Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84902 |
|---|---|
| ensemblid | ENSG00000121289.18 |
| hgncid | 25907 |
| symbol | CEP89 |
| name | centrosomal protein 89 |
| refseq_nuc | NM_032816.5 |
| refseq_prot | NP_116205.3 |
| ensembl_nuc | ENST00000305768.10 |
| ensembl_prot | ENSP00000306105.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 32875925 |
| end | 32971958 |
| strand | - |
| ver | v1.2 |
| region | chr19:32875925-32971958 |
| region5000 | chr19:32870925-32976958 |
| regionname0 | CEP89_chr19_32875925_32971958 |
| regionname5000 | CEP89_chr19_32870925_32976958 |
| 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 | 49 | 6 | 12 | 14 | 5 | 12 | 11 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001 | 0/0 | 783 | 126 | 17 | 21 | 79 | 2 | 7 | 62 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0002 | 0/0 | 783 | 90 | 18 | 9 | 52 | 3 | 8 | 39 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003 | 1/0 | 783 | 72 | 19 | 17 | 21 | 3 | 11 | 17 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0004 | 0/0 | 783 | 22 | 3 | 2 | 9 | 1 | 7 | 5 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0005 | 0/0 | 783 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0006 | 0/0 | 783 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0007 | 0/0 | 783 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0008 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0009 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0010 | 0/0 | 230 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0011 | 0/1 | 783 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0012 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0013 | 0/0 | 783 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0014 | 0/0 | 783 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0015 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| 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 | 2352 | 89 | 18 | 9 | 51 | 3 | 8 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0002 | 0/0 | 2352 | 80 | 16 | 10 | 50 | 1 | 3 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0003 | 0/0 | 2352 | 64 | 15 | 16 | 20 | 3 | 10 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0004 | 0/0 | 2352 | 45 | 1 | 10 | 29 | 1 | 4 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0005 | 0/0 | 2352 | 27 | 4 | 10 | 0 | 4 | 9 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0006 | 0/0 | 2352 | 22 | 3 | 2 | 9 | 1 | 7 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0007 | 0/0 | 2352 | 20 | 1 | 2 | 13 | 1 | 3 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0008 | 0/0 | 2352 | 12 | 12 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0009 | 0/0 | 2352 | 4 | 4 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0010 | 0/0 | 2352 | 4 | 2 | 1 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0011 | 0/0 | 2352 | 3 | 3 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0012 | 0/0 | 2352 | 2 | 1 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0013 | 1/0 | 2352 | 2 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0014 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0015 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0016 | 0/0 | 2352 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0017 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0018 | 0/1 | 2352 | 1 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0019 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0020 | 0/0 | 2372 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0021 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0022 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0023 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0024 | 0/0 | 2352 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| c0025 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3322 | 118 | 13 | 18 | 76 | 2 | 8 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0002 | 0/0 | 3323 | 78 | 19 | 9 | 40 | 3 | 7 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0003 | 0/1 | 3323 | 56 | 12 | 11 | 20 | 3 | 9 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0004 | 0/0 | 3323 | 20 | 1 | 2 | 13 | 1 | 3 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0005 | 0/0 | 3323 | 20 | 2 | 8 | 0 | 4 | 6 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0006 | 0/0 | 3322 | 12 | 12 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0007 | 0/0 | 3322 | 11 | 1 | 0 | 7 | 0 | 3 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0008 | 0/0 | 3323 | 9 | 0 | 0 | 9 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0009 | 0/0 | 3322 | 8 | 0 | 2 | 2 | 1 | 3 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0010 | 0/0 | 3322 | 5 | 5 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0011 | 0/0 | 3322 | 5 | 5 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0012 | 0/0 | 3322 | 4 | 4 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0013 | 0/0 | 3322 | 3 | 0 | 2 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0014 | 0/0 | 3323 | 2 | 2 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0015 | 0/0 | 3323 | 2 | 0 | 1 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0016 | 0/0 | 3322 | 2 | 0 | 1 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0017 | 0/0 | 3324 | 2 | 0 | 0 | 1 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0018 | 0/0 | 3323 | 2 | 0 | 0 | 2 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0019 | 0/0 | 3321 | 2 | 0 | 0 | 0 | 0 | 2 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0020 | 0/0 | 3322 | 2 | 0 | 1 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0021 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0022 | 0/0 | 3323 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0023 | 0/0 | 3322 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0024 | 0/0 | 3322 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0025 | 0/0 | 3322 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0026 | 0/0 | 3322 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0027 | 0/0 | 3323 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0028 | 0/0 | 3322 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0029 | 0/0 | 3322 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0030 | 0/0 | 3322 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0031 | 0/0 | 3322 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0032 | 0/0 | 3323 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0033 | 0/0 | 3322 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0034 | 0/0 | 3323 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0035 | 0/0 | 3323 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0036 | 0/0 | 3323 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0037 | 0/0 | 3323 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0038 | 0/0 | 3323 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0039 | 0/0 | 3323 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0040 | 0/0 | 3324 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0041 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0042 | 0/0 | 3323 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| t0043 | 0/0 | 3322 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0276 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0005 | 0/0 | 2352 | 27 | 4 | 10 | 0 | 4 | 9 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0000c0007 | 0/0 | 2352 | 20 | 1 | 2 | 13 | 1 | 3 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0000c0012 | 0/0 | 2352 | 2 | 1 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0002 | 0/0 | 2352 | 80 | 16 | 10 | 50 | 1 | 3 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0004 | 0/0 | 2352 | 45 | 1 | 10 | 29 | 1 | 4 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0016 | 0/0 | 2352 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0002c0001 | 0/0 | 2352 | 89 | 18 | 9 | 51 | 3 | 8 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0002c0025 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0003 | 0/0 | 2352 | 64 | 15 | 16 | 20 | 3 | 10 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0010 | 0/0 | 2352 | 4 | 2 | 1 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0013 | 1/0 | 2352 | 2 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0019 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0021 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0004c0006 | 0/0 | 2352 | 22 | 3 | 2 | 9 | 1 | 7 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0005c0008 | 0/0 | 2352 | 12 | 12 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0006c0009 | 0/0 | 2352 | 4 | 4 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0007c0011 | 0/0 | 2352 | 3 | 3 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0008c0015 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0009c0023 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0010c0020 | 0/0 | 2372 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0011c0018 | 0/1 | 2352 | 1 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0012c0017 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0013c0024 | 0/0 | 2352 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0014c0022 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0015c0014 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0005t0005 | 0/0 | 5674 | 20 | 2 | 8 | 0 | 4 | 6 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0000c0005t0019 | 0/0 | 5672 | 2 | 0 | 0 | 0 | 0 | 2 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0000c0005t0020 | 0/0 | 5673 | 2 | 0 | 1 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0000c0005t0023 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0000c0005t0041 | 0/0 | 5672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0000c0005t0042 | 0/0 | 5674 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0000c0007t0004 | 0/0 | 5674 | 19 | 1 | 2 | 12 | 1 | 3 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0000c0007t0033 | 0/0 | 5673 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0000c0012t0004 | 0/0 | 5674 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0000c0012t0021 | 0/0 | 5672 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0002t0001 | 0/0 | 5673 | 69 | 11 | 8 | 47 | 1 | 2 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0002t0010 | 0/0 | 5673 | 4 | 4 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0002t0015 | 0/0 | 5674 | 2 | 0 | 1 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0002t0016 | 0/0 | 5673 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0002t0024 | 0/0 | 5673 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0002t0028 | 0/0 | 5673 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0002t0031 | 0/0 | 5673 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0002t0043 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0004t0001 | 0/0 | 5673 | 44 | 1 | 10 | 28 | 1 | 4 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0004t0002 | 0/0 | 5674 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0001c0016t0030 | 0/0 | 5673 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0002c0001t0001 | 0/0 | 5673 | 2 | 0 | 0 | 1 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0002c0001t0002 | 0/0 | 5674 | 72 | 18 | 7 | 38 | 3 | 6 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0002c0001t0008 | 0/0 | 5674 | 9 | 0 | 0 | 9 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0002c0001t0016 | 0/0 | 5673 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0002c0001t0017 | 0/0 | 5675 | 2 | 0 | 0 | 1 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0002c0001t0018 | 0/0 | 5674 | 2 | 0 | 0 | 2 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0002c0001t0025 | 0/0 | 5673 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0002c0025t0002 | 0/0 | 5674 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0003t0002 | 0/0 | 5674 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0003t0003 | 0/0 | 5674 | 52 | 12 | 11 | 17 | 3 | 9 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0003t0010 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0003t0013 | 0/0 | 5673 | 3 | 0 | 2 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0003t0034 | 0/0 | 5674 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0003t0035 | 0/0 | 5674 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0003t0036 | 0/0 | 5674 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0003t0037 | 0/0 | 5674 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0003t0038 | 0/0 | 5674 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0003t0039 | 0/0 | 5674 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0003t0040 | 0/0 | 5675 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0010t0002 | 0/0 | 5674 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0010t0014 | 0/0 | 5674 | 2 | 2 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0010t0029 | 0/0 | 5673 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0013t0001 | 1/0 | 5673 | 1 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0013t0003 | 0/0 | 5674 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0019t0012 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0003c0021t0022 | 0/0 | 5674 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0004c0006t0007 | 0/0 | 5673 | 10 | 1 | 0 | 6 | 0 | 3 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0004c0006t0009 | 0/0 | 5673 | 8 | 0 | 2 | 2 | 1 | 3 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0004c0006t0011 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0004c0006t0026 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0004c0006t0027 | 0/0 | 5674 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0004c0006t0032 | 0/0 | 5674 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0005c0008t0006 | 0/0 | 5673 | 12 | 12 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0006c0009t0011 | 0/0 | 5673 | 4 | 4 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0007c0011t0012 | 0/0 | 5673 | 3 | 3 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0008c0015t0001 | 0/0 | 5673 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0009c0023t0007 | 0/0 | 5673 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0010c0020t0003 | 0/0 | 5694 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0011c0018t0003 | 0/1 | 5674 | 1 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0012c0017t0003 | 0/0 | 5674 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0013c0024t0002 | 0/0 | 5674 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0014c0022t0001 | 0/0 | 5673 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| a0015c0014t0002 | 0/0 | 5674 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | copy fasta | chr19 | 32870925 | 32976958 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0005t0005g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0019g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0019g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0020g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0020g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0023g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0041g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0005t0042g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0007t0033g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0012t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0000c0012t0021g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0010g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0010g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0010g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0015g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0015g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0016g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0024g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0028g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0031g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0002t0043g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0004t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0001c0016t0030g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0008g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0008g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0008g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0008g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0008g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0008g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0008g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0016g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0017g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0017g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0018g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0018g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0001t0025g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0002c0025t0002g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0010g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0013g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0013g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0013g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0034g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0035g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0036g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0037g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0038g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0039g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0003t0040g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0010t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0010t0014g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0010t0014g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0010t0029g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0013t0001g0276 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0013t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0019t0012g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0003c0021t0022g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0007g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0007g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0009g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0009g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0009g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0009g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0009g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0009g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0009g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0009g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0011g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0026g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0027g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0004c0006t0032g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0005c0008t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0005c0008t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0005c0008t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0005c0008t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0005c0008t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0005c0008t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0005c0008t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0005c0008t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0005c0008t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0005c0008t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0005c0008t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0005c0008t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0006c0009t0011g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0006c0009t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0006c0009t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0006c0009t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0007c0011t0012g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0007c0011t0012g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0007c0011t0012g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0008c0015t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0009c0023t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0010c0020t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0011c0018t0003g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0012c0017t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0013c0024t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0014c0022t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| a0015c0014t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0000 | c0007 | t0004 | g0278 | EUR | GBR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00099 | hp2 | a0000 | c0005 | t0005 | g0120 | EUR | GBR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00140 | hp1 | a0002 | c0001 | t0002 | g0360 | EUR | GBR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00140 | hp2 | a0003 | c0003 | t0003 | g0263 | EUR | GBR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00280 | hp1 | a0002 | c0001 | t0002 | g0355 | EUR | FIN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00280 | hp2 | a0000 | c0005 | t0005 | g0110 | EUR | FIN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00323 | hp1 | a0002 | c0001 | t0002 | g0162 | EUR | FIN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00323 | hp2 | a0001 | c0004 | t0001 | g0207 | EUR | FIN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00408 | hp1 | a0003 | c0003 | t0003 | g0236 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00408 | hp2 | a0001 | c0004 | t0001 | g0193 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00423 | hp1 | a0001 | c0004 | t0001 | g0202 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00423 | hp2 | a0003 | c0003 | t0003 | g0254 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00438 | hp2 | a0002 | c0001 | t0002 | g0339 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00544 | hp1 | a0002 | c0001 | t0002 | g0165 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00544 | hp2 | a0001 | c0004 | t0001 | g0167 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00597 | hp2 | a0001 | c0004 | t0001 | g0201 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00609 | hp1 | a0004 | c0006 | t0007 | g0135 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00609 | hp2 | a0001 | c0004 | t0001 | g0176 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00621 | hp1 | a0002 | c0001 | t0002 | g0150 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0169 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00639 | hp2 | a0003 | c0003 | t0003 | g0230 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00642 | hp1 | a0002 | c0001 | t0002 | g0319 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00642 | hp2 | a0001 | c0004 | t0001 | g0200 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00673 | hp1 | a0002 | c0001 | t0002 | g0336 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00673 | hp2 | a0001 | c0004 | t0001 | g0192 | EAS | CHS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00735 | hp1 | a0001 | c0004 | t0001 | g0177 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00735 | hp2 | a0003 | c0003 | t0039 | g0237 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00738 | hp1 | a0003 | c0003 | t0003 | g0235 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00738 | hp2 | a0000 | c0005 | t0005 | g0116 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00741 | hp1 | a0000 | c0005 | t0005 | g0108 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0180 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0048 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01070 | hp1 | a0002 | c0001 | t0016 | g0317 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01070 | hp2 | a0000 | c0005 | t0020 | g0121 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01071 | hp2 | a0002 | c0001 | t0002 | g0318 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01074 | hp1 | a0013 | c0024 | t0002 | g0324 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01074 | hp2 | a0000 | c0007 | t0004 | g0277 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01081 | hp1 | a0003 | c0003 | t0003 | g0222 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01081 | hp2 | a0000 | c0005 | t0005 | g0268 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01106 | hp1 | a0004 | c0006 | t0009 | g0270 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01106 | hp2 | a0000 | c0005 | t0005 | g0103 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01109 | hp1 | a0001 | c0002 | t0015 | g0021 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01109 | hp2 | a0003 | c0010 | t0029 | g0307 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01167 | hp1 | a0001 | c0004 | t0001 | g0075 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01167 | hp2 | a0003 | c0003 | t0003 | g0249 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01169 | hp1 | a0003 | c0003 | t0013 | g0271 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0195 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01175 | hp1 | a0000 | c0005 | t0005 | g0269 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01175 | hp2 | a0002 | c0001 | t0025 | g0148 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01192 | hp1 | a0000 | c0005 | t0042 | g0109 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01192 | hp2 | a0003 | c0003 | t0003 | g0239 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01243 | hp1 | a0000 | c0005 | t0005 | g0099 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0189 | AMR | PUR | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01257 | hp1 | a0002 | c0001 | t0002 | g0316 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01258 | hp1 | a0003 | c0003 | t0002 | g0265 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01261 | hp1 | a0001 | c0016 | t0030 | g0055 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0166 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01358 | hp1 | a0002 | c0001 | t0002 | g0314 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01358 | hp2 | a0000 | c0005 | t0005 | g0112 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01361 | hp1 | a0004 | c0006 | t0009 | g0137 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01433 | hp1 | a0003 | c0003 | t0003 | g0253 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01496 | hp1 | a0002 | c0001 | t0002 | g0361 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01496 | hp2 | a0003 | c0003 | t0013 | g0220 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0019 | EUR | IBS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01515 | hp2 | a0003 | c0003 | t0003 | g0221 | EUR | IBS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01516 | hp1 | a0004 | c0006 | t0009 | g0136 | EUR | IBS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01516 | hp2 | a0000 | c0005 | t0005 | g0098 | EUR | IBS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01517 | hp1 | a0000 | c0005 | t0005 | g0097 | EUR | IBS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01517 | hp2 | a0003 | c0003 | t0003 | g0244 | EUR | IBS | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01884 | hp1 | a0002 | c0001 | t0002 | g0352 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01884 | hp2 | a0000 | c0005 | t0023 | g0079 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01928 | hp1 | a0003 | c0003 | t0003 | g0241 | AMR | PEL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01928 | hp2 | a0000 | c0005 | t0005 | g0119 | AMR | PEL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01952 | hp1 | a0003 | c0003 | t0003 | g0256 | AMR | PEL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | PEL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01975 | hp1 | a0003 | c0003 | t0003 | g0250 | AMR | PEL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01975 | hp2 | a0001 | c0004 | t0001 | g0175 | AMR | PEL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01978 | hp1 | a0001 | c0004 | t0001 | g0199 | AMR | PEL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01978 | hp2 | a0003 | c0003 | t0003 | g0232 | AMR | PEL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01981 | hp1 | a0003 | c0003 | t0040 | g0231 | AMR | PEL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01981 | hp2 | a0002 | c0001 | t0002 | g0315 | AMR | PEL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02015 | hp1 | a0002 | c0001 | t0002 | g0333 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02015 | hp2 | a0001 | c0004 | t0002 | g0181 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02027 | hp1 | a0004 | c0006 | t0009 | g0141 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02027 | hp2 | a0002 | c0001 | t0002 | g0313 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02040 | hp2 | a0002 | c0001 | t0002 | g0159 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02055 | hp1 | a0005 | c0008 | t0006 | g0308 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02055 | hp2 | a0003 | c0003 | t0010 | g0218 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02056 | hp1 | a0012 | c0017 | t0003 | g0267 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02056 | hp2 | a0000 | c0007 | t0004 | g0281 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02080 | hp1 | a0002 | c0001 | t0002 | g0161 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02083 | hp1 | a0002 | c0001 | t0002 | g0335 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02083 | hp2 | a0004 | c0006 | t0009 | g0139 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02129 | hp1 | a0004 | c0006 | t0007 | g0133 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02132 | hp1 | a0002 | c0001 | t0002 | g0151 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02132 | hp2 | a0000 | c0007 | t0004 | g0283 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02135 | hp1 | a0002 | c0001 | t0002 | g0158 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02135 | hp2 | a0001 | c0004 | t0001 | g0191 | EAS | KHV | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0300 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02145 | hp2 | a0005 | c0008 | t0006 | g0089 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02155 | hp1 | a0002 | c0001 | t0002 | g0160 | EAS | CDX | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02155 | hp2 | a0003 | c0003 | t0036 | g0264 | EAS | CDX | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02165 | hp1 | a0000 | c0007 | t0004 | g0284 | EAS | CDX | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | CDX | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02257 | hp1 | a0002 | c0001 | t0002 | g0327 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02257 | hp2 | a0000 | c0012 | t0021 | g0015 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02258 | hp1 | a0002 | c0001 | t0002 | g0153 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0296 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0305 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02280 | hp2 | a0003 | c0003 | t0003 | g0214 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02293 | hp1 | a0003 | c0003 | t0003 | g0251 | AMR | PEL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02293 | hp2 | a0002 | c0001 | t0002 | g0371 | AMR | PEL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02451 | hp1 | a0002 | c0001 | t0002 | g0353 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0301 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02602 | hp1 | a0003 | c0003 | t0003 | g0261 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02602 | hp2 | a0002 | c0001 | t0017 | g0354 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02615 | hp1 | a0003 | c0003 | t0003 | g0248 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02615 | hp2 | a0003 | c0019 | t0012 | g0364 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02622 | hp1 | a0003 | c0003 | t0038 | g0229 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02622 | hp2 | a0004 | c0006 | t0026 | g0144 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02630 | hp1 | a0003 | c0003 | t0003 | g0217 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02630 | hp2 | a0007 | c0011 | t0012 | g0380 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02647 | hp1 | a0002 | c0001 | t0002 | g0328 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02647 | hp2 | a0003 | c0003 | t0003 | g0306 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02698 | hp1 | a0000 | c0005 | t0019 | g0114 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02698 | hp2 | a0004 | c0006 | t0009 | g0138 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02717 | hp1 | a0006 | c0009 | t0011 | g0124 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02717 | hp2 | a0002 | c0001 | t0002 | g0330 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02723 | hp1 | a0002 | c0001 | t0002 | g0320 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02723 | hp2 | a0005 | c0008 | t0006 | g0088 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02735 | hp2 | a0003 | c0003 | t0003 | g0238 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02738 | hp1 | a0000 | c0005 | t0005 | g0102 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02738 | hp2 | a0000 | c0007 | t0004 | g0291 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02809 | hp1 | a0003 | c0003 | t0003 | g0080 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02809 | hp2 | a0007 | c0011 | t0012 | g0375 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02818 | hp1 | a0002 | c0001 | t0002 | g0329 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02818 | hp2 | a0005 | c0008 | t0006 | g0090 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02886 | hp1 | a0005 | c0008 | t0006 | g0096 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02886 | hp2 | a0003 | c0010 | t0014 | g0168 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02897 | hp1 | a0015 | c0014 | t0002 | g0323 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02897 | hp2 | a0005 | c0008 | t0006 | g0095 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02922 | hp1 | a0008 | c0015 | t0001 | g0081 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02922 | hp2 | a0001 | c0002 | t0010 | g0377 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02965 | hp1 | a0003 | c0003 | t0003 | g0227 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02965 | hp2 | a0005 | c0008 | t0006 | g0087 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02970 | hp1 | a0003 | c0003 | t0003 | g0228 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02970 | hp2 | a0006 | c0009 | t0011 | g0312 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02976 | hp1 | a0003 | c0003 | t0003 | g0273 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02976 | hp2 | a0002 | c0001 | t0002 | g0311 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03017 | hp1 | a0003 | c0003 | t0003 | g0077 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03017 | hp2 | a0002 | c0001 | t0002 | g0345 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03041 | hp1 | a0001 | c0002 | t0010 | g0149 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03041 | hp2 | a0002 | c0001 | t0002 | g0073 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03098 | hp1 | a0002 | c0001 | t0002 | g0349 | AFR | MSL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0298 | AFR | MSL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03139 | hp1 | a0003 | c0003 | t0003 | g0213 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03139 | hp2 | a0005 | c0008 | t0006 | g0092 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03195 | hp1 | a0007 | c0011 | t0012 | g0379 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03195 | hp2 | a0002 | c0001 | t0002 | g0004 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03209 | hp1 | a0001 | c0002 | t0010 | g0376 | AFR | MSL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03209 | hp2 | a0003 | c0003 | t0003 | g0212 | AFR | MSL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03239 | hp1 | a0004 | c0006 | t0009 | g0142 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03239 | hp2 | a0000 | c0005 | t0019 | g0113 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0304 | AFR | MSL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03453 | hp2 | a0006 | c0009 | t0011 | g0123 | AFR | MSL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03486 | hp1 | a0005 | c0008 | t0006 | g0093 | AFR | MSL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0303 | AFR | MSL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03490 | hp1 | a0003 | c0003 | t0034 | g0076 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03490 | hp2 | a0004 | c0006 | t0007 | g0129 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03491 | hp1 | a0000 | c0005 | t0020 | g0107 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03491 | hp2 | a0000 | c0007 | t0004 | g0275 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03492 | hp1 | a0004 | c0006 | t0007 | g0134 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03492 | hp2 | a0000 | c0005 | t0005 | g0101 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03516 | hp1 | a0000 | c0005 | t0005 | g0117 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03516 | hp2 | a0001 | c0002 | t0010 | g0378 | AFR | ESN | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03540 | hp1 | a0003 | c0003 | t0037 | g0247 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03540 | hp2 | a0002 | c0001 | t0002 | g0351 | AFR | GWD | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03654 | hp1 | a0003 | c0003 | t0003 | g0233 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03654 | hp2 | a0000 | c0005 | t0005 | g0164 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03669 | hp1 | a0001 | c0004 | t0001 | g0182 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03669 | hp2 | a0003 | c0003 | t0003 | g0262 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03688 | hp1 | a0002 | c0001 | t0002 | g0334 | SAS | STU | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03688 | hp2 | a0003 | c0003 | t0003 | g0246 | SAS | STU | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03704 | hp1 | a0002 | c0001 | t0002 | g0331 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03704 | hp2 | a0001 | c0004 | t0001 | g0178 | SAS | PJL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03831 | hp1 | a0004 | c0006 | t0027 | g0140 | SAS | BEB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03831 | hp2 | a0002 | c0001 | t0002 | g0358 | SAS | BEB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03834 | hp1 | a0003 | c0003 | t0003 | g0234 | SAS | BEB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0332 | SAS | BEB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03927 | hp1 | a0000 | c0005 | t0005 | g0106 | SAS | BEB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03927 | hp2 | a0002 | c0001 | t0002 | g0356 | SAS | BEB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03942 | hp1 | a0003 | c0010 | t0002 | g0105 | SAS | BEB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03942 | hp2 | a0004 | c0006 | t0009 | g0146 | SAS | BEB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG04115 | hp1 | a0003 | c0003 | t0003 | g0243 | SAS | STU | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG04115 | hp2 | a0001 | c0002 | t0028 | g0054 | SAS | STU | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG04184 | hp1 | a0000 | c0005 | t0005 | g0104 | SAS | BEB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG04184 | hp2 | a0014 | c0022 | t0001 | g0196 | SAS | BEB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG04199 | hp1 | a0002 | c0001 | t0002 | g0325 | SAS | STU | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG04199 | hp2 | a0000 | c0005 | t0005 | g0100 | SAS | STU | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG04204 | hp1 | a0000 | c0007 | t0004 | g0294 | SAS | STU | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG04204 | hp2 | a0003 | c0003 | t0003 | g0245 | SAS | STU | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG04228 | hp1 | a0001 | c0004 | t0001 | g0197 | SAS | STU | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | STU | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18522 | hp1 | a0000 | c0005 | t0041 | g0111 | AFR | YRI | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18522 | hp2 | a0002 | c0001 | t0002 | g0326 | AFR | YRI | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18612 | hp1 | a0003 | c0003 | t0003 | g0215 | EAS | CHB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18612 | hp2 | a0002 | c0001 | t0002 | g0155 | EAS | CHB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18747 | hp1 | a0001 | c0002 | t0016 | g0023 | EAS | CHB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18747 | hp2 | a0001 | c0004 | t0001 | g0208 | EAS | CHB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18906 | hp1 | a0005 | c0008 | t0006 | g0094 | AFR | YRI | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18906 | hp2 | a0002 | c0001 | t0002 | g0004 | AFR | YRI | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18939 | hp1 | a0003 | c0003 | t0003 | g0365 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18939 | hp2 | a0002 | c0001 | t0002 | g0370 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18942 | hp2 | a0002 | c0001 | t0002 | g0341 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18943 | hp1 | a0002 | c0001 | t0002 | g0005 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18944 | hp1 | a0002 | c0001 | t0008 | g0007 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18944 | hp2 | a0000 | c0007 | t0004 | g0288 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18945 | hp1 | a0002 | c0001 | t0002 | g0005 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18945 | hp2 | a0003 | c0013 | t0003 | g0292 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18947 | hp1 | a0001 | c0002 | t0031 | g0053 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18947 | hp2 | a0001 | c0004 | t0001 | g0185 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18949 | hp1 | a0004 | c0006 | t0007 | g0274 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18949 | hp2 | a0000 | c0007 | t0004 | g0293 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18950 | hp1 | a0001 | c0004 | t0001 | g0204 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18950 | hp2 | a0002 | c0001 | t0018 | g0338 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18952 | hp1 | a0002 | c0001 | t0002 | g0359 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18953 | hp1 | a0002 | c0001 | t0002 | g0156 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18953 | hp2 | a0003 | c0003 | t0003 | g0257 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18954 | hp1 | a0001 | c0004 | t0001 | g0074 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18959 | hp1 | a0003 | c0003 | t0003 | g0223 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18959 | hp2 | a0001 | c0004 | t0001 | g0170 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18960 | hp1 | a0004 | c0006 | t0007 | g0131 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18961 | hp1 | a0004 | c0006 | t0007 | g0086 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18961 | hp2 | a0002 | c0001 | t0008 | g0009 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18962 | hp1 | a0001 | c0004 | t0001 | g0187 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0357 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18963 | hp2 | a0002 | c0001 | t0002 | g0367 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18964 | hp1 | a0002 | c0001 | t0002 | g0344 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18965 | hp1 | a0001 | c0004 | t0001 | g0194 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18965 | hp2 | a0002 | c0001 | t0002 | g0343 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18966 | hp1 | a0002 | c0001 | t0002 | g0363 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18967 | hp2 | a0004 | c0006 | t0032 | g0127 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18969 | hp1 | a0002 | c0001 | t0002 | g0154 