Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80321 |
| ensemblid | ENSG00000114107.9 |
| hgncid | 29972 |
| symbol | CEP70 |
| name | centrosomal protein 70 |
| refseq_nuc | NM_024491.4 |
| refseq_prot | NP_077817.2 |
| ensembl_nuc | ENST00000264982.8 |
| ensembl_prot | ENSP00000264982.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 138494344 |
| end | 138594260 |
| strand | - |
| ver | v1.2 |
| region | chr3:138494344-138594260 |
| region5000 | chr3:138489344-138599260 |
| regionname0 | CEP70_chr3_138494344_138594260 |
| regionname5000 | CEP70_chr3_138489344_138599260 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 597 | 118 | 16 | 23 | 59 | 5 | 15 | 44 | CEP70_chr3_138489344_138599260 | CEP70 | MFPVA others(592): Show |
chr3 | 138489344 | 138599260 |
| a0002 | 0/1 | 597 | 105 | 34 | 6 | 54 | 0 | 10 | 40 | CEP70_chr3_138489344_138599260 | CEP70 | MFPVA others(592): Show |
chr3 | 138489344 | 138599260 |
| a0003 | 1/0 | 597 | 89 | 31 | 19 | 13 | 9 | 16 | 10 | CEP70_chr3_138489344_138599260 | CEP70 | MFPVA others(592): Show |
chr3 | 138489344 | 138599260 |
| a0004 | 0/0 | 597 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | MFPVA others(592): Show |
chr3 | 138489344 | 138599260 |
| a0005 | 0/0 | 597 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | MFPVA others(592): Show |
chr3 | 138489344 | 138599260 |
| a0006 | 0/0 | 597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | MFPVA others(592): Show |
chr3 | 138489344 | 138599260 |
| a0007 | 0/0 | 597 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | MFPVA others(592): Show |
chr3 | 138489344 | 138599260 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1791 | 111 | 9 | 23 | 59 | 5 | 15 | CEP70_chr3_138489344_138599260 | CEP70 | ATGTT others(1786): Show |
chr3 | 138489344 | 138599260 | ||
| a0001c0004 | 0/0 | 1791 | 6 | 6 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | ATGTT others(1786): Show |
chr3 | 138489344 | 138599260 | ||
| a0001c0011 | 0/0 | 1791 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | ATGTT others(1786): Show |
chr3 | 138489344 | 138599260 | ||
| a0002c0002 | 0/1 | 1791 | 104 | 34 | 6 | 53 | 0 | 10 | CEP70_chr3_138489344_138599260 | CEP70 | ATGTT others(1786): Show |
chr3 | 138489344 | 138599260 | ||
| a0002c0012 | 0/0 | 1791 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | ATGTT others(1786): Show |
chr3 | 138489344 | 138599260 | ||
| a0003c0003 | 0/0 | 1791 | 81 | 25 | 19 | 13 | 8 | 16 | CEP70_chr3_138489344_138599260 | CEP70 | ATGTT others(1786): Show |
chr3 | 138489344 | 138599260 | ||
| a0003c0005 | 0/0 | 1791 | 6 | 6 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | ATGTT others(1786): Show |
chr3 | 138489344 | 138599260 | ||
| a0003c0007 | 1/0 | 1791 | 2 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | ATGTT others(1786): Show |
chr3 | 138489344 | 138599260 | ||
| a0004c0006 | 0/0 | 1791 | 3 | 2 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | ATGTT others(1786): Show |
chr3 | 138489344 | 138599260 | ||
| a0005c0010 | 0/0 | 1791 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | ATGTT others(1786): Show |
chr3 | 138489344 | 138599260 | ||
| a0006c0009 | 0/0 | 1791 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | ATGTT others(1786): Show |
chr3 | 138489344 | 138599260 | ||
| a0007c0008 | 0/0 | 1791 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | ATGTT others(1786): Show |
chr3 | 138489344 | 138599260 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2636 | 111 | 9 | 23 | 59 | 5 | 15 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2631): Show |
chr3 | 138489344 | 138599260 |
| a0001c0004t0004 | 0/0 | 2636 | 4 | 4 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2631): Show |
chr3 | 138489344 | 138599260 |
| a0001c0004t0006 | 0/0 | 2636 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2631): Show |
chr3 | 138489344 | 138599260 |
| a0001c0011t0001 | 0/0 | 2636 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2631): Show |
chr3 | 138489344 | 138599260 |
| a0002c0002t0001 | 0/0 | 2636 | 23 | 20 | 3 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2631): Show |
chr3 | 138489344 | 138599260 |
| a0002c0002t0002 | 0/1 | 2636 | 81 | 14 | 3 | 53 | 0 | 10 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2631): Show |
chr3 | 138489344 | 138599260 |
| a0002c0012t0002 | 0/0 | 2636 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2631): Show |
chr3 | 138489344 | 138599260 |
| a0003c0003t0001 | 0/0 | 2636 | 9 | 1 | 5 | 0 | 2 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2631): Show |
chr3 | 138489344 | 138599260 |
| a0003c0003t0003 | 0/0 | 2631 | 72 | 24 | 14 | 13 | 6 | 15 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2626): Show |
chr3 | 138489344 | 138599260 |
| a0003c0005t0003 | 0/0 | 2631 | 6 | 6 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2626): Show |
chr3 | 138489344 | 138599260 |
| a0003c0007t0003 | 0/0 | 2631 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2626): Show |
chr3 | 138489344 | 138599260 |
| a0003c0007t0004 | 1/0 | 2636 | 1 | 0 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2631): Show |
chr3 | 138489344 | 138599260 |
| a0004c0006t0005 | 0/0 | 2636 | 3 | 2 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2631): Show |
chr3 | 138489344 | 138599260 |
| a0005c0010t0004 | 0/0 | 2636 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2631): Show |
chr3 | 138489344 | 138599260 |
| a0006c0009t0004 | 0/0 | 2636 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2631): Show |
chr3 | 138489344 | 138599260 |
| a0007c0008t0001 | 0/0 | 2636 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | GTAGC others(2631): Show |
chr3 | 138489344 | 138599260 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0004t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0004t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0004t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0004t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0004t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0004t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0001c0011t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0266 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0002c0012t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0003t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0005t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0005t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0005t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0005t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0005t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0005t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0007t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0003c0007t0004g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0004c0006t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0004c0006t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0004c0006t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0005c0010t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0006c0009t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| a0007c0008t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0003 | c0003 | t0003 | g0062 | EUR | GBR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00280 | hp2 | a0003 | c0003 | t0003 | g0069 | EUR | FIN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00323 | hp1 | a0003 | c0007 | t0003 | g0044 | EUR | FIN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00323 | hp2 | a0003 | c0003 | t0003 | g0070 | EUR | FIN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0234 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00621 | hp1 | a0003 | c0003 | t0003 | g0046 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0072 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00673 | hp2 | a0003 | c0003 | t0003 | g0047 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00735 | hp1 | a0003 | c0003 | t0003 | g0092 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00735 | hp2 | a0004 | c0006 | t0005 | g0029 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01069 | hp1 | a0003 | c0003 | t0003 | g0068 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0066 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01099 | hp2 | a0003 | c0003 | t0003 | g0054 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01106 | hp2 | a0003 | c0003 | t0003 | g0043 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01109 | hp2 | a0003 | c0003 | t0003 | g0090 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01167 | hp1 | a0003 | c0003 | t0003 | g0101 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0026 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01169 | hp1 | a0003 | c0003 | t0003 | g0103 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01175 | hp1 | a0003 | c0003 | t0003 | g0011 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01243 | hp1 | a0005 | c0010 | t0004 | g0022 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01243 | hp2 | a0003 | c0003 | t0003 | g0097 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0032 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01256 | hp1 | a0003 | c0003 | t0003 | g0091 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01257 | hp2 | a0003 | c0003 | t0001 | g0071 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0074 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0239 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01433 | hp2 | a0003 | c0003 | t0003 | g0010 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01496 | hp1 | a0003 | c0003 | t0003 | g0038 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0201 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0073 | EUR | IBS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01516 | hp2 | a0003 | c0003 | t0003 | g0052 | EUR | IBS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01517 | hp1 | a0003 | c0003 | t0003 | g0051 | EUR | IBS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0267 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0220 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01891 | hp1 | a0004 | c0006 | t0005 | g0030 