13078750
|
C | T | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5616+5565C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078750 | ||||||
| chr18:13078818
|
G | A | 1 | a0001c0002t0001g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5616+5633G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078818 | ||||||
| chr18:13078819
|
A | T | 1 | a0005c0005t0001g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5616+5634A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078819 | ||||||
| chr18:13078849
|
A | T | 1 | a0013c0016t0003g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5616+5664A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078849 | ||||||
| chr18:13078987
|
T | C | 1 | a0022c0028t0001g0357 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5616+5802T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078987 | ||||||
| chr18:13078996
|
A | G | 1 | a0025c0021t0001g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5616+5811A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078996 | ||||||
| chr18:13079061
|
A | G | 1 | a0004c0004t0001g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5616+5876A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079061 | ||||||
| chr18:13079086
|
G | A | 1 | a0004c0004t0001g0183 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5616+5901G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079086 | ||||||
| chr18:13079345
|
A | G | 77 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(74): Show | 80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.5616+6160A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079345 | ||||||
| chr18:13079457
|
A | G | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.5616+6272A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079457 | ||||||
| chr18:13079552
|
G | C | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5616+6367G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079552 | ||||||
| chr18:13079604
|
G | A | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5616+6419G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079604 | ||||||
| chr18:13079645
|
A | T | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5616+6460A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079645 | ||||||
| chr18:13079649
|
C | A | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5616+6464C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079649 | ||||||
| chr18:13079675
|
C | T | 62 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(59): Show | 66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.5616+6490C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079675 | ||||||
| chr18:13079790
|
A | C | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5616+6605A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079790 | ||||||
| chr18:13079858
|
T | C | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.5616+6673T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079858 | ||||||
| chr18:13079911
|
T | C | 1 | a0006c0006t0002g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5616+6726T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079911 | ||||||
| chr18:13079993
|
G | A | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5616+6808G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079993 | ||||||
| chr18:13080181
|
C | T | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-6836C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080181 | ||||||
| chr18:13080231
|
G | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-6786G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080231 | ||||||
| chr18:13080284
|
C | A | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5617-6733C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080284 | ||||||
| chr18:13080313
|
T | C | 1 | a0010c0010t0002g0081 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.5617-6704T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080313 | ||||||
| chr18:13080381
|
T | A | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.5617-6636T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080381 | ||||||
| chr18:13080399
|
A | C | 3 | a0003c0003t0002g0064a0003c0003t0002g0065a0018c0017t0002g0009 | 4 | HG02080.hp1 HG02083.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.5617-6618A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080399 | ||||||
| chr18:13080563
|
T | C | 4 | a0002c0001t0001g0022a0002c0001t0001g0323a0002c0001t0001g0328others(1): Show | 5 | HG01099.hp1 HG01261.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-6454T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080563 | ||||||
| chr18:13080890
|
T | G | 78 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(75): Show | 81 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.5617-6127T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080890 | ||||||
| chr18:13080970
|
G | T | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-6047G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080970 | ||||||
| chr18:13081162
|
G | A | 2 | a0001c0002t0001g0258a0001c0002t0001g0268 | 2 | NA18985.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.5617-5855G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13081162 | ||||||
| chr18:13081304
|
T | C | 281 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(278): Show | 304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.5617-5713T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13081304 | ||||||
| chr18:13081322
|
T | C | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.5617-5695T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13081322 | ||||||
| chr18:13081565
|
G | C | 1 | a0004c0004t0001g0193 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5617-5452G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13081565 | ||||||
| chr18:13081614
|
G | GT | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.5617-5396dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13081614 | |||||
| chr18:13081795
|
G | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-5222G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13081795 | ||||||
| chr18:13081936
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5617-5081G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13081936 | ||||||
| chr18:13082013
|
T | A | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5617-5004T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082013 | ||||||
| chr18:13082102
|
C | G | 1 | a0010c0010t0002g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.5617-4915C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082102 | ||||||
| chr18:13082240
|
A | G | 1 | a0002c0001t0001g0021 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.5617-4777A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082240 | ||||||
| chr18:13082330
|
C | T | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-4687C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082330 | ||||||
| chr18:13082333
|
T | G | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-4684T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082333 | ||||||
| chr18:13082432
|
C | CT | 52 | a0001c0002t0001g0241a0001c0002t0001g0281a0002c0001t0001g0302others(49): Show | 52 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.5617-4560dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13082432 | |||||
| chr18:13082432
|
C | CTT | 18 | a0002c0001t0001g0303a0002c0001t0001g0360a0003c0003t0002g0050others(15): Show | 22 | HG00741.hp2 HG02071.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.5617-4561_5617-456 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13082432 | |||||
| chr18:13082432
|
C | CTTT | 6 | a0004c0004t0001g0185a0004c0004t0001g0200a0015c0012t0001g0011others(3): Show | 6 | HG00621.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.5617-4562_5617-456 others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13082432 | |||||
| chr18:13082432
|
CT | C | 87 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(84): Show | 91 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.5617-4560delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13082432 | |||||
| chr18:13082507
|
A | T | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5617-4510A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082507 | ||||||
| chr18:13082718
|
G | A | 1 | a0004c0004t0001g0174 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5617-4299G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082718 | ||||||
| chr18:13082783
|
T | A | 62 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(59): Show | 66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.5617-4234T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082783 | ||||||
| chr18:13083005
|
T | G | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-4012T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083005 | ||||||
| chr18:13083096
|
G | A | 1 | a0004c0004t0001g0192 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.5617-3921G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083096 | ||||||
| chr18:13083198
|
A | G | 3 | a0006c0006t0002g0042a0006c0006t0002g0043a0006c0006t0002g0044 | 3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5617-3819A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083198 | ||||||
| chr18:13083203
|
C | G | 1 | a0003c0003t0002g0085 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5617-3814C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083203 | ||||||
| chr18:13083389
|
C | T | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.5617-3628C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083389 | ||||||
| chr18:13083496
|
A | G | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-3521A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083496 | ||||||
| chr18:13083512
|
C | T | 1 | a0002c0001t0001g0330 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.5617-3505C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083512 | ||||||
| chr18:13083582
|
G | A | 1 | a0003c0003t0002g0061 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5617-3435G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083582 | ||||||
| chr18:13083644
|
A | G | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-3373A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083644 | ||||||
| chr18:13083673
|
C | T | 1 | a0032c0032t0001g0119 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5617-3344C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083673 | ||||||
| chr18:13083685
|
G | A | 1 | a0002c0001t0001g0286 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5617-3332G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083685 | ||||||
| chr18:13083868
|
T | A | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-3149T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083868 | ||||||
| chr18:13084059
|
G | C | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-2958G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084059 | ||||||
| chr18:13084116
|
G | A | 1 | a0001c0002t0001g0271 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.5617-2901G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084116 | ||||||
| chr18:13084164
|
A | G | 1 | a0001c0002t0001g0210 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5617-2853A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084164 | ||||||
| chr18:13084266
|
G | A | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-2751G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084266 | ||||||
| chr18:13084337
|
C | A | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5617-2680C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084337 | ||||||
| chr18:13084383
|
CT | C | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5617-2633delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084383 | ||||||
| chr18:13084385
|
G | C | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5617-2632G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084385 | ||||||
| chr18:13084434
|
C | T | 42 | a0001c0002t0001g0222a0004c0004t0001g0001a0004c0004t0001g0002others(39): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.5617-2583C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084434 | ||||||
| chr18:13084435
|
G | A | 3 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219 | 6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.5617-2582G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084435 | ||||||
| chr18:13084496
|
C | T | 3 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219 | 6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.5617-2521C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084496 | ||||||
| chr18:13084559
|
C | T | 5 | a0004c0004t0001g0174a0004c0004t0001g0175a0004c0004t0001g0206others(2): Show | 5 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-2458C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084559 | ||||||
| chr18:13084564
|
G | A | 1 | a0002c0022t0001g0307 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.5617-2453G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084564 | ||||||
| chr18:13084711
|
C | T | 1 | a0002c0001t0001g0328 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.5617-2306C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084711 | ||||||
| chr18:13084729
|