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18972 | hp1 | a0002 | c0001 | t0002 | g0369 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18974 | hp1 | a0003 | c0003 | t0003 | g0252 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18977 | hp1 | a0002 | c0001 | t0001 | g0350 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18977 | hp2 | a0000 | c0007 | t0004 | g0289 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18978 | hp1 | a0002 | c0001 | t0002 | g0372 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18978 | hp2 | a0001 | c0004 | t0001 | g0188 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18979 | hp1 | a0001 | c0004 | t0001 | g0206 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18979 | hp2 | a0003 | c0003 | t0003 | g0258 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18980 | hp1 | a0000 | c0007 | t0004 | g0285 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18980 | hp2 | a0002 | c0001 | t0002 | g0342 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18982 | hp1 | a0002 | c0001 | t0002 | g0340 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18983 | hp1 | a0003 | c0003 | t0003 | g0255 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18984 | hp1 | a0000 | c0007 | t0004 | g0282 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18986 | hp1 | a0001 | c0004 | t0001 | g0184 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18986 | hp2 | a0002 | c0001 | t0002 | g0152 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18991 | hp1 | a0002 | c0001 | t0002 | g0373 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18993 | hp2 | a0003 | c0003 | t0003 | g0219 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18994 | hp1 | a0002 | c0025 | t0002 | g0374 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18995 | hp1 | a0002 | c0001 | t0008 | g0014 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18995 | hp2 | a0001 | c0004 | t0001 | g0186 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18997 | hp2 | a0002 | c0001 | t0002 | g0322 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18999 | hp2 | a0003 | c0003 | t0003 | g0211 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19000 | hp1 | a0004 | c0006 | t0007 | g0128 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19002 | hp1 | a0001 | c0002 | t0015 | g0044 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19002 | hp2 | a0003 | c0003 | t0003 | g0242 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19003 | hp1 | a0000 | c0007 | t0004 | g0287 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19004 | hp1 | a0002 | c0001 | t0002 | g0368 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19004 | hp2 | a0000 | c0012 | t0004 | g0065 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19005 | hp2 | a0002 | c0001 | t0002 | g0348 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19007 | hp2 | a0001 | c0004 | t0001 | g0203 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19009 | hp2 | a0001 | c0004 | t0001 | g0174 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19010 | hp1 | a0001 | c0004 | t0001 | g0198 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19010 | hp2 | a0002 | c0001 | t0008 | g0006 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19011 | hp2 | a0002 | c0001 | t0008 | g0011 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19012 | hp1 | a0000 | c0007 | t0004 | g0290 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19012 | hp2 | a0002 | c0001 | t0002 | g0362 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19030 | hp1 | a0005 | c0008 | t0006 | g0210 | AFR | LWK | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19030 | hp2 | a0000 | c0005 | t0005 | g0115 | AFR | LWK | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19043 | hp1 | a0006 | c0009 | t0011 | g0125 | AFR | LWK | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19043 | hp2 | a0004 | c0006 | t0011 | g0143 | AFR | LWK | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19054 | hp1 | a0001 | c0004 | t0001 | g0171 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19054 | hp2 | a0003 | c0003 | t0003 | g0216 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19055 | hp2 | a0003 | c0003 | t0035 | g0259 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19057 | hp1 | a0000 | c0007 | t0004 | g0286 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19057 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19058 | hp2 | a0010 | c0020 | t0003 | g0122 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19060 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0190 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19063 | hp1 | a0003 | c0003 | t0013 | g0272 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19063 | hp2 | a0002 | c0001 | t0008 | g0010 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19068 | hp1 | a0001 | c0004 | t0001 | g0173 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0205 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19070 | hp2 | a0002 | c0001 | t0002 | g0157 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19074 | hp2 | a0009 | c0023 | t0007 | g0130 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19075 | hp1 | a0002 | c0001 | t0002 | g0163 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19078 | hp1 | a0001 | c0004 | t0001 | g0209 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19079 | hp1 | a0003 | c0003 | t0003 | g0225 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19079 | hp2 | a0002 | c0001 | t0008 | g0013 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19081 | hp1 | a0003 | c0003 | t0003 | g0260 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19082 | hp1 | a0002 | c0001 | t0017 | g0347 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19083 | hp1 | a0000 | c0007 | t0004 | g0078 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19083 | hp2 | a0001 | c0004 | t0001 | g0172 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19084 | hp1 | a0002 | c0001 | t0002 | g0126 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19084 | hp2 | a0001 | c0004 | t0001 | g0179 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19085 | hp1 | a0002 | c0001 | t0008 | g0012 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19087 | hp2 | a0002 | c0001 | t0002 | g0346 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19088 | hp1 | a0002 | c0001 | t0008 | g0008 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19091 | hp2 | a0002 | c0001 | t0018 | g0337 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19240 | hp1 | a0003 | c0021 | t0022 | g0266 | AFR | YRI | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0299 | AFR | YRI | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA20129 | hp1 | a0003 | c0010 | t0014 | g0366 | AFR | ASW | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ASW | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0183 | SAS | GIH | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA20905 | hp2 | a0004 | c0006 | t0007 | g0147 | SAS | GIH | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01123 | hp1 | a0000 | c0007 | t0004 | g0279 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG01123 | hp2 | a0001 | c0002 | t0024 | g0072 | AMR | CLM | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02109 | hp1 | a0001 | c0002 | t0043 | g0118 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0145 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0302 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02486 | hp2 | a0003 | c0003 | t0003 | g0224 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02559 | hp1 | a0002 | c0001 | t0002 | g0309 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG02559 | hp2 | a0000 | c0007 | t0004 | g0280 | AFR | ACB | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0297 | AFR | MSL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| HG03471 | hp2 | a0005 | c0008 | t0006 | g0091 | AFR | MSL | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18955 | hp1 | a0000 | c0007 | t0033 | g0295 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA20300 | hp1 | a0003 | c0003 | t0003 | g0226 | AFR | USA | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA20300 | hp2 | a0002 | c0001 | t0002 | g0321 | AFR | USA | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA21309 | hp1 | a0004 | c0006 | t0007 | g0132 | AFR | LWK | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| NA21309 | hp2 | a0002 | c0001 | t0002 | g0310 | AFR | LWK | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| homoSapiens_chm13v2 | hp1 | a0011 | c0018 | t0003 | g0240 | REF | REF | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| homoSapiens_grch38 | hp1 | a0003 | c0013 | t0001 | g0276 | REF | REF | CEP89_chr19_32870925_32976958 | CEP89 | chr19 | 32870925 | 32976958 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:32879164
|
A | G | 1 | a0000 | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
stop_lost | HIGH | c.2350T>C | p.Ter784Glnext*? | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2434/5673 | 2350/2352 | 784/783 | chr19 | 32879164 | ||
| chr19:32879178
|
T | A | 1 | a0000 | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
missense_variant | MODERATE | c.2336A>T | p.His779Leu | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2420/5673 | 2336/2352 | 779/783 | chr19 | 32879178 | ||
| chr19:32879193
|
T | C | 1 | a0011 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.2321A>G | p.Tyr774Cys | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2405/5673 | 2321/2352 | 774/783 | chr19 | 32879193 | ||
| chr19:32881908
|
G | A | 3 | a0004a0006a0009 | 27 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(24): Show |
missense_variant | MODERATE | c.2071C>T | p.Arg691Trp | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/19 | 2155/5673 | 2071/2352 | 691/783 | chr19 | 32881908 | ||
| chr19:32899981
|
A | G | 1 | a0012 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.1751T>C | p.Ile584Thr | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/19 | 1835/5673 | 1751/2352 | 584/783 | chr19 | 32899981 | ||
| chr19:32915421
|
C | T | 1 | a0007 | 3 | HG02630.hp2 HG02809.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.1481G>A | p.Arg494His | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/19 | 1565/5673 | 1481/2352 | 494/783 | chr19 | 32915421 | ||
| chr19:32923512
|
G | GGACTCGC others(13): Show |
1 | a0010 | 1 | NA19058.hp2 | frameshift_variant | HIGH | c.1175_1194dupGAATGT others(14): Show |
p.Gln399fs | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/19 | 1278/5673 | 1194/2352 | 398/783 | chr19 | 32923512 | ||
| chr19:32923514
|
A | G | 6 | a0000a0001a0007others(3): Show | 134 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(131): Show |
missense_variant | MODERATE | c.1193T>C | p.Val398Ala | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/19 | 1277/5673 | 1193/2352 | 398/783 | chr19 | 32923514 | ||
| chr19:32933646
|
T | A | 1 | a0010 | 1 | NA19058.hp2 | stop_gained | HIGH | c.691A>T | p.Arg231* | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/19 | 775/5673 | 691/2352 | 231/783 | chr19 | 32933646 | ||
| chr19:32948280
|
C | T | 1 | a0009 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.581G>A | p.Arg194Gln | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/19 | 665/5673 | 581/2352 | 194/783 | chr19 | 32948280 | ||
| chr19:32948281
|
G | A | 3 | a0002a0013a0015 | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
missense_variant | MODERATE | c.580C>T | p.Arg194Trp | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/19 | 664/5673 | 580/2352 | 194/783 | chr19 | 32948281 | ||
| chr19:32953635
|
C | T | 1 | a0014 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.472G>A | p.Ala158Thr | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/19 | 556/5673 | 472/2352 | 158/783 | chr19 | 32953635 | ||
| chr19:32959900
|
C | T | 2 | a0005a0006 | 16 | HG02055.hp1 HG02145.hp2 HG02717.hp1 others(13): Show |
missense_variant&splice_region_variant | MODERATE | c.305G>A | p.Arg102Gln | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/19 | 389/5673 | 305/2352 | 102/783 | chr19 | 32959900 | ||
| chr19:32960014
|
C | T | 1 | a0008 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.191G>A | p.Arg64Gln | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/19 | 275/5673 | 191/2352 | 64/783 | chr19 | 32960014 | ||
| chr19:32960032
|
G | T | 1 | a0015 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.173C>A | p.Ala58Glu | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/19 | 257/5673 | 173/2352 | 58/783 | chr19 | 32960032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:32879207
|
G | A | 1 | a0002c0025 | 1 | NA18994.hp1 | synonymous_variant | LOW | c.2307C>T | p.Cys769Cys | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2391/5673 | 2307/2352 | 769/783 | chr19 | 32879207 | ||
| chr19:32879255
|
A | C | 3 | a0000c0005a0000c0007a0000c0012 | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
synonymous_variant | LOW | c.2259T>G | p.Val753Val | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2343/5673 | 2259/2352 | 753/783 | chr19 | 32879255 | ||
| chr19:32899890
|
G | A | 23 | a0000c0005a0000c0012a0001c0002others(20): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
synonymous_variant | LOW | c.1842C>T | p.Asn614Asn | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/19 | 1926/5673 | 1842/2352 | 614/783 | chr19 | 32899890 | ||
| chr19:32923486
|
T | C | 1 | a0001c0016 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.1221A>G | p.Glu407Glu | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/19 | 1305/5673 | 1221/2352 | 407/783 | chr19 | 32923486 | ||
| chr19:32926205
|
G | C | 1 | a0003c0019 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.1149C>G | p.Leu383Leu | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/19 | 1233/5673 | 1149/2352 | 383/783 | chr19 | 32926205 | ||
| chr19:32953690
|
T | C | 1 | a0003c0021 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.417A>G | p.Glu139Glu | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/19 | 501/5673 | 417/2352 | 139/783 | chr19 | 32953690 | ||
| chr19:32953801
|
C | T | 11 | a0000c0012a0001c0002a0001c0016others(8): Show | 156 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(153): Show |
splice_region_variant&synonymous_variant | LOW | c.306G>A | p.Arg102Arg | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/19 | 390/5673 | 306/2352 | 102/783 | chr19 | 32953801 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:32876025
|
C | G | 1 | a0001c0002t0024 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3137G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 3137 | chr19 | 32876025 | |||||
| chr19:32876314
|
C | A | 6 | a0000c0005t0023a0001c0002t0010a0001c0002t0024others(3): Show | 10 | HG01123.hp2 HG01884.hp2 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2848G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2848 | chr19 | 32876314 | |||||
| chr19:32876327
|
T | C | 3 | a0000c0007t0004a0000c0007t0033a0000c0012t0004 | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2835A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2835 | chr19 | 32876327 | |||||
| chr19:32876532
|
C | A | 1 | a0003c0010t0029 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2630G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2630 | chr19 | 32876532 | |||||
| chr19:32876604
|
G | A | 1 | a0003c0003t0035 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2558C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2558 | chr19 | 32876604 | |||||
| chr19:32876706
|
G | A | 1 | a0002c0001t0025 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2456C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2456 | chr19 | 32876706 | |||||
| chr19:32876870
|
G | A | 1 | a0003c0003t0036 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2292C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2292 | chr19 | 32876870 | |||||
| chr19:32876970
|
G | C | 1 | a0003c0003t0034 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2192C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2192 | chr19 | 32876970 | |||||
| chr19:32876971
|
C | G | 1 | a0003c0003t0034 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2191G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2191 | chr19 | 32876971 | |||||
| chr19:32877029
|
G | A | 2 | a0000c0005t0041a0001c0016t0030 | 2 | HG01261.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2133C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2133 | chr19 | 32877029 | |||||
| chr19:32877065
|
G | A | 1 | a0003c0003t0038 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2097C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2097 | chr19 | 32877065 | |||||
| chr19:32877089
|
A | G | 3 | a0004c0006t0007a0004c0006t0032a0009c0023t0007 | 12 | HG00609.hp1 HG02129.hp1 HG03490.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2073T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2073 | chr19 | 32877089 | |||||
| chr19:32877160
|
C | T | 26 | a0001c0002t0016a0001c0004t0002a0002c0001t0002others(23): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*2002G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 2002 | chr19 | 32877160 | |||||
| chr19:32877245
|
C | T | 1 | a0001c0002t0028 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1917G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 1917 | chr19 | 32877245 | |||||
| chr19:32877387
|
C | T | 7 | a0000c0005t0005a0000c0005t0019a0000c0005t0020others(4): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1775G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 1775 | chr19 | 32877387 | |||||
| chr19:32877448
|
G | A | 3 | a0000c0007t0004a0000c0007t0033a0000c0012t0004 | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1714C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 1714 | chr19 | 32877448 | |||||
| chr19:32877653
|
C | A | 1 | a0001c0002t0031 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1509G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 1509 | chr19 | 32877653 | |||||
| chr19:32877655
|
C | T | 6 | a0000c0005t0005a0000c0005t0019a0000c0005t0020others(3): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1507G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 1507 | chr19 | 32877655 | |||||
| chr19:32877665
|
T | C | 3 | a0002c0001t0025a0003c0019t0012a0007c0011t0012 | 5 | HG01175.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1497A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 1497 | chr19 | 32877665 | |||||
| chr19:32877775
|
A | AT | 4 | a0001c0002t0015a0002c0001t0017a0003c0010t0014others(1): Show | 7 | HG01109.hp1 HG02602.hp2 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1386dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 1386 | chr19 | 32877775 | |||||
| chr19:32877776
|
T | A | 1 | a0002c0001t0018 | 2 | NA18950.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1386A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 1386 | chr19 | 32877776 | |||||
| chr19:32877823
|
A | C | 9 | a0001c0002t0010a0001c0002t0024a0001c0002t0043others(6): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1339T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 1339 | chr19 | 32877823 | |||||
| chr19:32877979
|
C | T | 7 | a0000c0005t0005a0000c0005t0019a0000c0005t0020others(4): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1183G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 1183 | chr19 | 32877979 | |||||
| chr19:32878000
|
G | A | 14 | a0003c0003t0003a0003c0003t0013a0003c0003t0034others(11): Show | 67 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1162C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 1162 | chr19 | 32878000 | |||||
| chr19:32878055
|
C | T | 9 | a0001c0002t0010a0001c0002t0024a0001c0002t0043others(6): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1107G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 1107 | chr19 | 32878055 | |||||
| chr19:32878122
|
G | A | 5 | a0000c0005t0005a0000c0005t0019a0000c0005t0020others(2): Show | 26 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1040C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 1040 | chr19 | 32878122 | |||||
| chr19:32878327
|
G | A | 1 | a0003c0003t0037 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*835C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 835 | chr19 | 32878327 | |||||
| chr19:32878340
|
G | A | 1 | a0004c0006t0026 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 822 | chr19 | 32878340 | |||||
| chr19:32878376
|
GT | G | 9 | a0000c0005t0005a0000c0005t0019a0000c0005t0020others(6): Show | 48 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*785delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 785 | chr19 | 32878376 | |||||
| chr19:32878377
|
T | A | 1 | a0000c0005t0023 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*785A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 785 | chr19 | 32878377 | |||||
| chr19:32878416
|
G | A | 5 | a0004c0006t0007a0004c0006t0009a0004c0006t0027others(2): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*746C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 746 | chr19 | 32878416 | |||||
| chr19:32878694
|
G | A | 1 | a0003c0003t0038 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 468 | chr19 | 32878694 | |||||
| chr19:32878705
|
C | A | 3 | a0000c0007t0004a0000c0007t0033a0000c0012t0004 | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*457G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 457 | chr19 | 32878705 | |||||
| chr19:32878749
|
A | C | 27 | a0000c0005t0005a0000c0005t0019a0000c0005t0020others(24): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*413T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 413 | chr19 | 32878749 | |||||
| chr19:32878893
|
T | C | 1 | a0003c0003t0039 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 269 | chr19 | 32878893 | |||||
| chr19:32878962
|
T | TA | 25 | a0000c0005t0020a0000c0007t0033a0001c0004t0002others(22): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*199dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 199 | chr19 | 32878962 | |||||
| chr19:32878962
|
T | TAA | 5 | a0000c0005t0005a0000c0005t0042a0000c0007t0004others(2): Show | 42 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*198_*199dupTT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 199 | chr19 | 32878962 | |||||
| chr19:32878978
|
T | A | 1 | a0000c0005t0042 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*184A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 184 | chr19 | 32878978 | |||||
| chr19:32878979
|
T | A | 7 | a0000c0005t0005a0000c0005t0019a0000c0005t0020others(4): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*183A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 183 | chr19 | 32878979 | |||||
| chr19:32878982
|
A | T | 1 | a0000c0005t0023 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*180T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 180 | chr19 | 32878982 | |||||
| chr19:32878984
|
A | C | 1 | a0003c0021t0022 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*178T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 178 | chr19 | 32878984 | |||||
| chr19:32879027
|
T | G | 1 | a0001c0002t0043 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*135A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 19/19 | 135 | chr19 | 32879027 | |||||
| chr19:32971930
|
C | T | 1 | a0000c0012t0021 | 1 | HG02257.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-56G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/19 | chr19 | 32971930 | ||||||
| chr19:32971942
|
A | G | 1 | a0002c0001t0008 | 9 | NA18944.hp1 NA18961.hp2 NA18995.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-68T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/19 | 68 | chr19 | 32971942 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:32879405
|
C | T | 1 | a0003c0010t0014g0366 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2136-27G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32879405 | ||||||
| chr19:32879457
|
A | G | 1 | a0004c0006t0007g0132 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2136-79T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32879457 | ||||||
| chr19:32879470
|
G | A | 22 | a0003c0003t0003g0211a0003c0003t0003g0215a0003c0003t0003g0216others(19): Show | 22 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.2136-92C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32879470 | ||||||
| chr19:32879558
|
G | C | 2 | a0001c0004t0001g0178a0001c0004t0001g0183 | 2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2136-180C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32879558 | ||||||
| chr19:32879640
|
A | G | 5 | a0002c0001t0025g0148a0003c0019t0012g0364a0007c0011t0012g0375others(2): Show | 5 | HG01175.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2136-262T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32879640 | ||||||
| chr19:32879660
|
T | C | 49 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.2136-282A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32879660 | ||||||
| chr19:32879680
|
C | T | 6 | a0004c0006t0011g0143a0004c0006t0026g0144a0006c0009t0011g0123others(3): Show | 6 | HG02622.hp2 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2136-302G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32879680 | ||||||
| chr19:32879783
|
C | T | 1 | a0000c0005t0005g0104 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2136-405G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32879783 | ||||||
| chr19:32879796
|
A | G | 49 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.2136-418T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32879796 | ||||||
| chr19:32879824
|
C | T | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.2136-446G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32879824 | ||||||
| chr19:32879840
|
C | G | 1 | a0003c0003t0003g0253 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2136-462G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32879840 | ||||||
| chr19:32879846
|
C | G | 3 | a0002c0001t0002g0367a0002c0001t0002g0368a0002c0001t0002g0369 | 3 | NA18963.hp2 NA18972.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2136-468G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32879846 | ||||||
| chr19:32879915
|
G | C | 2 | a0001c0002t0024g0072a0003c0003t0010g0218 | 2 | HG01123.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2136-537C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32879915 | ||||||
| chr19:32880046
|
G | A | 49 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.2136-668C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880046 | ||||||
| chr19:32880133
|
A | C | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.2136-755T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880133 | ||||||
| chr19:32880153
|
C | T | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2136-775G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880153 | ||||||
| chr19:32880154
|
G | C | 49 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.2136-776C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880154 | ||||||
| chr19:32880223
|
C | T | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2136-845G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880223 | ||||||
| chr19:32880239
|
G | A | 49 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.2136-861C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880239 | ||||||
| chr19:32880287
|
G | A | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2136-909C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880287 | ||||||
| chr19:32880328
|
T | C | 48 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.2136-950A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880328 | ||||||
| chr19:32880329
|
G | A | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2136-951C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880329 | ||||||
| chr19:32880342
|
CAG | C | 21 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.2136-966_2136-965d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880342 | ||||||
| chr19:32880499
|
C | T | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2136-1121G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880499 | ||||||
| chr19:32880625
|
C | A | 1 | a0013c0024t0002g0324 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2135+1219G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880625 | ||||||
| chr19:32880632
|
T | C | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2135+1212A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880632 | ||||||
| chr19:32880639
|
T | TA | 23 | a0001c0004t0001g0172a0001c0004t0001g0186a0001c0004t0001g0187others(20): Show | 23 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.2135+1204dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880639 | ||||||
| chr19:32880639
|
TA | T | 198 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0016others(195): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.2135+1204delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880639 | ||||||
| chr19:32880639
|
TAA | T | 41 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0040others(38): Show | 41 | HG01123.hp2 HG01167.hp2 HG01975.hp1 others(38): Show |
intron_variant | MODIFIER | c.2135+1203_2135+120 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880639 | ||||||
| chr19:32880639
|
TAAA | T | 29 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.2135+1202_2135+120 others(7): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880639 | ||||||
| chr19:32880639
|
TAAAA | T | 20 | a0000c0005t0020g0107a0000c0007t0004g0078a0000c0007t0004g0275others(17): Show | 20 | HG00099.hp1 HG01123.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.2135+1201_2135+120 others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880639 | ||||||
| chr19:32880640
|
A | T | 2 | a0006c0009t0011g0123a0006c0009t0011g0124 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2135+1204T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880640 | ||||||
| chr19:32880829
|
A | G | 5 | a0002c0001t0025g0148a0003c0019t0012g0364a0007c0011t0012g0375others(2): Show | 5 | HG01175.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2135+1015T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32880829 | ||||||
| chr19:32881300
|
A | C | 28 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.2135+544T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32881300 | ||||||
| chr19:32881307
|
G | GTAATAA | 4 | a0001c0004t0001g0206a0001c0004t0001g0207a0001c0004t0001g0208others(1): Show | 4 | HG00323.hp2 NA18747.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2135+531_2135+536d others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32881307 | ||||||
| chr19:32881307
|
GTAA | G | 75 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.2135+534_2135+536d others(5): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32881307 | ||||||
| chr19:32881337
|
G | T | 49 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.2135+507C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32881337 | ||||||
| chr19:32881368
|
A | G | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2135+476T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32881368 | ||||||
| chr19:32881590
|
A | AG | 3 | a0001c0002t0010g0376a0001c0002t0010g0377a0001c0002t0010g0378 | 3 | HG02922.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2135+253dupC | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32881590 | ||||||
| chr19:32881640
|
G | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.2135+204C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32881640 | ||||||
| chr19:32881695
|
T | C | 75 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.2135+149A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32881695 | ||||||
| chr19:32881717
|
T | G | 2 | a0003c0003t0003g0242a0003c0003t0003g0252 | 2 | NA18974.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2135+127A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32881717 | ||||||
| chr19:32881775
|
G | T | 2 | a0004c0006t0011g0143a0004c0006t0026g0144 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2135+69C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32881775 | ||||||
| chr19:32881780
|
A | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.2135+64T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 18/18 | chr19 | 32881780 | ||||||
| chr19:32882038
|
A | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-25T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882038 | ||||||
| chr19:32882068
|
A | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-55T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882068 | ||||||
| chr19:32882134
|
G | A | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1966-121C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882134 | ||||||
| chr19:32882294
|
A | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-281T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882294 | ||||||
| chr19:32882305
|
C | G | 261 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(258): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1966-292G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882305 | ||||||
| chr19:32882420
|
A | C | 5 | a0001c0004t0001g0173a0001c0004t0001g0186a0001c0004t0001g0187others(2): Show | 5 | NA18962.hp1 NA18965.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1966-407T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882420 | ||||||
| chr19:32882424
|
G | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-411C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882424 | ||||||
| chr19:32882495
|
G | A | 1 | a0002c0001t0002g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1966-482C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882495 | ||||||
| chr19:32882561
|
C | CA | 25 | a0000c0005t0042g0109a0001c0002t0001g0057a0001c0002t0001g0069others(22): Show | 25 | HG01192.hp1 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1966-549dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882561 | ||||||
| chr19:32882624
|
A | G | 2 | a0000c0005t0005g0110a0000c0005t0019g0113 | 2 | HG00280.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1966-611T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882624 | ||||||
| chr19:32882628
|
G | A | 1 | a0002c0001t0002g0004 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1966-615C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882628 | ||||||
| chr19:32882634
|
T | C | 27 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(24): Show | 27 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.1966-621A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882634 | ||||||
| chr19:32882728
|
T | C | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1966-715A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882728 | ||||||
| chr19:32882729
|
T | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-716A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882729 | ||||||
| chr19:32882734
|
A | G | 2 | a0003c0003t0003g0248a0003c0003t0037g0247 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1966-721T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882734 | ||||||
| chr19:32882743
|
A | G | 1 | a0000c0007t0004g0281 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1966-730T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882743 | ||||||
| chr19:32882792
|
T | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-779A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882792 | ||||||
| chr19:32882878
|
C | T | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-865G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882878 | ||||||
| chr19:32882920
|
G | A | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1966-907C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882920 | ||||||
| chr19:32882923
|
A | G | 1 | a0003c0003t0003g0365 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1966-910T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32882923 | ||||||
| chr19:32883008
|
A | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-995T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883008 | ||||||
| chr19:32883015
|
C | T | 1 | a0003c0010t0014g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1966-1002G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883015 | ||||||
| chr19:32883016
|
A | G | 75 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1966-1003T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883016 | ||||||
| chr19:32883084
|
A | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-1071T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883084 | ||||||
| chr19:32883099
|
C | T | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-1086G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883099 | ||||||
| chr19:32883105
|
G | A | 28 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1966-1092C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883105 | ||||||
| chr19:32883119
|
CCCAAAGT others(4): Show |
C | 1 | a0000c0005t0005g0116 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1966-1117_1966-110 others(15): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883119 | ||||||
| chr19:32883147
|
A | C | 379 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(376): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1966-1134T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883147 | ||||||
| chr19:32883209
|
C | T | 2 | a0003c0003t0003g0242a0003c0003t0003g0252 | 2 | NA18974.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1966-1196G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883209 | ||||||
| chr19:32883216
|
A | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-1203T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883216 | ||||||
| chr19:32883376
|
G | A | 66 | a0003c0003t0003g0003a0003c0003t0003g0077a0003c0003t0003g0080others(63): Show | 67 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1966-1363C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883376 | ||||||
| chr19:32883396
|
G | T | 66 | a0003c0003t0003g0003a0003c0003t0003g0077a0003c0003t0003g0080others(63): Show | 67 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1966-1383C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883396 | ||||||
| chr19:32883503
|
C | G | 1 | a0003c0003t0036g0264 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1966-1490G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883503 | ||||||
| chr19:32883522
|
C | A | 12 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(9): Show | 12 | HG00609.hp1 HG02129.hp1 HG03490.hp2 others(9): Show |
intron_variant | MODIFIER | c.1966-1509G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883522 | ||||||
| chr19:32883547
|
C | T | 88 | a0001c0004t0002g0181a0002c0001t0002g0004a0002c0001t0002g0005others(85): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1966-1534G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883547 | ||||||
| chr19:32883588
|
T | C | 2 | a0004c0006t0009g0139a0004c0006t0009g0141 | 2 | HG02027.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1966-1575A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883588 | ||||||
| chr19:32883654
|
G | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-1641C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883654 | ||||||
| chr19:32883698
|
T | C | 28 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1966-1685A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883698 | ||||||
| chr19:32883908
|
T | C | 1 | a0001c0002t0001g0034 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1966-1895A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883908 | ||||||
| chr19:32883943
|
T | C | 1 | a0002c0001t0002g0321 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1966-1930A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883943 | ||||||
| chr19:32883956
|
G | A | 1 | a0001c0004t0001g0198 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1966-1943C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32883956 | ||||||
| chr19:32884034
|
G | A | 75 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1966-2021C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884034 | ||||||
| chr19:32884075
|
C | T | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-2062G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884075 | ||||||
| chr19:32884435
|
C | T | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1966-2422G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884435 | ||||||
| chr19:32884637
|
T | C | 21 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(18): Show | 21 | HG01123.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1966-2624A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884637 | ||||||
| chr19:32884652
|
T | C | 2 | a0004c0006t0009g0136a0004c0006t0009g0137 | 2 | HG01361.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1966-2639A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884652 | ||||||
| chr19:32884700
|
G | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-2687C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884700 | ||||||
| chr19:32884702
|
G | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-2689C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884702 | ||||||
| chr19:32884726
|
G | A | 21 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1966-2713C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884726 | ||||||
| chr19:32884740
|
T | A | 1 | a0000c0005t0019g0114 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1966-2727A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884740 | ||||||
| chr19:32884741
|
T | A | 27 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(24): Show | 27 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.1966-2728A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884741 | ||||||
| chr19:32884753
|
T | C | 1 | a0003c0003t0003g0080 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1966-2740A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884753 | ||||||
| chr19:32884757
|
G | A | 1 | a0001c0002t0043g0118 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1966-2744C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884757 | ||||||
| chr19:32884844
|
C | T | 21 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1966-2831G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884844 | ||||||
| chr19:32884873
|
TA | T | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1966-2861delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884873 | ||||||
| chr19:32884928
|
T | C | 1 | a0003c0003t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1965+2824A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884928 | ||||||
| chr19:32884947
|
G | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+2805C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884947 | ||||||
| chr19:32884969
|
T | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+2783A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32884969 | ||||||
| chr19:32885082
|
T | G | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1965+2670A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885082 | ||||||
| chr19:32885113
|
C | T | 1 | a0006c0009t0011g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1965+2639G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885113 | ||||||
| chr19:32885114
|
G | A | 66 | a0003c0003t0003g0003a0003c0003t0003g0077a0003c0003t0003g0080others(63): Show | 67 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1965+2638C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885114 | ||||||
| chr19:32885182
|
T | C | 12 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1965+2570A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885182 | ||||||
| chr19:32885214
|
T | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+2538A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885214 | ||||||
| chr19:32885295
|
C | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+2457G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885295 | ||||||
| chr19:32885297
|
G | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+2455C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885297 | ||||||
| chr19:32885297
|
G | C | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1965+2455C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885297 | ||||||
| chr19:32885333
|
A | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+2419T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885333 | ||||||
| chr19:32885353
|
C | A | 3 | a0001c0002t0043g0118a0003c0010t0014g0168a0003c0010t0014g0366 | 3 | HG02109.hp1 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1965+2399G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885353 | ||||||
| chr19:32885446
|
G | A | 1 | a0001c0004t0001g0145 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1965+2306C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885446 | ||||||
| chr19:32885489
|
T | C | 1 | a0000c0007t0004g0291 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1965+2263A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885489 | ||||||
| chr19:32885495
|
A | AT | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+2256dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885495 | ||||||
| chr19:32885555
|
C | A | 1 | a0003c0010t0014g0366 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1965+2197G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885555 | ||||||
| chr19:32885613
|
T | C | 75 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1965+2139A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885613 | ||||||
| chr19:32885642
|
G | A | 1 | a0002c0001t0002g0343 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1965+2110C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885642 | ||||||
| chr19:32885691
|
A | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+2061T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885691 | ||||||
| chr19:32885977
|
G | T | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+1775C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885977 | ||||||
| chr19:32885978
|
T | A | 1 | a0005c0008t0006g0090 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1965+1774A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32885978 | ||||||
| chr19:32886013
|
C | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+1739G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32886013 | ||||||
| chr19:32886057
|
T | C | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1965+1695A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32886057 | ||||||
| chr19:32886114
|
C | A | 1 | a0003c0003t0003g0260 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1965+1638G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32886114 | ||||||
| chr19:32886147
|
T | C | 75 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1965+1605A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32886147 | ||||||
| chr19:32886331
|
A | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+1421T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32886331 | ||||||
| chr19:32886384
|
C | G | 1 | a0000c0005t0005g0116 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1965+1368G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32886384 | ||||||
| chr19:32886422
|
T | C | 27 | a0000c0005t0041g0111a0001c0002t0010g0149a0001c0002t0010g0376others(24): Show | 27 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1965+1330A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32886422 | ||||||
| chr19:32886462
|
G | A | 1 | a0004c0006t0007g0135 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1965+1290C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32886462 | ||||||
| chr19:32886630
|
C | T | 27 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(24): Show | 27 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.1965+1122G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32886630 | ||||||
| chr19:32886743
|
A | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+1009T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32886743 | ||||||
| chr19:32886761
|
G | GA | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+990dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32886761 | ||||||
| chr19:32886860
|
C | T | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+892G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32886860 | ||||||
| chr19:32887017
|
A | AC | 5 | a0002c0001t0025g0148a0003c0019t0012g0364a0007c0011t0012g0375others(2): Show | 5 | HG01175.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1965+734_1965+735i others(3): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32887017 | ||||||
| chr19:32887018
|
A | C | 22 | a0001c0002t0001g0002a0001c0002t0010g0149a0001c0002t0010g0376others(19): Show | 23 | HG01123.hp2 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1965+734T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32887018 | ||||||
| chr19:32887029
|
C | A | 1 | a0005c0008t0006g0308 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1965+723G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32887029 | ||||||
| chr19:32887029
|
C | CA | 19 | a0001c0002t0001g0061a0001c0002t0010g0149a0001c0002t0010g0376others(16): Show | 19 | HG01123.hp2 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1965+722dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32887029 | ||||||
| chr19:32887029
|
C | CAA | 37 | a0003c0019t0012g0364a0004c0006t0007g0086a0004c0006t0007g0128others(34): Show | 37 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.1965+721_1965+722d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32887029 | ||||||
| chr19:32887029
|
CA | C | 49 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1965+722delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32887029 | ||||||
| chr19:32887062
|
T | A | 57 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0016others(54): Show | 60 | HG00597.hp1 HG00621.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1965+690A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32887062 | ||||||
| chr19:32887163
|
C | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1965+589G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32887163 | ||||||
| chr19:32887341
|
G | C | 330 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(327): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1965+411C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32887341 | ||||||
| chr19:32887560
|
G | T | 1 | a0000c0005t0020g0121 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1965+192C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32887560 | ||||||
| chr19:32887657
|
G | A | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1965+95C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 17/18 | chr19 | 32887657 | ||||||
| chr19:32888337
|
T | C | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1876-496A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32888337 | ||||||
| chr19:32888556
|
A | G | 75 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1876-715T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32888556 | ||||||
| chr19:32888585
|
A | G | 21 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(18): Show | 21 | HG01123.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1876-744T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32888585 | ||||||
| chr19:32888670
|
G | A | 1 | a0003c0003t0036g0264 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1876-829C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32888670 | ||||||
| chr19:32888682
|
C | CA | 6 | a0000c0007t0004g0291a0001c0004t0001g0172a0003c0010t0014g0168others(3): Show | 6 | HG02622.hp2 HG02738.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1876-842dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32888682 | ||||||
| chr19:32888794
|
T | C | 17 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0010g0218others(14): Show | 17 | HG01123.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1876-953A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32888794 | ||||||
| chr19:32888935
|
G | T | 2 | a0002c0001t0002g0157a0002c0001t0002g0165 | 2 | HG00544.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1876-1094C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32888935 | ||||||
| chr19:32888956
|
C | T | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1876-1115G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32888956 | ||||||
| chr19:32889271
|
G | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-1430C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32889271 | ||||||
| chr19:32889276
|
C | T | 1 | a0001c0004t0001g0180 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1876-1435G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32889276 | ||||||
| chr19:32889418
|
T | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-1577A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32889418 | ||||||
| chr19:32889591
|
T | C | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1876-1750A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32889591 | ||||||
| chr19:32889594
|
G | T | 16 | a0000c0007t0004g0078a0000c0007t0004g0281a0000c0007t0004g0282others(13): Show | 16 | HG02056.hp2 HG02132.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.1876-1753C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32889594 | ||||||
| chr19:32889682
|
G | A | 3 | a0002c0001t0002g0331a0003c0003t0002g0265a0013c0024t0002g0324 | 3 | HG01074.hp1 HG01258.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1876-1841C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32889682 | ||||||
| chr19:32889716
|
C | G | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1876-1875G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32889716 | ||||||
| chr19:32889719
|
C | T | 1 | a0001c0004t0001g0167 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1876-1878G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32889719 | ||||||
| chr19:32889926
|
A | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-2085T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32889926 | ||||||
| chr19:32890331
|
C | T | 1 | a0002c0001t0017g0354 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1876-2490G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890331 | ||||||
| chr19:32890405
|
CCAAA | C | 28 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1876-2568_1876-256 others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890405 | ||||||
| chr19:32890422
|
C | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-2581G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890422 | ||||||
| chr19:32890538
|
C | T | 1 | a0001c0004t0001g0209 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1876-2697G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890538 | ||||||
| chr19:32890549
|
G | A | 230 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(227): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1876-2708C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890549 | ||||||
| chr19:32890573
|
C | T | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1876-2732G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890573 | ||||||
| chr19:32890583
|
G | A | 1 | a0000c0007t0004g0287 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1876-2742C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890583 | ||||||
| chr19:32890652
|
T | C | 2 | a0002c0001t0002g0331a0013c0024t0002g0324 | 2 | HG01074.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1876-2811A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890652 | ||||||
| chr19:32890680
|
G | A | 1 | a0003c0003t0035g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1876-2839C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890680 | ||||||
| chr19:32890683
|
G | A | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1876-2842C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890683 | ||||||
| chr19:32890704
|
T | C | 49 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1876-2863A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890704 | ||||||
| chr19:32890745
|
G | A | 1 | a0003c0003t0003g0222 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1876-2904C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890745 | ||||||
| chr19:32890804
|
G | A | 2 | a0001c0002t0001g0037a0001c0002t0001g0038 | 2 | HG02080.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1876-2963C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890804 | ||||||
| chr19:32890814
|
G | A | 231 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(228): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1876-2973C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890814 | ||||||
| chr19:32890844
|
T | C | 233 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1876-3003A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890844 | ||||||
| chr19:32890884
|
C | G | 1 | a0001c0004t0002g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1876-3043G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890884 | ||||||
| chr19:32890917
|
C | T | 1 | a0003c0003t0003g0225 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1876-3076G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890917 | ||||||
| chr19:32890943
|
G | A | 1 | a0004c0006t0027g0140 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1876-3102C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32890943 | ||||||
| chr19:32891003
|
C | T | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1876-3162G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891003 | ||||||
| chr19:32891008
|
G | A | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0082 | 3 | HG01069.hp2 HG01071.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1876-3167C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891008 | ||||||
| chr19:32891114
|
G | A | 233 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1876-3273C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891114 | ||||||
| chr19:32891124
|
A | G | 3 | a0004c0006t0011g0143a0004c0006t0026g0144a0006c0009t0011g0312 | 3 | HG02622.hp2 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1876-3283T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891124 | ||||||
| chr19:32891184
|
G | A | 1 | a0002c0001t0025g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1876-3343C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891184 | ||||||
| chr19:32891197
|
C | T | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1876-3356G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891197 | ||||||
| chr19:32891204
|
A | C | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1876-3363T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891204 | ||||||
| chr19:32891204
|
A | G | 1 | a0003c0003t0010g0218 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1876-3363T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891204 | ||||||
| chr19:32891336
|
G | T | 1 | a0005c0008t0006g0090 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1876-3495C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891336 | ||||||
| chr19:32891340
|
C | A | 1 | a0001c0002t0024g0072 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1876-3499G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891340 | ||||||
| chr19:32891343
|
G | GCACA | 4 | a0000c0007t0004g0275a0000c0007t0004g0277a0000c0007t0004g0278others(1): Show | 4 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1876-3506_1876-350 others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891343 | ||||||
| chr19:32891343
|
G | GCACACA | 17 | a0000c0007t0004g0078a0000c0007t0004g0280a0000c0007t0004g0281others(14): Show | 17 | HG02056.hp2 HG02132.hp2 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.1876-3508_1876-350 others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891343 | ||||||
| chr19:32891343
|
G | GCACACAC others(5): Show |
1 | a0001c0002t0001g0033 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1876-3514_1876-350 others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891343 | ||||||
| chr19:32891354
|
A | C | 49 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1876-3513T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891354 | ||||||
| chr19:32891360
|
C | T | 1 | a0001c0004t0001g0166 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1876-3519G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891360 | ||||||
| chr19:32891361
|
A | C | 1 | a0001c0002t0043g0118 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1876-3520T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891361 | ||||||
| chr19:32891790
|
T | G | 75 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1876-3949A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891790 | ||||||
| chr19:32891807
|
GAA | G | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1876-3968_1876-396 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891807 | ||||||
| chr19:32891837
|
A | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-3996T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891837 | ||||||
| chr19:32891882
|
TA | T | 27 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(24): Show | 27 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1876-4042delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891882 | ||||||
| chr19:32891884
|
A | T | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4043T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32891884 | ||||||
| chr19:32892070
|
G | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4229C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892070 | ||||||
| chr19:32892091
|
A | AAT | 21 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1876-4252_1876-425 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892091 | ||||||
| chr19:32892091
|
AAT | A | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1876-4252_1876-425 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892091 | ||||||
| chr19:32892106
|
ATT | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4267_1876-426 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892106 | ||||||
| chr19:32892109
|
T | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4268A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892109 | ||||||
| chr19:32892111
|
G | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4270C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892111 | ||||||
| chr19:32892113
|
C | T | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4272G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892113 | ||||||
| chr19:32892117
|
C | T | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4276G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892117 | ||||||
| chr19:32892131
|
T | TAC | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4291_1876-429 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892131 | ||||||
| chr19:32892143
|
CAT | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4304_1876-430 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892143 | ||||||
| chr19:32892161
|
TACATATA others(5): Show |
T | 1 | a0012c0017t0003g0267 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1876-4332_1876-432 others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892161 | ||||||
| chr19:32892189
|
A | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4348T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892189 | ||||||
| chr19:32892202
|
C | CAT | 43 | a0000c0007t0004g0282a0000c0007t0004g0285a0000c0007t0004g0286others(40): Show | 45 | HG00597.hp1 HG00597.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.1876-4363_1876-436 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
C | CATAT | 34 | a0000c0005t0023g0079a0000c0007t0004g0275a0000c0007t0004g0278others(31): Show | 34 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1876-4365_1876-436 others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
C | CATATAT | 8 | a0000c0007t0004g0277a0000c0007t0004g0281a0001c0002t0001g0025others(5): Show | 8 | HG01074.hp2 HG02056.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.1876-4367_1876-436 others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
C | CATATATA others(3): Show |
1 | a0000c0007t0004g0287 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1876-4371_1876-436 others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
C | CATATATA others(5): Show |
1 | a0000c0007t0033g0295 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1876-4373_1876-436 others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
CAT | C | 14 | a0000c0007t0004g0280a0001c0002t0001g0002a0001c0002t0001g0017others(11): Show | 15 | HG00438.hp1 HG01109.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.1876-4363_1876-436 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
CATAT | C | 10 | a0001c0002t0001g0032a0001c0002t0001g0085a0001c0004t0001g0169others(7): Show | 10 | HG00639.hp1 HG00673.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1876-4365_1876-436 others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
CATATAT | C | 19 | a0001c0004t0001g0075a0001c0004t0001g0175a0001c0004t0001g0177others(16): Show | 20 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1876-4367_1876-436 others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
CATATATA others(1): Show |
C | 34 | a0002c0001t0002g0315a0002c0001t0002g0316a0002c0001t0002g0318others(31): Show | 34 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1876-4369_1876-436 others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
CATATATA others(3): Show |
C | 34 | a0002c0001t0002g0314a0002c0001t0002g0349a0003c0003t0003g0077others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1876-4371_1876-436 others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
CATATATA others(5): Show |
C | 11 | a0002c0001t0002g0126a0002c0001t0002g0150a0002c0001t0002g0158others(8): Show | 11 | HG00621.hp1 HG01109.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1876-4373_1876-436 others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
CATATATA others(7): Show |
C | 81 | a0001c0004t0002g0181a0002c0001t0002g0004a0002c0001t0002g0005others(78): Show | 83 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1876-4375_1876-436 others(18): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
CATATATA others(9): Show |
C | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1876-4377_1876-436 others(20): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
CATATATA others(11): Show |
C | 30 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1876-4379_1876-436 others(22): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
CATATATA others(13): Show |
C | 22 | a0001c0002t0024g0072a0001c0002t0043g0118a0002c0001t0025g0148others(19): Show | 22 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1876-4381_1876-436 others(24): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892202
|
CATATATA others(17): Show |
C | 1 | a0001c0002t0001g0019 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1876-4385_1876-436 others(28): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892202 | ||||||
| chr19:32892282
|
G | A | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1876-4441C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892282 | ||||||
| chr19:32892282
|
G | C | 1 | a0007c0011t0012g0379 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1876-4441C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892282 | ||||||
| chr19:32892306
|
C | CT | 47 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(44): Show | 47 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.1876-4466dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892306 | ||||||
| chr19:32892389
|
T | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4548A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892389 | ||||||
| chr19:32892464
|
A | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4623T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892464 | ||||||
| chr19:32892498
|
G | T | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1876-4657C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892498 | ||||||
| chr19:32892502
|
C | T | 1 | a0005c0008t0006g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1876-4661G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892502 | ||||||
| chr19:32892503
|
G | A | 49 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1876-4662C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892503 | ||||||
| chr19:32892574
|
G | A | 1 | a0001c0002t0001g0002 | 2 | NA18963.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1876-4733C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892574 | ||||||
| chr19:32892629
|
C | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4788G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892629 | ||||||
| chr19:32892676
|
G | GA | 16 | a0001c0002t0001g0027a0001c0002t0001g0036a0001c0002t0001g0083others(13): Show | 16 | HG00621.hp1 HG02135.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.1876-4836dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892676 | ||||||
| chr19:32892676
|
GA | G | 46 | a0000c0005t0023g0079a0000c0005t0041g0111a0000c0007t0004g0078others(43): Show | 46 | HG00099.hp1 HG00609.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.1876-4836delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892676 | ||||||
| chr19:32892676
|
GAA | G | 46 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(43): Show | 46 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1876-4837_1876-483 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892676 | ||||||
| chr19:32892689
|
A | C | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1876-4848T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892689 | ||||||
| chr19:32892690
|
A | C | 1 | a0006c0009t0011g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1876-4849T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892690 | ||||||
| chr19:32892703
|
C | T | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-4862G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892703 | ||||||
| chr19:32892746
|
G | A | 1 | a0003c0010t0002g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1876-4905C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892746 | ||||||
| chr19:32892798
|
A | G | 2 | a0003c0010t0014g0168a0003c0010t0014g0366 | 2 | HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1876-4957T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892798 | ||||||
| chr19:32892852
|
C | T | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1876-5011G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892852 | ||||||
| chr19:32892853
|
G | A | 1 | a0003c0003t0003g0306 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1876-5012C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892853 | ||||||
| chr19:32892999
|
A | G | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1876-5158T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32892999 | ||||||
| chr19:32893057
|
A | T | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1876-5216T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32893057 | ||||||
| chr19:32893107
|
G | GA | 64 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0016others(61): Show | 67 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.1876-5267dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32893107 | ||||||
| chr19:32893107
|
GA | G | 32 | a0002c0001t0025g0148a0003c0019t0012g0364a0004c0006t0007g0086others(29): Show | 32 | HG00609.hp1 HG01106.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1876-5267delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32893107 | ||||||
| chr19:32893156
|
C | A | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1876-5315G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32893156 | ||||||
| chr19:32893464
|
T | C | 1 | a0003c0003t0003g0246 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1876-5623A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32893464 | ||||||
| chr19:32893597
|
A | G | 1 | a0004c0006t0027g0140 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1876-5756T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32893597 | ||||||
| chr19:32893622
|
C | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1876-5781G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32893622 | ||||||
| chr19:32893623
|
G | A | 3 | a0004c0006t0007g0129a0004c0006t0007g0134a0004c0006t0007g0147 | 3 | HG03490.hp2 HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1876-5782C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32893623 | ||||||
| chr19:32893757
|
A | G | 21 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0277others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1876-5916T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32893757 | ||||||
| chr19:32893802
|
G | T | 88 | a0001c0004t0002g0181a0002c0001t0002g0004a0002c0001t0002g0005others(85): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1876-5961C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32893802 | ||||||
| chr19:32893847
|
C | A | 49 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1876-6006G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32893847 | ||||||
| chr19:32893958
|
C | T | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1875+5899G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32893958 | ||||||
| chr19:32894036
|
A | T | 49 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1875+5821T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32894036 | ||||||
| chr19:32894392
|
G | A | 4 | a0001c0004t0001g0206a0001c0004t0001g0207a0001c0004t0001g0208others(1): Show | 4 | HG00323.hp2 NA18747.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1875+5465C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32894392 | ||||||
| chr19:32894446
|
T | C | 5 | a0002c0001t0002g0359a0002c0001t0002g0367a0002c0001t0002g0368others(2): Show | 5 | NA18939.hp2 NA18952.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.1875+5411A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32894446 | ||||||
| chr19:32894467
|
C | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1875+5390G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32894467 | ||||||
| chr19:32894683
|
T | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1875+5174A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32894683 | ||||||
| chr19:32894812
|
C | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1875+5045G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32894812 | ||||||
| chr19:32894818
|
C | T | 1 | a0000c0007t0033g0295 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1875+5039G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32894818 | ||||||
| chr19:32894902
|
T | C | 75 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1875+4955A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32894902 | ||||||
| chr19:32895066
|
C | T | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1875+4791G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895066 | ||||||
| chr19:32895327
|
A | G | 1 | a0001c0004t0001g0180 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1875+4530T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895327 | ||||||
| chr19:32895403
|
G | A | 1 | a0003c0003t0003g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1875+4454C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895403 | ||||||
| chr19:32895446
|
C | G | 1 | a0001c0016t0030g0055 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1875+4411G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895446 | ||||||
| chr19:32895466
|
C | T | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1875+4391G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895466 | ||||||
| chr19:32895615
|
A | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1875+4242T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895615 | ||||||
| chr19:32895643
|
A | G | 2 | a0001c0004t0001g0075a0001c0004t0001g0195 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1875+4214T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895643 | ||||||
| chr19:32895650
|
T | C | 27 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(24): Show | 27 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.1875+4207A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895650 | ||||||
| chr19:32895731
|
A | G | 1 | a0005c0008t0006g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1875+4126T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895731 | ||||||
| chr19:32895750
|
TA | T | 83 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1875+4106delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895750 | ||||||
| chr19:32895750
|
TAA | T | 67 | a0000c0012t0021g0015a0003c0003t0003g0003a0003c0003t0003g0077others(64): Show | 68 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1875+4105_1875+410 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895750 | ||||||
| chr19:32895752
|
A | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1875+4105T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895752 | ||||||
| chr19:32895819
|
T | A | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1875+4038A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895819 | ||||||
| chr19:32895911
|
A | G | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1875+3946T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32895911 | ||||||
| chr19:32896006
|
G | T | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1875+3851C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32896006 | ||||||
| chr19:32896361
|
G | A | 75 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1875+3496C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32896361 | ||||||
| chr19:32896373
|
G | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1875+3484C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32896373 | ||||||
| chr19:32896415
|
T | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1875+3442A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32896415 | ||||||
| chr19:32896728
|
C | T | 1 | a0005c0008t0006g0096 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1875+3129G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32896728 | ||||||
| chr19:32896779
|
C | T | 48 | a0000c0005t0023g0079a0000c0007t0004g0078a0000c0007t0004g0275others(45): Show | 48 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.1875+3078G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32896779 | ||||||
| chr19:32896783
|
T | C | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1875+3074A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32896783 | ||||||
| chr19:32896867
|
T | A | 26 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(23): Show | 26 | HG01123.hp2 HG01175.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1875+2990A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32896867 | ||||||
| chr19:32896990
|
G | C | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1875+2867C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32896990 | ||||||
| chr19:32897025
|
G | T | 75 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1875+2832C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32897025 | ||||||
| chr19:32897535
|
T | C | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1875+2322A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32897535 | ||||||
| chr19:32897748
|
G | A | 1 | a0001c0002t0001g0039 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1875+2109C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32897748 | ||||||
| chr19:32897978
|
C | G | 2 | a0001c0002t0001g0070a0001c0002t0001g0071 | 2 | NA18952.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1875+1879G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32897978 | ||||||
| chr19:32898056
|
A | G | 1 | a0001c0002t0001g0056 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1875+1801T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32898056 | ||||||
| chr19:32898275
|
G | C | 86 | a0001c0002t0001g0029a0002c0001t0002g0004a0002c0001t0002g0005others(83): Show | 88 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1875+1582C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32898275 | ||||||
| chr19:32898397
|
G | A | 1 | a0002c0001t0025g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1875+1460C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32898397 | ||||||
| chr19:32898421
|
T | G | 28 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.1875+1436A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32898421 | ||||||
| chr19:32898473
|
C | A | 1 | a0002c0001t0008g0010 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1875+1384G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32898473 | ||||||
| chr19:32898620
|
A | G | 2 | a0001c0002t0024g0072a0003c0003t0010g0218 | 2 | HG01123.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1875+1237T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32898620 | ||||||
| chr19:32898760
|
T | C | 1 | a0003c0003t0003g0226 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1875+1097A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32898760 | ||||||
| chr19:32898830
|
C | T | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1875+1027G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32898830 | ||||||
| chr19:32898877
|
A | G | 325 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(322): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1875+980T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32898877 | ||||||
| chr19:32898881
|
T | TA | 197 | a0000c0005t0005g0102a0000c0005t0005g0106a0000c0005t0005g0269others(194): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1875+975dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32898881 | ||||||
| chr19:32898881
|
T | TAA | 122 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(119): Show | 125 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1875+974_1875+975d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32898881 | ||||||
| chr19:32898881
|
T | TAAA | 8 | a0001c0002t0001g0019a0001c0002t0001g0032a0001c0002t0001g0083others(5): Show | 8 | HG01515.hp1 HG03098.hp2 HG04228.hp1 others(5): Show |
intron_variant | MODIFIER | c.1875+973_1875+975d others(5): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32898881 | ||||||
| chr19:32899049
|
T | G | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1875+808A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32899049 | ||||||
| chr19:32899131
|
A | AT | 57 | a0000c0007t0004g0294a0000c0012t0004g0065a0001c0002t0001g0001others(54): Show | 60 | HG00438.hp1 HG00621.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1875+725dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32899131 | ||||||
| chr19:32899131
|
A | ATT | 9 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0040others(6): Show | 9 | HG00597.hp1 HG01433.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.1875+724_1875+725d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32899131 | ||||||
| chr19:32899131
|
A | ATTTCC | 92 | a0001c0002t0001g0029a0002c0001t0001g0332a0002c0001t0002g0004others(89): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1875+725_1875+726i others(7): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32899131 | ||||||
| chr19:32899131
|
A | ATTTCCT | 133 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(130): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1875+725_1875+726i others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32899131 | ||||||
| chr19:32899225
|
C | T | 1 | a0001c0002t0010g0376 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1875+632G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32899225 | ||||||
| chr19:32899581
|
C | CAATCTAC others(8): Show |
2 | a0004c0006t0007g0129a0004c0006t0007g0134 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1875+261_1875+275d others(17): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32899581 | ||||||
| chr19:32899611
|
G | A | 1 | a0005c0008t0006g0088 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1875+246C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32899611 | ||||||
| chr19:32899641
|
T | C | 1 | a0006c0009t0011g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1875+216A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32899641 | ||||||
| chr19:32899787
|
T | A | 33 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(30): Show | 33 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1875+70A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 16/18 | chr19 | 32899787 | ||||||
| chr19:32900100
|
T | G | 66 | a0003c0003t0003g0003a0003c0003t0003g0077a0003c0003t0003g0080others(63): Show | 67 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1734-102A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900100 | ||||||
| chr19:32900215
|
G | C | 1 | a0003c0003t0003g0214 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1734-217C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900215 | ||||||
| chr19:32900246
|
A | AT | 12 | a0000c0007t0004g0287a0000c0007t0004g0293a0001c0002t0001g0059others(9): Show | 12 | HG02630.hp2 HG02809.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.1734-249dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900246 | ||||||
| chr19:32900246
|
A | ATTT | 87 | a0002c0001t0001g0332a0002c0001t0002g0004a0002c0001t0002g0005others(84): Show | 89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1734-251_1734-249d others(5): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900246 | ||||||
| chr19:32900246
|
A | ATTTTT | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1734-253_1734-249d others(7): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900246 | ||||||
| chr19:32900246
|
AT | A | 85 | a0000c0007t0004g0283a0001c0002t0001g0082a0001c0004t0001g0169others(82): Show | 86 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1734-249delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900246 | ||||||
| chr19:32900251
|
T | G | 1 | a0005c0008t0006g0096 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1734-253A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900251 | ||||||
| chr19:32900301
|
G | A | 2 | a0002c0001t0002g0359a0002c0001t0002g0370 | 2 | NA18939.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1734-303C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900301 | ||||||
| chr19:32900340
|
G | A | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1734-342C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900340 | ||||||
| chr19:32900395
|
G | A | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1734-397C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900395 | ||||||
| chr19:32900437
|
A | T | 1 | a0002c0001t0002g0334 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1734-439T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900437 | ||||||
| chr19:32900439
|
T | A | 129 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(126): Show | 132 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1734-441A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900439 | ||||||
| chr19:32900441
|
T | A | 1 | a0007c0011t0012g0375 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1734-443A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900441 | ||||||
| chr19:32900525
|
A | G | 1 | a0004c0006t0007g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1734-527T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900525 | ||||||
| chr19:32900628
|
A | G | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1733+617T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900628 | ||||||
| chr19:32900778
|
T | C | 66 | a0003c0003t0003g0003a0003c0003t0003g0077a0003c0003t0003g0080others(63): Show | 67 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1733+467A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900778 | ||||||
| chr19:32900796
|
A | T | 4 | a0003c0003t0003g0212a0003c0003t0003g0213a0003c0003t0003g0214others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1733+449T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900796 | ||||||
| chr19:32900832
|
C | A | 104 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(101): Show | 105 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1733+413G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900832 | ||||||