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0036 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02004 | hp1 | a0003 | c0003 | t0003 | g0084 | AMR | PEL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0218 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0226 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0236 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02080 | hp1 | a0003 | c0003 | t0003 | g0042 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0272 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02145 | hp1 | a0003 | c0003 | t0003 | g0067 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02148 | hp1 | a0003 | c0003 | t0003 | g0060 | AMR | PEL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CDX | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0235 | EAS | CDX | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02258 | hp1 | a0001 | c0004 | t0004 | g0108 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0025 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02280 | hp1 | a0003 | c0005 | t0003 | g0087 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0205 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0219 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02451 | hp2 | a0003 | c0005 | t0003 | g0077 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02572 | hp1 | a0003 | c0003 | t0003 | g0107 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0211 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02602 | hp1 | a0003 | c0003 | t0003 | g0011 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02615 | hp2 | a0001 | c0004 | t0006 | g0028 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02622 | hp1 | a0003 | c0003 | t0003 | g0100 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02622 | hp2 | a0003 | c0003 | t0003 | g0212 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02630 | hp2 | a0003 | c0003 | t0003 | g0003 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02647 | hp1 | a0003 | c0003 | t0003 | g0105 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02683 | hp1 | a0003 | c0003 | t0003 | g0053 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0244 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02723 | hp2 | a0003 | c0003 | t0003 | g0012 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02738 | hp1 | a0003 | c0003 | t0001 | g0059 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02818 | hp1 | a0003 | c0003 | t0003 | g0058 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02818 | hp2 | a0003 | c0003 | t0003 | g0094 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0196 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02895 | hp2 | a0003 | c0003 | t0003 | g0012 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02897 | hp1 | a0003 | c0003 | t0003 | g0102 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02897 | hp2 | a0003 | c0003 | t0003 | g0093 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02922 | hp1 | a0003 | c0005 | t0003 | g0057 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0208 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02965 | hp1 | a0003 | c0003 | t0003 | g0096 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02970 | hp1 | a0003 | c0003 | t0003 | g0056 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0200 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03041 | hp2 | a0001 | c0004 | t0004 | g0109 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03098 | hp1 | a0003 | c0003 | t0003 | g0075 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03098 | hp2 | a0003 | c0003 | t0003 | g0055 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03130 | hp1 | a0003 | c0003 | t0003 | g0003 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03139 | hp2 | a0001 | c0011 | t0001 | g0110 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03195 | hp2 | a0001 | c0004 | t0004 | g0214 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03225 | hp1 | a0003 | c0003 | t0003 | g0106 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03225 | hp2 | a0006 | c0009 | t0004 | g0216 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03239 | hp2 | a0003 | c0003 | t0003 | g0009 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03453 | hp1 | a0001 | c0004 | t0006 | g0031 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03453 | hp2 | a0003 | c0003 | t0003 | g0003 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0024 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03486 | hp2 | a0003 | c0003 | t0003 | g0099 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03490 | hp1 | a0003 | c0003 | t0003 | g0009 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03516 | hp2 | a0001 | c0004 | t0004 | g0215 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03579 | hp1 | a0003 | c0003 | t0003 | g0104 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0203 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0260 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03669 | hp1 | a0003 | c0003 | t0003 | g0083 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03688 | hp1 | a0003 | c0003 | t0003 | g0061 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0265 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03704 | hp2 | a0003 | c0003 | t0003 | g0040 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03710 | hp2 | a0003 | c0003 | t0003 | g0086 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03831 | hp1 | a0003 | c0003 | t0003 | g0065 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0020 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03834 | hp1 | a0003 | c0003 | t0003 | g0045 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0233 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03927 | hp1 | a0003 | c0003 | t0003 | g0213 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0264 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03942 | hp2 | a0003 | c0003 | t0003 | g0063 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG04115 | hp1 | a0003 | c0003 | t0003 | g0089 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG04199 | hp1 | a0003 | c0003 | t0003 | g0064 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0020 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | CHB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | CHB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18939 | hp2 | a0003 | c0003 | t0003 | g0041 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18941 | hp1 | a0002 | c0012 | t0002 | g0269 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0245 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18957 | hp2 | a0003 | c0003 | t0003 | g0113 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18968 | hp2 | a0003 | c0003 | t0003 | g0033 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18980 | hp2 | a0003 | c0003 | t0003 | g0112 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18986 | hp2 | a0003 | c0003 | t0003 | g0049 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19002 | hp1 | a0003 | c0003 | t0003 | g0114 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19005 | hp1 | a0003 | c0003 | t0003 | g0085 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0221 | AFR | LWK | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0194 | AFR | LWK | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19082 | hp2 | a0003 | c0003 | t0003 | g0080 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19086 | hp2 | a0003 | c0003 | t0003 | g0081 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19087 | hp2 | a0003 | c0003 | t0003 | g0082 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0259 | AFR | YRI | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA19240 | hp2 | a0003 | c0003 | t0003 | g0076 | AFR | YRI | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA20129 | hp1 | a0003 | c0005 | t0003 | g0078 | AFR | ASW | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0204 | AFR | ASW | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA20752 | hp2 | a0003 | c0003 | t0003 | g0048 | EUR | TSI | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA20805 | hp2 | a0003 | c0003 | t0001 | g0191 | EUR | TSI | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA20905 | hp1 | a0003 | c0003 | t0003 | g0095 | SAS | GIH | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA20905 | hp2 | a0007 | c0008 | t0001 | g0189 | SAS | GIH | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0035 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0202 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02559 | hp1 | a0003 | c0003 | t0003 | g0098 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG02559 | hp2 | a0003 | c0005 | t0003 | g0088 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG03471 | hp2 | a0003 | c0005 | t0003 | g0079 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0210 | AFR | USA | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| HG06807 | hp2 | a0004 | c0006 | t0005 | g0027 | AFR | USA | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| NA21309 | hp2 | a0003 | c0003 | t0003 | g0010 | AFR | LWK | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0266 | REF | REF | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| homoSapiens | grch38p0 | a0003 | c0007 | t0004 | g0050 | REF | REF | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:138500152 | T | C | 1 | a0002 | 104 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
missense_variant | MODERATE | c.1610A>G | p.Asn537Ser | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/18 | 1781/2636 | 1610/1794 | 537/597 | chr3 | 138500152 | |||
| chr3:138500549 | A | G | 1 | a0005 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1387T>C | p.Phe463Leu | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 15/18 | 1558/2636 | 1387/1794 | 463/597 | chr3 | 138500549 | |||
| chr3:138500832 | A | T | 1 | a0004 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.1271T>A | p.Leu424His | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 14/18 | 1442/2636 | 1271/1794 | 424/597 | chr3 | 138500832 | |||