G | A | 2 | a0006c0006t0001g0356a0006c0006t0001g0358 | 2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.5617-2288G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084729 | ||||||
| chr18:13084762
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5617-2255G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084762 | ||||||
| chr18:13084786
|
G | A | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-2231G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084786 | ||||||
| chr18:13084820
|
C | CT | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0018others(70): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.5617-2186dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13084820 | |||||
| chr18:13084904
|
C | T | 6 | a0011c0011t0001g0283a0011c0011t0001g0284a0011c0011t0001g0288others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.5617-2113C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084904 | ||||||
| chr18:13084961
|
G | A | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5617-2056G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084961 | ||||||
| chr18:13084981
|
A | G | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00408.hp1 HG00544.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.5617-2036A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084981 | ||||||
| chr18:13084991
|
G | GT | 11 | a0002c0001t0001g0315a0002c0001t0001g0360a0003c0003t0002g0106others(8): Show | 11 | HG01515.hp1 HG02145.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.5617-2012dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13084991 | |||||
| chr18:13084991
|
GT | G | 7 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(4): Show | 7 | HG01167.hp1 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.5617-2012delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13084991 | |||||
| chr18:13085114
|
C | T | 1 | a0002c0001t0001g0286 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5617-1903C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085114 | ||||||
| chr18:13085115
|
G | A | 1 | a0005c0005t0001g0139 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5617-1902G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085115 | ||||||
| chr18:13085121
|
G | A | 1 | a0003c0003t0002g0110 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.5617-1896G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085121 | ||||||
| chr18:13085130
|
G | A | 127 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(124): Show | 133 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.5617-1887G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085130 | ||||||
| chr18:13085170
|
G | A | 1 | a0001c0002t0001g0279 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.5617-1847G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085170 | ||||||
| chr18:13085175
|
T | C | 19 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(16): Show | 20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.5617-1842T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085175 | ||||||
| chr18:13085237
|
G | A | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.5617-1780G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085237 | ||||||
| chr18:13085383
|
GA | G | 133 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(130): Show | 139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.5617-1632delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13085383 | |||||
| chr18:13085438
|
G | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-1579G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085438 | ||||||
| chr18:13085472
|
G | A | 1 | a0011c0011t0001g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5617-1545G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085472 | ||||||
| chr18:13085473
|
T | C | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-1544T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085473 | ||||||
| chr18:13085496
|
T | G | 63 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(60): Show | 67 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.5617-1521T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085496 | ||||||
| chr18:13085756
|
T | TCTGTTTT others(15): Show |
3 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0265 | 3 | HG02040.hp2 NA18974.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.5617-1250_5617-122 others(26): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13085756 | |||||
| chr18:13085804
|
G | T | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5617-1213G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085804 | ||||||
| chr18:13085825
|
C | T | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5617-1192C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085825 | ||||||
| chr18:13085874
|
C | T | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5617-1143C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085874 | ||||||
| chr18:13085910
|
G | GT | 5 | a0003c0003t0002g0108a0009c0009t0001g0003a0009c0009t0001g0218others(2): Show | 8 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.5617-1097dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13085910 | |||||
| chr18:13085998
|
A | G | 1 | a0027c0024t0001g0359 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5617-1019A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085998 | ||||||
| chr18:13086032
|
C | T | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5617-985C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086032 | ||||||
| chr18:13086335
|
A | C | 1 | a0002c0023t0001g0296 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5617-682A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086335 | ||||||
| chr18:13086365
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5617-652G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086365 | ||||||
| chr18:13086476
|
G | T | 1 | a0001c0002t0001g0268 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.5617-541G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086476 | ||||||
| chr18:13086620
|
T | C | 1 | a0006c0006t0002g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5617-397T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086620 | ||||||
| chr18:13086703
|
C | CTA | 9 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(6): Show | 9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.5617-311_5617-310d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13086703 | |||||
| chr18:13086742
|
A | G | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-275A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086742 | ||||||
| chr18:13086947
|
C | T | 1 | a0002c0001t0001g0309 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.5617-70C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086947 | ||||||
| chr18:13087286
|
A | G | 3 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124 | 3 | HG02630.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.5877+9A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 31/44 | chr18 | 13087286 | ||||||
| chr18:13087405
|
T | G | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5878-126T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 31/44 | chr18 | 13087405 | ||||||
| chr18:13087454
|
C | T | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5878-77C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 31/44 | chr18 | 13087454 | ||||||
| chr18:13087790
|
A | G | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.5993+144A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13087790 | ||||||
| chr18:13087816
|
G | A | 281 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(278): Show | 304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.5993+170G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13087816 | ||||||
| chr18:13087824
|
C | T | 1 | a0001c0002t0001g0233 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.5993+178C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13087824 | ||||||
| chr18:13087960
|
A | G | 1 | a0004c0004t0001g0204 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.5993+314A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13087960 | ||||||
| chr18:13088059
|
C | T | 1 | a0001c0002t0001g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.5993+413C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088059 | ||||||
| chr18:13088082
|
A | G | 35 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(32): Show | 37 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.5993+436A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088082 | ||||||
| chr18:13088157
|
T | G | 2 | a0003c0003t0002g0077a0003c0003t0002g0103 | 2 | HG00140.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.5993+511T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088157 | ||||||
| chr18:13088319
|
G | A | 19 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(16): Show | 20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.5993+673G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088319 | ||||||
| chr18:13088526
|
T | A | 1 | a0003c0003t0005g0100 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.5993+880T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088526 | ||||||
| chr18:13088667
|
C | T | 2 | a0001c0002t0001g0242a0002c0001t0001g0291 | 2 | HG01081.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.5994-789C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088667 | ||||||
| chr18:13088674
|
T | C | 244 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(241): Show | 257 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.5994-782T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088674 | ||||||
| chr18:13088681
|
T | C | 1 | a0022c0028t0001g0357 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5994-775T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088681 | ||||||
| chr18:13088895
|
A | T | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5994-561A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088895 | ||||||
| chr18:13088916
|
T | G | 2 | a0004c0004t0001g0002a0004c0004t0001g0196 | 5 | NA18942.hp1 NA18983.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.5994-540T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088916 | ||||||
| chr18:13088931
|
A | G | 2 | a0002c0001t0001g0336a0026c0025t0001g0300 | 2 | HG00738.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.5994-525A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088931 | ||||||
| chr18:13089030
|
C | T | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5994-426C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089030 | ||||||
| chr18:13089039
|
A | C | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5994-417A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089039 | ||||||
| chr18:13089149
|
A | G | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5994-307A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089149 | ||||||
| chr18:13089280
|
T | C | 1 | a0003c0003t0002g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5994-176T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089280 | ||||||
| chr18:13089355
|
A | G | 6 | a0006c0006t0001g0356a0006c0006t0001g0358a0013c0016t0003g0216others(3): Show | 6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.5994-101A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089355 | ||||||
| chr18:13089373
|
C | T | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5994-83C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089373 | ||||||
| chr18:13089441
|
A | T | 9 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(6): Show | 9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.5994-15A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089441 | ||||||
| chr18:13089580
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6103+15G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13089580 | ||||||
| chr18:13089786
|
C | G | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.6103+221C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13089786 | ||||||
| chr18:13089825
|
A | G | 1 | a0001c0002t0001g0249 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6103+260A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13089825 | ||||||
| chr18:13089909
|
T | A | 1 | a0001c0002t0001g0277 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.6103+344T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13089909 | ||||||
| chr18:13090506
|
G | A | 32 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(29): Show | 34 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.6103+941G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13090506 | ||||||
| chr18:13090668
|
C | A | 133 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(130): Show | 139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.6103+1103C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13090668 | ||||||
| chr18:13090686
|
G | A | 1 | a0004c0004t0001g0197 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.6103+1121G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13090686 | ||||||
| chr18:13090829
|
A | G | 1 | a0005c0005t0001g0148 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.6103+1264A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13090829 | ||||||
| chr18:13090951
|
G | T | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6103+1386G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13090951 | ||||||