| chr19:32900888
|
C | CTT | 13 | a0003c0003t0010g0218a0005c0008t0006g0087a0005c0008t0006g0088others(10): Show | 13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1733+355_1733+356d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900888 | ||||||
| chr19:32900888
|
C | CTTTTTT | 110 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(107): Show | 113 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1733+351_1733+356d others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900888 | ||||||
| chr19:32900888
|
C | CTTTTTTT | 13 | a0001c0002t0001g0028a0001c0002t0001g0036a0001c0002t0001g0058others(10): Show | 13 | HG01361.hp2 HG01433.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1733+350_1733+356d others(9): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900888 | ||||||
| chr19:32900888
|
CT | C | 35 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1733+356delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900888 | ||||||
| chr19:32900947
|
G | A | 125 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(122): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1733+298C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900947 | ||||||
| chr19:32900954
|
C | T | 4 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0010t0014g0168others(1): Show | 4 | HG01123.hp2 HG02109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1733+291G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32900954 | ||||||
| chr19:32901043
|
C | G | 1 | a0001c0002t0001g0016 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1733+202G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32901043 | ||||||
| chr19:32901050
|
C | A | 121 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(118): Show | 124 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1733+195G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32901050 | ||||||
| chr19:32901104
|
C | A | 126 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(123): Show | 128 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1733+141G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32901104 | ||||||
| chr19:32901181
|
C | T | 125 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(122): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1733+64G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 15/18 | chr19 | 32901181 | ||||||
| chr19:32901569
|
C | T | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1566-157G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32901569 | ||||||
| chr19:32901584
|
C | T | 125 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(122): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1566-172G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32901584 | ||||||
| chr19:32901623
|
A | G | 3 | a0001c0002t0043g0118a0003c0010t0014g0168a0003c0010t0014g0366 | 3 | HG02109.hp1 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1566-211T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32901623 | ||||||
| chr19:32901653
|
G | A | 1 | a0002c0001t0025g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1566-241C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32901653 | ||||||
| chr19:32901797
|
G | A | 1 | a0003c0003t0003g0222 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1566-385C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32901797 | ||||||
| chr19:32901845
|
G | A | 129 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(126): Show | 132 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1566-433C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32901845 | ||||||
| chr19:32901965
|
CCA | C | 21 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1566-555_1566-554d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32901965 | ||||||
| chr19:32901996
|
G | GTC | 3 | a0003c0003t0003g0236a0003c0003t0003g0273a0003c0003t0036g0264 | 3 | HG00408.hp1 HG02155.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1566-586_1566-585d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32901996 | ||||||
| chr19:32902004
|
C | CTGTGTGT others(1): Show |
7 | a0001c0002t0001g0036a0001c0002t0001g0063a0001c0002t0028g0054others(4): Show | 7 | HG00408.hp2 HG04115.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.1566-593_1566-592i others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902004 | ||||||
| chr19:32902004
|
C | CTGTGTGT others(3): Show |
10 | a0001c0002t0001g0028a0001c0002t0001g0038a0001c0002t0001g0056others(7): Show | 10 | HG01433.hp2 HG01952.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1566-593_1566-592i others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902004 | ||||||
| chr19:32902004
|
C | CTGTGTGT others(5): Show |
22 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0027others(19): Show | 24 | HG00597.hp2 HG00609.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1566-593_1566-592i others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902004 | ||||||
| chr19:32902004
|
C | CTGTGTGT others(7): Show |
33 | a0001c0002t0001g0002a0001c0002t0001g0016a0001c0002t0001g0018others(30): Show | 34 | HG00544.hp2 HG00597.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1566-593_1566-592i others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902004 | ||||||
| chr19:32902004
|
C | CTGTGTGT others(9): Show |
15 | a0001c0002t0001g0017a0001c0002t0001g0033a0001c0002t0001g0035others(12): Show | 15 | HG00323.hp2 HG00423.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1566-593_1566-592i others(18): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902004 | ||||||
| chr19:32902004
|
C | CTGTGTGT others(11): Show |
4 | a0001c0002t0001g0022a0001c0002t0001g0029a0001c0004t0001g0203others(1): Show | 4 | HG04184.hp2 NA18964.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1566-593_1566-592i others(20): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902004 | ||||||
| chr19:32902004
|
C | CTGTGTGT others(13): Show |
5 | a0001c0002t0001g0025a0001c0002t0001g0043a0001c0002t0001g0070others(2): Show | 5 | HG00673.hp2 HG02135.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566-593_1566-592i others(22): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902004 | ||||||
| chr19:32902004
|
C | CTGTGTGT others(15): Show |
8 | a0001c0002t0001g0030a0001c0002t0001g0032a0001c0002t0001g0034others(5): Show | 8 | HG00438.hp1 HG00642.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1566-593_1566-592i others(24): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902004 | ||||||
| chr19:32902004
|
C | CTGTGTGT others(17): Show |
1 | a0001c0002t0001g0024 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1566-593_1566-592i others(26): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902004 | ||||||
| chr19:32902004
|
C | G | 1 | a0008c0015t0001g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1566-592G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902004 | ||||||
| chr19:32902006
|
C | CTGTGTGT others(7): Show |
1 | a0001c0004t0001g0166 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1566-595_1566-594i others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902006 | ||||||
| chr19:32902006
|
C | CTGTGTGT others(11): Show |
1 | a0001c0004t0001g0170 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1566-595_1566-594i others(20): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902006 | ||||||
| chr19:32902006
|
C | G | 109 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(106): Show | 112 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1566-594G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902006 | ||||||
| chr19:32902008
|
C | CTGTGTGT others(5): Show |
4 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0303others(1): Show | 4 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1566-597_1566-596i others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902008 | ||||||
| chr19:32902008
|
C | CTGTGTGT others(7): Show |
2 | a0001c0002t0001g0302a0001c0002t0001g0304 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1566-597_1566-596i others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902008 | ||||||
| chr19:32902008
|
C | CTGTGTGT others(9): Show |
3 | a0001c0002t0001g0296a0001c0002t0001g0297a0001c0002t0001g0298 | 3 | HG02258.hp2 HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1566-597_1566-596i others(18): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902008 | ||||||
| chr19:32902008
|
C | CTGTGTGT others(15): Show |
1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1566-597_1566-596i others(24): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902008 | ||||||
| chr19:32902008
|
C | G | 111 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(108): Show | 114 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1566-596G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902008 | ||||||
| chr19:32902010
|
C | CTCTCTCT others(1): Show |
17 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(14): Show | 17 | HG00609.hp1 HG01361.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.1566-599_1566-598i others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTCTCTCT others(3): Show |
2 | a0004c0006t0009g0270a0004c0006t0027g0140 | 2 | HG01106.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1566-599_1566-598i others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTCTCTGT others(3): Show |
6 | a0002c0001t0002g0335a0002c0001t0002g0339a0002c0001t0002g0345others(3): Show | 6 | HG00438.hp2 HG02083.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1566-599_1566-598i others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTCTCTGT others(5): Show |
2 | a0002c0001t0002g0309a0002c0001t0002g0310 | 2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1566-599_1566-598i others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTCTCTGT others(7): Show |
2 | a0002c0001t0002g0159a0002c0001t0025g0148 | 2 | HG01175.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1566-599_1566-598i others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTCTGTGT others(1): Show |
12 | a0002c0001t0002g0073a0002c0001t0002g0155a0002c0001t0002g0158others(9): Show | 12 | HG00140.hp1 HG01496.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1566-599_1566-598i others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTCTGTGT others(3): Show |
29 | a0002c0001t0002g0313a0002c0001t0002g0321a0002c0001t0002g0333others(26): Show | 29 | HG00280.hp1 HG00673.hp1 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.1566-599_1566-598i others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTCTGTGT others(5): Show |
34 | a0000c0005t0005g0115a0000c0005t0005g0117a0002c0001t0001g0332others(31): Show | 35 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.1566-599_1566-598i others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTCTGTGT others(7): Show |
6 | a0002c0001t0002g0150a0002c0001t0002g0319a0002c0001t0002g0349others(3): Show | 6 | HG00621.hp1 HG00642.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1566-599_1566-598i others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTCTGTGT others(9): Show |
1 | a0002c0001t0002g0153 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1566-599_1566-598i others(18): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTGTGTG | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566-604_1566-599d others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTGTGTGT others(3): Show |
18 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0103others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1566-608_1566-599d others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTGTGTGT others(5): Show |
8 | a0000c0005t0005g0100a0000c0005t0005g0101a0000c0005t0005g0102others(5): Show | 8 | HG00544.hp1 HG01358.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1566-610_1566-599d others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTGTGTGT others(7): Show |
1 | a0000c0005t0041g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1566-612_1566-599d others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | CTGTGTGT others(13): Show |
1 | a0000c0005t0005g0116 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1566-618_1566-599d others(22): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
C | G | 122 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(119): Show | 125 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1566-598G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
CTG | C | 3 | a0000c0005t0005g0099a0003c0010t0014g0168a0003c0010t0014g0366 | 3 | HG01243.hp1 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1566-600_1566-599d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902010
|
CTGTGTG | C | 15 | a0002c0001t0002g0005a0002c0001t0002g0163a0002c0001t0002g0322others(12): Show | 16 | HG02630.hp2 HG02809.hp2 HG03195.hp1 others(13): Show |
intron_variant | MODIFIER | c.1566-604_1566-599d others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902010 | ||||||
| chr19:32902012
|
G | C | 68 | a0000c0005t0023g0079a0001c0002t0043g0118a0002c0001t0002g0331others(65): Show | 69 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1566-600C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902012 | ||||||
| chr19:32902014
|
G | C | 67 | a0003c0003t0003g0003a0003c0003t0003g0077a0003c0003t0003g0080others(64): Show | 68 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1566-602C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902014 | ||||||
| chr19:32902016
|
G | C | 65 | a0001c0002t0024g0072a0003c0003t0003g0003a0003c0003t0003g0077others(62): Show | 66 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.1566-604C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902016 | ||||||
| chr19:32902018
|
G | C | 13 | a0001c0002t0024g0072a0002c0001t0002g0005a0002c0001t0002g0163others(10): Show | 14 | HG01123.hp2 NA18942.hp2 NA18943.hp1 others(11): Show |
intron_variant | MODIFIER | c.1566-606C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902018 | ||||||
| chr19:32902034
|
G | GTGTGTGT others(14): Show |
1 | a0001c0002t0001g0083 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1566-623_1566-622i others(23): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902034 | ||||||
| chr19:32902046
|
A | G | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1566-634T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902046 | ||||||
| chr19:32902048
|
G | A | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1566-636C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902048 | ||||||
| chr19:32902126
|
A | T | 3 | a0002c0001t0002g0155a0002c0001t0002g0309a0002c0001t0002g0310 | 3 | HG02559.hp1 NA18612.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1566-714T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902126 | ||||||
| chr19:32902147
|
T | C | 103 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(100): Show | 104 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1566-735A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902147 | ||||||
| chr19:32902345
|
C | A | 3 | a0004c0006t0011g0143a0004c0006t0026g0144a0006c0009t0011g0312 | 3 | HG02622.hp2 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1566-933G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902345 | ||||||
| chr19:32902372
|
A | G | 1 | a0001c0002t0031g0053 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1566-960T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902372 | ||||||
| chr19:32902475
|
T | G | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1566-1063A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902475 | ||||||
| chr19:32902531
|
C | A | 2 | a0004c0006t0009g0136a0004c0006t0009g0137 | 2 | HG01361.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1566-1119G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902531 | ||||||
| chr19:32902560
|
C | T | 13 | a0003c0003t0010g0218a0005c0008t0006g0087a0005c0008t0006g0088others(10): Show | 13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1566-1148G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902560 | ||||||
| chr19:32902698
|
A | C | 1 | a0001c0002t0001g0085 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1566-1286T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902698 | ||||||
| chr19:32902705
|
G | T | 91 | a0002c0001t0001g0332a0002c0001t0002g0004a0002c0001t0002g0005others(88): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1566-1293C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902705 | ||||||
| chr19:32902738
|
G | A | 35 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1566-1326C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902738 | ||||||
| chr19:32902792
|
C | T | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1566-1380G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902792 | ||||||
| chr19:32902801
|
C | T | 3 | a0002c0001t0002g0005a0002c0001t0002g0341a0002c0001t0002g0342 | 4 | NA18942.hp2 NA18943.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566-1389G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902801 | ||||||
| chr19:32902873
|
A | G | 1 | a0002c0001t0002g0313 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1566-1461T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32902873 | ||||||
| chr19:32903184
|
G | GA | 122 | a0000c0007t0004g0282a0000c0007t0004g0291a0000c0012t0004g0065others(119): Show | 125 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1566-1773dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32903184 | ||||||
| chr19:32903184
|
GA | G | 228 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(225): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1566-1773delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32903184 | ||||||
| chr19:32903215
|
A | G | 1 | a0006c0009t0011g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1566-1803T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32903215 | ||||||
| chr19:32903282
|
T | G | 33 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(30): Show | 33 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1566-1870A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32903282 | ||||||
| chr19:32903447
|
A | T | 1 | a0002c0001t0002g0126 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1566-2035T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32903447 | ||||||
| chr19:32903511
|
G | A | 128 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(125): Show | 131 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1566-2099C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32903511 | ||||||
| chr19:32903637
|
G | T | 3 | a0007c0011t0012g0375a0007c0011t0012g0379a0007c0011t0012g0380 | 3 | HG02630.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1566-2225C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32903637 | ||||||
| chr19:32903676
|
A | C | 1 | a0001c0004t0001g0170 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1566-2264T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32903676 | ||||||
| chr19:32903684
|
G | T | 1 | a0001c0002t0043g0118 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1566-2272C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32903684 | ||||||
| chr19:32903699
|
G | T | 4 | a0002c0001t0002g0320a0002c0001t0002g0327a0002c0001t0002g0328others(1): Show | 4 | HG02257.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566-2287C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32903699 | ||||||
| chr19:32903755
|
G | A | 35 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1566-2343C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32903755 | ||||||
| chr19:32903807
|
A | G | 1 | a0004c0006t0007g0133 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1566-2395T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32903807 | ||||||
| chr19:32903941
|
C | T | 129 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(126): Show | 132 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1566-2529G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32903941 | ||||||
| chr19:32904017
|
G | A | 4 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0010t0014g0168others(1): Show | 4 | HG01123.hp2 HG02109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1566-2605C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904017 | ||||||
| chr19:32904067
|
G | A | 2 | a0001c0004t0001g0206a0001c0004t0001g0208 | 2 | NA18747.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1566-2655C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904067 | ||||||
| chr19:32904081
|
G | T | 1 | a0000c0005t0005g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1566-2669C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904081 | ||||||
| chr19:32904131
|
G | A | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1566-2719C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904131 | ||||||
| chr19:32904132
|
C | T | 1 | a0002c0001t0002g0157 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1566-2720G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904132 | ||||||
| chr19:32904155
|
G | T | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1566-2743C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904155 | ||||||
| chr19:32904470
|
C | T | 3 | a0006c0009t0011g0123a0006c0009t0011g0124a0006c0009t0011g0125 | 3 | HG02717.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1566-3058G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904470 | ||||||
| chr19:32904507
|
G | A | 292 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(289): Show | 298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.1566-3095C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904507 | ||||||
| chr19:32904535
|
T | A | 3 | a0006c0009t0011g0123a0006c0009t0011g0124a0006c0009t0011g0125 | 3 | HG02717.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1566-3123A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904535 | ||||||
| chr19:32904566
|
T | C | 65 | a0003c0003t0003g0003a0003c0003t0003g0077a0003c0003t0003g0080others(62): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1566-3154A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904566 | ||||||
| chr19:32904596
|
C | CTT | 80 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(77): Show | 81 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1566-3186_1566-318 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904596 | ||||||
| chr19:32904653
|
G | A | 12 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1566-3241C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904653 | ||||||
| chr19:32904694
|
C | T | 1 | a0003c0003t0003g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1566-3282G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904694 | ||||||
| chr19:32904740
|
C | T | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1566-3328G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32904740 | ||||||
| chr19:32905269
|
G | A | 1 | a0001c0002t0001g0036 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1566-3857C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32905269 | ||||||
| chr19:32905321
|
T | C | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1566-3909A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32905321 | ||||||
| chr19:32905466
|
C | T | 1 | a0000c0005t0005g0164 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1566-4054G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32905466 | ||||||
| chr19:32905476
|
A | G | 3 | a0000c0007t0004g0278a0000c0007t0004g0279a0000c0007t0004g0280 | 3 | HG00099.hp1 HG01123.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1566-4064T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32905476 | ||||||
| chr19:32905491
|
A | AT | 100 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0082others(97): Show | 102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1566-4080dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32905491 | ||||||
| chr19:32905491
|
A | ATTT | 26 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(23): Show | 26 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1566-4082_1566-408 others(7): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32905491 | ||||||
| chr19:32905491
|
AT | A | 65 | a0003c0003t0003g0003a0003c0003t0003g0077a0003c0003t0003g0080others(62): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1566-4080delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32905491 | ||||||
| chr19:32905646
|
A | G | 2 | a0002c0001t0002g0352a0002c0001t0002g0353 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1566-4234T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32905646 | ||||||
| chr19:32905935
|
G | A | 1 | a0001c0004t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1566-4523C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32905935 | ||||||
| chr19:32905938
|
T | C | 3 | a0001c0004t0001g0166a0001c0004t0001g0167a0014c0022t0001g0196 | 3 | HG00544.hp2 HG01261.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1566-4526A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32905938 | ||||||
| chr19:32905953
|
G | C | 1 | a0001c0004t0001g0209 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1566-4541C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32905953 | ||||||
| chr19:32906124
|
A | G | 33 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(30): Show | 33 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1566-4712T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32906124 | ||||||
| chr19:32906287
|
G | A | 46 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0166others(43): Show | 46 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.1566-4875C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32906287 | ||||||
| chr19:32906316
|
C | G | 10 | a0001c0002t0001g0296a0001c0002t0001g0297a0001c0002t0001g0298others(7): Show | 10 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1566-4904G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32906316 | ||||||
| chr19:32906633
|
C | T | 121 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(118): Show | 124 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1566-5221G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32906633 | ||||||
| chr19:32906738
|
G | A | 21 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1566-5326C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32906738 | ||||||
| chr19:32906759
|
A | C | 83 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(80): Show | 84 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1566-5347T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32906759 | ||||||
| chr19:32906799
|
A | G | 104 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(101): Show | 105 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1566-5387T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32906799 | ||||||
| chr19:32906882
|
G | A | 3 | a0001c0002t0043g0118a0003c0010t0014g0168a0003c0010t0014g0366 | 3 | HG02109.hp1 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1566-5470C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32906882 | ||||||
| chr19:32906991
|
G | A | 2 | a0003c0010t0014g0168a0003c0010t0014g0366 | 2 | HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1566-5579C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32906991 | ||||||
| chr19:32907003
|
C | A | 1 | a0002c0001t0002g0165 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1566-5591G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32907003 | ||||||
| chr19:32907113
|
G | A | 125 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(122): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1566-5701C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32907113 | ||||||
| chr19:32907230
|
G | A | 5 | a0001c0002t0001g0031a0001c0002t0001g0040a0001c0002t0001g0041others(2): Show | 5 | HG00597.hp1 NA18997.hp1 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1566-5818C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32907230 | ||||||
| chr19:32907237
|
T | C | 2 | a0000c0007t0004g0287a0000c0007t0004g0289 | 2 | NA18977.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1566-5825A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32907237 | ||||||
| chr19:32907315
|
T | C | 87 | a0002c0001t0001g0332a0002c0001t0002g0004a0002c0001t0002g0005others(84): Show | 89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1566-5903A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32907315 | ||||||
| chr19:32907383
|
A | C | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1566-5971T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32907383 | ||||||
| chr19:32907455
|
A | AT | 71 | a0000c0005t0023g0079a0000c0012t0021g0015a0001c0002t0001g0296others(68): Show | 71 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1566-6044dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32907455 | ||||||
| chr19:32907455
|
AT | A | 102 | a0001c0002t0001g0068a0001c0002t0001g0083a0001c0002t0024g0072others(99): Show | 103 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1566-6044delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32907455 | ||||||
| chr19:32907513
|
G | A | 3 | a0001c0002t0001g0032a0002c0001t0002g0360a0002c0001t0002g0361 | 3 | HG00140.hp1 HG01496.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1566-6101C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32907513 | ||||||
| chr19:32907565
|
C | T | 129 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(126): Show | 132 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1566-6153G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32907565 | ||||||
| chr19:32907671
|
T | C | 229 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(226): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1566-6259A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32907671 | ||||||
| chr19:32907950
|
CAA | C | 33 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(30): Show | 33 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1566-6540_1566-653 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32907950 | ||||||
| chr19:32908050
|
CTG | C | 33 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(30): Show | 33 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1566-6640_1566-663 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32908050 | ||||||
| chr19:32908290
|
C | G | 2 | a0003c0003t0003g0233a0003c0003t0003g0234 | 2 | HG03654.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1566-6878G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32908290 | ||||||
| chr19:32908397
|
G | A | 1 | a0001c0004t0002g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1565+6940C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32908397 | ||||||
| chr19:32908438
|
G | A | 112 | a0002c0001t0001g0332a0002c0001t0002g0004a0002c0001t0002g0005others(109): Show | 114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1565+6899C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32908438 | ||||||
| chr19:32908445
|
T | C | 2 | a0004c0006t0007g0129a0004c0006t0007g0134 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1565+6892A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32908445 | ||||||
| chr19:32908673
|
C | T | 1 | a0001c0016t0030g0055 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1565+6664G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32908673 | ||||||
| chr19:32909128
|
C | T | 1 | a0002c0001t0008g0009 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1565+6209G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32909128 | ||||||
| chr19:32909227
|
G | C | 82 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(79): Show | 83 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1565+6110C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32909227 | ||||||
| chr19:32909329
|
C | T | 1 | a0004c0006t0032g0127 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1565+6008G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32909329 | ||||||
| chr19:32909491
|
C | T | 103 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(100): Show | 104 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1565+5846G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32909491 | ||||||
| chr19:32909726
|
C | T | 1 | a0000c0005t0005g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1565+5611G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32909726 | ||||||
| chr19:32909824
|
C | A | 1 | a0003c0003t0003g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1565+5513G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32909824 | ||||||
| chr19:32909961
|
A | G | 19 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(16): Show | 19 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1565+5376T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32909961 | ||||||
| chr19:32910253
|
G | A | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1565+5084C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910253 | ||||||
| chr19:32910265
|
C | CAG | 67 | a0000c0005t0041g0111a0001c0002t0024g0072a0003c0003t0003g0003others(64): Show | 68 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1565+5070_1565+507 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910265 | ||||||
| chr19:32910265
|
C | CAGAG | 115 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(112): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1565+5068_1565+507 others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910265 | ||||||
| chr19:32910265
|
C | CAGAGAG | 7 | a0000c0005t0005g0103a0002c0001t0002g0325a0002c0001t0002g0329others(4): Show | 7 | HG01074.hp1 HG01106.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1565+5066_1565+507 others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910265 | ||||||
| chr19:32910265
|
C | CAGAGAGA others(3): Show |
1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1565+5062_1565+507 others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910265 | ||||||
| chr19:32910265
|
C | CAGAGAGA others(5): Show |
1 | a0002c0001t0002g0152 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1565+5060_1565+507 others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910265 | ||||||
| chr19:32910288
|
AGC | A | 10 | a0001c0002t0001g0034a0001c0004t0001g0075a0001c0004t0001g0169others(7): Show | 10 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1565+5047_1565+504 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910288 | ||||||
| chr19:32910293
|
G | A | 1 | a0001c0002t0024g0072 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1565+5044C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910293 | ||||||
| chr19:32910294
|
A | C | 10 | a0001c0002t0001g0034a0001c0004t0001g0075a0001c0004t0001g0169others(7): Show | 10 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1565+5043T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910294 | ||||||
| chr19:32910298
|
AGAGG | A | 118 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(115): Show | 121 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1565+5035_1565+503 others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910298 | ||||||
| chr19:32910302
|
G | A | 10 | a0001c0002t0001g0034a0001c0004t0001g0075a0001c0004t0001g0169others(7): Show | 10 | HG00639.hp1 HG00735.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1565+5035C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910302 | ||||||
| chr19:32910316
|
A | G | 1 | a0002c0025t0002g0374 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1565+5021T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910316 | ||||||
| chr19:32910441
|
A | G | 1 | a0002c0001t0002g0309 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1565+4896T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910441 | ||||||
| chr19:32910668
|
AAATTTTT others(3): Show |
A | 88 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(85): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1565+4659_1565+466 others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910668 | ||||||
| chr19:32910699
|
A | T | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1565+4638T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910699 | ||||||
| chr19:32910744
|
G | T | 105 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(102): Show | 106 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1565+4593C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910744 | ||||||
| chr19:32910780
|
G | C | 1 | a0002c0001t0002g0351 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1565+4557C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910780 | ||||||
| chr19:32910826
|
C | T | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1565+4511G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910826 | ||||||
| chr19:32910928
|
T | G | 30 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1565+4409A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32910928 | ||||||
| chr19:32911113
|
G | A | 88 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(85): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1565+4224C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911113 | ||||||
| chr19:32911194
|
G | A | 105 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(102): Show | 106 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1565+4143C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911194 | ||||||
| chr19:32911260
|
T | A | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1565+4077A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911260 | ||||||
| chr19:32911394
|
T | C | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1565+3943A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911394 | ||||||
| chr19:32911395
|
G | A | 66 | a0003c0003t0003g0003a0003c0003t0003g0077a0003c0003t0003g0080others(63): Show | 67 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1565+3942C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911395 | ||||||
| chr19:32911459
|
C | G | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1565+3878G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911459 | ||||||
| chr19:32911513
|
T | C | 230 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(227): Show | 233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.1565+3824A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911513 | ||||||
| chr19:32911554
|
G | A | 1 | a0004c0006t0011g0143 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1565+3783C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911554 | ||||||
| chr19:32911686
|
T | A | 3 | a0002c0001t0002g0309a0002c0001t0002g0310a0002c0001t0025g0148 | 3 | HG01175.hp2 HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1565+3651A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911686 | ||||||
| chr19:32911735
|
T | C | 1 | a0003c0003t0003g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1565+3602A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911735 | ||||||
| chr19:32911794
|
T | C | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1565+3543A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911794 | ||||||
| chr19:32911795
|
G | A | 125 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(122): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1565+3542C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911795 | ||||||
| chr19:32911862
|
G | A | 3 | a0007c0011t0012g0375a0007c0011t0012g0379a0007c0011t0012g0380 | 3 | HG02630.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1565+3475C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911862 | ||||||
| chr19:32911877
|
G | A | 3 | a0001c0002t0043g0118a0003c0010t0014g0168a0003c0010t0014g0366 | 3 | HG02109.hp1 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1565+3460C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911877 | ||||||
| chr19:32911901
|
T | C | 91 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(88): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1565+3436A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911901 | ||||||
| chr19:32911983
|
T | A | 105 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(102): Show | 106 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1565+3354A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32911983 | ||||||
| chr19:32912018
|
G | A | 125 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(122): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1565+3319C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32912018 | ||||||
| chr19:32912139
|
G | A | 10 | a0001c0002t0001g0296a0001c0002t0001g0297a0001c0002t0001g0298others(7): Show | 10 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1565+3198C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32912139 | ||||||
| chr19:32912202
|
C | CAA | 21 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1565+3133_1565+313 others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32912202 | ||||||
| chr19:32912262
|
T | C | 1 | a0001c0004t0001g0145 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1565+3075A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32912262 | ||||||
| chr19:32912341
|
G | A | 2 | a0001c0002t0001g0032a0001c0002t0028g0054 | 2 | HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1565+2996C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32912341 | ||||||
| chr19:32912499
|
C | G | 84 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(81): Show | 85 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1565+2838G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32912499 | ||||||
| chr19:32912600
|
G | A | 125 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(122): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1565+2737C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32912600 | ||||||
| chr19:32912612
|
G | A | 2 | a0001c0002t0001g0050a0001c0002t0001g0056 | 2 | HG02129.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1565+2725C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32912612 | ||||||
| chr19:32912765
|
G | A | 1 | a0001c0002t0043g0118 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1565+2572C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32912765 | ||||||
| chr19:32912791
|
C | A | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1565+2546G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32912791 | ||||||
| chr19:32912813
|
C | T | 1 | a0004c0006t0009g0139 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1565+2524G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32912813 | ||||||
| chr19:32912837
|
T | G | 84 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(81): Show | 85 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1565+2500A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32912837 | ||||||
| chr19:32913036
|
G | A | 30 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1565+2301C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913036 | ||||||
| chr19:32913051
|
A | T | 32 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(29): Show | 32 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1565+2286T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913051 | ||||||
| chr19:32913058
|
A | T | 32 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(29): Show | 32 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1565+2279T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913058 | ||||||
| chr19:32913061
|
T | A | 45 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0166others(42): Show | 45 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1565+2276A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913061 | ||||||
| chr19:32913062
|
A | T | 13 | a0000c0007t0004g0287a0005c0008t0006g0087a0005c0008t0006g0088others(10): Show | 13 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1565+2275T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913062 | ||||||
| chr19:32913192
|
C | A | 1 | a0008c0015t0001g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1565+2145G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913192 | ||||||
| chr19:32913228
|
A | C | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1565+2109T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913228 | ||||||
| chr19:32913288
|