| chr3:138505372 | C | T | 1 | a0006 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1144G>A | p.Asp382Asn | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/18 | 1315/2636 | 1144/1794 | 382/597 | chr3 | 138505372 | |||
| chr3:138570379 | C | T | 6 | a0001 a0002 a0004 others(3): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
missense_variant | MODERATE | c.404G>A | p.Ser135Asn | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/18 | 575/2636 | 404/1794 | 135/597 | chr3 | 138570379 | |||
| chr3:138570472 | C | T | 1 | a0007 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.311G>A | p.Arg104Gln | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/18 | 482/2636 | 311/1794 | 104/597 | chr3 | 138570472 | |||
| chr3:138572893 | C | T | 1 | a0004 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.35G>A | p.Ser12Asn | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/18 | 206/2636 | 35/1794 | 12/597 | chr3 | 138572893 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:138500827 | A | G | 1 | a0001c0011 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.1276T>C | p.Leu426Leu | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 14/18 | 1447/2636 | 1276/1794 | 426/597 | chr3 | 138500827 | |||
| chr3:138525558 | C | T | 3 | a0003c0003 a0003c0005 a0004c0006 |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
synonymous_variant | LOW | c.876G>A | p.Thr292Thr | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/18 | 1047/2636 | 876/1794 | 292/597 | chr3 | 138525558 | |||
| chr3:138570321 | T | C | 5 | a0001c0001 a0001c0011 a0002c0012 others(2): Show |
120 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(117): Show |
synonymous_variant | LOW | c.462A>G | p.Leu154Leu | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/18 | 633/2636 | 462/1794 | 154/597 | chr3 | 138570321 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:138494450 | C | T | 2 | a0002c0002t0002 a0002c0012t0002 |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*565G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 18/18 | 565 | chr3 | 138494450 | ||||||
| chr3:138494867 | T | C | 6 | a0001c0001t0001 a0001c0004t0006 a0001c0011t0001 others(3): Show |
147 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*148A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 18/18 | 148 | chr3 | 138494867 | ||||||
| chr3:138495007 | ATTTGT | A | 3 | a0003c0003t0003 a0003c0005t0003 a0003c0007t0003 |
79 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*3_*7delACAAA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 18/18 | 3 | chr3 | 138495007 | ||||||
| chr3:138591865 | C | T | 2 | a0001c0004t0006 a0004c0006t0005 |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-17G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/18 | 18938 | chr3 | 138591865 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:138495552 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02698.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1733-476T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138495552 | |||||||
| chr3:138495652 | G | C | 67 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(64): Show |
78 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1733-576C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138495652 | |||||||
| chr3:138495669 | C | T | 1 | a0003c0003t0003g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1733-593G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138495669 | |||||||
| chr3:138495790 | T | G | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1733-714A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138495790 | |||||||
| chr3:138495862 | C | A | 1 | a0006c0009t0004g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1733-786G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138495862 | |||||||
| chr3:138495984 | C | A | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1733-908G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138495984 | |||||||
| chr3:138496196 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1733-1120C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496196 | |||||||
| chr3:138496203 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1733-1127G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496203 | |||||||
| chr3:138496272 | C | T | 152 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(149): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1733-1196G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496272 | |||||||
| chr3:138496318 | CT | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1733-1243delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496318 | |||||||
| chr3:138496351 | T | C | 2 | a0003c0003t0003g0093 a0003c0003t0003g0094 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1733-1275A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496351 | |||||||
| chr3:138496445 | G | A | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1733-1369C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496445 | |||||||
| chr3:138496535 | A | T | 1 | a0001c0004t0006g0031 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1733-1459T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496535 | |||||||
| chr3:138496618 | G | A | 1 | a0002c0002t0002g0239 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1732+1413C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496618 | |||||||
| chr3:138496673 | C | A | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1732+1358G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496673 | |||||||
| chr3:138496703 | A | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1732+1328T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496703 | |||||||
| chr3:138496779 | C | T | 1 | a0002c0002t0002g0238 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1732+1252G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496779 | |||||||
| chr3:138496935 | T | G | 74 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0002g0002 others(71): Show |
85 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1732+1096A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496935 | |||||||
| chr3:138497149 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1732+882A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497149 | |||||||
| chr3:138497331 | T | TA | 14 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(11): Show |
14 | HG00741.hp2 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1732+699dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497331 | |||||||
| chr3:138497388 | C | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1732+643G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497388 | |||||||
| chr3:138497715 | A | G | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1732+316T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497715 | |||||||
| chr3:138497763 | T | C | 1 | a0002c0002t0002g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1732+268A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497763 | |||||||
| chr3:138497871 | A | C | 24 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(21): Show |
26 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.1732+160T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497871 | |||||||
| chr3:138497890 | G | A | 5 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0141 others(2): Show |
5 | HG02071.hp2 NA18947.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1732+141C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497890 | |||||||
| chr3:138497928 | C | G | 1 | a0003c0003t0003g0033 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1732+103G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497928 | |||||||
| chr3:138498244 | TTTTC | T | 3 | a0002c0002t0002g0220 a0002c0002t0002g0265 a0002c0002t0002g0267 |
3 | HG01884.hp1 HG01884.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1653-138_1653-135d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498244 | |||||||
| chr3:138498383 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1653-273T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498383 | |||||||
| chr3:138498576 | C | T | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1653-466G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498576 | |||||||
| chr3:138498578 | C | T | 1 | a0003c0003t0003g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1653-468G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498578 | |||||||
| chr3:138498683 | C | T | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1653-573G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498683 | |||||||
| chr3:138498897 | T | G | 1 | a0003c0003t0001g0072 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1653-787A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498897 | |||||||
| chr3:138498914 | C | T | 2 | a0002c0002t0002g0035 a0002c0002t0002g0036 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1653-804G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498914 | |||||||
| chr3:138499146 | C | T | 13 | a0003c0003t0003g0012 a0003c0003t0003g0038 a0003c0003t0003g0101 others(10): Show |
14 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1652+964G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499146 | |||||||
| chr3:138499169 | G | C | 1 | a0002c0002t0001g0018 | 2 | HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1652+941C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499169 | |||||||
| chr3:138499266 | T | TG | 72 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(69): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1652+843dupC | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499266 | |||||||
| chr3:138499357 | T | A | 2 | a0003c0003t0003g0068 a0003c0003t0003g0070 |
2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1652+753A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499357 | |||||||
| chr3:138499493 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1652+617T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499493 | |||||||
| chr3:138499559 | A | G | 1 | a0003c0003t0003g0092 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1652+551T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499559 | |||||||