| chr18:13090983
|
A | G | 137 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(134): Show | 146 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.6104-1394A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13090983 | ||||||
| chr18:13091250
|
A | G | 1 | a0010c0010t0002g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.6104-1127A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091250 | ||||||
| chr18:13091402
|
A | G | 1 | a0001c0002t0001g0270 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.6104-975A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091402 | ||||||
| chr18:13091454
|
G | A | 1 | a0002c0001t0001g0308 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.6104-923G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091454 | ||||||
| chr18:13091471
|
G | GT | 281 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(278): Show | 304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.6104-906_6104-905i others(3): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091471 | ||||||
| chr18:13091479
|
A | C | 5 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.6104-898A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091479 | ||||||
| chr18:13091523
|
T | C | 1 | a0025c0021t0001g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6104-854T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091523 | ||||||
| chr18:13091662
|
T | C | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.6104-715T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091662 | ||||||
| chr18:13091965
|
A | T | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6104-412A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091965 | ||||||
| chr18:13091989
|
A | G | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.6104-388A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091989 | ||||||
| chr18:13092025
|
G | A | 3 | a0003c0003t0002g0096a0016c0015t0002g0040a0016c0015t0002g0041 | 3 | HG02895.hp1 HG02897.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.6104-352G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13092025 | ||||||
| chr18:13092162
|
A | G | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.6104-215A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13092162 | ||||||
| chr18:13092220
|
G | A | 1 | a0001c0002t0001g0222 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6104-157G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13092220 | ||||||
| chr18:13092243
|
C | G | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6104-134C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13092243 | ||||||
| chr18:13092274
|
A | G | 1 | a0004c0004t0001g0179 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.6104-103A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13092274 | ||||||
| chr18:13092290
|
A | G | 1 | a0002c0001t0001g0317 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6104-87A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13092290 | ||||||
| chr18:13092770
|
T | G | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6254+243T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13092770 | ||||||
| chr18:13092777
|
C | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6254+250C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13092777 | ||||||
| chr18:13092857
|
A | G | 3 | a0005c0005t0001g0138a0005c0005t0001g0170a0005c0005t0001g0171 | 3 | NA18956.hp2 NA18977.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.6254+330A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13092857 | ||||||
| chr18:13092951
|
G | A | 3 | a0002c0001t0001g0324a0002c0001t0001g0325a0002c0001t0001g0332 | 3 | NA18998.hp1 NA19004.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.6254+424G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13092951 | ||||||
| chr18:13093190
|
C | T | 1 | a0029c0036t0001g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.6254+663C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093190 | ||||||
| chr18:13093337
|
C | T | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6254+810C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093337 | ||||||
| chr18:13093354
|
T | C | 12 | a0005c0005t0001g0151a0005c0005t0001g0153a0005c0005t0001g0154others(9): Show | 12 | HG01884.hp2 HG02717.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.6254+827T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093354 | ||||||
| chr18:13093366
|
C | T | 68 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(65): Show | 71 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.6254+839C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093366 | ||||||
| chr18:13093384
|
C | T | 19 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(16): Show | 20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.6254+857C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093384 | ||||||
| chr18:13093424
|
C | T | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.6254+897C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093424 | ||||||
| chr18:13093426
|
G | T | 2 | a0001c0002t0001g0212a0001c0033t0001g0211 | 2 | HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.6254+899G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093426 | ||||||
| chr18:13093522
|
A | G | 33 | a0005c0005t0001g0013a0005c0005t0001g0015a0005c0005t0001g0116others(30): Show | 35 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.6254+995A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093522 | ||||||
| chr18:13093712
|
T | C | 2 | a0001c0002t0001g0212a0001c0033t0001g0211 | 2 | HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.6254+1185T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093712 | ||||||
| chr18:13093775
|
G | A | 293 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(290): Show | 316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.6254+1248G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093775 | ||||||
| chr18:13093797
|
G | A | 236 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(233): Show | 246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.6254+1270G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093797 | ||||||
| chr18:13093943
|
G | A | 3 | a0006c0006t0001g0356a0006c0006t0001g0358a0022c0028t0001g0357 | 3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6254+1416G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093943 | ||||||
| chr18:13094017
|
C | T | 1 | a0001c0002t0001g0254 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6255-1486C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094017 | ||||||
| chr18:13094045
|
G | T | 1 | a0003c0003t0002g0061 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6255-1458G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094045 | ||||||
| chr18:13094133
|
G | A | 293 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(290): Show | 316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.6255-1370G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094133 | ||||||
| chr18:13094291
|
C | T | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6255-1212C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094291 | ||||||
| chr18:13094802
|
C | T | 215 | a0002c0001t0001g0019a0002c0001t0001g0021a0002c0001t0001g0022others(212): Show | 235 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.6255-701C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094802 | ||||||
| chr18:13094805
|
C | T | 1 | a0003c0003t0002g0088 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.6255-698C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094805 | ||||||
| chr18:13094821
|
AC | A | 128 | a0002c0001t0001g0019a0002c0001t0001g0021a0002c0001t0001g0022others(125): Show | 136 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.6255-680delC | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chr18 | 13094821 | |||||
| chr18:13094885
|
C | A | 75 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(72): Show | 78 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.6255-618C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094885 | ||||||
| chr18:13094997
|
A | G | 4 | a0004c0004t0001g0174a0004c0004t0001g0175a0004c0004t0001g0206others(1): Show | 4 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.6255-506A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094997 | ||||||
| chr18:13095109
|
T | C | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.6255-394T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095109 | ||||||
| chr18:13095131
|
G | C | 1 | a0036c0020t0001g0355 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6255-372G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095131 | ||||||
| chr18:13095196
|
C | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6255-307C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095196 | ||||||
| chr18:13095212
|
G | A | 1 | a0009c0009t0001g0003 | 4 | HG00621.hp2 NA18970.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.6255-291G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095212 | ||||||
| chr18:13095249
|
G | A | 4 | a0001c0002t0001g0238a0001c0002t0001g0241a0001c0002t0001g0242others(1): Show | 4 | NA18946.hp1 NA18984.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.6255-254G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095249 | ||||||
| chr18:13095293
|
C | T | 1 | a0001c0002t0001g0226 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.6255-210C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095293 | ||||||
| chr18:13095319
|
A | G | 4 | a0002c0001t0001g0022a0002c0001t0001g0323a0002c0001t0001g0328others(1): Show | 5 | HG01099.hp1 HG01261.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.6255-184A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095319 | ||||||
| chr18:13095402
|
A | T | 127 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(124): Show | 133 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.6255-101A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095402 | ||||||
| chr18:13095477
|
T | G | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6255-26T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095477 | ||||||
| chr18:13095726
|
C | T | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6433+45C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/44 | chr18 | 13095726 | ||||||
| chr18:13095988
|
C | A | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6434-196C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/44 | chr18 | 13095988 | ||||||
| chr18:13095989
|
CAAGCAGT others(1): Show |
C | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6434-193_6434-186d others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/44 | INFO_REALIGN_3_PRIME | chr18 | 13095989 | |||||
| chr18:13096404
|
G | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6557+97G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096404 | ||||||
| chr18:13096437
|
T | C | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.6557+130T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096437 | ||||||
| chr18:13096689
|
C | T | 1 | a0001c0002t0001g0032 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6557+382C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096689 | ||||||
| chr18:13096704
|
G | T | 1 | a0001c0002t0001g0033 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6557+397G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096704 | ||||||
| chr18:13096713
|
G | A | 1 | a0002c0001t0001g0342 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6557+406G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096713 | ||||||
| chr18:13096726
|
G | C | 1 | a0006c0006t0002g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6557+419G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096726 | ||||||
| chr18:13096818
|
C | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6557+511C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096818 | ||||||
| chr18:13097208
|
C | T | 133 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(130): Show | 139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.6557+901C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097208 | ||||||
| chr18:13097411
|
A | T | 1 | a0003c0003t0002g0093 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.6557+1104A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097411 | ||||||
| chr18:13097523
|
C | G | 8 | a0007c0007t0002g0006a0007c0007t0002g0024a0007c0007t0002g0026others(5): Show | 9 | HG01952.hp2 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.6557+1216C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097523 | ||||||
| chr18:13097528
|
G | C | 1 | a0002c0001t0001g0323 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.6557+1221G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097528 | ||||||
| chr18:13097627
|
CT | C | 7 | a0001c0002t0001g0229a0001c0002t0001g0265a0001c0002t0001g0272others(4): Show | 7 | HG00673.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.6557+1334delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chr18 | 13097627 | |||||
| chr18:13097649
|
AT | A | 7 | a0005c0005t0001g0134a0006c0006t0001g0356a0006c0006t0001g0358others(4): Show | 7 | HG01515.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.6557+1356delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chr18 | 13097649 | |||||
| chr18:13097651
|