CATAT | C | 4 | a0001c0002t0043g0118a0002c0001t0002g0373a0002c0001t0018g0337others(1): Show | 4 | HG02109.hp1 NA18950.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.1565+2045_1565+204 others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913288 | ||||||
| chr19:32913298
|
TATATATA others(8): Show |
T | 1 | a0003c0003t0003g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1565+2024_1565+203 others(19): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913298 | ||||||
| chr19:32913299
|
ATATATAT | A | 5 | a0004c0006t0011g0143a0004c0006t0026g0144a0006c0009t0011g0123others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565+2031_1565+203 others(11): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913299 | ||||||
| chr19:32913301
|
ATATAT | A | 13 | a0000c0005t0005g0106a0003c0010t0014g0168a0003c0010t0014g0366others(10): Show | 13 | HG02145.hp2 HG02723.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.1565+2031_1565+203 others(9): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913301 | ||||||
| chr19:32913301
|
ATATATT | A | 23 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(20): Show | 23 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1565+2030_1565+203 others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913301 | ||||||
| chr19:32913303
|
A | T | 2 | a0002c0001t0002g0355a0002c0001t0017g0354 | 2 | HG00280.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1565+2034T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913303 | ||||||
| chr19:32913303
|
ATAT | A | 4 | a0000c0007t0004g0078a0000c0007t0004g0275a0000c0007t0004g0293others(1): Show | 4 | HG03491.hp2 NA18945.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565+2031_1565+203 others(7): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913303 | ||||||
| chr19:32913303
|
ATATTT | A | 3 | a0001c0004t0001g0200a0002c0001t0002g0309a0002c0001t0002g0310 | 3 | HG00642.hp2 HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1565+2029_1565+203 others(9): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913303 | ||||||
| chr19:32913303
|
ATATTTTT | A | 21 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1565+2027_1565+203 others(11): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913303 | ||||||
| chr19:32913304
|
TATTTTTT others(2): Show |
T | 65 | a0003c0003t0003g0003a0003c0003t0003g0077a0003c0003t0003g0080others(62): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1565+2024_1565+203 others(13): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913304 | ||||||
| chr19:32913305
|
A | T | 79 | a0000c0005t0005g0117a0000c0005t0005g0119a0000c0005t0005g0268others(76): Show | 81 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1565+2032T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913305 | ||||||
| chr19:32913305
|
ATTT | A | 6 | a0000c0007t0004g0283a0000c0007t0004g0285a0000c0007t0004g0287others(3): Show | 6 | HG02132.hp2 NA18944.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1565+2029_1565+203 others(7): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913305 | ||||||
| chr19:32913307
|
T | A | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1565+2030A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913307 | ||||||
| chr19:32913308
|
TTTTTG | T | 122 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(119): Show | 125 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1565+2024_1565+202 others(9): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913308 | ||||||
| chr19:32913308
|
TTTTTGTT others(7): Show |
T | 21 | a0002c0001t0002g0004a0002c0001t0002g0073a0002c0001t0002g0126others(18): Show | 22 | HG00140.hp1 HG01496.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.1565+2015_1565+202 others(18): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913308 | ||||||
| chr19:32913309
|
T | A | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1565+2028A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913309 | ||||||
| chr19:32913310
|
TTTG | T | 11 | a0000c0007t0004g0277a0000c0007t0004g0278a0000c0007t0004g0279others(8): Show | 11 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1565+2024_1565+202 others(7): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913310 | ||||||
| chr19:32913311
|
TTGTTGTT others(7): Show |
T | 64 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0005others(61): Show | 65 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1565+2012_1565+202 others(18): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913311 | ||||||
| chr19:32913312
|
TGTTG | T | 13 | a0003c0010t0014g0168a0003c0010t0014g0366a0005c0008t0006g0087others(10): Show | 13 | HG02145.hp2 HG02723.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.1565+2021_1565+202 others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913312 | ||||||
| chr19:32913312
|
TGTTGTTG others(3): Show |
T | 3 | a0002c0001t0002g0373a0002c0001t0018g0337a0002c0001t0018g0338 | 3 | NA18950.hp2 NA18991.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1565+2015_1565+202 others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913312 | ||||||
| chr19:32913313
|
G | T | 60 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(57): Show | 60 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1565+2024C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913313 | ||||||
| chr19:32913316
|
G | T | 89 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1565+2021C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913316 | ||||||
| chr19:32913319
|
G | A | 1 | a0003c0003t0003g0243 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1565+2018C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913319 | ||||||
| chr19:32913319
|
G | T | 1 | a0000c0005t0005g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1565+2018C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913319 | ||||||
| chr19:32913363
|
A | T | 32 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(29): Show | 32 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1565+1974T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913363 | ||||||
| chr19:32913412
|
T | C | 2 | a0000c0007t0004g0078a0001c0002t0010g0149 | 2 | HG03041.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1565+1925A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913412 | ||||||
| chr19:32913447
|
G | C | 32 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(29): Show | 32 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1565+1890C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913447 | ||||||
| chr19:32913453
|
T | C | 1 | a0001c0002t0024g0072 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1565+1884A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913453 | ||||||
| chr19:32913598
|
G | A | 2 | a0002c0001t0002g0309a0002c0001t0002g0310 | 2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1565+1739C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913598 | ||||||
| chr19:32913639
|
C | CT | 260 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(257): Show | 264 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.1565+1697dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913639 | ||||||
| chr19:32913704
|
T | C | 84 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(81): Show | 85 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1565+1633A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913704 | ||||||
| chr19:32913725
|
G | A | 21 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1565+1612C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913725 | ||||||
| chr19:32913764
|
G | A | 2 | a0001c0002t0001g0026a0004c0006t0009g0139 | 2 | HG02083.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1565+1573C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913764 | ||||||
| chr19:32913764
|
G | T | 2 | a0000c0005t0023g0079a0003c0010t0029g0307 | 2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1565+1573C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913764 | ||||||
| chr19:32913776
|
T | C | 1 | a0003c0003t0013g0271 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1565+1561A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913776 | ||||||
| chr19:32913866
|
C | T | 3 | a0001c0002t0001g0039a0001c0002t0001g0045a0001c0002t0031g0053 | 3 | HG00621.hp2 NA18947.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1565+1471G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913866 | ||||||
| chr19:32913929
|
G | A | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1565+1408C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913929 | ||||||
| chr19:32913946
|
C | T | 4 | a0001c0004t0001g0169a0001c0004t0001g0177a0001c0004t0001g0182others(1): Show | 4 | HG00639.hp1 HG00735.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565+1391G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32913946 | ||||||
| chr19:32914125
|
T | C | 1 | a0005c0008t0006g0090 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1565+1212A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32914125 | ||||||
| chr19:32914190
|
T | C | 32 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(29): Show | 32 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1565+1147A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32914190 | ||||||
| chr19:32914469
|
G | A | 1 | a0005c0008t0006g0090 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1565+868C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32914469 | ||||||
| chr19:32914618
|
C | T | 1 | a0001c0002t0024g0072 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1565+719G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32914618 | ||||||
| chr19:32914633
|
A | G | 92 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(89): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1565+704T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32914633 | ||||||
| chr19:32914851
|
G | A | 209 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(206): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1565+486C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32914851 | ||||||
| chr19:32914893
|
G | A | 128 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(125): Show | 131 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1565+444C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32914893 | ||||||
| chr19:32914935
|
T | C | 209 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(206): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1565+402A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32914935 | ||||||
| chr19:32915185
|
G | A | 129 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(126): Show | 132 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1565+152C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 14/18 | chr19 | 32915185 | ||||||
| chr19:32915536
|
A | G | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1385-19T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915536 | ||||||
| chr19:32915567
|
A | C | 1 | a0002c0001t0002g0362 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1385-50T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915567 | ||||||
| chr19:32915578
|
G | T | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1385-61C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915578 | ||||||
| chr19:32915587
|
G | C | 120 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(117): Show | 123 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1385-70C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915587 | ||||||
| chr19:32915588
|
G | A | 2 | a0001c0002t0001g0042a0001c0002t0001g0052 | 2 | HG02165.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1385-71C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915588 | ||||||
| chr19:32915625
|
T | G | 1 | a0001c0002t0001g0052 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1385-108A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915625 | ||||||
| chr19:32915643
|
A | G | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1385-126T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915643 | ||||||
| chr19:32915744
|
C | T | 2 | a0002c0001t0002g0352a0002c0001t0002g0353 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1385-227G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915744 | ||||||
| chr19:32915809
|
T | C | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1385-292A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915809 | ||||||
| chr19:32915918
|
GA | G | 15 | a0000c0012t0021g0015a0001c0002t0001g0305a0001c0002t0010g0149others(12): Show | 15 | HG00621.hp1 HG01516.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1385-402delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915918 | ||||||
| chr19:32915918
|
GAA | G | 290 | a0000c0005t0005g0102a0000c0012t0004g0065a0001c0002t0001g0001others(287): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.1385-403_1385-402d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915918 | ||||||
| chr19:32915918
|
GAAA | G | 34 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(31): Show | 34 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1385-404_1385-402d others(5): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915918 | ||||||
| chr19:32915920
|
A | G | 2 | a0002c0001t0002g0150a0002c0001t0002g0158 | 2 | HG00621.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1385-403T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915920 | ||||||
| chr19:32915975
|
T | C | 4 | a0002c0001t0002g0004a0002c0001t0002g0153a0002c0001t0002g0311others(1): Show | 5 | HG02258.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1385-458A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915975 | ||||||
| chr19:32915992
|
G | A | 129 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(126): Show | 132 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1385-475C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32915992 | ||||||
| chr19:32916087
|
G | T | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1385-570C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32916087 | ||||||
| chr19:32916205
|
A | G | 374 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(371): Show | 380 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(377): Show |
intron_variant | MODIFIER | c.1385-688T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32916205 | ||||||
| chr19:32916587
|
A | C | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1385-1070T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32916587 | ||||||
| chr19:32916750
|
C | T | 150 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(147): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1385-1233G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32916750 | ||||||
| chr19:32916846
|
G | T | 1 | a0002c0001t0025g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1385-1329C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32916846 | ||||||
| chr19:32916879
|
G | A | 150 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(147): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1384+1345C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32916879 | ||||||
| chr19:32916922
|
C | T | 2 | a0000c0005t0005g0106a0000c0005t0042g0109 | 2 | HG01192.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1384+1302G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32916922 | ||||||
| chr19:32916923
|
G | T | 1 | a0002c0001t0002g0158 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1384+1301C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32916923 | ||||||
| chr19:32917032
|
T | C | 13 | a0003c0003t0010g0218a0005c0008t0006g0087a0005c0008t0006g0088others(10): Show | 13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1384+1192A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917032 | ||||||
| chr19:32917034
|
G | C | 8 | a0001c0002t0001g0028a0001c0002t0001g0030a0001c0002t0001g0042others(5): Show | 8 | HG00438.hp1 HG02165.hp2 NA18974.hp2 others(5): Show |
intron_variant | MODIFIER | c.1384+1190C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917034 | ||||||
| chr19:32917047
|
C | G | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1384+1177G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917047 | ||||||
| chr19:32917098
|
A | C | 1 | a0003c0021t0022g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1384+1126T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917098 | ||||||
| chr19:32917268
|
G | A | 2 | a0003c0003t0003g0245a0006c0009t0011g0312 | 2 | HG02970.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1384+956C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917268 | ||||||
| chr19:32917291
|
G | A | 1 | a0001c0002t0024g0072 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1384+933C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917291 | ||||||
| chr19:32917303
|
T | G | 1 | a0006c0009t0011g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1384+921A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917303 | ||||||
| chr19:32917368
|
C | T | 2 | a0000c0005t0005g0097a0000c0005t0005g0098 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1384+856G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917368 | ||||||
| chr19:32917504
|
C | T | 64 | a0003c0003t0003g0003a0003c0003t0003g0077a0003c0003t0003g0080others(61): Show | 65 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1384+720G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917504 | ||||||
| chr19:32917529
|
T | C | 30 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1384+695A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917529 | ||||||
| chr19:32917682
|
G | A | 4 | a0001c0004t0001g0206a0001c0004t0001g0207a0001c0004t0001g0208others(1): Show | 4 | HG00323.hp2 NA18747.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384+542C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917682 | ||||||
| chr19:32917717
|
G | A | 1 | a0003c0003t0003g0223 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1384+507C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917717 | ||||||
| chr19:32917792
|
C | T | 2 | a0003c0003t0003g0215a0003c0003t0003g0216 | 2 | NA18612.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1384+432G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917792 | ||||||
| chr19:32917948
|
A | C | 1 | a0002c0001t0002g0351 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1384+276T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917948 | ||||||
| chr19:32917998
|
G | C | 92 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(89): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1384+226C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32917998 | ||||||
| chr19:32918032
|
T | C | 1 | a0003c0010t0002g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1384+192A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32918032 | ||||||
| chr19:32918071
|
C | T | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1384+153G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32918071 | ||||||
| chr19:32918073
|
T | C | 1 | a0000c0005t0005g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1384+151A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32918073 | ||||||
| chr19:32918142
|
GC | G | 121 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(118): Show | 124 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1384+81delG | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32918142 | ||||||
| chr19:32918148
|
G | A | 129 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(126): Show | 132 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1384+76C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32918148 | ||||||
| chr19:32918155
|
G | C | 150 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(147): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1384+69C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 13/18 | chr19 | 32918155 | ||||||
| chr19:32918507
|
G | T | 150 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(147): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1269-168C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918507 | ||||||
| chr19:32918509
|
C | T | 21 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1269-170G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918509 | ||||||
| chr19:32918524
|
G | A | 2 | a0000c0005t0005g0268a0000c0005t0005g0269 | 2 | HG01081.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1269-185C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918524 | ||||||
| chr19:32918531
|
C | A | 1 | a0000c0005t0005g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1269-192G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918531 | ||||||
| chr19:32918582
|
T | C | 1 | a0006c0009t0011g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1269-243A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918582 | ||||||
| chr19:32918785
|
A | G | 3 | a0002c0001t0002g0320a0002c0001t0002g0327a0002c0001t0002g0349 | 3 | HG02257.hp1 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1269-446T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918785 | ||||||
| chr19:32918866
|
T | A | 208 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(205): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1269-527A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918866 | ||||||
| chr19:32918868
|
TTTTC | T | 8 | a0000c0012t0021g0015a0001c0002t0010g0149a0001c0002t0010g0376others(5): Show | 8 | HG02257.hp2 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1269-533_1269-530d others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918868 | ||||||
| chr19:32918869
|
T | A | 1 | a0004c0006t0007g0274 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1269-530A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918869 | ||||||
| chr19:32918878
|
CT | C | 154 | a0001c0002t0024g0072a0001c0002t0043g0118a0002c0001t0001g0332others(151): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1269-540delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918878 | ||||||
| chr19:32918882
|
T | TC | 4 | a0000c0005t0005g0117a0000c0005t0023g0079a0005c0008t0006g0089others(1): Show | 4 | HG01884.hp2 HG02145.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1269-544_1269-543i others(3): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918882 | ||||||
| chr19:32918883
|
T | C | 45 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(42): Show | 45 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1269-544A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918883 | ||||||
| chr19:32918884
|
C | T | 49 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(46): Show | 49 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.1269-545G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918884 | ||||||
| chr19:32918884
|
CT | C | 126 | a0000c0007t0004g0284a0000c0012t0004g0065a0001c0002t0001g0001others(123): Show | 129 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1269-546delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918884 | ||||||
| chr19:32918885
|
T | C | 5 | a0002c0001t0001g0350a0002c0001t0002g0152a0002c0001t0002g0340others(2): Show | 5 | NA18974.hp1 NA18977.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1269-546A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918885 | ||||||
| chr19:32918887
|
T | C | 1 | a0005c0008t0006g0092 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1269-548A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918887 | ||||||
| chr19:32918978
|
G | A | 129 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(126): Show | 132 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1269-639C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32918978 | ||||||
| chr19:32919042
|
G | A | 92 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(89): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1269-703C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32919042 | ||||||
| chr19:32919102
|
G | A | 4 | a0002c0001t0002g0309a0002c0001t0002g0310a0002c0001t0025g0148others(1): Show | 4 | HG01175.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1269-763C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32919102 | ||||||
| chr19:32919373
|
G | A | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1269-1034C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32919373 | ||||||
| chr19:32919383
|
T | C | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1269-1044A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32919383 | ||||||
| chr19:32919473
|
C | T | 1 | a0002c0001t0002g0073 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1269-1134G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32919473 | ||||||
| chr19:32919482
|
T | C | 69 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0003g0003others(66): Show | 70 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1269-1143A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32919482 | ||||||
| chr19:32919616
|
C | T | 2 | a0003c0010t0014g0168a0003c0010t0014g0366 | 2 | HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1269-1277G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32919616 | ||||||
| chr19:32919825
|
T | C | 7 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(4): Show | 7 | HG02630.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1269-1486A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32919825 | ||||||
| chr19:32919926
|
G | A | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1269-1587C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32919926 | ||||||
| chr19:32919945
|
C | T | 121 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(118): Show | 124 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1269-1606G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32919945 | ||||||
| chr19:32920098
|
C | T | 1 | a0006c0009t0011g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1269-1759G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920098 | ||||||
| chr19:32920141
|
G | A | 2 | a0003c0010t0014g0168a0003c0010t0014g0366 | 2 | HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1269-1802C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920141 | ||||||
| chr19:32920152
|
C | G | 92 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(89): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1269-1813G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920152 | ||||||
| chr19:32920220
|
T | C | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1269-1881A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920220 | ||||||
| chr19:32920233
|
T | G | 208 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(205): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1269-1894A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920233 | ||||||
| chr19:32920457
|
C | T | 5 | a0001c0004t0001g0201a0001c0004t0001g0202a0001c0004t0001g0203others(2): Show | 5 | HG00423.hp1 HG00597.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.1269-2118G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920457 | ||||||
| chr19:32920463
|
T | A | 92 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(89): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1269-2124A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920463 | ||||||
| chr19:32920544
|
C | G | 3 | a0003c0003t0003g0212a0003c0003t0003g0213a0003c0003t0003g0214 | 3 | HG02280.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1269-2205G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920544 | ||||||
| chr19:32920546
|
C | T | 2 | a0001c0004t0001g0204a0001c0004t0001g0205 | 2 | NA18950.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1269-2207G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920546 | ||||||
| chr19:32920567
|
T | C | 88 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(85): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1269-2228A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920567 | ||||||
| chr19:32920628
|
C | T | 4 | a0001c0004t0001g0172a0001c0004t0001g0174a0001c0004t0001g0184others(1): Show | 4 | NA18947.hp2 NA18986.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1269-2289G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920628 | ||||||
| chr19:32920650
|
T | A | 3 | a0000c0005t0005g0100a0000c0005t0019g0114a0003c0010t0002g0105 | 3 | HG02698.hp1 HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1269-2311A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920650 | ||||||
| chr19:32920670
|
G | A | 208 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(205): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1269-2331C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920670 | ||||||
| chr19:32920671
|
A | T | 1 | a0001c0002t0001g0300 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1269-2332T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920671 | ||||||
| chr19:32920764
|
G | A | 129 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(126): Show | 132 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1269-2425C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920764 | ||||||
| chr19:32920833
|
C | T | 3 | a0006c0009t0011g0123a0006c0009t0011g0124a0006c0009t0011g0125 | 3 | HG02717.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1269-2494G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920833 | ||||||
| chr19:32920955
|
C | T | 3 | a0007c0011t0012g0375a0007c0011t0012g0379a0007c0011t0012g0380 | 3 | HG02630.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1268+2484G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920955 | ||||||
| chr19:32920956
|
G | A | 1 | a0008c0015t0001g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1268+2483C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32920956 | ||||||
| chr19:32921013
|
T | C | 21 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1268+2426A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921013 | ||||||
| chr19:32921120
|
G | T | 1 | a0003c0003t0037g0247 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1268+2319C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921120 | ||||||
| chr19:32921221
|
C | CA | 95 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(92): Show | 97 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1268+2217dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921221 | ||||||
| chr19:32921229
|
AAAAG | A | 126 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(123): Show | 129 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1268+2206_1268+220 others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921229 | ||||||
| chr19:32921233
|
G | A | 107 | a0001c0002t0024g0072a0001c0002t0043g0118a0002c0001t0002g0309others(104): Show | 108 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1268+2206C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921233 | ||||||
| chr19:32921237
|
G | A | 126 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(123): Show | 129 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1268+2202C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921237 | ||||||
| chr19:32921276
|
G | A | 21 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1268+2163C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921276 | ||||||
| chr19:32921286
|
T | G | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1268+2153A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921286 | ||||||
| chr19:32921356
|
T | C | 3 | a0006c0009t0011g0123a0006c0009t0011g0124a0006c0009t0011g0125 | 3 | HG02717.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1268+2083A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921356 | ||||||
| chr19:32921513
|
A | T | 3 | a0006c0009t0011g0123a0006c0009t0011g0124a0006c0009t0011g0125 | 3 | HG02717.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1268+1926T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921513 | ||||||
| chr19:32921514
|
T | C | 1 | a0002c0001t0002g0126 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1268+1925A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921514 | ||||||
| chr19:32921607
|
G | C | 150 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(147): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1268+1832C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921607 | ||||||
| chr19:32921835
|
G | A | 22 | a0000c0005t0005g0104a0004c0006t0007g0086a0004c0006t0007g0128others(19): Show | 22 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.1268+1604C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921835 | ||||||
| chr19:32921860
|
G | A | 129 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(126): Show | 132 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1268+1579C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921860 | ||||||
| chr19:32921876
|
T | A | 2 | a0003c0003t0003g0248a0003c0003t0037g0247 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1268+1563A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921876 | ||||||
| chr19:32921942
|
G | A | 129 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(126): Show | 132 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1268+1497C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32921942 | ||||||
| chr19:32922053
|
T | C | 16 | a0002c0001t0002g0004a0002c0001t0002g0073a0002c0001t0002g0153others(13): Show | 17 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1268+1386A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922053 | ||||||
| chr19:32922095
|
C | T | 1 | a0003c0010t0014g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1268+1344G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922095 | ||||||
| chr19:32922096
|
G | A | 21 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1268+1343C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922096 | ||||||
| chr19:32922107
|
C | A | 2 | a0002c0001t0002g0352a0002c0001t0002g0353 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1268+1332G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922107 | ||||||
| chr19:32922113
|
T | A | 2 | a0002c0001t0002g0352a0002c0001t0002g0353 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1268+1326A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922113 | ||||||
| chr19:32922125
|
T | C | 6 | a0000c0007t0004g0283a0000c0007t0004g0285a0000c0007t0004g0287others(3): Show | 6 | HG02132.hp2 NA18944.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1268+1314A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922125 | ||||||
| chr19:32922263
|
C | T | 12 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1268+1176G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922263 | ||||||
| chr19:32922312
|
C | T | 150 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(147): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1268+1127G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922312 | ||||||
| chr19:32922340
|
G | C | 208 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(205): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1268+1099C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922340 | ||||||
| chr19:32922389
|
A | T | 1 | a0002c0001t0025g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1268+1050T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922389 | ||||||
| chr19:32922586
|
G | A | 2 | a0002c0001t0002g0352a0002c0001t0002g0353 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1268+853C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922586 | ||||||
| chr19:32922696
|
A | G | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1268+743T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922696 | ||||||
| chr19:32922702
|
G | C | 1 | a0002c0001t0002g0343 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1268+737C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922702 | ||||||
| chr19:32922703
|
C | T | 1 | a0002c0001t0002g0343 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1268+736G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922703 | ||||||
| chr19:32922708
|
T | C | 151 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(148): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1268+731A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922708 | ||||||
| chr19:32922719
|
G | A | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1268+720C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922719 | ||||||
| chr19:32922756
|
G | A | 3 | a0007c0011t0012g0375a0007c0011t0012g0379a0007c0011t0012g0380 | 3 | HG02630.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1268+683C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922756 | ||||||
| chr19:32922807
|
C | T | 2 | a0001c0004t0001g0179a0001c0004t0001g0190 | 2 | NA19060.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1268+632G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922807 | ||||||
| chr19:32922847
|
CA | C | 235 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(232): Show | 238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.1268+591delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32922847 | ||||||
| chr19:32923032
|
G | A | 1 | a0003c0003t0003g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1268+407C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32923032 | ||||||
| chr19:32923139
|
G | C | 221 | a0000c0005t0023g0079a0000c0007t0004g0281a0000c0007t0004g0284others(218): Show | 226 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.1268+300C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32923139 | ||||||
| chr19:32923232
|
A | T | 16 | a0000c0007t0004g0078a0000c0007t0004g0281a0000c0007t0004g0282others(13): Show | 16 | HG02056.hp2 HG02132.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.1268+207T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32923232 | ||||||
| chr19:32923326
|
C | T | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1268+113G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32923326 | ||||||
| chr19:32923335
|
A | G | 12 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1268+104T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32923335 | ||||||
| chr19:32923349
|
T | G | 1 | a0010c0020t0003g0122 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1268+90A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32923349 | ||||||
| chr19:32923357
|
T | C | 1 | a0001c0004t0001g0180 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1268+82A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 12/18 | chr19 | 32923357 | ||||||
| chr19:32923766
|
A | T | 1 | a0014c0022t0001g0196 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1165-224T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32923766 | ||||||
| chr19:32924004
|
C | CT | 15 | a0000c0005t0005g0102a0000c0005t0005g0106a0000c0005t0005g0115others(12): Show | 15 | HG01257.hp2 HG02145.hp2 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1165-463dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32924004 | ||||||
| chr19:32924004
|
CT | C | 24 | a0001c0002t0001g0017a0001c0004t0001g0180a0002c0001t0002g0309others(21): Show | 24 | HG00609.hp1 HG01069.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1165-463delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32924004 | ||||||
| chr19:32924021
|
T | A | 1 | a0010c0020t0003g0122 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1165-479A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32924021 | ||||||
| chr19:32924443
|
C | G | 29 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1165-901G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32924443 | ||||||
| chr19:32924509
|
C | T | 1 | a0002c0001t0002g0351 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1165-967G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32924509 | ||||||
| chr19:32924534
|
G | T | 2 | a0001c0004t0001g0178a0001c0004t0001g0183 | 2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1165-992C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32924534 | ||||||
| chr19:32925078
|
A | G | 1 | a0001c0004t0001g0176 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1164+1112T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925078 | ||||||
| chr19:32925260
|
AC | A | 197 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(194): Show | 201 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1164+929delG | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925260 | ||||||
| chr19:32925285
|
G | C | 27 | a0003c0010t0014g0168a0003c0010t0014g0366a0004c0006t0007g0086others(24): Show | 27 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.1164+905C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925285 | ||||||
| chr19:32925356
|
C | T | 2 | a0001c0002t0001g0042a0001c0002t0001g0043 | 2 | NA19081.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1164+834G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925356 | ||||||
| chr19:32925398
|
T | A | 1 | a0002c0001t0001g0350 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1164+792A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925398 | ||||||
| chr19:32925423
|
G | A | 1 | a0005c0008t0006g0095 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1164+767C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925423 | ||||||
| chr19:32925436
|
T | G | 8 | a0000c0012t0021g0015a0001c0002t0010g0149a0001c0002t0010g0376others(5): Show | 8 | HG02257.hp2 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1164+754A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925436 | ||||||
| chr19:32925485
|
C | CT | 15 | a0000c0005t0005g0099a0000c0005t0005g0103a0000c0005t0005g0106others(12): Show | 15 | HG01106.hp2 HG01109.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1164+704dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925485 | ||||||
| chr19:32925485
|
CT | C | 18 | a0000c0005t0005g0100a0000c0005t0023g0079a0001c0004t0001g0074others(15): Show | 18 | HG00609.hp2 HG01081.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1164+704delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925485 | ||||||
| chr19:32925485
|
CTT | C | 81 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(78): Show | 83 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1164+703_1164+704d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925485 | ||||||
| chr19:32925505
|
T | TC | 7 | a0004c0006t0009g0136a0004c0006t0009g0137a0004c0006t0009g0138others(4): Show | 7 | HG01106.hp1 HG01361.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1164+684_1164+685i others(3): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925505 | ||||||
| chr19:32925506
|
T | C | 124 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(121): Show | 127 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.1164+684A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925506 | ||||||
| chr19:32925506
|
T | TC | 31 | a0001c0002t0001g0061a0001c0004t0001g0166a0003c0010t0014g0168others(28): Show | 31 | HG00609.hp1 HG01261.hp2 HG02129.hp1 others(28): Show |
intron_variant | MODIFIER | c.1164+683dupG | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925506 | ||||||
| chr19:32925613
|
T | C | 197 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(194): Show | 201 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1164+577A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925613 | ||||||
| chr19:32925722
|
A | G | 1 | a0000c0007t0004g0291 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1164+468T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925722 | ||||||
| chr19:32925779
|
C | T | 197 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(194): Show | 201 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1164+411G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925779 | ||||||
| chr19:32925780
|
G | A | 1 | a0000c0005t0005g0120 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1164+410C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925780 | ||||||
| chr19:32925841
|
C | T | 26 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(23): Show | 26 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1164+349G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925841 | ||||||
| chr19:32925895
|
G | C | 68 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(65): Show | 68 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1164+295C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925895 | ||||||
| chr19:32925956