| chr3:138499724 | C | T | 3 | a0002c0002t0001g0018 a0002c0002t0001g0193 a0002c0002t0001g0194 |
4 | HG02257.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1652+386G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499724 | |||||||
| chr3:138499772 | A | C | 1 | a0002c0002t0002g0235 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1652+338T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499772 | |||||||
| chr3:138499783 | T | TAC | 5 | a0001c0001t0001g0125 a0001c0001t0001g0277 a0001c0004t0004g0214 others(2): Show |
5 | HG01261.hp2 HG02071.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1652+325_1652+326d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | |||||||
| chr3:138499783 | T | TACAC | 70 | a0001c0001t0001g0137 a0003c0003t0001g0025 a0003c0003t0001g0026 others(67): Show |
74 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1652+323_1652+326d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | |||||||
| chr3:138499783 | T | TACACAC | 12 | a0002c0002t0002g0243 a0003c0003t0003g0003 a0003c0003t0003g0049 others(9): Show |
14 | HG01243.hp2 HG02559.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1652+321_1652+326d others(8): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | |||||||
| chr3:138499783 | T | TACACACA others(1): Show |
65 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(62): Show |
76 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1652+319_1652+326d others(10): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | |||||||
| chr3:138499783 | T | TACACACA others(3): Show |
5 | a0002c0002t0002g0034 a0002c0002t0002g0250 a0002c0002t0002g0264 others(2): Show |
5 | HG02027.hp1 HG02129.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1652+317_1652+326d others(12): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | |||||||
| chr3:138499783 | T | TACACACA others(5): Show |
1 | a0002c0002t0002g0239 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1652+315_1652+326d others(14): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | |||||||
| chr3:138499783 | T | TACACACA others(11): Show |
16 | a0002c0002t0001g0018 a0002c0002t0001g0195 a0002c0002t0001g0196 others(13): Show |
17 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.1652+309_1652+326d others(20): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | |||||||
| chr3:138499783 | T | TACACACA others(13): Show |
5 | a0002c0002t0001g0019 a0002c0002t0001g0193 a0002c0002t0001g0194 others(2): Show |
6 | HG02257.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1652+307_1652+326d others(22): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | |||||||
| chr3:138499783 | T | TACACACA others(17): Show |
2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1652+326_1652+327i others(26): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | |||||||
| chr3:138499783 | T | TACACACA others(19): Show |
1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1652+326_1652+327i others(28): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | |||||||
| chr3:138499810 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1652+300A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499810 | |||||||
| chr3:138499867 | C | A | 82 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(79): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1652+243G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499867 | |||||||
| chr3:138500076 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1652+34A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138500076 | |||||||
| chr3:138500593 | AAG | A | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.1369-28_1369-27del others(2): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 14/17 | chr3 | 138500593 | |||||||
| chr3:138500725 | T | G | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1368+10A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 14/17 | chr3 | 138500725 | |||||||
| chr3:138501011 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1222-130G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501011 | |||||||
| chr3:138501050 | T | A | 1 | a0001c0001t0001g0161 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1222-169A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501050 | |||||||
| chr3:138501065 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-184G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501065 | |||||||
| chr3:138501081 | A | G | 59 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(56): Show |
62 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1222-200T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501081 | |||||||
| chr3:138501295 | T | A | 1 | a0003c0003t0003g0045 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1222-414A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501295 | |||||||
| chr3:138501296 | C | G | 1 | a0003c0003t0003g0045 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1222-415G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501296 | |||||||
| chr3:138501400 | C | T | 3 | a0003c0003t0003g0051 a0003c0003t0003g0052 a0003c0003t0003g0091 |
3 | HG01256.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1222-519G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501400 | |||||||
| chr3:138501432 | T | C | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222-551A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501432 | |||||||
| chr3:138501482 | A | G | 1 | a0003c0003t0003g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1222-601T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501482 | |||||||
| chr3:138501498 | G | C | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1222-617C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501498 | |||||||
| chr3:138501528 | G | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-647C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501528 | |||||||
| chr3:138501588 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-707T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501588 | |||||||
| chr3:138501652 | G | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-771C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501652 | |||||||
| chr3:138501664 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1222-783T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501664 | |||||||
| chr3:138501737 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1222-856C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501737 | |||||||
| chr3:138501747 | G | A | 7 | a0003c0003t0003g0009 a0003c0003t0003g0061 a0003c0003t0003g0062 others(4): Show |
8 | HG00140.hp1 HG03239.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1222-866C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501747 | |||||||
| chr3:138501897 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-1016A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501897 | |||||||
| chr3:138502010 | T | C | 1 | a0002c0002t0002g0259 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1222-1129A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502010 | |||||||
| chr3:138502089 | G | C | 2 | a0003c0003t0003g0075 a0003c0003t0003g0090 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1222-1208C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502089 | |||||||
| chr3:138502451 | T | C | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1222-1570A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502451 | |||||||
| chr3:138502539 | GA | G | 69 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(66): Show |
80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1222-1659delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502539 | |||||||
| chr3:138502744 | C | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA18975.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1222-1863G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502744 | |||||||
| chr3:138502769 | A | G | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1222-1888T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502769 | |||||||
| chr3:138502840 | C | A | 1 | a0003c0003t0003g0033 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1222-1959G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502840 | |||||||
| chr3:138502846 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-1965G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502846 | |||||||
| chr3:138502881 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-2000T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502881 | |||||||
| chr3:138503266 | A | G | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1221+2029T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138503266 | |||||||
| chr3:138503338 | A | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1221+1957T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138503338 | |||||||
| chr3:138503455 | C | T | 6 | a0002c0002t0001g0019 a0002c0002t0001g0200 a0002c0002t0001g0201 others(3): Show |
7 | HG01123.hp2 HG01496.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1221+1840G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138503455 | |||||||
| chr3:138503552 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1221+1743A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138503552 | |||||||
| chr3:138503710 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1221+1585G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138503710 | |||||||
| chr3:138503884 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1221+1411G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138503884 | |||||||
| chr3:138504155 | A | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0118 others(8): Show |
13 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1221+1140T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504155 | |||||||
| chr3:138504172 | A | G | 84 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0003c0003t0001g0025 others(81): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1221+1123T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504172 | |||||||
| chr3:138504220 | G | C | 1 | a0001c0001t0001g0143 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1221+1075C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504220 | |||||||