T | TA | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6557+1344_6557+134 others(5): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097651 | ||||||
| chr18:13097652
|
T | A | 67 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(64): Show | 71 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.6557+1345T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097652 | ||||||
| chr18:13097655
|
T | A | 5 | a0002c0001t0001g0309a0015c0012t0001g0011a0015c0012t0001g0114others(2): Show | 5 | HG01256.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.6557+1348T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097655 | ||||||
| chr18:13097728
|
G | A | 1 | a0007c0007t0002g0024 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6557+1421G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097728 | ||||||
| chr18:13097789
|
A | C | 293 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(290): Show | 316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.6557+1482A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097789 | ||||||
| chr18:13097838
|
C | T | 75 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(72): Show | 78 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.6557+1531C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097838 | ||||||
| chr18:13097854
|
A | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6557+1547A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097854 | ||||||
| chr18:13097869
|
G | A | 7 | a0002c0001t0001g0303a0002c0001t0001g0304a0002c0001t0001g0305others(4): Show | 7 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(4): Show |
intron_variant | MODIFIER | c.6557+1562G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097869 | ||||||
| chr18:13098012
|
A | G | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6558-1464A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098012 | ||||||
| chr18:13098071
|
G | A | 2 | a0004c0004t0001g0191a0004c0004t0001g0194 | 2 | NA18993.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.6558-1405G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098071 | ||||||
| chr18:13098120
|
C | T | 5 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.6558-1356C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098120 | ||||||
| chr18:13098139
|
C | T | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6558-1337C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098139 | ||||||
| chr18:13098174
|
G | A | 6 | a0004c0004t0001g0174a0004c0004t0001g0175a0004c0004t0001g0206others(3): Show | 6 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.6558-1302G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098174 | ||||||
| chr18:13098194
|
G | A | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.6558-1282G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098194 | ||||||
| chr18:13098206
|
T | G | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.6558-1270T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098206 | ||||||
| chr18:13098247
|
G | C | 1 | a0002c0001t0001g0321 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.6558-1229G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098247 | ||||||
| chr18:13098297
|
T | G | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6558-1179T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098297 | ||||||
| chr18:13098359
|
C | T | 5 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.6558-1117C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098359 | ||||||
| chr18:13098406
|
GCTCCTCA others(33): Show |
G | 36 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(33): Show | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.6558-1042_6558-100 others(44): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chr18 | 13098406 | |||||
| chr18:13098440
|
G | A | 5 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(2): Show | 8 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.6558-1036G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098440 | ||||||
| chr18:13098482
|
CGCTCCTC others(109): Show |
C | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6558-984_6558-869d others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chr18 | 13098482 | |||||
| chr18:13098513
|
G | A | 6 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.6558-963G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098513 | ||||||
| chr18:13098584
|
C | T | 4 | a0004c0004t0001g0014a0004c0004t0001g0184a0004c0004t0001g0188others(1): Show | 5 | NA18949.hp1 NA18965.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.6558-892C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098584 | ||||||
| chr18:13098586
|
G | T | 1 | a0005c0005t0001g0125 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.6558-890G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098586 | ||||||
| chr18:13098598
|
T | C | 288 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(285): Show | 311 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.6558-878T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098598 | ||||||
| chr18:13098599
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6558-877G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098599 | ||||||
| chr18:13098639
|
G | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6558-837G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098639 | ||||||
| chr18:13098678
|
C | T | 1 | a0001c0002t0001g0253 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.6558-798C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098678 | ||||||
| chr18:13098722
|
C | G | 1 | a0005c0005t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6558-754C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098722 | ||||||
| chr18:13098752
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6558-724G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098752 | ||||||
| chr18:13098768
|
C | T | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.6558-708C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098768 | ||||||
| chr18:13098772
|
C | CG | 12 | a0001c0002t0001g0249a0001c0002t0001g0252a0001c0002t0001g0254others(9): Show | 12 | HG00280.hp2 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.6558-700dupG | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chr18 | 13098772 | |||||
| chr18:13098785
|
G | A | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.6558-691G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098785 | ||||||
| chr18:13098864
|
C | T | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.6558-612C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098864 | ||||||
| chr18:13098907
|
C | T | 1 | a0002c0001t0001g0311 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.6558-569C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098907 | ||||||
| chr18:13098927
|
C | T | 1 | a0001c0002t0001g0267 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.6558-549C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098927 | ||||||
| chr18:13098935
|
C | T | 1 | a0003c0003t0002g0069 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.6558-541C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098935 | ||||||
| chr18:13099006
|
C | T | 1 | a0002c0001t0001g0321 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.6558-470C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099006 | ||||||
| chr18:13099041
|
G | A | 1 | a0003c0003t0002g0010 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.6558-435G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099041 | ||||||
| chr18:13099049
|
G | A | 2 | a0004c0004t0001g0178a0004c0004t0001g0179 | 2 | NA18974.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.6558-427G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099049 | ||||||
| chr18:13099060
|
A | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6558-416A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099060 | ||||||
| chr18:13099102
|
G | C | 1 | a0002c0001t0001g0308 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.6558-374G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099102 | ||||||
| chr18:13099130
|
G | A | 1 | a0031c0038t0002g0070 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.6558-346G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099130 | ||||||
| chr18:13099149
|
C | G | 1 | a0001c0002t0001g0210 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.6558-327C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099149 | ||||||
| chr18:13099161
|
G | A | 1 | a0008c0008t0001g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6558-315G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099161 | ||||||
| chr18:13099175
|
AGGGAGG | A | 3 | a0001c0045t0001g0269a0016c0015t0002g0040a0016c0015t0002g0041 | 3 | HG02572.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.6558-283_6558-278d others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chr18 | 13099175 | |||||
| chr18:13099199
|
A | G | 2 | a0001c0002t0001g0275a0001c0002t0001g0279 | 2 | NA18956.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.6558-277A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099199 | ||||||
| chr18:13099250
|
C | T | 62 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(59): Show | 66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.6558-226C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099250 | ||||||
| chr18:13099283
|
C | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6558-193C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099283 | ||||||
| chr18:13099323
|
C | T | 1 | a0004c0004t0001g0197 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.6558-153C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099323 | ||||||
| chr18:13099700
|
A | G | 1 | a0004c0004t0001g0197 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.6663+119A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/44 | chr18 | 13099700 | ||||||
| chr18:13099824
|
A | G | 2 | a0001c0002t0001g0210a0001c0002t0001g0213 | 2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.6663+243A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/44 | chr18 | 13099824 | ||||||
| chr18:13100006
|
G | A | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6664-299G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/44 | chr18 | 13100006 | ||||||
| chr18:13100011
|
T | C | 2 | a0004c0004t0001g0206a0004c0004t0001g0207 | 2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.6664-294T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/44 | chr18 | 13100011 | ||||||
| chr18:13100099
|
G | A | 1 | a0036c0020t0001g0355 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6664-206G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/44 | chr18 | 13100099 | ||||||
| chr18:13100252
|
G | A | 5 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.6664-53G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/44 | chr18 | 13100252 | ||||||
| chr18:13100663
|
T | C | 1 | a0006c0006t0001g0358 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.6871+151T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13100663 | ||||||
| chr18:13100723
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6871+211G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13100723 | ||||||
| chr18:13100770
|
G | A | 1 | a0032c0032t0001g0119 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6871+258G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13100770 | ||||||
| chr18:13101143
|
C | T | 1 | a0003c0003t0002g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.6871+631C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101143 | ||||||
| chr18:13101161
|
T | A | 1 | a0005c0005t0001g0127 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.6871+649T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101161 | ||||||
| chr18:13101169
|
A | G | 281 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(278): Show | 304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.6871+657A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101169 | ||||||
| chr18:13101228
|
A | G | 6 | a0011c0011t0001g0283a0011c0011t0001g0284a0011c0011t0001g0288others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.6871+716A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101228 | ||||||
| chr18:13101253
|
A | G | 2 | a0005c0005t0001g0162a0005c0005t0001g0163 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.6871+741A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101253 | ||||||
| chr18:13101372
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6871+860G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101372 | ||||||
| chr18:13101435
|
A | G | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6871+923A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101435 | ||||||
| chr18:13101471
|
T | C | 5 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.6871+959T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101471 | ||||||
| chr18:13101510
|
G | A | 2 | a0006c0006t0001g0356a0006c0006t0001g0358 | 2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.6871+998G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101510 | ||||||
| chr18:13101652
|
A | G | 1 | a0003c0003t0002g0065 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6871+1140A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101652 | ||||||
| chr18:13101761
|