|
C | T | 1 | a0002c0001t0002g0348 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1164+234G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32925956 | ||||||
| chr19:32926025
|
C | G | 1 | a0001c0002t0001g0296 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1164+165G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32926025 | ||||||
| chr19:32926053
|
C | T | 2 | a0002c0001t0002g0360a0002c0001t0002g0361 | 2 | HG00140.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1164+137G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32926053 | ||||||
| chr19:32926138
|
C | T | 26 | a0003c0010t0014g0168a0003c0010t0014g0366a0004c0006t0007g0086others(23): Show | 26 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.1164+52G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 11/18 | chr19 | 32926138 | ||||||
| chr19:32926403
|
C | G | 198 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(195): Show | 202 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1081-130G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 10/18 | chr19 | 32926403 | ||||||
| chr19:32926407
|
T | C | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1081-134A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 10/18 | chr19 | 32926407 | ||||||
| chr19:32926537
|
C | A | 2 | a0004c0006t0011g0143a0004c0006t0026g0144 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1081-264G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 10/18 | chr19 | 32926537 | ||||||
| chr19:32926613
|
G | A | 13 | a0002c0001t0001g0350a0002c0001t0002g0005a0002c0001t0002g0163others(10): Show | 14 | NA18942.hp2 NA18943.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.1080+321C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 10/18 | chr19 | 32926613 | ||||||
| chr19:32926615
|
G | A | 1 | a0003c0003t0003g0263 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1080+319C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 10/18 | chr19 | 32926615 | ||||||
| chr19:32926625
|
G | A | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1080+309C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 10/18 | chr19 | 32926625 | ||||||
| chr19:32926665
|
G | A | 1 | a0002c0001t0002g0158 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1080+269C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 10/18 | chr19 | 32926665 | ||||||
| chr19:32926677
|
T | G | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1080+257A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 10/18 | chr19 | 32926677 | ||||||
| chr19:32926809
|
G | A | 2 | a0003c0003t0003g0215a0003c0003t0003g0216 | 2 | NA18612.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1080+125C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 10/18 | chr19 | 32926809 | ||||||
| chr19:32926851
|
C | T | 2 | a0004c0006t0011g0143a0004c0006t0026g0144 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1080+83G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 10/18 | chr19 | 32926851 | ||||||
| chr19:32927113
|
C | CACCCACC others(1): Show |
35 | a0003c0010t0014g0168a0003c0010t0014g0366a0004c0006t0007g0086others(32): Show | 35 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.1030-137_1030-130d others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927113 | ||||||
| chr19:32927131
|
C | CCCAT | 81 | a0000c0005t0005g0101a0000c0005t0020g0107a0002c0001t0001g0332others(78): Show | 83 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1030-151_1030-148d others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927131 | ||||||
| chr19:32927131
|
CCCAT | C | 193 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(190): Show | 197 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1030-151_1030-148d others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927131 | ||||||
| chr19:32927161
|
C | T | 3 | a0001c0002t0001g0039a0001c0002t0001g0045a0001c0002t0031g0053 | 3 | HG00621.hp2 NA18947.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1030-177G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927161 | ||||||
| chr19:32927165
|
T | C | 10 | a0001c0002t0001g0039a0001c0002t0001g0045a0001c0002t0031g0053others(7): Show | 10 | HG00438.hp2 HG00621.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1030-181A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927165 | ||||||
| chr19:32927169
|
C | T | 7 | a0002c0001t0002g0335a0002c0001t0002g0339a0002c0001t0002g0359others(4): Show | 7 | HG00438.hp2 HG02083.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.1030-185G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927169 | ||||||
| chr19:32927246
|
G | A | 1 | a0002c0001t0002g0309 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1030-262C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927246 | ||||||
| chr19:32927269
|
T | G | 198 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(195): Show | 202 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1030-285A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927269 | ||||||
| chr19:32927401
|
C | CAT | 6 | a0000c0005t0023g0079a0002c0001t0002g0352a0002c0001t0002g0353others(3): Show | 6 | HG01496.hp2 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1030-419_1030-418d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927401 | ||||||
| chr19:32927648
|
G | A | 88 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(85): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1030-664C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927648 | ||||||
| chr19:32927657
|
T | C | 88 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(85): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1030-673A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927657 | ||||||
| chr19:32927683
|
C | A | 192 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(189): Show | 196 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1030-699G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927683 | ||||||
| chr19:32927777
|
G | T | 1 | a0003c0003t0013g0220 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1030-793C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927777 | ||||||
| chr19:32927902
|
GCTTTTTT others(9): Show |
G | 3 | a0001c0004t0001g0074a0001c0004t0001g0171a0001c0004t0001g0198 | 3 | NA18954.hp1 NA19010.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1030-934_1030-919d others(18): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927902 | ||||||
| chr19:32927903
|
CT | C | 179 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(176): Show | 182 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1030-920delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927903 | ||||||
| chr19:32927903
|
CTT | C | 156 | a0000c0005t0005g0120a0000c0005t0020g0121a0002c0001t0001g0332others(153): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1030-921_1030-920d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927903 | ||||||
| chr19:32927917
|
T | C | 2 | a0002c0001t0008g0010a0002c0001t0017g0347 | 2 | NA19063.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1030-933A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927917 | ||||||
| chr19:32927918
|
T | C | 4 | a0001c0004t0001g0169a0001c0004t0001g0174a0004c0006t0009g0141others(1): Show | 4 | HG00639.hp1 HG02027.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1030-934A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927918 | ||||||
| chr19:32927919
|
C | T | 4 | a0001c0004t0001g0169a0001c0004t0001g0174a0004c0006t0009g0141others(1): Show | 4 | HG00639.hp1 HG02027.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1030-935G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927919 | ||||||
| chr19:32927920
|
T | C | 6 | a0001c0002t0001g0020a0001c0002t0001g0063a0001c0004t0001g0205others(3): Show | 6 | HG01257.hp2 HG02897.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.1030-936A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927920 | ||||||
| chr19:32927934
|
T | C | 3 | a0001c0004t0001g0074a0001c0004t0001g0171a0001c0004t0001g0198 | 3 | NA18954.hp1 NA19010.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1030-950A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32927934 | ||||||
| chr19:32928035
|
C | T | 1 | a0001c0002t0010g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1030-1051G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32928035 | ||||||
| chr19:32928340
|
G | A | 44 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(41): Show | 44 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.1030-1356C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32928340 | ||||||
| chr19:32928477
|
C | A | 1 | a0001c0004t0001g0172 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1030-1493G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32928477 | ||||||
| chr19:32928504
|
A | G | 30 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(27): Show | 30 | HG00280.hp2 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1030-1520T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32928504 | ||||||
| chr19:32928522
|
T | C | 1 | a0010c0020t0003g0122 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1030-1538A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32928522 | ||||||
| chr19:32928622
|
C | A | 1 | a0001c0002t0024g0072 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1030-1638G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32928622 | ||||||
| chr19:32928654
|
C | G | 153 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(150): Show | 157 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1030-1670G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32928654 | ||||||
| chr19:32928664
|
C | T | 1 | a0006c0009t0011g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1030-1680G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32928664 | ||||||
| chr19:32928773
|
C | T | 2 | a0001c0002t0024g0072a0001c0002t0043g0118 | 2 | HG01123.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1030-1789G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32928773 | ||||||
| chr19:32929330
|
G | A | 3 | a0007c0011t0012g0375a0007c0011t0012g0379a0007c0011t0012g0380 | 3 | HG02630.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1029+2099C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32929330 | ||||||
| chr19:32929475
|
G | A | 1 | a0002c0001t0002g0161 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1029+1954C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32929475 | ||||||
| chr19:32929559
|
G | A | 90 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(87): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1029+1870C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32929559 | ||||||
| chr19:32929577
|
T | C | 1 | a0004c0006t0007g0131 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1029+1852A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32929577 | ||||||
| chr19:32929601
|
T | TA | 83 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0005others(80): Show | 84 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1029+1827dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32929601 | ||||||
| chr19:32929601
|
TA | T | 11 | a0001c0002t0001g0017a0001c0002t0001g0025a0002c0001t0002g0073others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1029+1827delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32929601 | ||||||
| chr19:32929613
|
A | AG | 3 | a0006c0009t0011g0123a0006c0009t0011g0124a0006c0009t0011g0125 | 3 | HG02717.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1029+1815_1029+181 others(5): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32929613 | ||||||
| chr19:32929982
|
G | A | 1 | a0003c0003t0003g0250 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1029+1447C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32929982 | ||||||
| chr19:32930007
|
C | CTTCCTTT others(3): Show |
1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1029+1412_1029+142 others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32930007 | ||||||
| chr19:32930021
|
C | CT | 13 | a0000c0005t0005g0102a0000c0005t0005g0106a0000c0007t0004g0275others(10): Show | 13 | HG00438.hp2 HG00642.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1029+1407dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32930021 | ||||||
| chr19:32930021
|
CT | C | 7 | a0001c0002t0024g0072a0002c0001t0002g0309a0002c0001t0002g0310others(4): Show | 7 | HG01123.hp2 HG01175.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1029+1407delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32930021 | ||||||
| chr19:32930034
|
T | A | 69 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(66): Show | 69 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1029+1395A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32930034 | ||||||
| chr19:32930231
|
T | G | 12 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1029+1198A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32930231 | ||||||
| chr19:32930251
|
C | T | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1029+1178G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32930251 | ||||||
| chr19:32930580
|
T | C | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1029+849A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32930580 | ||||||
| chr19:32930621
|
CTG | C | 3 | a0006c0009t0011g0123a0006c0009t0011g0124a0006c0009t0011g0125 | 3 | HG02717.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1029+806_1029+807d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32930621 | ||||||
| chr19:32930708
|
G | A | 16 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(13): Show | 16 | HG00609.hp1 HG02129.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.1029+721C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32930708 | ||||||
| chr19:32930833
|
A | T | 1 | a0004c0006t0007g0132 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1029+596T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32930833 | ||||||
| chr19:32930886
|
A | AT | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1029+542dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32930886 | ||||||
| chr19:32930896
|
T | A | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1029+533A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32930896 | ||||||
| chr19:32930963
|
A | G | 247 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(244): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1029+466T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32930963 | ||||||
| chr19:32931092
|
GT | G | 90 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(87): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1029+336delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32931092 | ||||||
| chr19:32931228
|
T | A | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1029+201A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32931228 | ||||||
| chr19:32931251
|
C | T | 1 | a0001c0004t0001g0203 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1029+178G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 9/18 | chr19 | 32931251 | ||||||
| chr19:32931710
|
G | T | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.887-139C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32931710 | ||||||
| chr19:32931725
|
T | C | 2 | a0000c0005t0005g0115a0000c0005t0005g0117 | 2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.887-154A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32931725 | ||||||
| chr19:32931751
|
C | T | 8 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0040others(5): Show | 8 | HG00597.hp1 NA18942.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.887-180G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32931751 | ||||||
| chr19:32931775
|
C | T | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.887-204G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32931775 | ||||||
| chr19:32931785
|
A | G | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.887-214T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32931785 | ||||||
| chr19:32931910
|
G | A | 3 | a0007c0011t0012g0375a0007c0011t0012g0379a0007c0011t0012g0380 | 3 | HG02630.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.887-339C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32931910 | ||||||
| chr19:32932182
|
C | CA | 66 | a0003c0003t0002g0265a0003c0003t0003g0003a0003c0003t0003g0077others(63): Show | 67 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.887-612dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32932182 | ||||||
| chr19:32932192
|
A | G | 1 | a0000c0005t0005g0103 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.887-621T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32932192 | ||||||
| chr19:32932207
|
A | C | 1 | a0000c0005t0005g0116 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.887-636T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32932207 | ||||||
| chr19:32932238
|
G | T | 3 | a0006c0009t0011g0123a0006c0009t0011g0124a0006c0009t0011g0125 | 3 | HG02717.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.887-667C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32932238 | ||||||
| chr19:32932303
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.887-732T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32932303 | ||||||
| chr19:32932443
|
A | C | 1 | a0002c0001t0002g0334 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.887-872T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32932443 | ||||||
| chr19:32932596
|
T | C | 144 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(141): Show | 148 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.886+855A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32932596 | ||||||
| chr19:32932661
|
C | A | 2 | a0000c0005t0005g0115a0000c0005t0005g0117 | 2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.886+790G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32932661 | ||||||
| chr19:32932785
|
TA | T | 91 | a0001c0002t0001g0045a0002c0001t0001g0332a0002c0001t0001g0350others(88): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.886+665delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32932785 | ||||||
| chr19:32932799
|
A | C | 1 | a0007c0011t0012g0375 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.886+652T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32932799 | ||||||
| chr19:32932819
|
G | A | 69 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0002g0265others(66): Show | 70 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.886+632C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32932819 | ||||||
| chr19:32933002
|
C | G | 1 | a0002c0001t0002g0313 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.886+449G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32933002 | ||||||
| chr19:32933010
|
G | T | 2 | a0002c0001t0002g0309a0002c0001t0002g0310 | 2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.886+441C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32933010 | ||||||
| chr19:32933063
|
AT | A | 144 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(141): Show | 148 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.886+387delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32933063 | ||||||
| chr19:32933107
|
T | G | 1 | a0001c0002t0043g0118 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.886+344A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32933107 | ||||||
| chr19:32933120
|
G | A | 12 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.886+331C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32933120 | ||||||
| chr19:32933178
|
G | A | 3 | a0007c0011t0012g0375a0007c0011t0012g0379a0007c0011t0012g0380 | 3 | HG02630.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.886+273C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32933178 | ||||||
| chr19:32933381
|
T | C | 1 | a0003c0010t0014g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.886+70A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 8/18 | chr19 | 32933381 | ||||||
| chr19:32934045
|
G | A | 2 | a0004c0006t0007g0129a0004c0006t0007g0134 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.668-376C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32934045 | ||||||
| chr19:32934142
|
C | T | 1 | a0003c0003t0003g0260 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.668-473G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32934142 | ||||||
| chr19:32934186
|
GT | G | 144 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(141): Show | 148 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.668-518delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32934186 | ||||||
| chr19:32934754
|
T | C | 1 | a0002c0001t0002g0334 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.668-1085A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32934754 | ||||||
| chr19:32934855
|
G | A | 29 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.668-1186C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32934855 | ||||||
| chr19:32934911
|
G | A | 1 | a0001c0002t0001g0061 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.668-1242C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32934911 | ||||||
| chr19:32935040
|
G | C | 1 | a0001c0002t0016g0023 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.668-1371C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32935040 | ||||||
| chr19:32935243
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.668-1574C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32935243 | ||||||
| chr19:32935456
|
A | G | 52 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.668-1787T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32935456 | ||||||
| chr19:32935631
|
C | T | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.668-1962G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32935631 | ||||||
| chr19:32935704
|
C | T | 69 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(66): Show | 69 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.667+1927G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32935704 | ||||||
| chr19:32935853
|
C | G | 74 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(71): Show | 77 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.667+1778G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32935853 | ||||||
| chr19:32936105
|
C | T | 1 | a0003c0003t0003g0253 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.667+1526G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32936105 | ||||||
| chr19:32936199
|
G | A | 1 | a0000c0007t0004g0291 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.667+1432C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32936199 | ||||||
| chr19:32936290
|
C | T | 4 | a0002c0001t0002g0309a0002c0001t0002g0310a0002c0001t0025g0148others(1): Show | 4 | HG01175.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+1341G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32936290 | ||||||
| chr19:32936388
|
G | T | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+1243C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32936388 | ||||||
| chr19:32936402
|
G | T | 144 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(141): Show | 148 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.667+1229C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32936402 | ||||||
| chr19:32936419
|
G | A | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.667+1212C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32936419 | ||||||
| chr19:32936578
|
A | G | 52 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.667+1053T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32936578 | ||||||
| chr19:32936628
|
T | C | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.667+1003A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32936628 | ||||||
| chr19:32936800
|
T | C | 1 | a0003c0003t0003g0249 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.667+831A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32936800 | ||||||
| chr19:32936927
|
G | A | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.667+704C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32936927 | ||||||
| chr19:32937077
|
G | A | 23 | a0003c0010t0014g0168a0003c0010t0014g0366a0004c0006t0007g0086others(20): Show | 23 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.667+554C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32937077 | ||||||
| chr19:32937260
|
T | G | 235 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(232): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.667+371A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32937260 | ||||||
| chr19:32937374
|
C | T | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+257G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32937374 | ||||||
| chr19:32937444
|
C | T | 144 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(141): Show | 148 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.667+187G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32937444 | ||||||
| chr19:32937517
|
G | T | 144 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(141): Show | 148 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.667+114C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 7/18 | chr19 | 32937517 | ||||||
| chr19:32938002
|
AT | A | 147 | a0000c0005t0005g0102a0001c0002t0010g0149a0001c0004t0001g0074others(144): Show | 148 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.625-330delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32938002 | ||||||
| chr19:32938002
|
ATT | A | 146 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(143): Show | 148 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.625-331_625-330del others(2): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32938002 | ||||||
| chr19:32938002
|
ATTT | A | 60 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(57): Show | 63 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.625-332_625-330del others(3): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32938002 | ||||||
| chr19:32938091
|
G | T | 2 | a0002c0001t0002g0352a0002c0001t0002g0353 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.625-418C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32938091 | ||||||
| chr19:32938563
|
C | T | 1 | a0000c0007t0004g0078 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.625-890G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32938563 | ||||||
| chr19:32938582
|
T | C | 1 | a0000c0005t0005g0104 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.625-909A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32938582 | ||||||
| chr19:32938901
|
G | A | 1 | a0000c0007t0004g0277 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.624+956C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32938901 | ||||||
| chr19:32939077
|
T | A | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.624+780A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32939077 | ||||||
| chr19:32939182
|
T | C | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.624+675A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32939182 | ||||||
| chr19:32939487
|
G | A | 5 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0301others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.624+370C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32939487 | ||||||
| chr19:32939557
|
G | A | 1 | a0001c0004t0001g0172 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.624+300C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32939557 | ||||||
| chr19:32939571
|
G | A | 1 | a0003c0003t0003g0241 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.624+286C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32939571 | ||||||
| chr19:32939590
|
A | T | 3 | a0002c0001t0008g0012a0002c0001t0008g0013a0002c0001t0008g0014 | 3 | NA18995.hp1 NA19079.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.624+267T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32939590 | ||||||
| chr19:32939676
|
CA | C | 143 | a0000c0007t0004g0282a0000c0012t0004g0065a0000c0012t0021g0015others(140): Show | 147 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.624+180delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32939676 | ||||||
| chr19:32939707
|
T | G | 1 | a0001c0004t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.624+150A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32939707 | ||||||
| chr19:32939722
|
C | T | 12 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.624+135G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32939722 | ||||||
| chr19:32939758
|
C | T | 1 | a0003c0003t0013g0271 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.624+99G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32939758 | ||||||
| chr19:32939840
|
A | T | 28 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.624+17T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 6/18 | chr19 | 32939840 | ||||||
| chr19:32939910
|
T | G | 235 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(232): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.596-25A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32939910 | ||||||
| chr19:32939942
|
A | G | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.596-57T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32939942 | ||||||
| chr19:32940254
|
T | C | 1 | a0002c0001t0002g0311 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.596-369A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32940254 | ||||||
| chr19:32940266
|
C | T | 74 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(71): Show | 77 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.596-381G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32940266 | ||||||
| chr19:32940267
|
G | T | 1 | a0002c0001t0002g0311 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.596-382C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32940267 | ||||||
| chr19:32940271
|
T | C | 1 | a0002c0001t0002g0311 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.596-386A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32940271 | ||||||
| chr19:32940273
|
T | C | 374 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(371): Show | 380 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(377): Show |
intron_variant | MODIFIER | c.596-388A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32940273 | ||||||
| chr19:32940332
|
C | T | 3 | a0007c0011t0012g0375a0007c0011t0012g0379a0007c0011t0012g0380 | 3 | HG02630.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.596-447G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32940332 | ||||||
| chr19:32940536
|
G | A | 1 | a0001c0004t0001g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.596-651C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32940536 | ||||||
| chr19:32940577
|
T | G | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.596-692A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32940577 | ||||||
| chr19:32940765
|
C | CT | 11 | a0001c0002t0001g0027a0001c0002t0001g0028a0002c0001t0002g0316others(8): Show | 11 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.596-881dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32940765 | ||||||
| chr19:32940784
|
C | T | 6 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(3): Show | 6 | HG02809.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-899G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32940784 | ||||||
| chr19:32940785
|
G | A | 23 | a0003c0010t0014g0168a0003c0010t0014g0366a0004c0006t0007g0086others(20): Show | 23 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.596-900C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32940785 | ||||||
| chr19:32940820
|
G | A | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.596-935C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32940820 | ||||||
| chr19:32940909
|
C | T | 90 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(87): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.596-1024G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32940909 | ||||||
| chr19:32941116
|
A | C | 52 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.596-1231T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32941116 | ||||||
| chr19:32941313
|
G | T | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.596-1428C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32941313 | ||||||
| chr19:32941360
|
G | A | 12 | a0001c0002t0001g0296a0001c0002t0001g0297a0001c0002t0001g0298others(9): Show | 12 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.596-1475C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32941360 | ||||||
| chr19:32941560
|
G | A | 1 | a0004c0006t0007g0133 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.596-1675C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32941560 | ||||||
| chr19:32941760
|
T | C | 1 | a0001c0002t0010g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.596-1875A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32941760 | ||||||
| chr19:32941788
|
G | A | 16 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(13): Show | 16 | HG02055.hp1 HG02145.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.596-1903C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32941788 | ||||||
| chr19:32941803
|
T | C | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.596-1918A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32941803 | ||||||
| chr19:32941843
|
G | A | 1 | a0001c0002t0001g0038 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.596-1958C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32941843 | ||||||
| chr19:32941851
|
C | T | 1 | a0004c0006t0007g0133 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.596-1966G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32941851 | ||||||
| chr19:32941927
|
A | G | 1 | a0001c0002t0001g0030 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.596-2042T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32941927 | ||||||
| chr19:32941952
|
A | G | 1 | a0001c0002t0015g0044 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.596-2067T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32941952 | ||||||
| chr19:32942426
|
T | C | 7 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(4): Show | 7 | HG02630.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.596-2541A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32942426 | ||||||
| chr19:32942581
|
T | TAAAGATT others(327): Show |
1 | a0001c0004t0002g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.596-2697_596-2696i others(336): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32942581 | ||||||
| chr19:32942649
|
G | A | 63 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(60): Show | 66 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.596-2764C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32942649 | ||||||
| chr19:32942786
|
A | G | 90 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(87): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.596-2901T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32942786 | ||||||
| chr19:32942843
|
T | C | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.596-2958A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32942843 | ||||||
| chr19:32942849
|
C | CT | 26 | a0000c0007t0033g0295a0001c0002t0001g0029a0001c0002t0001g0057others(23): Show | 26 | HG00544.hp1 HG00544.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.596-2965dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32942849 | ||||||
| chr19:32942849
|
CT | C | 29 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.596-2965delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32942849 | ||||||
| chr19:32942895
|
G | C | 70 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0002g0265others(67): Show | 71 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.596-3010C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32942895 | ||||||
| chr19:32942939
|
G | A | 1 | a0000c0005t0041g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.596-3054C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32942939 | ||||||
| chr19:32942940
|
A | G | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.596-3055T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32942940 | ||||||
| chr19:32943164
|
T | C | 3 | a0007c0011t0012g0375a0007c0011t0012g0379a0007c0011t0012g0380 | 3 | HG02630.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.596-3279A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32943164 | ||||||
| chr19:32943220
|
T | C | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.596-3335A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32943220 | ||||||
| chr19:32943230
|
C | T | 16 | a0000c0007t0004g0078a0000c0007t0004g0281a0000c0007t0004g0282others(13): Show | 16 | HG02056.hp2 HG02132.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.596-3345G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32943230 | ||||||
| chr19:32943310
|
T | C | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.596-3425A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32943310 | ||||||
| chr19:32943340
|
C | T | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.596-3455G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32943340 | ||||||
| chr19:32943520
|
G | A | 1 | a0002c0001t0002g0314 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.596-3635C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32943520 | ||||||
| chr19:32943525
|
C | T | 63 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(60): Show | 66 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.596-3640G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32943525 | ||||||
| chr19:32943533
|
G | A | 1 | a0004c0006t0009g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.596-3648C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32943533 | ||||||
| chr19:32943735
|
G | C | 1 | a0003c0003t0036g0264 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.596-3850C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32943735 | ||||||
| chr19:32943790
|
A | G | 1 | a0001c0002t0001g0085 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.596-3905T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32943790 | ||||||
| chr19:32943957
|
G | T | 1 | a0001c0002t0024g0072 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.596-4072C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32943957 | ||||||
| chr19:32944155
|
T | C | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.595+4111A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944155 | ||||||
| chr19:32944164
|
C | T | 3 | a0000c0007t0004g0278a0000c0007t0004g0279a0000c0007t0004g0280 | 3 | HG00099.hp1 HG01123.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.595+4102G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944164 | ||||||
| chr19:32944205
|
C | G | 1 | a0001c0004t0001g0176 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.595+4061G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944205 | ||||||
| chr19:32944218
|
T | C | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.595+4048A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944218 | ||||||
| chr19:32944220
|
T | TAAAAAAA others(1): Show |
21 | a0001c0004t0001g0186a0003c0010t0014g0168a0003c0010t0014g0366others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.595+4038_595+4045d others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944220 | ||||||
| chr19:32944220
|
T | TAAAAAAA others(2): Show |
38 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(35): Show | 38 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.595+4037_595+4045d others(11): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944220 | ||||||
| chr19:32944220
|
T | TAAAAAAA others(3): Show |
16 | a0000c0005t0023g0079a0001c0004t0001g0174a0001c0004t0001g0182others(13): Show | 16 | HG00673.hp2 HG01257.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.595+4036_595+4045d others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944220 | ||||||
| chr19:32944220
|
T | TAAAAAAA others(4): Show |
75 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(72): Show | 77 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.595+4035_595+4045d others(13): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944220 | ||||||
| chr19:32944220
|
T | TAAAAAAA others(5): Show |
20 | a0002c0001t0002g0159a0002c0001t0002g0160a0002c0001t0002g0161others(17): Show | 20 | HG02027.hp2 HG02040.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.595+4034_595+4045d others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944220 | ||||||
| chr19:32944220
|
T | TAAAAAAA others(9): Show |
4 | a0001c0002t0010g0149a0002c0001t0002g0309a0002c0001t0025g0148others(1): Show | 4 | HG01175.hp2 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+4030_595+4045d others(18): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944220 | ||||||
| chr19:32944220
|
T | TAAAAAAA others(10): Show |
4 | a0001c0002t0010g0377a0001c0002t0010g0378a0002c0001t0002g0310others(1): Show | 4 | HG02630.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+4029_595+4045d others(19): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944220 | ||||||
| chr19:32944220
|
T | TAAAAAAA others(11): Show |
2 | a0001c0002t0010g0376a0007c0011t0012g0379 | 2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.595+4045_595+4046i others(20): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944220 | ||||||
| chr19:32944220
|
T | TAAAAAAA others(13): Show |
3 | a0006c0009t0011g0123a0006c0009t0011g0124a0006c0009t0011g0125 | 3 | HG02717.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.595+4045_595+4046i others(22): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944220 | ||||||
| chr19:32944220
|
T | TAAAAAAA others(14): Show |
13 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0102others(10): Show | 13 | HG00099.hp2 HG00738.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.595+4045_595+4046i others(23): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944220 | ||||||
| chr19:32944220
|
T | TAAAAAAA others(15): Show |
12 | a0000c0005t0005g0099a0000c0005t0005g0100a0000c0005t0005g0103others(9): Show | 12 | HG00280.hp2 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.595+4045_595+4046i others(24): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944220 | ||||||
| chr19:32944220
|
T | TAAAAAAA others(16): Show |
1 | a0000c0005t0005g0101 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.595+4045_595+4046i others(25): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944220 | ||||||
| chr19:32944220
|
T | TAAAAAAA others(17): Show |
1 | a0000c0005t0005g0164 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.595+4045_595+4046i others(26): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944220 | ||||||
| chr19:32944235
|
A | G | 2 | a0004c0006t0007g0129a0004c0006t0007g0134 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.595+4031T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944235 | ||||||
| chr19:32944237
|
AG | A | 134 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(131): Show | 138 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.595+4028delC | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944237 | ||||||
| chr19:32944238
|
G | A | 78 | a0001c0002t0001g0027a0001c0002t0001g0041a0001c0002t0001g0057others(75): Show | 78 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.595+4028C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944238 | ||||||
| chr19:32944240
|
C | G | 69 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(66): Show | 69 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.595+4026G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944240 | ||||||
| chr19:32944241
|
T | A | 69 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(66): Show | 69 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.595+4025A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944241 | ||||||
| chr19:32944281
|
G | T | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.595+3985C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944281 | ||||||
| chr19:32944286
|
A | G | 1 | a0003c0003t0038g0229 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.595+3980T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944286 | ||||||