| chr3:138504279 | G | A | 1 | a0002c0002t0002g0248 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1221+1016C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504279 | |||||||
| chr3:138504282 | T | G | 1 | a0002c0002t0002g0248 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1221+1013A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504282 | |||||||
| chr3:138504283 | A | G | 1 | a0002c0002t0002g0248 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1221+1012T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504283 | |||||||
| chr3:138504439 | T | C | 1 | a0002c0002t0002g0270 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1221+856A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504439 | |||||||
| chr3:138504825 | G | T | 2 | a0003c0003t0003g0101 a0003c0003t0003g0103 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1221+470C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504825 | |||||||
| chr3:138504833 | C | A | 2 | a0003c0003t0003g0101 a0003c0003t0003g0103 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1221+462G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504833 | |||||||
| chr3:138504841 | C | CAGAAAAT others(15): Show |
1 | a0002c0002t0002g0235 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1221+432_1221+453d others(24): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504841 | |||||||
| chr3:138504863 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1221+432C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504863 | |||||||
| chr3:138504917 | G | A | 1 | a0003c0003t0003g0038 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1221+378C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504917 | |||||||
| chr3:138505098 | C | T | 1 | a0003c0003t0003g0094 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1221+197G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138505098 | |||||||
| chr3:138505181 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1221+114G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138505181 | |||||||
| chr3:138505621 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1051-156A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138505621 | |||||||
| chr3:138505719 | C | G | 1 | a0001c0001t0001g0135 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1051-254G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138505719 | |||||||
| chr3:138505935 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0128 a0001c0001t0001g0187 |
5 | HG01123.hp1 HG01257.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051-470G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138505935 | |||||||
| chr3:138505960 | A | G | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1051-495T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138505960 | |||||||
| chr3:138505964 | C | T | 1 | a0001c0004t0004g0215 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1051-499G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138505964 | |||||||
| chr3:138505978 | C | T | 5 | a0003c0003t0003g0075 a0003c0003t0003g0090 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01109.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051-513G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138505978 | |||||||
| chr3:138506058 | ACTAT | A | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1051-597_1051-594d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506058 | |||||||
| chr3:138506308 | A | C | 4 | a0002c0002t0002g0236 a0002c0002t0002g0256 a0002c0002t0002g0257 others(1): Show |
4 | HG00408.hp2 HG02074.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051-843T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506308 | |||||||
| chr3:138506616 | A | G | 2 | a0003c0003t0003g0010 a0003c0003t0003g0011 |
4 | HG01175.hp1 HG01433.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051-1151T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506616 | |||||||
| chr3:138506690 | T | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1051-1225A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506690 | |||||||
| chr3:138506697 | A | T | 1 | a0002c0002t0002g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1051-1232T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506697 | |||||||
| chr3:138506795 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1051-1330C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506795 | |||||||
| chr3:138506824 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1051-1359C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506824 | |||||||
| chr3:138506948 | G | A | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1051-1483C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506948 | |||||||
| chr3:138506953 | G | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1050+1486C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506953 | |||||||
| chr3:138507068 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1050+1371G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507068 | |||||||
| chr3:138507080 | A | C | 1 | a0002c0002t0002g0233 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1050+1359T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507080 | |||||||
| chr3:138507507 | A | G | 1 | a0003c0003t0001g0072 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1050+932T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507507 | |||||||
| chr3:138507539 | T | C | 1 | a0002c0002t0002g0274 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1050+900A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507539 | |||||||
| chr3:138507645 | C | T | 1 | a0003c0003t0001g0059 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1050+794G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507645 | |||||||
| chr3:138507832 | GT | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1050+606delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507832 | |||||||
| chr3:138507882 | T | A | 1 | a0002c0002t0002g0249 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1050+557A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507882 | |||||||
| chr3:138507887 | A | T | 2 | a0003c0003t0003g0093 a0003c0003t0003g0094 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1050+552T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507887 | |||||||
| chr3:138507934 | A | C | 4 | a0002c0002t0001g0207 a0002c0002t0001g0208 a0002c0002t0001g0209 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1050+505T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507934 | |||||||
| chr3:138507992 | C | T | 1 | a0002c0002t0002g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1050+447G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507992 | |||||||
| chr3:138508081 | G | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1050+358C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138508081 | |||||||
| chr3:138508188 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1050+251C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138508188 | |||||||
| chr3:138508191 | A | T | 163 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(160): Show |
180 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1050+248T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138508191 | |||||||
| chr3:138508347 | T | A | 5 | a0002c0002t0002g0240 a0002c0002t0002g0241 a0002c0002t0002g0242 others(2): Show |
5 | NA18947.hp2 NA18949.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.1050+92A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138508347 | |||||||
| chr3:138508709 | A | G | 1 | a0003c0003t0003g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.945-165T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508709 | |||||||
| chr3:138508729 | A | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-185T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508729 | |||||||
| chr3:138508736 | A | T | 2 | a0003c0003t0003g0063 a0003c0003t0003g0064 |
2 | HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.945-192T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508736 | |||||||
| chr3:138508737 | T | A | 3 | a0003c0005t0003g0057 a0003c0005t0003g0087 a0003c0005t0003g0088 |
3 | HG02280.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.945-193A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508737 | |||||||
| chr3:138508761 | T | G | 1 | a0001c0001t0001g0017 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.945-217A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508761 | |||||||
| chr3:138508765 | G | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-221C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508765 | |||||||
| chr3:138508878 | C | T | 1 | a0002c0002t0002g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.945-334G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508878 | |||||||
| chr3:138508884 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-340G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508884 | |||||||
| chr3:138509011 | G | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.945-467C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509011 | |||||||
| chr3:138509013 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.945-469C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509013 | |||||||
| chr3:138509101 | T | G | 4 | a0002c0002t0001g0019 a0002c0002t0001g0200 a0002c0002t0001g0203 others(1): Show |
5 | HG01123.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.945-557A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509101 | |||||||
| chr3:138509163 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-619C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509163 | |||||||
| chr3:138509225 | C | T | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.945-681G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509225 | |||||||
| chr3:138509255 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02698.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.945-711C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509255 | |||||||