C | T | 1 | a0002c0001t0001g0346 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.6871+1249C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101761 | ||||||
| chr18:13101903
|
T | G | 137 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(134): Show | 146 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.6871+1391T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101903 | ||||||
| chr18:13102005
|
C | T | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6871+1493C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102005 | ||||||
| chr18:13102329
|
G | A | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.6872-1180G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102329 | ||||||
| chr18:13102405
|
C | G | 5 | a0001c0002t0001g0210a0001c0002t0001g0212a0001c0002t0001g0213others(2): Show | 5 | HG01109.hp2 HG02132.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.6872-1104C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102405 | ||||||
| chr18:13102473
|
A | G | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.6872-1036A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102473 | ||||||
| chr18:13102825
|
C | A | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6872-684C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102825 | ||||||
| chr18:13102842
|
T | C | 1 | a0004c0004t0001g0192 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6872-667T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102842 | ||||||
| chr18:13102861
|
A | G | 2 | a0003c0003t0002g0050a0028c0042t0002g0107 | 2 | HG02074.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.6872-648A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102861 | ||||||
| chr18:13102958
|
G | T | 1 | a0002c0001t0001g0360 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6872-551G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102958 | ||||||
| chr18:13103310
|
A | C | 1 | a0005c0005t0001g0170 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.6872-199A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13103310 | ||||||
| chr18:13103328
|
A | G | 1 | a0003c0003t0002g0057 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.6872-181A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13103328 | ||||||
| chr18:13103661
|
A | G | 5 | a0003c0003t0002g0045a0009c0009t0001g0003a0009c0009t0001g0218others(2): Show | 8 | HG00621.hp2 HG02129.hp1 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.6951+73A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13103661 | ||||||
| chr18:13103815
|
A | T | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.6951+227A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13103815 | ||||||
| chr18:13104042
|
G | A | 3 | a0006c0006t0001g0356a0006c0006t0001g0358a0022c0028t0001g0357 | 3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6951+454G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104042 | ||||||
| chr18:13104252
|
A | C | 1 | a0001c0045t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.6951+664A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104252 | ||||||
| chr18:13104252
|
A | G | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.6951+664A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104252 | ||||||
| chr18:13104330
|
AGTCT | A | 63 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(60): Show | 67 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.6952-653_6952-650d others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104330 | ||||||
| chr18:13104544
|
C | T | 2 | a0005c0005t0001g0144a0005c0005t0001g0145 | 2 | NA18982.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.6952-440C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104544 | ||||||
| chr18:13104618
|
AT | A | 4 | a0005c0005t0001g0116a0005c0005t0001g0117a0005c0005t0001g0128others(1): Show | 4 | HG01071.hp2 HG01255.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.6952-365delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104618 | ||||||
| chr18:13104687
|
A | C | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6952-297A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104687 | ||||||
| chr18:13104901
|
G | A | 4 | a0001c0002t0001g0267a0001c0002t0001g0274a0006c0006t0001g0356others(1): Show | 4 | HG01192.hp2 HG01515.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.6952-83G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104901 | ||||||
| chr18:13105336
|
A | G | 2 | a0004c0004t0001g0206a0004c0004t0001g0207 | 2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.7047+257A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105336 | ||||||
| chr18:13105364
|
G | A | 1 | a0036c0020t0001g0355 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.7047+285G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105364 | ||||||
| chr18:13105450
|
C | T | 1 | a0002c0001t0001g0301 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7047+371C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105450 | ||||||
| chr18:13105541
|
G | A | 62 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(59): Show | 66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.7047+462G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105541 | ||||||
| chr18:13105572
|
C | T | 9 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(6): Show | 9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.7047+493C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105572 | ||||||
| chr18:13105651
|
G | A | 5 | a0004c0004t0001g0174a0004c0004t0001g0175a0004c0004t0001g0206others(2): Show | 5 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.7047+572G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105651 | ||||||
| chr18:13105731
|
T | G | 1 | a0002c0001t0001g0337 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.7047+652T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105731 | ||||||
| chr18:13105851
|
T | C | 3 | a0006c0006t0001g0356a0006c0006t0001g0358a0022c0028t0001g0357 | 3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.7047+772T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105851 | ||||||
| chr18:13106256
|
C | T | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7047+1177C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106256 | ||||||
| chr18:13106257
|
G | A | 1 | a0035c0044t0001g0165 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.7047+1178G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106257 | ||||||
| chr18:13106338
|
T | C | 293 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(290): Show | 316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.7047+1259T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106338 | ||||||
| chr18:13106374
|
GCTACCAC others(82): Show |
G | 1 | a0000c0035t0001g0264 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.7047+1308_7047+139 others(93): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13106374 | |||||
| chr18:13106403
|
CACTCACC others(73): Show |
C | 1 | a0001c0045t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.7047+1350_7047+142 others(84): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13106403 | |||||
| chr18:13106428
|
CCACACAA others(8): Show |
C | 66 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(63): Show | 69 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.7047+1350_7047+136 others(19): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106428 | ||||||
| chr18:13106447
|
A | C | 66 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(63): Show | 69 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.7047+1368A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106447 | ||||||
| chr18:13106452
|
CACCCCAC others(2): Show |
C | 66 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(63): Show | 69 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.7047+1375_7047+138 others(13): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13106452 | |||||
| chr18:13106462
|
A | C | 66 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(63): Show | 69 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.7047+1383A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106462 | ||||||
| chr18:13106465
|
T | C | 66 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(63): Show | 69 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.7047+1386T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106465 | ||||||
| chr18:13106477
|
TACCACTA others(49): Show |
T | 66 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(63): Show | 69 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.7047+1402_7047+145 others(60): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13106477 | |||||
| chr18:13106480
|
C | T | 1 | a0000c0035t0001g0264 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.7047+1401C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106480 | ||||||
| chr18:13106483
|
T | C | 1 | a0000c0035t0001g0264 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.7047+1404T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106483 | ||||||
| chr18:13106509
|
T | TACC | 5 | a0009c0009t0001g0220a0015c0012t0001g0011a0015c0012t0001g0114others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.7047+1455_7047+145 others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13106509 | |||||
| chr18:13106509
|
T | TACCACCA others(8): Show |
6 | a0011c0011t0001g0283a0011c0011t0001g0284a0011c0011t0001g0288others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.7047+1443_7047+145 others(19): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13106509 | |||||
| chr18:13106519
|
A | G | 2 | a0004c0004t0001g0002a0004c0004t0001g0196 | 5 | NA18942.hp1 NA18983.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.7047+1440A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106519 | ||||||
| chr18:13106533
|
C | T | 7 | a0000c0035t0001g0264a0001c0002t0001g0210a0001c0002t0001g0212others(4): Show | 7 | HG01109.hp2 HG02132.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.7047+1454C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106533 | ||||||
| chr18:13106834
|
A | T | 1 | a0002c0001t0001g0333 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.7047+1755A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106834 | ||||||
| chr18:13106996
|
T | A | 5 | a0005c0005t0001g0013a0005c0005t0001g0126a0014c0014t0001g0012others(2): Show | 6 | HG02132.hp1 NA18944.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.7047+1917T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106996 | ||||||
| chr18:13107181
|
C | G | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.7047+2102C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107181 | ||||||
| chr18:13107231
|
G | A | 2 | a0001c0002t0001g0263a0010c0010t0002g0079 | 2 | HG01928.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.7047+2152G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107231 | ||||||
| chr18:13107255
|
A | C | 18 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(15): Show | 18 | HG01167.hp1 HG01884.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.7047+2176A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107255 | ||||||
| chr18:13107337
|
T | A | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.7047+2258T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107337 | ||||||
| chr18:13107434
|
GA | G | 3 | a0006c0006t0002g0042a0006c0006t0002g0043a0006c0006t0002g0044 | 3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7047+2358delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13107434 | |||||
| chr18:13107518
|
A | G | 1 | a0005c0005t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.7047+2439A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107518 | ||||||
| chr18:13107560
|
A | G | 2 | a0003c0003t0002g0077a0003c0003t0002g0103 | 2 | HG00140.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.7047+2481A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107560 | ||||||
| chr18:13107571
|
G | A | 1 | a0032c0032t0001g0119 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.7047+2492G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107571 | ||||||
| chr18:13107760
|
C | T | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7047+2681C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107760 | ||||||
| chr18:13107795
|
A | G | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.7047+2716A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107795 | ||||||
| chr18:13107858
|
C | T | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7047+2779C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107858 | ||||||
| chr18:13107859
|
G | A | 6 | a0011c0011t0001g0283a0011c0011t0001g0284a0011c0011t0001g0288others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.7047+2780G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107859 | ||||||
| chr18:13107883
|
C | A | 1 | a0007c0007t0002g0023 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.7047+2804C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107883 | ||||||
| chr18:13107883
|
C | CA | 14 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(11): Show | 14 | HG01167.hp1 HG01515.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.7047+2820dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13107883 | |||||
| chr18:13107883
|
CA | C | 163 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(160): Show | 179 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.7047+2820delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13107883 | |||||