| chr19:32944540
|
T | C | 1 | a0001c0002t0001g0056 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.595+3726A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944540 | ||||||
| chr19:32944670
|
AG | A | 23 | a0003c0010t0014g0168a0003c0010t0014g0366a0004c0006t0007g0086others(20): Show | 23 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.595+3595delC | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944670 | ||||||
| chr19:32944859
|
A | G | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.595+3407T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944859 | ||||||
| chr19:32944903
|
G | T | 1 | a0001c0004t0001g0200 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.595+3363C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32944903 | ||||||
| chr19:32945051
|
C | T | 3 | a0004c0006t0007g0086a0004c0006t0007g0133a0009c0023t0007g0130 | 3 | HG02129.hp1 NA18961.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.595+3215G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945051 | ||||||
| chr19:32945133
|
A | C | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.595+3133T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945133 | ||||||
| chr19:32945199
|
G | A | 1 | a0005c0008t0006g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.595+3067C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945199 | ||||||
| chr19:32945200
|
C | G | 1 | a0005c0008t0006g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.595+3066G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945200 | ||||||
| chr19:32945215
|
C | T | 90 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(87): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.595+3051G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945215 | ||||||
| chr19:32945284
|
C | CA | 72 | a0000c0007t0004g0281a0000c0007t0004g0293a0000c0007t0033g0295others(69): Show | 72 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.595+2981dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945284 | ||||||
| chr19:32945284
|
CA | C | 163 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(160): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.595+2981delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945284 | ||||||
| chr19:32945284
|
CAA | C | 16 | a0001c0002t0001g0031a0001c0002t0001g0068a0001c0002t0001g0082others(13): Show | 16 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.595+2980_595+2981d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945284 | ||||||
| chr19:32945381
|
G | A | 74 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(71): Show | 77 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.595+2885C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945381 | ||||||
| chr19:32945461
|
G | A | 68 | a0003c0003t0002g0265a0003c0003t0003g0003a0003c0003t0003g0077others(65): Show | 69 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.595+2805C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945461 | ||||||
| chr19:32945484
|
C | T | 74 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(71): Show | 77 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.595+2782G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945484 | ||||||
| chr19:32945580
|
G | A | 1 | a0003c0003t0003g0249 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.595+2686C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945580 | ||||||
| chr19:32945670
|
T | A | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.595+2596A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945670 | ||||||
| chr19:32945781
|
A | G | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.595+2485T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945781 | ||||||
| chr19:32945835
|
C | T | 74 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(71): Show | 77 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.595+2431G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945835 | ||||||
| chr19:32945915
|
C | T | 2 | a0001c0002t0001g0042a0001c0002t0001g0043 | 2 | NA19081.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.595+2351G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32945915 | ||||||
| chr19:32946104
|
T | C | 1 | a0014c0022t0001g0196 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.595+2162A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32946104 | ||||||
| chr19:32946347
|
G | A | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.595+1919C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32946347 | ||||||
| chr19:32946383
|
T | C | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.595+1883A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32946383 | ||||||
| chr19:32946422
|
G | A | 9 | a0003c0003t0003g0080a0003c0003t0003g0212a0003c0003t0003g0213others(6): Show | 9 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.595+1844C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32946422 | ||||||
| chr19:32946571
|
G | C | 90 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(87): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.595+1695C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32946571 | ||||||
| chr19:32946729
|
G | A | 2 | a0001c0004t0001g0166a0001c0004t0001g0167 | 2 | HG00544.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.595+1537C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32946729 | ||||||
| chr19:32946768
|
T | C | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.595+1498A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32946768 | ||||||
| chr19:32946933
|
A | AT | 146 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(143): Show | 150 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.595+1332dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32946933 | ||||||
| chr19:32946982
|
C | T | 3 | a0001c0002t0010g0376a0001c0002t0010g0377a0001c0002t0010g0378 | 3 | HG02922.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.595+1284G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32946982 | ||||||
| chr19:32947102
|
C | A | 2 | a0002c0001t0002g0309a0002c0001t0002g0310 | 2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.595+1164G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32947102 | ||||||
| chr19:32947133
|
T | C | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.595+1133A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32947133 | ||||||
| chr19:32947302
|
G | C | 1 | a0000c0005t0005g0108 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.595+964C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32947302 | ||||||
| chr19:32947426
|
CA | C | 146 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(143): Show | 150 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.595+839delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32947426 | ||||||
| chr19:32947568
|
G | A | 50 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(47): Show | 50 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.595+698C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32947568 | ||||||
| chr19:32947604
|
C | T | 1 | a0000c0007t0004g0285 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.595+662G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32947604 | ||||||
| chr19:32947833
|
T | A | 1 | a0001c0004t0001g0183 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.595+433A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32947833 | ||||||
| chr19:32947856
|
AATGGTGC others(14): Show |
A | 1 | a0003c0003t0013g0272 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.595+389_595+409del others(21): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32947856 | ||||||
| chr19:32947987
|
T | C | 1 | a0005c0008t0006g0093 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.595+279A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32947987 | ||||||
| chr19:32948252
|
T | C | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.595+14A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32948252 | ||||||
| chr19:32948261
|
T | C | 1 | a0001c0002t0031g0053 | 1 | NA18947.hp1 | splice_region_variant&intron_variant | LOW | c.595+5A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 5/18 | chr19 | 32948261 | ||||||
| chr19:32948376
|
T | G | 1 | a0001c0002t0024g0072 | 1 | HG01123.hp2 | splice_region_variant&intron_variant | LOW | c.493-8A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32948376 | ||||||
| chr19:32948484
|
C | T | 46 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(43): Show | 46 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.493-116G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32948484 | ||||||
| chr19:32948579
|
G | A | 70 | a0001c0002t0024g0072a0001c0002t0043g0118a0003c0003t0002g0265others(67): Show | 71 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.493-211C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32948579 | ||||||
| chr19:32948632
|
C | A | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-264G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32948632 | ||||||
| chr19:32948643
|
C | A | 4 | a0002c0001t0002g0321a0002c0001t0002g0329a0002c0001t0002g0330others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-275G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32948643 | ||||||
| chr19:32948688
|
C | T | 1 | a0003c0003t0013g0271 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.493-320G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32948688 | ||||||
| chr19:32948733
|
C | T | 1 | a0003c0010t0014g0366 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.493-365G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32948733 | ||||||
| chr19:32948742
|
T | C | 2 | a0000c0005t0005g0115a0000c0005t0005g0117 | 2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.493-374A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32948742 | ||||||
| chr19:32949029
|
G | A | 1 | a0001c0002t0001g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.493-661C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32949029 | ||||||
| chr19:32949185
|
C | T | 2 | a0001c0002t0001g0037a0001c0002t0001g0038 | 2 | HG02080.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.493-817G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32949185 | ||||||
| chr19:32949257
|
C | T | 1 | a0003c0003t0003g0249 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.493-889G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32949257 | ||||||
| chr19:32949293
|
C | T | 90 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(87): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.493-925G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32949293 | ||||||
| chr19:32949446
|
C | T | 63 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(60): Show | 66 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.493-1078G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32949446 | ||||||
| chr19:32949473
|
C | T | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-1105G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32949473 | ||||||
| chr19:32949562
|
T | G | 2 | a0001c0002t0024g0072a0001c0002t0043g0118 | 2 | HG01123.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.493-1194A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32949562 | ||||||
| chr19:32949594
|
G | A | 1 | a0003c0003t0002g0265 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.493-1226C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32949594 | ||||||
| chr19:32949635
|
T | C | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.493-1267A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32949635 | ||||||
| chr19:32949692
|
T | G | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.493-1324A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32949692 | ||||||
| chr19:32949891
|
G | A | 1 | a0008c0015t0001g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.493-1523C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32949891 | ||||||
| chr19:32949911
|
G | A | 15 | a0002c0001t0002g0150a0002c0001t0002g0151a0002c0001t0002g0152others(12): Show | 15 | HG00544.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.493-1543C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32949911 | ||||||
| chr19:32950020
|
C | CT | 7 | a0002c0001t0002g0325a0003c0003t0002g0265a0003c0003t0003g0077others(4): Show | 7 | HG00140.hp2 HG01258.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.493-1653dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32950020 | ||||||
| chr19:32950020
|
CT | C | 12 | a0000c0005t0023g0079a0001c0002t0001g0068a0001c0002t0010g0149others(9): Show | 12 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.493-1653delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32950020 | ||||||
| chr19:32950057
|
G | A | 1 | a0006c0009t0011g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.493-1689C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32950057 | ||||||
| chr19:32950324
|
T | C | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.493-1956A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32950324 | ||||||
| chr19:32950413
|
C | G | 1 | a0002c0001t0002g0331 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.493-2045G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32950413 | ||||||
| chr19:32950649
|
A | G | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.493-2281T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32950649 | ||||||
| chr19:32950666
|
A | C | 1 | a0000c0005t0005g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.493-2298T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32950666 | ||||||
| chr19:32950818
|
G | A | 42 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0169others(39): Show | 42 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.493-2450C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32950818 | ||||||
| chr19:32950901
|
T | C | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.493-2533A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32950901 | ||||||
| chr19:32951029
|
T | G | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.492+2586A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951029 | ||||||
| chr19:32951096
|
A | C | 145 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(142): Show | 149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.492+2519T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951096 | ||||||
| chr19:32951107
|
T | C | 68 | a0003c0003t0002g0265a0003c0003t0003g0003a0003c0003t0003g0077others(65): Show | 69 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.492+2508A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951107 | ||||||
| chr19:32951511
|
TTA | T | 6 | a0000c0007t0004g0278a0000c0007t0004g0279a0002c0001t0002g0326others(3): Show | 6 | HG00099.hp1 HG01123.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.492+2102_492+2103d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951511 | ||||||
| chr19:32951511
|
TTATA | T | 64 | a0000c0005t0023g0079a0002c0001t0001g0332a0002c0001t0001g0350others(61): Show | 65 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.492+2100_492+2103d others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951511 | ||||||
| chr19:32951511
|
TTATATAT others(3): Show |
T | 4 | a0003c0003t0003g0221a0003c0003t0003g0244a0003c0003t0003g0245others(1): Show | 4 | HG01515.hp2 HG01517.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+2094_492+2103d others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951511 | ||||||
| chr19:32951511
|
TTATATAT others(5): Show |
T | 59 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0037others(56): Show | 60 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.492+2092_492+2103d others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951511 | ||||||
| chr19:32951511
|
TTATATAT others(7): Show |
T | 72 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(69): Show | 75 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.492+2090_492+2103d others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951511 | ||||||
| chr19:32951511
|
TTATATAT others(9): Show |
T | 1 | a0001c0002t0001g0062 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.492+2088_492+2103d others(18): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951511 | ||||||
| chr19:32951520
|
TATATATA others(9): Show |
T | 7 | a0000c0012t0021g0015a0003c0003t0003g0212a0003c0003t0003g0213others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.492+2079_492+2094d others(18): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951520 | ||||||
| chr19:32951530
|
T | C | 1 | a0003c0003t0003g0248 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.492+2085A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951530 | ||||||
| chr19:32951530
|
T | TACAC | 5 | a0001c0004t0001g0186a0001c0004t0001g0187a0001c0004t0001g0188others(2): Show | 5 | HG02622.hp2 NA18962.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+2084_492+2085i others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951530 | ||||||
| chr19:32951530
|
T | TACACACA others(3): Show |
1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.492+2084_492+2085i others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951530 | ||||||
| chr19:32951532
|
T | C | 30 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0037others(27): Show | 30 | HG00280.hp1 HG01109.hp2 HG01515.hp2 others(27): Show |
intron_variant | MODIFIER | c.492+2083A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951532 | ||||||
| chr19:32951532
|
T | TAC | 4 | a0001c0004t0001g0167a0001c0004t0001g0202a0002c0001t0025g0148others(1): Show | 4 | HG00423.hp1 HG00544.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+2082_492+2083i others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951532 | ||||||
| chr19:32951532
|
T | TACAC | 29 | a0000c0005t0005g0106a0000c0005t0042g0109a0001c0004t0001g0145others(26): Show | 29 | HG00323.hp2 HG00408.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.492+2082_492+2083i others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951532 | ||||||
| chr19:32951532
|
T | TACACAC | 8 | a0000c0005t0005g0268a0000c0005t0005g0269a0001c0004t0001g0075others(5): Show | 8 | HG00642.hp2 HG01081.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.492+2082_492+2083i others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951532 | ||||||
| chr19:32951532
|
T | TACACACA others(1): Show |
3 | a0001c0004t0001g0074a0001c0004t0001g0171a0001c0004t0001g0199 | 3 | HG01978.hp1 NA18954.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.492+2082_492+2083i others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951532 | ||||||
| chr19:32951532
|
TATAC | T | 11 | a0001c0004t0001g0169a0002c0001t0002g0004a0002c0001t0002g0073others(8): Show | 12 | HG00639.hp1 HG01884.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.492+2079_492+2082d others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951532 | ||||||
| chr19:32951534
|
T | C | 196 | a0000c0005t0005g0106a0000c0005t0005g0268a0000c0005t0005g0269others(193): Show | 200 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.492+2081A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TAC | 15 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0007t0004g0078others(12): Show | 15 | HG01261.hp2 HG01516.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.492+2079_492+2080d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TACAC | 6 | a0000c0005t0005g0110a0000c0005t0019g0113a0000c0007t0004g0282others(3): Show | 6 | HG00280.hp2 HG02970.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.492+2077_492+2080d others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TACACAC | 14 | a0000c0005t0005g0099a0000c0005t0005g0100a0000c0005t0005g0102others(11): Show | 14 | HG00741.hp1 HG01243.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.492+2075_492+2080d others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TACACACA others(1): Show |
13 | a0000c0005t0005g0101a0000c0005t0005g0103a0000c0005t0005g0104others(10): Show | 13 | HG00738.hp2 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.492+2073_492+2080d others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TACACACA others(3): Show |
1 | a0005c0008t0006g0093 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.492+2071_492+2080d others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TATACAC | 3 | a0001c0004t0001g0170a0004c0006t0007g0135a0009c0023t0007g0130 | 3 | HG00609.hp1 NA18959.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.492+2080_492+2081i others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TATACACA others(3): Show |
3 | a0004c0006t0007g0132a0004c0006t0007g0147a0005c0008t0006g0092 | 3 | HG03139.hp2 NA20905.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.492+2080_492+2081i others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TATATACA others(1): Show |
6 | a0004c0006t0007g0086a0004c0006t0007g0131a0004c0006t0007g0133others(3): Show | 6 | HG02056.hp1 HG02129.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+2080_492+2081i others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TATATACA others(5): Show |
1 | a0007c0011t0012g0379 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.492+2080_492+2081i others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TATATATA others(5): Show |
2 | a0007c0011t0012g0375a0007c0011t0012g0380 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.492+2080_492+2081i others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TATATATA others(7): Show |
1 | a0001c0002t0010g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492+2080_492+2081i others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TATATATA others(15): Show |
4 | a0001c0002t0010g0377a0006c0009t0011g0123a0006c0009t0011g0124others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+2080_492+2081i others(24): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TATATATA others(15): Show |
1 | a0001c0002t0010g0376 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.492+2080_492+2081i others(24): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951534
|
T | TATATATA others(17): Show |
1 | a0001c0002t0010g0378 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.492+2080_492+2081i others(26): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951534 | ||||||
| chr19:32951567
|
G | A | 1 | a0004c0006t0007g0132 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.492+2048C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951567 | ||||||
| chr19:32951600
|
G | C | 68 | a0003c0003t0002g0265a0003c0003t0003g0003a0003c0003t0003g0077others(65): Show | 69 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.492+2015C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951600 | ||||||
| chr19:32951648
|
A | G | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.492+1967T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951648 | ||||||
| chr19:32951734
|
A | G | 2 | a0001c0004t0001g0191a0001c0004t0001g0192 | 2 | HG00673.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.492+1881T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951734 | ||||||
| chr19:32951775
|
T | C | 91 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(88): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.492+1840A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951775 | ||||||
| chr19:32951863
|
T | C | 1 | a0004c0006t0027g0140 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.492+1752A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951863 | ||||||
| chr19:32951959
|
G | A | 1 | a0003c0003t0003g0245 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.492+1656C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951959 | ||||||
| chr19:32951974
|
G | A | 23 | a0003c0010t0014g0168a0003c0010t0014g0366a0004c0006t0007g0086others(20): Show | 23 | HG00609.hp1 HG01106.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.492+1641C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951974 | ||||||
| chr19:32951978
|
A | G | 71 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(68): Show | 71 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.492+1637T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32951978 | ||||||
| chr19:32952034
|
T | C | 1 | a0001c0002t0001g0068 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.492+1581A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952034 | ||||||
| chr19:32952091
|
C | A | 3 | a0002c0001t0002g0367a0002c0001t0002g0368a0002c0001t0002g0369 | 3 | NA18963.hp2 NA18972.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.492+1524G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952091 | ||||||
| chr19:32952310
|
G | A | 2 | a0002c0001t0002g0309a0002c0001t0002g0310 | 2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.492+1305C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952310 | ||||||
| chr19:32952319
|
G | GA | 180 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(177): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.492+1295dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952319 | ||||||
| chr19:32952319
|
G | GAA | 6 | a0001c0002t0001g0028a0001c0002t0001g0061a0003c0003t0003g0219others(3): Show | 6 | HG02486.hp2 HG03688.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.492+1294_492+1295d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952319 | ||||||
| chr19:32952352
|
G | A | 3 | a0007c0011t0012g0375a0007c0011t0012g0379a0007c0011t0012g0380 | 3 | HG02630.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.492+1263C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952352 | ||||||
| chr19:32952373
|
C | T | 12 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.492+1242G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952373 | ||||||
| chr19:32952413
|
G | C | 5 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(2): Show | 5 | HG00741.hp1 HG01243.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.492+1202C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952413 | ||||||
| chr19:32952475
|
C | A | 74 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(71): Show | 77 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.492+1140G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952475 | ||||||
| chr19:32952482
|
TA | T | 94 | a0000c0005t0005g0097a0001c0002t0001g0002a0001c0002t0001g0033others(91): Show | 97 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.492+1132delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952482 | ||||||
| chr19:32952483
|
A | T | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.492+1132T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952483 | ||||||
| chr19:32952497
|
G | A | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.492+1118C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952497 | ||||||
| chr19:32952568
|
A | T | 90 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(87): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.492+1047T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952568 | ||||||
| chr19:32952661
|
T | G | 4 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+954A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952661 | ||||||
| chr19:32952698
|
G | A | 1 | a0001c0002t0001g0069 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.492+917C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952698 | ||||||
| chr19:32952709
|
G | A | 1 | a0004c0006t0026g0144 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.492+906C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952709 | ||||||
| chr19:32952795
|
T | C | 1 | a0008c0015t0001g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.492+820A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952795 | ||||||
| chr19:32952863
|
C | T | 1 | a0006c0009t0011g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.492+752G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952863 | ||||||
| chr19:32952899
|
G | T | 1 | a0002c0001t0002g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.492+716C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952899 | ||||||
| chr19:32952903
|
C | CA | 119 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(116): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.492+711dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952903 | ||||||
| chr19:32952903
|
C | CAA | 6 | a0000c0005t0005g0102a0000c0005t0005g0119a0000c0007t0004g0280others(3): Show | 6 | HG01358.hp1 HG01928.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.492+710_492+711dup others(2): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952903 | ||||||
| chr19:32952918
|
A | AAG | 6 | a0000c0012t0021g0015a0001c0002t0001g0027a0001c0002t0001g0057others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.492+696_492+697ins others(2): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952918 | ||||||
| chr19:32952918
|
A | AG | 144 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(141): Show | 148 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.492+696_492+697ins others(1): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952918 | ||||||
| chr19:32952918
|
A | G | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | NA19085.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.492+697T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952918 | ||||||
| chr19:32952920
|
A | G | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.492+695T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32952920 | ||||||
| chr19:32953103
|
G | C | 1 | a0003c0010t0014g0366 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.492+512C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32953103 | ||||||
| chr19:32953161
|
G | A | 151 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(148): Show | 155 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.492+454C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32953161 | ||||||
| chr19:32953249
|
G | A | 1 | a0008c0015t0001g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.492+366C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32953249 | ||||||
| chr19:32953550
|
A | G | 71 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(68): Show | 71 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.492+65T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32953550 | ||||||
| chr19:32953583
|
G | A | 1 | a0002c0001t0002g0315 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.492+32C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 4/18 | chr19 | 32953583 | ||||||
| chr19:32953862
|
A | G | 16 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(13): Show | 16 | HG02055.hp1 HG02145.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.306-61T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32953862 | ||||||
| chr19:32953867
|
CT | C | 103 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(100): Show | 103 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.306-67delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32953867 | ||||||
| chr19:32953867
|
CTT | C | 148 | a0000c0005t0005g0268a0000c0005t0005g0269a0000c0012t0004g0065others(145): Show | 152 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.306-68_306-67delAA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32953867 | ||||||
| chr19:32953970
|
G | A | 1 | a0008c0015t0001g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.306-169C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32953970 | ||||||
| chr19:32953982
|
C | T | 90 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(87): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.306-181G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32953982 | ||||||
| chr19:32954020
|
C | T | 2 | a0001c0002t0024g0072a0001c0002t0043g0118 | 2 | HG01123.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.306-219G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954020 | ||||||
| chr19:32954031
|
G | C | 1 | a0001c0004t0001g0170 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.306-230C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954031 | ||||||
| chr19:32954036
|
T | C | 71 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0005others(68): Show | 72 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.306-235A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954036 | ||||||
| chr19:32954162
|
T | C | 258 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(255): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.306-361A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954162 | ||||||
| chr19:32954174
|
G | A | 152 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(149): Show | 156 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.306-373C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954174 | ||||||
| chr19:32954194
|
T | C | 2 | a0001c0002t0024g0072a0001c0002t0043g0118 | 2 | HG01123.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.306-393A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954194 | ||||||
| chr19:32954328
|
A | C | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.306-527T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954328 | ||||||
| chr19:32954361
|
T | C | 2 | a0003c0003t0003g0248a0003c0003t0037g0247 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.306-560A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954361 | ||||||
| chr19:32954363
|
T | G | 2 | a0003c0003t0003g0248a0003c0003t0037g0247 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.306-562A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954363 | ||||||
| chr19:32954367
|
T | C | 12 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.306-566A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954367 | ||||||
| chr19:32954372
|
G | GT | 155 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(152): Show | 159 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.306-572dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954372 | ||||||
| chr19:32954534
|
G | A | 1 | a0001c0004t0001g0172 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.306-733C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954534 | ||||||
| chr19:32954555
|
G | A | 1 | a0001c0002t0001g0030 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.306-754C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954555 | ||||||
| chr19:32954586
|
C | G | 7 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(4): Show | 7 | HG02630.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.306-785G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954586 | ||||||
| chr19:32954590
|
G | T | 1 | a0008c0015t0001g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.306-789C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954590 | ||||||
| chr19:32954635
|
G | A | 1 | a0001c0002t0001g0038 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.306-834C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954635 | ||||||
| chr19:32954713
|
G | GGGT | 74 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(71): Show | 77 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.306-913_306-912ins others(3): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954713 | ||||||
| chr19:32954725
|
T | C | 152 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(149): Show | 156 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.306-924A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954725 | ||||||
| chr19:32954758
|
G | A | 1 | a0000c0005t0005g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.306-957C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954758 | ||||||
| chr19:32954827
|
G | GCTAATTT others(303): Show |
1 | a0000c0005t0019g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.306-1027_306-1026i others(312): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954827 | ||||||
| chr19:32954827
|
G | GCTAATTT others(306): Show |
1 | a0000c0005t0005g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.306-1027_306-1026i others(315): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954827 | ||||||
| chr19:32954827
|
G | GCTAATTT others(313): Show |
1 | a0000c0005t0005g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.306-1027_306-1026i others(322): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954827 | ||||||
| chr19:32954827
|
G | GCTAATTT others(328): Show |
1 | a0000c0005t0041g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.306-1027_306-1026i others(337): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954827 | ||||||
| chr19:32954827
|
G | GCTAATTT others(329): Show |
8 | a0000c0005t0005g0102a0000c0005t0005g0110a0000c0005t0005g0115others(5): Show | 8 | HG00099.hp2 HG00280.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.306-1027_306-1026i others(338): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954827 | ||||||
| chr19:32954827
|
G | GCTAATTT others(330): Show |
8 | a0000c0005t0005g0100a0000c0005t0005g0101a0000c0005t0005g0106others(5): Show | 8 | HG00741.hp1 HG01175.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.306-1027_306-1026i others(339): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954827 | ||||||
| chr19:32954827
|
G | GCTAATTT others(331): Show |
6 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0104others(3): Show | 6 | HG00738.hp2 HG01081.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.306-1027_306-1026i others(340): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954827 | ||||||
| chr19:32954827
|
G | GCTAATTT others(335): Show |
1 | a0000c0005t0005g0103 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.306-1027_306-1026i others(344): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32954827 | ||||||
| chr19:32955044
|
G | T | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.306-1243C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955044 | ||||||
| chr19:32955065
|
G | T | 12 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.306-1264C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955065 | ||||||
| chr19:32955076
|
C | T | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.306-1275G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955076 | ||||||
| chr19:32955333
|
A | G | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.306-1532T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955333 | ||||||
| chr19:32955379
|
T | G | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.306-1578A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955379 | ||||||
| chr19:32955391
|
G | GT | 4 | a0000c0012t0021g0015a0001c0004t0001g0199a0002c0001t0002g0163others(1): Show | 4 | HG01978.hp1 HG02257.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.306-1591dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955391 | ||||||
| chr19:32955511
|
T | C | 1 | a0001c0004t0001g0173 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.306-1710A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955511 | ||||||
| chr19:32955603
|
T | C | 1 | a0003c0003t0003g0249 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.306-1802A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955603 | ||||||
| chr19:32955606
|
C | T | 2 | a0002c0001t0008g0012a0002c0001t0008g0014 | 2 | NA18995.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.306-1805G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955606 | ||||||
| chr19:32955741
|
T | C | 68 | a0003c0003t0002g0265a0003c0003t0003g0003a0003c0003t0003g0077others(65): Show | 69 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.306-1940A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955741 | ||||||
| chr19:32955761
|
G | A | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.306-1960C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955761 | ||||||
| chr19:32955783
|
A | G | 152 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(149): Show | 156 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.306-1982T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955783 | ||||||
| chr19:32955785
|
G | A | 152 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(149): Show | 156 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.306-1984C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955785 | ||||||
| chr19:32955848
|
A | G | 152 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(149): Show | 156 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.306-2047T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955848 | ||||||
| chr19:32955959
|
C | A | 7 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(4): Show | 7 | HG02630.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.306-2158G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955959 | ||||||
| chr19:32955982
|
T | G | 1 | a0003c0003t0003g0365 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.306-2181A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32955982 | ||||||
| chr19:32956049
|
C | CT | 40 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(37): Show | 40 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.306-2249dupA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956049 | ||||||
| chr19:32956049
|
C | CTT | 14 | a0000c0005t0005g0100a0000c0005t0005g0101a0000c0005t0005g0102others(11): Show | 14 | HG02717.hp1 HG02723.hp2 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.306-2250_306-2249d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956049 | ||||||
| chr19:32956049
|
CT | C | 22 | a0000c0007t0004g0078a0000c0007t0004g0281a0000c0007t0004g0282others(19): Show | 22 | HG00323.hp1 HG01169.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.306-2249delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956049 | ||||||
| chr19:32956049
|
CTTTTTTT others(3): Show |
C | 151 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(148): Show | 155 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.306-2258_306-2249d others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956049 | ||||||
| chr19:32956095
|
C | A | 3 | a0000c0007t0004g0078a0000c0007t0004g0293a0003c0013t0003g0292 | 3 | NA18945.hp2 NA18949.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.306-2294G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956095 | ||||||
| chr19:32956115
|
G | T | 4 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.306-2314C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956115 | ||||||
| chr19:32956130
|
A | G | 1 | a0002c0001t0002g0319 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.306-2329T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956130 | ||||||
| chr19:32956149
|
G | A | 152 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(149): Show | 156 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.306-2348C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956149 | ||||||
| chr19:32956212
|
C | T | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.306-2411G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956212 | ||||||
| chr19:32956244
|
C | T | 1 | a0003c0003t0034g0076 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.306-2443G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956244 | ||||||
| chr19:32956343
|
C | T | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.306-2542G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956343 | ||||||
| chr19:32956350
|
G | A | 12 | a0004c0006t0007g0086a0004c0006t0007g0128a0004c0006t0007g0129others(9): Show | 12 | HG00609.hp1 HG02129.hp1 HG03490.hp2 others(9): Show |
intron_variant | MODIFIER | c.306-2549C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956350 | ||||||
| chr19:32956522
|
G | T | 2 | a0002c0001t0002g0341a0002c0001t0002g0342 | 2 | NA18942.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.306-2721C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956522 | ||||||
| chr19:32956688
|
T | C | 1 | a0001c0002t0001g0022 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.306-2887A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956688 | ||||||
| chr19:32956712
|
G | C | 7 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(4): Show | 7 | HG02630.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.306-2911C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956712 | ||||||
| chr19:32956743
|
T | C | 1 | a0000c0005t0019g0114 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.306-2942A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956743 | ||||||