| chr3:138509359 | A | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-815T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509359 | |||||||
| chr3:138509518 | A | G | 7 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0036 others(4): Show |
9 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.945-974T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509518 | |||||||
| chr3:138509539 | G | A | 184 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(181): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.945-995C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509539 | |||||||
| chr3:138509579 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-1035G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509579 | |||||||
| chr3:138509852 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-1308T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509852 | |||||||
| chr3:138509906 | C | A | 182 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(179): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.945-1362G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509906 | |||||||
| chr3:138509985 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-1441A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509985 | |||||||
| chr3:138510251 | T | TA | 79 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(76): Show |
90 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.945-1708dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510251 | |||||||
| chr3:138510276 | T | C | 82 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(79): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.945-1732A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510276 | |||||||
| chr3:138510349 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.945-1805G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510349 | |||||||
| chr3:138510433 | C | CA | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(81): Show |
96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.945-1890dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510433 | |||||||
| chr3:138510574 | C | G | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.945-2030G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510574 | |||||||
| chr3:138510636 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-2092C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510636 | |||||||
| chr3:138510662 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-2118A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510662 | |||||||
| chr3:138510719 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-2175G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510719 | |||||||
| chr3:138510772 | G | C | 2 | a0002c0002t0002g0035 a0002c0002t0002g0036 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.945-2228C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510772 | |||||||
| chr3:138510843 | A | T | 2 | a0002c0002t0002g0035 a0002c0002t0002g0036 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.945-2299T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510843 | |||||||
| chr3:138510856 | C | CT | 7 | a0002c0002t0002g0034 a0002c0002t0002g0226 a0002c0002t0002g0241 others(4): Show |
7 | HG00408.hp2 HG01256.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.945-2313dupA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510856 | |||||||
| chr3:138510856 | CT | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
116 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.945-2313delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510856 | |||||||
| chr3:138510883 | C | T | 82 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(79): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.945-2339G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510883 | |||||||
| chr3:138510892 | G | A | 5 | a0002c0002t0002g0222 a0002c0002t0002g0224 a0002c0002t0002g0225 others(2): Show |
5 | HG02071.hp1 NA18747.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.945-2348C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510892 | |||||||
| chr3:138511026 | T | TTTG | 183 | a0001c0001t0001g0133 a0001c0004t0004g0108 a0001c0004t0004g0109 others(180): Show |
202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.945-2485_945-2483d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511026 | |||||||
| chr3:138511060 | A | G | 7 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0036 others(4): Show |
9 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.945-2516T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511060 | |||||||
| chr3:138511163 | G | GC | 23 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(20): Show |
27 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.945-2620dupG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511163 | |||||||
| chr3:138511168 | C | A | 1 | a0001c0001t0001g0135 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.945-2624G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511168 | |||||||
| chr3:138511245 | C | A | 1 | a0003c0005t0003g0079 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.945-2701G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511245 | |||||||
| chr3:138511286 | C | G | 2 | a0003c0003t0003g0083 a0003c0003t0003g0084 |
2 | HG02004.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.945-2742G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511286 | |||||||
| chr3:138511300 | T | C | 2 | a0001c0004t0004g0214 a0001c0004t0004g0215 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.945-2756A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511300 | |||||||
| chr3:138511337 | T | C | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.945-2793A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511337 | |||||||
| chr3:138511393 | G | C | 3 | a0003c0003t0003g0042 a0003c0003t0003g0046 a0003c0003t0003g0047 |
3 | HG00621.hp1 HG00673.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.945-2849C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511393 | |||||||
| chr3:138511473 | C | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-2929G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511473 | |||||||
| chr3:138511566 | A | G | 184 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(181): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.945-3022T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511566 | |||||||
| chr3:138511604 | C | T | 1 | a0003c0003t0003g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.945-3060G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511604 | |||||||
| chr3:138511657 | T | C | 82 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(79): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.945-3113A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511657 | |||||||
| chr3:138511788 | A | G | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.945-3244T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511788 | |||||||
| chr3:138512113 | T | C | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.945-3569A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512113 | |||||||
| chr3:138512421 | T | C | 67 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(64): Show |
78 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.945-3877A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512421 | |||||||
| chr3:138512504 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.945-3960G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512504 | |||||||
| chr3:138512576 | C | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-4032G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512576 | |||||||
| chr3:138512604 | A | C | 1 | a0002c0002t0001g0194 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.945-4060T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512604 | |||||||
| chr3:138512620 | T | C | 1 | a0003c0003t0003g0062 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.945-4076A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512620 | |||||||
| chr3:138512756 | C | A | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.945-4212G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512756 | |||||||
| chr3:138512796 | A | G | 1 | a0002c0002t0002g0271 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.945-4252T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512796 | |||||||
| chr3:138512893 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-4349G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512893 | |||||||
| chr3:138512920 | C | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-4376G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512920 | |||||||
| chr3:138512980 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.945-4436T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512980 | |||||||
| chr3:138513231 | C | A | 1 | a0002c0002t0001g0204 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.945-4687G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513231 | |||||||
| chr3:138513373 | C | G | 1 | a0001c0004t0004g0215 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.945-4829G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513373 | |||||||
| chr3:138513474 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.945-4930G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513474 | |||||||
| chr3:138513525 | T | TC | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.945-4982dupG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513525 | |||||||
| chr3:138513563 | G | A | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.945-5019C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513563 | |||||||
| chr3:138513952 | T | TA | 91 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(88): Show |
104 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.945-5409dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513952 | |||||||
| chr3:138513965 | C | A | 8 | a0003c0003t0001g0025 a0003c0003t0001g0059 a0003c0003t0001g0066 others(5): Show |
8 | HG00639.hp1 HG01071.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.945-5421G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513965 | |||||||