| chr18:13107883
|
CAA | C | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.7047+2819_7047+282 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13107883 | |||||
| chr18:13107977
|
G | C | 2 | a0006c0006t0001g0356a0006c0006t0001g0358 | 2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.7047+2898G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107977 | ||||||
| chr18:13108021
|
A | G | 1 | a0002c0001t0001g0346 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.7047+2942A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108021 | ||||||
| chr18:13108313
|
TTAAAC | T | 4 | a0002c0001t0001g0342a0002c0001t0001g0343a0002c0001t0001g0360others(1): Show | 4 | HG02976.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.7047+3239_7047+324 others(9): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13108313 | |||||
| chr18:13108375
|
A | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7047+3296A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108375 | ||||||
| chr18:13108524
|
C | T | 10 | a0006c0006t0002g0025a0007c0007t0002g0006a0007c0007t0002g0023others(7): Show | 11 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.7047+3445C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108524 | ||||||
| chr18:13108538
|
A | C | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7047+3459A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108538 | ||||||
| chr18:13108544
|
C | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7047+3465C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108544 | ||||||
| chr18:13108594
|
G | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7047+3515G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108594 | ||||||
| chr18:13108766
|
T | C | 1 | a0003c0003t0002g0056 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.7047+3687T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108766 | ||||||
| chr18:13108909
|
A | T | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7047+3830A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108909 | ||||||
| chr18:13108916
|
C | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7047+3837C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108916 | ||||||
| chr18:13109170
|
G | A | 77 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(74): Show | 80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.7047+4091G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109170 | ||||||
| chr18:13109219
|
T | C | 36 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(33): Show | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.7047+4140T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109219 | ||||||
| chr18:13109280
|
A | G | 42 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(39): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.7047+4201A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109280 | ||||||
| chr18:13109481
|
C | T | 10 | a0006c0006t0002g0025a0007c0007t0002g0006a0007c0007t0002g0023others(7): Show | 11 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.7048-4105C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109481 | ||||||
| chr18:13109546
|
A | C | 1 | a0002c0001t0001g0335 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.7048-4040A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109546 | ||||||
| chr18:13109556
|
A | G | 137 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(134): Show | 146 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.7048-4030A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109556 | ||||||
| chr18:13109649
|
G | A | 2 | a0011c0011t0001g0283a0011c0011t0001g0284 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.7048-3937G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109649 | ||||||
| chr18:13109756
|
AG | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7048-3829delG | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109756 | ||||||
| chr18:13109836
|
C | T | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7048-3750C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109836 | ||||||
| chr18:13109880
|
T | C | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.7048-3706T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109880 | ||||||
| chr18:13109977
|
G | A | 2 | a0001c0002t0001g0255a0001c0002t0001g0265 | 2 | NA18974.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.7048-3609G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109977 | ||||||
| chr18:13109986
|
G | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7048-3600G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109986 | ||||||
| chr18:13110149
|
C | G | 2 | a0006c0006t0001g0356a0006c0006t0001g0358 | 2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.7048-3437C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110149 | ||||||
| chr18:13110272
|
C | T | 42 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(39): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.7048-3314C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110272 | ||||||
| chr18:13110431
|
A | AT | 5 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(2): Show | 8 | HG00621.hp2 NA18522.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.7048-3141dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13110431 | |||||
| chr18:13110431
|
AT | A | 98 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(95): Show | 101 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.7048-3141delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13110431 | |||||
| chr18:13110558
|
G | A | 1 | a0005c0005t0001g0127 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.7048-3028G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110558 | ||||||
| chr18:13110584
|
G | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7048-3002G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110584 | ||||||
| chr18:13110659
|
A | G | 1 | a0005c0005t0001g0148 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.7048-2927A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110659 | ||||||
| chr18:13110847
|
G | A | 1 | a0010c0010t0002g0081 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.7048-2739G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110847 | ||||||
| chr18:13110859
|
C | T | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.7048-2727C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110859 | ||||||
| chr18:13110987
|
G | A | 1 | a0005c0005t0001g0135 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.7048-2599G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110987 | ||||||
| chr18:13111110
|
C | T | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.7048-2476C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111110 | ||||||
| chr18:13111194
|
G | A | 6 | a0011c0011t0001g0283a0011c0011t0001g0284a0011c0011t0001g0288others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.7048-2392G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111194 | ||||||
| chr18:13111243
|
G | A | 1 | a0007c0007t0002g0023 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.7048-2343G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111243 | ||||||
| chr18:13111283
|
C | T | 3 | a0004c0004t0001g0178a0004c0004t0001g0179a0004c0004t0004g0177 | 3 | HG00558.hp2 NA18974.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.7048-2303C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111283 | ||||||
| chr18:13111405
|
G | A | 6 | a0003c0003t0002g0055a0003c0003t0002g0063a0005c0005t0001g0122others(3): Show | 6 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.7048-2181G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111405 | ||||||
| chr18:13111420
|
C | T | 1 | a0006c0006t0002g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.7048-2166C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111420 | ||||||
| chr18:13111752
|
C | T | 1 | a0011c0011t0001g0289 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7048-1834C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111752 | ||||||
| chr18:13111824
|
A | T | 4 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(1): Show | 4 | HG03041.hp1 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.7048-1762A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111824 | ||||||
| chr18:13111834
|
A | G | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7048-1752A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111834 | ||||||
| chr18:13111835
|
G | A | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7048-1751G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111835 | ||||||
| chr18:13111836
|
A | G | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7048-1750A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111836 | ||||||
| chr18:13112047
|
G | A | 1 | a0004c0004t0001g0175 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.7048-1539G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112047 | ||||||
| chr18:13112215
|
G | A | 3 | a0005c0005t0001g0135a0005c0005t0001g0136a0005c0005t0001g0137 | 3 | HG00099.hp2 HG01099.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.7048-1371G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112215 | ||||||
| chr18:13112240
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7048-1346G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112240 | ||||||
| chr18:13112411
|
C | T | 1 | a0004c0004t0001g0183 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.7048-1175C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112411 | ||||||
| chr18:13112605
|
T | A | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7048-981T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112605 | ||||||
| chr18:13112673
|
T | C | 1 | a0005c0005t0001g0170 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.7048-913T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112673 | ||||||
| chr18:13112680
|
G | A | 3 | a0005c0005t0001g0151a0016c0015t0002g0040a0016c0015t0002g0041 | 3 | HG02895.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.7048-906G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112680 | ||||||
| chr18:13112884
|
C | G | 1 | a0002c0001t0001g0330 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.7048-702C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112884 | ||||||
| chr18:13112982
|
A | G | 1 | a0002c0001t0001g0293 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.7048-604A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112982 | ||||||
| chr18:13112992
|
T | C | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.7048-594T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112992 | ||||||
| chr18:13113090
|
T | C | 2 | a0006c0006t0002g0043a0006c0006t0002g0044 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7048-496T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113090 | ||||||
| chr18:13113095
|
G | A | 1 | a0002c0001t0001g0310 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7048-491G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113095 | ||||||
| chr18:13113111
|
G | A | 1 | a0006c0006t0002g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.7048-475G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113111 | ||||||
| chr18:13113117
|
C | G | 19 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(16): Show | 20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.7048-469C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113117 | ||||||
| chr18:13113134
|
C | T | 1 | a0005c0005t0001g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7048-452C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113134 | ||||||
| chr18:13113153
|
C | G | 1 | a0003c0003t0002g0110 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7048-433C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113153 | ||||||
| chr18:13113198
|
C | T | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.7048-388C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113198 | ||||||
| chr18:13113209
|
A | G | 1 | a0036c0020t0001g0355 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.7048-377A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113209 | ||||||
| chr18:13113294
|
T | C | 3 | a0019c0019t0001g0166a0019c0019t0001g0167a0035c0044t0001g0165 | 3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.7048-292T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113294 | ||||||
| chr18:13113447
|
T | C | 3 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219 | 6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.7048-139T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113447 | ||||||
| chr18:13113462
|
A | G | 1 | a0013c0029t0003g0215 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7048-124A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113462 | ||||||
| chr18:13113879
|
C | T | 1 | a0006c0006t0002g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7167+174C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/44 | chr18 | 13113879 | ||||||
| chr18:13113998
|
T | A | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7168-132T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/44 | chr18 | 13113998 | ||||||
| chr18:13114026
|
T | C | 2 | a0006c0006t0001g0356a0006c0006t0001g0358 | 2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.7168-104T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/44 | chr18 | 13114026 | ||||||