| chr19:32956761
|
A | G | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.306-2960T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956761 | ||||||
| chr19:32956892
|
C | T | 152 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(149): Show | 156 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.305+3008G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956892 | ||||||
| chr19:32956898
|
T | C | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.305+3002A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32956898 | ||||||
| chr19:32957039
|
C | T | 30 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(27): Show | 33 | HG01361.hp2 HG01433.hp2 HG01952.hp2 others(30): Show |
intron_variant | MODIFIER | c.305+2861G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32957039 | ||||||
| chr19:32957169
|
A | T | 2 | a0004c0006t0011g0143a0004c0006t0026g0144 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.305+2731T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32957169 | ||||||
| chr19:32957182
|
C | T | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.305+2718G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32957182 | ||||||
| chr19:32957193
|
T | C | 2 | a0001c0002t0024g0072a0001c0002t0043g0118 | 2 | HG01123.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.305+2707A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32957193 | ||||||
| chr19:32957298
|
A | G | 254 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(251): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.305+2602T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32957298 | ||||||
| chr19:32957417
|
C | CA | 299 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(296): Show | 305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.305+2482_305+2483i others(3): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32957417 | ||||||
| chr19:32957446
|
C | A | 6 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0301others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.305+2454G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32957446 | ||||||
| chr19:32957547
|
T | C | 153 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(150): Show | 157 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.305+2353A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32957547 | ||||||
| chr19:32957589
|
G | C | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.305+2311C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32957589 | ||||||
| chr19:32957690
|
G | A | 1 | a0003c0003t0003g0250 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.305+2210C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32957690 | ||||||
| chr19:32957848
|
T | C | 1 | a0006c0009t0011g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.305+2052A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32957848 | ||||||
| chr19:32958013
|
T | TC | 20 | a0000c0007t0004g0078a0001c0004t0001g0199a0002c0001t0002g0319others(17): Show | 20 | HG00642.hp1 HG01175.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.305+1886dupG | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32958013 | ||||||
| chr19:32958013
|
T | TCC | 60 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(57): Show | 63 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.305+1885_305+1886d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32958013 | ||||||
| chr19:32958015
|
C | CCCG | 65 | a0003c0003t0002g0265a0003c0003t0003g0003a0003c0003t0003g0077others(62): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.305+1884_305+1885i others(5): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32958015 | ||||||
| chr19:32958121
|
G | A | 1 | a0000c0005t0005g0116 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.305+1779C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32958121 | ||||||
| chr19:32958273
|
T | C | 98 | a0002c0001t0001g0332a0002c0001t0002g0004a0002c0001t0002g0005others(95): Show | 100 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.305+1627A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32958273 | ||||||
| chr19:32958478
|
A | AG | 270 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(267): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.305+1421_305+1422i others(3): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32958478 | ||||||
| chr19:32958552
|
G | A | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.305+1348C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32958552 | ||||||
| chr19:32958593
|
C | T | 151 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(148): Show | 155 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.305+1307G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32958593 | ||||||
| chr19:32958620
|
A | C | 1 | a0001c0002t0001g0031 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.305+1280T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32958620 | ||||||
| chr19:32959044
|
A | AC | 3 | a0002c0001t0002g0150a0002c0001t0002g0369a0013c0024t0002g0324 | 3 | HG00621.hp1 HG01074.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.305+855_305+856ins others(1): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959044 | ||||||
| chr19:32959045
|
A | C | 113 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(110): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.305+855T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959045 | ||||||
| chr19:32959046
|
C | A | 118 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(115): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.305+854G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959046 | ||||||
| chr19:32959046
|
CA | C | 72 | a0000c0012t0021g0015a0001c0002t0043g0118a0003c0003t0002g0265others(69): Show | 73 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.305+853delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959046 | ||||||
| chr19:32959046
|
CAA | C | 75 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(72): Show | 78 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.305+852_305+853del others(2): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959046 | ||||||
| chr19:32959047
|
A | C | 1 | a0004c0006t0007g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.305+853T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959047 | ||||||
| chr19:32959048
|
A | C | 3 | a0002c0001t0002g0150a0002c0001t0002g0369a0013c0024t0002g0324 | 3 | HG00621.hp1 HG01074.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.305+852T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959048 | ||||||
| chr19:32959049
|
A | C | 114 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(111): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.305+851T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959049 | ||||||
| chr19:32959050
|
A | C | 67 | a0003c0003t0002g0265a0003c0003t0003g0003a0003c0003t0003g0077others(64): Show | 68 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.305+850T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959050 | ||||||
| chr19:32959051
|
A | C | 1 | a0006c0009t0011g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.305+849T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959051 | ||||||
| chr19:32959083
|
C | T | 3 | a0007c0011t0012g0375a0007c0011t0012g0379a0007c0011t0012g0380 | 3 | HG02630.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.305+817G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959083 | ||||||
| chr19:32959120
|
T | G | 3 | a0003c0003t0003g0222a0003c0003t0003g0224a0003c0003t0013g0220 | 3 | HG01081.hp1 HG01496.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.305+780A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959120 | ||||||
| chr19:32959137
|
A | G | 16 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(13): Show | 16 | HG02055.hp1 HG02145.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.305+763T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959137 | ||||||
| chr19:32959268
|
C | T | 76 | a0002c0001t0001g0332a0002c0001t0002g0004a0002c0001t0002g0073others(73): Show | 77 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.305+632G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959268 | ||||||
| chr19:32959269
|
G | A | 2 | a0001c0002t0001g0017a0001c0002t0015g0021 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.305+631C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959269 | ||||||
| chr19:32959423
|
C | T | 1 | a0001c0002t0016g0023 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.305+477G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959423 | ||||||
| chr19:32959707
|
A | G | 1 | a0013c0024t0002g0324 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.305+193T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959707 | ||||||
| chr19:32959830
|
C | T | 12 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.305+70G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 3/18 | chr19 | 32959830 | ||||||
| chr19:32960086
|
A | G | 4 | a0002c0001t0001g0350a0002c0001t0002g0322a0002c0001t0002g0362others(1): Show | 4 | NA18977.hp1 NA18997.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-28T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32960086 | ||||||
| chr19:32960173
|
A | G | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.147-115T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32960173 | ||||||
| chr19:32960293
|
G | T | 59 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(56): Show | 59 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.147-235C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32960293 | ||||||
| chr19:32960357
|
C | T | 29 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.147-299G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32960357 | ||||||
| chr19:32960535
|
C | T | 1 | a0008c0015t0001g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.147-477G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32960535 | ||||||
| chr19:32960598
|
A | C | 29 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.147-540T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32960598 | ||||||
| chr19:32960633
|
C | A | 2 | a0000c0005t0005g0115a0000c0005t0005g0117 | 2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.147-575G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32960633 | ||||||
| chr19:32960749
|
ACTATGAG others(1): Show |
A | 3 | a0002c0001t0002g0162a0002c0001t0002g0345a0002c0001t0002g0356 | 3 | HG00323.hp1 HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.147-699_147-692del others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32960749 | ||||||
| chr19:32960809
|
C | CA | 205 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(202): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.147-752dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32960809 | ||||||
| chr19:32961058
|
A | G | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.147-1000T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961058 | ||||||
| chr19:32961135
|
G | A | 1 | a0003c0003t0003g0225 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.147-1077C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961135 | ||||||
| chr19:32961142
|
G | C | 15 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(12): Show | 15 | HG02055.hp1 HG02145.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.147-1084C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961142 | ||||||
| chr19:32961156
|
G | C | 151 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(148): Show | 155 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.147-1098C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961156 | ||||||
| chr19:32961187
|
G | A | 151 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(148): Show | 155 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.147-1129C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961187 | ||||||
| chr19:32961291
|
C | T | 151 | a0000c0012t0004g0065a0000c0012t0021g0015a0001c0002t0001g0001others(148): Show | 155 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.147-1233G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961291 | ||||||
| chr19:32961357
|
T | C | 1 | a0001c0002t0001g0057 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.147-1299A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961357 | ||||||
| chr19:32961414
|
C | CA | 151 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(148): Show | 155 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.147-1357dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961414 | ||||||
| chr19:32961448
|
G | A | 63 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(60): Show | 63 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.147-1390C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961448 | ||||||
| chr19:32961528
|
G | C | 1 | a0001c0002t0043g0118 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.147-1470C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961528 | ||||||
| chr19:32961533
|
C | T | 74 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(71): Show | 75 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.147-1475G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961533 | ||||||
| chr19:32961557
|
C | T | 1 | a0003c0003t0010g0218 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.147-1499G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961557 | ||||||
| chr19:32961578
|
C | CA | 146 | a0000c0005t0005g0116a0000c0012t0004g0065a0001c0002t0001g0001others(143): Show | 150 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.147-1521dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961578 | ||||||
| chr19:32961578
|
C | CAA | 10 | a0000c0012t0021g0015a0001c0002t0001g0302a0001c0002t0043g0118others(7): Show | 10 | HG01261.hp1 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.147-1522_147-1521d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961578 | ||||||
| chr19:32961578
|
C | CAAA | 15 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(12): Show | 15 | HG02055.hp1 HG02145.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.147-1523_147-1521d others(5): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961578 | ||||||
| chr19:32961637
|
C | A | 1 | a0003c0003t0003g0253 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.147-1579G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961637 | ||||||
| chr19:32961704
|
C | T | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.147-1646G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961704 | ||||||
| chr19:32961754
|
C | T | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.147-1696G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961754 | ||||||
| chr19:32961793
|
G | A | 16 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(13): Show | 16 | HG02055.hp1 HG02145.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.147-1735C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961793 | ||||||
| chr19:32961800
|
C | T | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.147-1742G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32961800 | ||||||
| chr19:32962049
|
C | CA | 14 | a0000c0005t0005g0117a0000c0007t0004g0078a0001c0004t0001g0199others(11): Show | 14 | HG00423.hp2 HG01952.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.147-1992dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32962049 | ||||||
| chr19:32962049
|
C | CAA | 102 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(99): Show | 104 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.147-1993_147-1992d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32962049 | ||||||
| chr19:32962049
|
CA | C | 77 | a0000c0005t0023g0079a0000c0012t0004g0065a0001c0002t0001g0001others(74): Show | 80 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.147-1992delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32962049 | ||||||
| chr19:32962064
|
A | G | 2 | a0004c0006t0009g0136a0004c0006t0009g0137 | 2 | HG01361.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.147-2006T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32962064 | ||||||
| chr19:32962266
|
G | C | 1 | a0002c0001t0002g0349 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.147-2208C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32962266 | ||||||
| chr19:32962621
|
G | A | 48 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(45): Show | 48 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.147-2563C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32962621 | ||||||
| chr19:32962689
|
T | C | 7 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(4): Show | 7 | HG02630.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.147-2631A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32962689 | ||||||
| chr19:32962748
|
T | C | 59 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(56): Show | 59 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.147-2690A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32962748 | ||||||
| chr19:32962753
|
T | C | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.147-2695A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32962753 | ||||||
| chr19:32962802
|
C | T | 1 | a0003c0019t0012g0364 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.147-2744G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32962802 | ||||||
| chr19:32962915
|
T | C | 59 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(56): Show | 59 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.147-2857A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32962915 | ||||||
| chr19:32963097
|
T | G | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.147-3039A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963097 | ||||||
| chr19:32963135
|
C | G | 102 | a0002c0001t0001g0332a0002c0001t0002g0004a0002c0001t0002g0005others(99): Show | 104 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.147-3077G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963135 | ||||||
| chr19:32963259
|
A | C | 1 | a0006c0009t0011g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.146+3101T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963259 | ||||||
| chr19:32963343
|
G | A | 93 | a0000c0012t0021g0015a0001c0002t0010g0149a0001c0002t0010g0376others(90): Show | 94 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.146+3017C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963343 | ||||||
| chr19:32963536
|
C | T | 76 | a0000c0005t0023g0079a0000c0012t0004g0065a0001c0002t0001g0001others(73): Show | 79 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.146+2824G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963536 | ||||||
| chr19:32963541
|
G | A | 2 | a0001c0002t0024g0072a0001c0002t0043g0118 | 2 | HG01123.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.146+2819C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963541 | ||||||
| chr19:32963629
|
C | T | 91 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(88): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.146+2731G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963629 | ||||||
| chr19:32963636
|
A | T | 1 | a0002c0001t0002g0314 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.146+2724T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963636 | ||||||
| chr19:32963869
|
C | A | 1 | a0003c0019t0012g0364 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.146+2491G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963869 | ||||||
| chr19:32963892
|
C | CCA | 4 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0070others(1): Show | 4 | NA18952.hp2 NA18966.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.146+2466_146+2467d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963892 | ||||||
| chr19:32963892
|
C | CCACA | 53 | a0000c0005t0005g0164a0000c0005t0023g0079a0001c0002t0001g0016others(50): Show | 53 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.146+2464_146+2467d others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963892 | ||||||
| chr19:32963892
|
C | CCACACA | 43 | a0000c0005t0005g0098a0000c0005t0005g0099a0000c0005t0005g0100others(40): Show | 46 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.146+2462_146+2467d others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963892 | ||||||
| chr19:32963892
|
CCA | C | 86 | a0000c0012t0021g0015a0003c0003t0002g0265a0003c0003t0003g0003others(83): Show | 87 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.146+2466_146+2467d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963892 | ||||||
| chr19:32963892
|
CCACA | C | 72 | a0001c0002t0024g0072a0001c0002t0043g0118a0001c0004t0001g0074others(69): Show | 72 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.146+2464_146+2467d others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963892 | ||||||
| chr19:32963892
|
CCACACA | C | 86 | a0002c0001t0001g0332a0002c0001t0001g0350a0002c0001t0002g0004others(83): Show | 88 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.146+2462_146+2467d others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963892 | ||||||
| chr19:32963892
|
CCACACAC others(3): Show |
C | 3 | a0002c0001t0002g0310a0002c0001t0025g0148a0003c0019t0012g0364 | 3 | HG01175.hp2 HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.146+2458_146+2467d others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963892 | ||||||
| chr19:32963892
|
CCACACAC others(7): Show |
C | 1 | a0002c0001t0002g0309 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.146+2454_146+2467d others(16): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963892 | ||||||
| chr19:32963920
|
G | A | 76 | a0000c0005t0023g0079a0000c0012t0004g0065a0001c0002t0001g0001others(73): Show | 79 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.146+2440C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963920 | ||||||
| chr19:32963941
|
A | AAC | 10 | a0000c0007t0004g0281a0000c0007t0004g0282a0002c0001t0002g0314others(7): Show | 10 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.146+2417_146+2418d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963941 | ||||||
| chr19:32963941
|
AAC | A | 107 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0100others(104): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.146+2417_146+2418d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963941 | ||||||
| chr19:32963941
|
AACAC | A | 34 | a0000c0007t0004g0294a0001c0002t0001g0304a0001c0002t0024g0072others(31): Show | 34 | HG00609.hp1 HG01123.hp2 HG02027.hp1 others(31): Show |
intron_variant | MODIFIER | c.146+2415_146+2418d others(6): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963941 | ||||||
| chr19:32963941
|
AACACAC | A | 16 | a0000c0005t0005g0268a0000c0005t0005g0269a0001c0002t0001g0022others(13): Show | 16 | HG00280.hp1 HG01081.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.146+2413_146+2418d others(8): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963941 | ||||||
| chr19:32963941
|
AACACACA others(1): Show |
A | 60 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(57): Show | 63 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.146+2411_146+2418d others(10): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963941 | ||||||
| chr19:32963941
|
AACACACA others(3): Show |
A | 16 | a0001c0002t0010g0376a0001c0002t0010g0377a0001c0002t0010g0378others(13): Show | 16 | HG00639.hp1 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.146+2409_146+2418d others(12): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963941 | ||||||
| chr19:32963941
|
AACACACA others(5): Show |
A | 107 | a0000c0012t0021g0015a0001c0002t0010g0149a0001c0004t0001g0074others(104): Show | 108 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.146+2407_146+2418d others(14): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963941 | ||||||
| chr19:32963941
|
AACACACA others(9): Show |
A | 1 | a0003c0003t0003g0260 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.146+2403_146+2418d others(18): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32963941 | ||||||
| chr19:32964072
|
T | C | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.146+2288A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964072 | ||||||
| chr19:32964084
|
T | C | 1 | a0002c0001t0002g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.146+2276A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964084 | ||||||
| chr19:32964176
|
AT | A | 76 | a0000c0012t0021g0015a0001c0002t0001g0085a0001c0002t0010g0149others(73): Show | 77 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.146+2183delA | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964176 | ||||||
| chr19:32964274
|
C | T | 16 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(13): Show | 16 | HG02055.hp1 HG02145.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.146+2086G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964274 | ||||||
| chr19:32964275
|
G | T | 1 | a0002c0001t0002g0313 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.146+2085C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964275 | ||||||
| chr19:32964282
|
G | C | 2 | a0001c0002t0024g0072a0001c0002t0043g0118 | 2 | HG01123.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.146+2078C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964282 | ||||||
| chr19:32964614
|
T | C | 1 | a0002c0001t0002g0165 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.146+1746A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964614 | ||||||
| chr19:32964630
|
G | A | 1 | a0002c0001t0002g0356 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.146+1730C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964630 | ||||||
| chr19:32964683
|
C | T | 93 | a0000c0012t0021g0015a0001c0002t0010g0149a0001c0002t0010g0376others(90): Show | 94 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.146+1677G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964683 | ||||||
| chr19:32964714
|
G | T | 16 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(13): Show | 16 | HG02055.hp1 HG02145.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.146+1646C>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964714 | ||||||
| chr19:32964763
|
A | C | 2 | a0001c0004t0001g0166a0001c0004t0001g0167 | 2 | HG00544.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.146+1597T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964763 | ||||||
| chr19:32964839
|
G | GAT | 3 | a0003c0003t0003g0212a0003c0003t0003g0213a0003c0003t0003g0214 | 3 | HG02280.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.146+1519_146+1520d others(4): Show |
CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964839 | ||||||
| chr19:32964988
|
C | T | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.146+1372G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964988 | ||||||
| chr19:32964991
|
T | G | 93 | a0000c0012t0021g0015a0001c0002t0010g0149a0001c0002t0010g0376others(90): Show | 94 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.146+1369A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32964991 | ||||||
| chr19:32965020
|
C | G | 2 | a0000c0005t0005g0097a0000c0005t0005g0098 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.146+1340G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32965020 | ||||||
| chr19:32965106
|
A | T | 74 | a0001c0002t0010g0149a0001c0002t0010g0376a0001c0002t0010g0377others(71): Show | 75 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.146+1254T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32965106 | ||||||
| chr19:32965136
|
C | T | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.146+1224G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32965136 | ||||||
| chr19:32965273
|
T | C | 196 | a0000c0012t0021g0015a0001c0002t0010g0149a0001c0002t0010g0376others(193): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.146+1087A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32965273 | ||||||
| chr19:32965564
|
T | C | 1 | a0000c0007t0033g0295 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.146+796A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32965564 | ||||||
| chr19:32965691
|
G | A | 16 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(13): Show | 16 | HG02055.hp1 HG02145.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.146+669C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32965691 | ||||||
| chr19:32965737
|
T | C | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.146+623A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32965737 | ||||||
| chr19:32965746
|
A | T | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.146+614T>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32965746 | ||||||
| chr19:32965808
|
A | G | 77 | a0000c0005t0023g0079a0000c0012t0004g0065a0001c0002t0001g0001others(74): Show | 80 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.146+552T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32965808 | ||||||
| chr19:32966109
|
T | A | 7 | a0003c0003t0002g0265a0003c0003t0003g0077a0003c0003t0003g0261others(4): Show | 7 | HG00140.hp2 HG01258.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.146+251A>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32966109 | ||||||
| chr19:32966126
|
C | T | 2 | a0002c0001t0002g0309a0002c0001t0002g0310 | 2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.146+234G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 2/18 | chr19 | 32966126 | ||||||
| chr19:32966731
|
T | G | 1 | a0002c0001t0008g0012 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.40-265A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32966731 | ||||||
| chr19:32966732
|
C | G | 1 | a0002c0001t0008g0012 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.40-266G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32966732 | ||||||
| chr19:32966807
|
G | A | 59 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(56): Show | 59 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.40-341C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32966807 | ||||||
| chr19:32966847
|
G | A | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.40-381C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32966847 | ||||||
| chr19:32966869
|
G | C | 16 | a0005c0008t0006g0087a0005c0008t0006g0088a0005c0008t0006g0089others(13): Show | 16 | HG02055.hp1 HG02145.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.40-403C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32966869 | ||||||
| chr19:32966915
|
G | A | 1 | a0004c0006t0009g0146 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.40-449C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32966915 | ||||||
| chr19:32967036
|
A | G | 27 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.40-570T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967036 | ||||||
| chr19:32967082
|
T | C | 331 | a0000c0005t0023g0079a0000c0012t0004g0065a0000c0012t0021g0015others(328): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.40-616A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967082 | ||||||
| chr19:32967186
|
T | C | 1 | a0012c0017t0003g0267 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.40-720A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967186 | ||||||
| chr19:32967227
|
C | T | 184 | a0000c0012t0021g0015a0001c0002t0010g0149a0001c0002t0010g0376others(181): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.40-761G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967227 | ||||||
| chr19:32967277
|
G | A | 2 | a0001c0002t0001g0070a0001c0002t0001g0071 | 2 | NA18952.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.40-811C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967277 | ||||||
| chr19:32967289
|
T | C | 71 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(68): Show | 71 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.40-823A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967289 | ||||||
| chr19:32967310
|
C | T | 20 | a0002c0001t0002g0309a0002c0001t0002g0310a0002c0001t0025g0148others(17): Show | 20 | HG01175.hp2 HG02055.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.40-844G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967310 | ||||||
| chr19:32967331
|
C | A | 63 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(60): Show | 66 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.40-865G>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967331 | ||||||
| chr19:32967345
|
G | A | 1 | a0002c0001t0002g0165 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.40-879C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967345 | ||||||
| chr19:32967421
|
G | A | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.40-955C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967421 | ||||||
| chr19:32967506
|
G | GA | 85 | a0000c0005t0005g0268a0000c0005t0005g0269a0000c0005t0023g0079others(82): Show | 86 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.40-1041dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967506 | ||||||
| chr19:32967506
|
GA | G | 73 | a0001c0002t0001g0296a0001c0002t0001g0297a0001c0002t0001g0298others(70): Show | 73 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.40-1041delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967506 | ||||||
| chr19:32967573
|
G | C | 71 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0145others(68): Show | 71 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.40-1107C>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967573 | ||||||
| chr19:32967711
|
C | G | 1 | a0002c0001t0002g0311 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.40-1245G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967711 | ||||||
| chr19:32967912
|
GA | G | 4 | a0002c0001t0002g0309a0002c0001t0002g0310a0002c0001t0025g0148others(1): Show | 4 | HG01175.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.40-1447delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32967912 | ||||||
| chr19:32968219
|
C | T | 1 | a0002c0001t0002g0150 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.40-1753G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32968219 | ||||||
| chr19:32968240
|
G | A | 1 | a0002c0001t0002g0358 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.40-1774C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32968240 | ||||||
| chr19:32968280
|
T | G | 75 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(72): Show | 78 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.40-1814A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32968280 | ||||||
| chr19:32968304
|
G | A | 2 | a0002c0001t0002g0360a0002c0001t0002g0361 | 2 | HG00140.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.40-1838C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32968304 | ||||||
| chr19:32968392
|
T | G | 257 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(254): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.40-1926A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32968392 | ||||||
| chr19:32968511
|
A | G | 348 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(345): Show | 354 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.40-2045T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32968511 | ||||||
| chr19:32968686
|
A | G | 358 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(355): Show | 364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.40-2220T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32968686 | ||||||
| chr19:32968778
|
T | C | 10 | a0001c0002t0001g0296a0001c0002t0001g0297a0001c0002t0001g0298others(7): Show | 10 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.40-2312A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32968778 | ||||||
| chr19:32968813
|
T | TG | 4 | a0001c0004t0001g0200a0002c0001t0002g0362a0002c0001t0002g0363others(1): Show | 4 | HG00642.hp2 NA18966.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.40-2348dupC | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32968813 | ||||||
| chr19:32968837
|
A | G | 4 | a0001c0002t0010g0149a0002c0001t0002g0309a0002c0001t0025g0148others(1): Show | 4 | HG01175.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.40-2371T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32968837 | ||||||
| chr19:32968999
|
C | G | 155 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(152): Show | 156 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.40-2533G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32968999 | ||||||
| chr19:32968999
|
C | T | 203 | a0000c0005t0005g0164a0000c0012t0004g0065a0001c0002t0001g0001others(200): Show | 208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.40-2533G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32968999 | ||||||
| chr19:32969049
|
G | A | 1 | a0003c0003t0003g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.40-2583C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969049 | ||||||
| chr19:32969090
|
C | T | 79 | a0000c0005t0005g0268a0000c0005t0005g0269a0000c0012t0021g0015others(76): Show | 80 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.40-2624G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969090 | ||||||
| chr19:32969143
|
G | A | 1 | a0005c0008t0006g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.40-2677C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969143 | ||||||
| chr19:32969207
|
T | G | 79 | a0000c0005t0005g0268a0000c0005t0005g0269a0000c0012t0021g0015others(76): Show | 80 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.39+2629A>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969207 | ||||||
| chr19:32969290
|
C | T | 63 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(60): Show | 66 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.39+2546G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969290 | ||||||
| chr19:32969365
|
G | A | 3 | a0000c0005t0005g0119a0000c0005t0005g0120a0000c0005t0020g0121 | 3 | HG00099.hp2 HG01070.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.39+2471C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969365 | ||||||
| chr19:32969531
|
A | G | 141 | a0000c0005t0005g0164a0001c0002t0001g0357a0001c0002t0010g0149others(138): Show | 143 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.39+2305T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969531 | ||||||
| chr19:32969570
|
G | A | 76 | a0000c0005t0005g0268a0000c0005t0005g0269a0001c0002t0010g0376others(73): Show | 77 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.39+2266C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969570 | ||||||
| chr19:32969630
|
A | G | 115 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(112): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.39+2206T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969630 | ||||||
| chr19:32969643
|
C | T | 1 | a0004c0006t0007g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.39+2193G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969643 | ||||||
| chr19:32969786
|
G | A | 5 | a0001c0004t0001g0201a0001c0004t0001g0202a0001c0004t0001g0203others(2): Show | 5 | HG00423.hp1 HG00597.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+2050C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969786 | ||||||
| chr19:32969843
|
C | G | 5 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(2): Show | 5 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+1993G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969843 | ||||||
| chr19:32969906
|
G | A | 1 | a0007c0011t0012g0380 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.39+1930C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969906 | ||||||
| chr19:32969964
|
G | A | 10 | a0001c0002t0001g0296a0001c0002t0001g0297a0001c0002t0001g0298others(7): Show | 10 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.39+1872C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969964 | ||||||
| chr19:32969984
|
C | T | 1 | a0001c0002t0001g0016 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.39+1852G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32969984 | ||||||
| chr19:32970027
|
T | C | 141 | a0000c0005t0005g0164a0001c0002t0001g0357a0001c0002t0010g0149others(138): Show | 143 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.39+1809A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32970027 | ||||||
| chr19:32970039
|
C | T | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.39+1797G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32970039 | ||||||
| chr19:32970203
|
C | T | 63 | a0000c0012t0004g0065a0001c0002t0001g0001a0001c0002t0001g0002others(60): Show | 66 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.39+1633G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32970203 | ||||||
| chr19:32970278
|
G | A | 4 | a0001c0004t0001g0206a0001c0004t0001g0207a0001c0004t0001g0208others(1): Show | 4 | HG00323.hp2 NA18747.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+1558C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32970278 | ||||||
| chr19:32970490
|
C | CA | 77 | a0000c0005t0005g0268a0000c0005t0005g0269a0001c0002t0010g0376others(74): Show | 78 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.39+1345dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32970490 | ||||||
| chr19:32970620
|
C | T | 3 | a0002c0001t0002g0367a0002c0001t0002g0368a0002c0001t0002g0369 | 3 | NA18963.hp2 NA18972.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.39+1216G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32970620 | ||||||
| chr19:32970640
|
G | A | 1 | a0003c0010t0014g0366 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.39+1196C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32970640 | ||||||
| chr19:32970814
|
A | C | 6 | a0002c0001t0008g0006a0002c0001t0008g0007a0002c0001t0008g0008others(3): Show | 6 | NA18944.hp1 NA18961.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+1022T>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32970814 | ||||||
| chr19:32970942
|
A | G | 348 | a0000c0005t0005g0097a0000c0005t0005g0098a0000c0005t0005g0099others(345): Show | 354 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.39+894T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32970942 | ||||||
| chr19:32971048
|
A | G | 1 | a0003c0003t0003g0080 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.39+788T>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32971048 | ||||||
| chr19:32971177
|
G | A | 1 | a0001c0002t0001g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.39+659C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32971177 | ||||||
| chr19:32971372
|
C | T | 1 | a0000c0012t0021g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.39+464G>A | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32971372 | ||||||
| chr19:32971373
|
G | A | 4 | a0002c0001t0002g0367a0002c0001t0002g0368a0002c0001t0002g0369others(1): Show | 4 | NA18939.hp2 NA18963.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+463C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32971373 | ||||||
| chr19:32971531
|
C | G | 1 | a0000c0005t0023g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.39+305G>C | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32971531 | ||||||
| chr19:32971626
|
T | C | 1 | a0003c0003t0003g0306 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.39+210A>G | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32971626 | ||||||
| chr19:32971646
|
G | A | 1 | a0003c0010t0029g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.39+190C>T | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32971646 | ||||||
| chr19:32971658
|
T | TA | 74 | a0001c0002t0001g0357a0002c0001t0001g0332a0002c0001t0001g0350others(71): Show | 76 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.39+177dupT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32971658 | ||||||
| chr19:32971658
|
T | TAA | 10 | a0001c0002t0010g0376a0001c0002t0010g0377a0001c0002t0010g0378others(7): Show | 10 | HG02293.hp2 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+176_39+177dupTT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32971658 | ||||||
| chr19:32971658
|
TA | T | 66 | a0000c0007t0004g0078a0000c0012t0004g0065a0001c0002t0001g0001others(63): Show | 70 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.39+177delT | CEP89 | ENSG00000121289.18 | transcript | ENST00000305768.10 | protein_coding | 1/18 | chr19 | 32971658 |