| chr3:138514004 | G | A | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.945-5460C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514004 | |||||||
| chr3:138514202 | T | C | 2 | a0002c0002t0002g0021 a0002c0002t0002g0234 |
3 | HG00544.hp1 HG00558.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.945-5658A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514202 | |||||||
| chr3:138514234 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-5690C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514234 | |||||||
| chr3:138514496 | C | T | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.945-5952G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514496 | |||||||
| chr3:138514781 | G | C | 82 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(79): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.945-6237C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514781 | |||||||
| chr3:138514849 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.945-6305C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514849 | |||||||
| chr3:138514877 | T | C | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.945-6333A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514877 | |||||||
| chr3:138514961 | A | G | 80 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(77): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.945-6417T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514961 | |||||||
| chr3:138515039 | G | A | 2 | a0001c0004t0004g0214 a0001c0004t0004g0215 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.945-6495C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515039 | |||||||
| chr3:138515059 | CAAG | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-6518_945-6516d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515059 | |||||||
| chr3:138515062 | G | C | 181 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(178): Show |
200 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.945-6518C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515062 | |||||||
| chr3:138515170 | T | C | 1 | a0002c0002t0002g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.945-6626A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515170 | |||||||
| chr3:138515298 | C | T | 1 | a0003c0003t0003g0112 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.945-6754G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515298 | |||||||
| chr3:138515404 | C | G | 1 | a0002c0002t0001g0206 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.945-6860G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515404 | |||||||
| chr3:138515467 | C | CA | 87 | a0001c0001t0001g0135 a0001c0001t0001g0152 a0001c0001t0001g0169 others(84): Show |
93 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.945-6924dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515467 | |||||||
| chr3:138515467 | C | CAA | 28 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0020 others(25): Show |
33 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.945-6925_945-6924d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515467 | |||||||
| chr3:138515467 | C | CAAA | 39 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0021 others(36): Show |
45 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.945-6926_945-6924d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515467 | |||||||
| chr3:138515467 | C | CAAAA | 8 | a0002c0002t0002g0037 a0002c0002t0002g0224 a0002c0002t0002g0227 others(5): Show |
8 | HG01433.hp1 NA18968.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.945-6927_945-6924d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515467 | |||||||
| chr3:138515471 | A | G | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.945-6927T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515471 | |||||||
| chr3:138515472 | A | G | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.945-6928T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515472 | |||||||
| chr3:138515569 | GA | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-7026delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515569 | |||||||
| chr3:138515612 | A | G | 180 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(177): Show |
199 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.945-7068T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515612 | |||||||
| chr3:138515616 | T | C | 1 | a0003c0003t0003g0069 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.945-7072A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515616 | |||||||
| chr3:138515684 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-7140T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515684 | |||||||
| chr3:138515725 | C | T | 58 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(55): Show |
67 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.945-7181G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515725 | |||||||
| chr3:138515734 | C | T | 159 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0002g0002 others(156): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.945-7190G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515734 | |||||||
| chr3:138515756 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-7212A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515756 | |||||||
| chr3:138515763 | G | A | 82 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(79): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.945-7219C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515763 | |||||||
| chr3:138515769 | G | A | 2 | a0002c0002t0002g0260 a0002c0002t0002g0264 |
2 | HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.945-7225C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515769 | |||||||
| chr3:138515872 | A | G | 4 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.945-7328T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515872 | |||||||
| chr3:138515910 | T | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.945-7366A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515910 | |||||||
| chr3:138515941 | C | G | 1 | a0002c0002t0002g0006 | 3 | HG02735.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.945-7397G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515941 | |||||||
| chr3:138515952 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-7408G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515952 | |||||||
| chr3:138516102 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.945-7558G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516102 | |||||||
| chr3:138516133 | A | G | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.945-7589T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516133 | |||||||
| chr3:138516136 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.945-7592C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516136 | |||||||
| chr3:138516361 | T | A | 3 | a0002c0002t0002g0228 a0002c0002t0002g0229 a0002c0002t0002g0230 |
3 | NA18965.hp1 NA18975.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.945-7817A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516361 | |||||||
| chr3:138516385 | T | G | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.945-7841A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516385 | |||||||
| chr3:138516393 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-7849G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516393 | |||||||
| chr3:138516399 | G | A | 1 | a0003c0003t0003g0112 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.945-7855C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516399 | |||||||
| chr3:138516410 | G | A | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.945-7866C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516410 | |||||||
| chr3:138516443 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.945-7899A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516443 | |||||||
| chr3:138516535 | A | AC | 9 | a0001c0001t0001g0158 a0001c0001t0001g0184 a0001c0001t0001g0276 others(6): Show |
9 | HG00621.hp1 HG02080.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.945-7992dupG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516535 | |||||||
| chr3:138516572 | G | A | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.945-8028C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516572 | |||||||
| chr3:138516616 | A | G | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.945-8072T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516616 | |||||||
| chr3:138516665 | C | T | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.945-8121G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516665 | |||||||
| chr3:138516750 | G | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-8206C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516750 | |||||||
| chr3:138516775 | G | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-8231C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516775 | |||||||
| chr3:138516797 | CAT | C | 59 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(56): Show |
68 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.945-8255_945-8254d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516797 | |||||||
| chr3:138516811 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.945-8267G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516811 | |||||||
| chr3:138517276 | G | A | 6 | a0003c0003t0003g0051 a0003c0003t0003g0052 a0003c0003t0003g0054 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.944+8214C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517276 | |||||||
| chr3:138517402 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+8088T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517402 | |||||||
| chr3:138517449 | C | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+8041G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517449 | |||||||
| chr3:138517455 | G | A | 95 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(92): Show |
108 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.944+8035C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517455 | |||||||