| chr18:13114047
|
A | ATG | 4 | a0001c0002t0001g0018a0001c0002t0001g0267a0001c0002t0001g0274others(1): Show | 5 | HG01192.hp2 HG02004.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.7168-82_7168-81dup others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chr18 | 13114047 | |||||
| chr18:13114047
|
A | G | 42 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(39): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.7168-83A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/44 | chr18 | 13114047 | ||||||
| chr18:13114053
|
G | T | 1 | a0002c0001t0001g0020 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.7168-77G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/44 | chr18 | 13114053 | ||||||
| chr18:13114442
|
T | C | 13 | a0005c0005t0001g0151a0005c0005t0001g0153a0005c0005t0001g0154others(10): Show | 13 | HG01884.hp2 HG02717.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.7289+191T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13114442 | ||||||
| chr18:13114715
|
A | G | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.7289+464A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13114715 | ||||||
| chr18:13115011
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7289+760G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115011 | ||||||
| chr18:13115021
|
A | T | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7289+770A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115021 | ||||||
| chr18:13115061
|
A | G | 5 | a0003c0003t0002g0007a0003c0003t0002g0058a0003c0003t0002g0059others(2): Show | 6 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.7289+810A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115061 | ||||||
| chr18:13115102
|
A | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7289+851A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115102 | ||||||
| chr18:13115172
|
A | G | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.7289+921A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115172 | ||||||
| chr18:13115264
|
C | T | 1 | a0003c0003t0002g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.7289+1013C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115264 | ||||||
| chr18:13115305
|
C | T | 1 | a0003c0003t0002g0094 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.7289+1054C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115305 | ||||||
| chr18:13115310
|
T | C | 1 | a0005c0005t0001g0148 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.7289+1059T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115310 | ||||||
| chr18:13115359
|
G | A | 1 | a0005c0005t0001g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.7290-1018G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115359 | ||||||
| chr18:13115447
|
C | T | 24 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(21): Show | 25 | HG01891.hp2 HG01952.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.7290-930C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115447 | ||||||
| chr18:13115460
|
T | C | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7290-917T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115460 | ||||||
| chr18:13115461
|
A | C | 1 | a0005c0005t0001g0134 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7290-916A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115461 | ||||||
| chr18:13115511
|
C | T | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.7290-866C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115511 | ||||||
| chr18:13115520
|
G | A | 3 | a0006c0006t0002g0042a0006c0006t0002g0043a0006c0006t0002g0044 | 3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7290-857G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115520 | ||||||
| chr18:13115693
|
C | T | 1 | a0002c0001t0001g0335 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.7290-684C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115693 | ||||||
| chr18:13115708
|
A | G | 8 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(5): Show | 8 | HG01167.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.7290-669A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115708 | ||||||
| chr18:13115750
|
TCA | T | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.7290-624_7290-623d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | INFO_REALIGN_3_PRIME | chr18 | 13115750 | |||||
| chr18:13115814
|
G | T | 2 | a0002c0001t0001g0320a0002c0001t0001g0321 | 2 | NA19060.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.7290-563G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115814 | ||||||
| chr18:13115873
|
A | G | 1 | a0002c0001t0001g0286 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7290-504A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115873 | ||||||
| chr18:13115917
|
G | A | 1 | a0003c0003t0002g0072 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.7290-460G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115917 | ||||||
| chr18:13115997
|
T | C | 6 | a0006c0006t0001g0356a0006c0006t0001g0358a0013c0016t0003g0216others(3): Show | 6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.7290-380T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115997 | ||||||
| chr18:13116002
|
T | A | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7290-375T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116002 | ||||||
| chr18:13116013
|
C | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7290-364C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116013 | ||||||
| chr18:13116152
|
C | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.7290-225C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116152 | ||||||
| chr18:13116236
|
C | T | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.7290-141C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116236 | ||||||
| chr18:13116319
|
A | G | 2 | a0005c0005t0001g0127a0005c0005t0001g0140 | 2 | HG02015.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.7290-58A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116319 | ||||||
| chr18:13116324
|
T | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7290-53T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116324 | ||||||
| chr18:13116359
|
C | T | 17 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(14): Show | 18 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.7290-18C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116359 | ||||||
| chr18:13116597
|
A | T | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7416+94A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13116597 | ||||||
| chr18:13116673
|
G | C | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7416+170G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13116673 | ||||||
| chr18:13116710
|
T | C | 4 | a0006c0006t0002g0035a0006c0006t0002g0036a0006c0006t0002g0038others(1): Show | 4 | HG02647.hp1 HG02723.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.7416+207T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13116710 | ||||||
| chr18:13116799
|
C | T | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.7416+296C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13116799 | ||||||
| chr18:13117059
|
C | CA | 88 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(85): Show | 93 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.7417-511dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | INFO_REALIGN_3_PRIME | chr18 | 13117059 | |||||
| chr18:13117246
|
G | A | 72 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(69): Show | 75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.7417-339G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117246 | ||||||
| chr18:13117291
|
C | T | 9 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(6): Show | 9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.7417-294C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117291 | ||||||
| chr18:13117348
|
T | A | 3 | a0003c0003t0002g0010a0003c0003t0002g0061a0003c0003t0002g0086 | 4 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.7417-237T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117348 | ||||||
| chr18:13117372
|
G | A | 2 | a0002c0001t0001g0292a0002c0001t0001g0294 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.7417-213G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117372 | ||||||
| chr18:13117442
|
T | C | 1 | a0006c0006t0002g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.7417-143T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117442 | ||||||
| chr18:13117540
|
A | C | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7417-45A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117540 | ||||||
| chr18:13117568
|
C | T | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7417-17C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117568 | ||||||
| chr18:13117570
|
T | A | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7417-15T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117570 | ||||||
| chr18:13117831
|
G | A | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7475+188G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13117831 | ||||||
| chr18:13118156
|
G | A | 9 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(6): Show | 9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.7475+513G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118156 | ||||||
| chr18:13118179
|
G | A | 1 | a0002c0001t0001g0301 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7475+536G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118179 | ||||||
| chr18:13118293
|
GTCTC | G | 121 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(118): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.7475+653_7475+656d others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13118293 | |||||
| chr18:13118628
|
A | T | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7475+985A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118628 | ||||||
| chr18:13118648
|
T | C | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7475+1005T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118648 | ||||||
| chr18:13118709
|
A | T | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7475+1066A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118709 | ||||||
| chr18:13118764
|
A | G | 3 | a0002c0001t0001g0310a0002c0001t0001g0316a0002c0001t0001g0318 | 3 | HG01361.hp1 HG01928.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.7475+1121A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118764 | ||||||
| chr18:13118787
|
G | A | 4 | a0005c0005t0001g0122a0005c0005t0001g0123a0005c0005t0001g0124others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.7475+1144G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118787 | ||||||
| chr18:13118796
|
T | A | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7475+1153T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118796 | ||||||
| chr18:13118798
|
ACAT | A | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7475+1174_7475+117 others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13118798 | |||||
| chr18:13118807
|
T | A | 1 | a0001c0002t0001g0273 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.7475+1164T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118807 | ||||||
| chr18:13118819
|
T | A | 2 | a0016c0015t0002g0040a0016c0015t0002g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7475+1176T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118819 | ||||||
| chr18:13119107
|
A | G | 1 | a0003c0003t0002g0108 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.7475+1464A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119107 | ||||||
| chr18:13119157
|
A | T | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.7475+1514A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119157 | ||||||
| chr18:13119307
|
A | G | 1 | a0001c0002t0001g0248 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.7475+1664A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119307 | ||||||
| chr18:13119337
|
T | A | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7475+1694T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119337 | ||||||
| chr18:13119453
|
A | T | 73 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(70): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7475+1810A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119453 | ||||||
| chr18:13119459
|
T | C | 1 | a0001c0002t0001g0271 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.7475+1816T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119459 | ||||||
| chr18:13119463
|
C | G | 1 | a0003c0003t0002g0085 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.7475+1820C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119463 | ||||||
| chr18:13119614
|
C | T | 41 | a0004c0004t0001g0001a0004c0004t0001g0002a0004c0004t0001g0005others(38): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.7475+1971C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119614 | ||||||
| chr18:13119658
|
C | T | 1 | a0002c0001t0001g0301 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7475+2015C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119658 | ||||||
| chr18:13119730
|
A | T | 1 | a0003c0003t0002g0056 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.7475+2087A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119730 | ||||||
| chr18:13119744
|
A | T | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7475+2101A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119744 | ||||||
| chr18:13119745
|
T | A | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7475+2102T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119745 | ||||||
| chr18:13119862
|
C | T | 1 | a0002c0001t0001g0295 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.7475+2219C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119862 | ||||||
| chr18:13119899
|
A | G | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.7475+2256A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119899 | ||||||
| chr18:13120332
|
A | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7475+2689A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13120332 | ||||||
| chr18:13120384
|
G | T | 114 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(111): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.7475+2741G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13120384 | ||||||
| chr18:13120417
|
C | G | 1 | a0029c0036t0001g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7475+2774C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13120417 | ||||||
| chr18:13120466
|
G | T | 1 | a0003c0003t0002g0058 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.7475+2823G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13120466 | ||||||
| chr18:13120653
|
G | C | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7475+3010G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13120653 | ||||||
| chr18:13120680
|
G | A | 1 | a0002c0001t0001g0020 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.7475+3037G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13120680 | ||||||
| chr18:13121062
|
C | T | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7475+3419C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121062 | ||||||
| chr18:13121151
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-3481G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121151 | ||||||
| chr18:13121161
|
T | C | 1 | a0001c0002t0001g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.7476-3471T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121161 | ||||||
| chr18:13121221
|
T | A | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-3411T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121221 | ||||||
| chr18:13121294
|
A | G | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.7476-3338A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121294 | ||||||
| chr18:13121432
|
C | T | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-3200C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121432 | ||||||
| chr18:13121626
|
C | A | 1 | a0003c0003t0002g0099 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.7476-3006C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121626 | ||||||
| chr18:13121668
|
C | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-2964C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121668 | ||||||
| chr18:13121681
|
C | T | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-2951C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121681 | ||||||
| chr18:13121682
|
T | C | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-2950T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121682 | ||||||
| chr18:13121683
|
C | T | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-2949C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121683 | ||||||
| chr18:13121772
|
A | G | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-2860A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121772 | ||||||
| chr18:13121802
|
G | T | 1 | a0025c0021t0001g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.7476-2830G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121802 | ||||||
| chr18:13121805
|
T | A | 1 | a0005c0005t0001g0208 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.7476-2827T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121805 | ||||||
| chr18:13121871
|
C | T | 2 | a0002c0001t0001g0360a0002c0001t0001g0361 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.7476-2761C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121871 | ||||||
| chr18:13121881
|
T | C | 1 | a0003c0003t0002g0094 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.7476-2751T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121881 | ||||||
| chr18:13121989
|
C | T | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-2643C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121989 | ||||||
| chr18:13122017
|
G | A | 1 | a0036c0020t0001g0355 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.7476-2615G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122017 | ||||||
| chr18:13122060
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-2572G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122060 | ||||||
| chr18:13122151
|
C | T | 1 | a0025c0021t0001g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.7476-2481C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122151 | ||||||
| chr18:13122213
|
A | G | 1 | a0009c0009t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.7476-2419A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122213 | ||||||
| chr18:13122355
|
C | T | 1 | a0005c0005t0001g0137 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.7476-2277C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122355 | ||||||
| chr18:13122411
|
A | T | 2 | a0013c0016t0003g0216a0013c0016t0003g0217 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.7476-2221A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122411 | ||||||
| chr18:13122484
|
G | A | 1 | a0007c0007t0002g0026 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.7476-2148G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122484 | ||||||
| chr18:13122529
|
T | C | 1 | a0002c0001t0001g0314 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7476-2103T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122529 | ||||||
| chr18:13122580
|
GA | G | 283 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(280): Show | 306 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.7476-2041delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13122580 | |||||
| chr18:13122619
|
G | A | 21 | a0006c0006t0002g0025a0006c0006t0002g0034a0006c0006t0002g0035others(18): Show | 22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.7476-2013G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122619 | ||||||
| chr18:13122711
|
T | G | 3 | a0013c0016t0003g0216a0013c0016t0003g0217a0013c0029t0003g0215 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.7476-1921T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122711 | ||||||
| chr18:13122739
|
C | T | 1 | a0005c0005t0001g0161 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.7476-1893C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122739 | ||||||
| chr18:13122760
|
A | G | 4 | a0009c0009t0001g0003a0009c0009t0001g0218a0009c0009t0001g0219others(1): Show | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.7476-1872A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122760 | ||||||
| chr18:13122832
|
C | CGT | 6 | a0005c0005t0001g0124a0005c0005t0001g0125a0009c0009t0001g0003others(3): Show | 9 | HG00621.hp2 HG01167.hp1 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.7476-1773_7476-177 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13122832 | |||||
| chr18:13122832
|
C | CGTGT | 8 | a0008c0008t0001g0129a0008c0008t0001g0130a0008c0008t0001g0131others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.7476-1775_7476-177 others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13122832 | |||||
| chr18:13122832
|
CGTGTGT | C | 149 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(146): Show | 164 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.7476-1777_7476-177 others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13122832 | |||||
| chr18:13122832
|
CGTGTGTG others(1): Show |
C | 103 | a0002c0001t0001g0019a0002c0001t0001g0020a0002c0001t0001g0021others(100): Show | 108 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.7476-1779_7476-177 others(12): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13122832 | |||||
| chr18:13122832
|
CGTGTGTG others(3): Show |
C | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-1781_7476-177 others(14): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13122832 | |||||
| chr18:13122850
|
T | A | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-1782T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122850 | ||||||
| chr18:13122878
|
T | C | 1 | a0004c0004t0001g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1754T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122878 | ||||||
| chr18:13122881
|
A | T | 1 | a0004c0004t0001g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1751A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122881 | ||||||
| chr18:13122897
|
G | T | 1 | a0004c0004t0001g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1735G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122897 | ||||||
| chr18:13122900
|
C | G | 1 | a0004c0004t0001g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1732C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122900 | ||||||
| chr18:13122901
|
T | A | 1 | a0004c0004t0001g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1731T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122901 | ||||||
| chr18:13122902
|
T | G | 1 | a0004c0004t0001g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1730T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122902 | ||||||
| chr18:13122903
|
T | A | 1 | a0004c0004t0001g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1729T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122903 | ||||||
| chr18:13122909
|
A | T | 1 | a0004c0004t0001g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1723A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122909 | ||||||
| chr18:13122912
|
T | A | 1 | a0004c0004t0001g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1720T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122912 | ||||||
| chr18:13123319
|
C | A | 1 | a0005c0005t0001g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.7476-1313C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123319 | ||||||
| chr18:13123319
|
C | G | 8 | a0005c0005t0001g0153a0005c0005t0001g0154a0005c0005t0001g0155others(5): Show | 8 | HG01884.hp2 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.7476-1313C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123319 | ||||||
| chr18:13123556
|
T | C | 1 | a0031c0038t0002g0070 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.7476-1076T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123556 | ||||||
| chr18:13123578
|
C | T | 1 | a0005c0005t0001g0285 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.7476-1054C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123578 | ||||||
| chr18:13123591
|
T | G | 1 | a0001c0034t0001g0246 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-1041T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123591 | ||||||
| chr18:13123632
|
C | T | 3 | a0019c0019t0001g0166a0019c0019t0001g0167a0035c0044t0001g0165 | 3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.7476-1000C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123632 | ||||||
| chr18:13123646
|
C | G | 277 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(274): Show | 297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.7476-986C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123646 | ||||||
| chr18:13123876
|
C | T | 9 | a0002c0001t0001g0338a0002c0001t0001g0339a0002c0001t0001g0340others(6): Show | 9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.7476-756C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123876 | ||||||
| chr18:13123877
|
C | G | 289 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(286): Show | 312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.7476-755C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123877 | ||||||
| chr18:13123939
|
C | T | 1 | a0001c0002t0001g0272 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.7476-693C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123939 | ||||||
| chr18:13124043
|
C | G | 1 | a0000c0035t0001g0264 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.7476-589C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13124043 | ||||||
| chr18:13124156
|
G | A | 1 | a0005c0005t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7476-476G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13124156 | ||||||
| chr18:13124416
|
C | T | 77 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(74): Show | 80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.7476-216C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13124416 | ||||||
| chr18:13124447
|
G | A | 4 | a0015c0012t0001g0011a0015c0012t0001g0114a0015c0012t0001g0115others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-185G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13124447 | ||||||
| chr18:13124610
|
T | C | 68 | a0000c0035t0001g0264a0001c0002t0001g0016a0001c0002t0001g0017others(65): Show | 71 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.7476-22T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13124610 |