| chr3:138517578 | A | G | 1 | a0002c0002t0002g0270 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.944+7912T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517578 | |||||||
| chr3:138517593 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+7897G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517593 | |||||||
| chr3:138517788 | A | T | 91 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(88): Show |
104 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.944+7702T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517788 | |||||||
| chr3:138517794 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+7696C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517794 | |||||||
| chr3:138517854 | G | A | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.944+7636C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517854 | |||||||
| chr3:138518003 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.944+7487G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518003 | |||||||
| chr3:138518011 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0192 |
2 | NA18957.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.944+7479C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518011 | |||||||
| chr3:138518017 | A | G | 180 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(177): Show |
199 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.944+7473T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518017 | |||||||
| chr3:138518044 | C | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+7446G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518044 | |||||||
| chr3:138518044 | C | T | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.944+7446G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518044 | |||||||
| chr3:138518117 | C | T | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.944+7373G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518117 | |||||||
| chr3:138518118 | G | A | 1 | a0003c0003t0001g0191 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.944+7372C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518118 | |||||||
| chr3:138518132 | G | A | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG01175.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.944+7358C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518132 | |||||||
| chr3:138518151 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.944+7339C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518151 | |||||||
| chr3:138518209 | C | T | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.944+7281G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518209 | |||||||
| chr3:138518323 | T | C | 1 | a0002c0002t0002g0221 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.944+7167A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518323 | |||||||
| chr3:138518327 | T | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+7163A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518327 | |||||||
| chr3:138518350 | G | A | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.944+7140C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518350 | |||||||
| chr3:138518373 | C | T | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.944+7117G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518373 | |||||||
| chr3:138518789 | A | T | 1 | a0002c0002t0002g0249 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.944+6701T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518789 | |||||||
| chr3:138518828 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+6662G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518828 | |||||||
| chr3:138518845 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+6645C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518845 | |||||||
| chr3:138518884 | G | A | 2 | a0002c0002t0001g0019 a0002c0002t0001g0211 |
3 | HG02572.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.944+6606C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518884 | |||||||
| chr3:138518903 | G | C | 1 | a0002c0002t0002g0270 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.944+6587C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518903 | |||||||
| chr3:138519057 | C | T | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+6433G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519057 | |||||||
| chr3:138519158 | G | T | 1 | a0006c0009t0004g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.944+6332C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519158 | |||||||
| chr3:138519225 | C | T | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+6265G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519225 | |||||||
| chr3:138519236 | G | C | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.944+6254C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519236 | |||||||
| chr3:138519253 | ACT | A | 80 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(77): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.944+6235_944+6236d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519253 | |||||||
| chr3:138519260 | A | C | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.944+6230T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519260 | |||||||
| chr3:138519262 | T | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.944+6228A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519262 | |||||||
| chr3:138519314 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+6176G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519314 | |||||||
| chr3:138519459 | G | T | 1 | a0003c0003t0001g0026 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.944+6031C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519459 | |||||||
| chr3:138519568 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+5922G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519568 | |||||||
| chr3:138519589 | A | G | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.944+5901T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519589 | |||||||
| chr3:138519611 | C | A | 3 | a0003c0003t0003g0097 a0003c0003t0003g0098 a0003c0003t0003g0099 |
3 | HG01243.hp2 HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.944+5879G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519611 | |||||||
| chr3:138519639 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.944+5851A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519639 | |||||||
| chr3:138519707 | G | A | 5 | a0001c0001t0001g0156 a0003c0003t0003g0055 a0003c0005t0003g0077 others(2): Show |
5 | HG02451.hp2 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.944+5783C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519707 | |||||||
| chr3:138519726 | T | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+5764A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519726 | |||||||
| chr3:138519729 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.944+5761A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519729 | |||||||
| chr3:138519738 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+5752T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519738 | |||||||
| chr3:138519747 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+5743C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519747 | |||||||
| chr3:138519778 | C | T | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.944+5712G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519778 | |||||||
| chr3:138520109 | C | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+5381G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520109 | |||||||
| chr3:138520230 | A | G | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+5260T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520230 | |||||||
| chr3:138520233 | G | A | 2 | a0003c0003t0003g0093 a0003c0003t0003g0094 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.944+5257C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520233 | |||||||
| chr3:138520329 | G | A | 4 | a0001c0001t0001g0172 a0004c0006t0005g0027 a0004c0006t0005g0029 others(1): Show |
4 | HG00735.hp2 HG01891.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.944+5161C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520329 | |||||||
| chr3:138520347 | C | T | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.944+5143G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520347 | |||||||
| chr3:138520355 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+5135A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520355 | |||||||
| chr3:138520362 | C | G | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.944+5128G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520362 | |||||||
| chr3:138520463 | T | C | 180 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(177): Show |
199 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.944+5027A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520463 | |||||||
| chr3:138520542 | C | T | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.944+4948G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520542 | |||||||
| chr3:138520683 | A | G | 2 | a0003c0003t0003g0093 a0003c0003t0003g0094 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.944+4807T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520683 | |||||||
| chr3:138520827 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+4663G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520827 | |||||||
| chr3:138520933 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+4557A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520933 | |||||||
| chr3:138520947 | T | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.944+4543A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520947 | |||||||
| chr3:138520966 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0117 |
3 | NA18961.hp1 NA19064.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.944+4524C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520966 | |||||||
| chr3:138521056 | T | C | 180 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(177): Show |
199 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.944+4434A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521056 | |||||||
| chr3:138521057 | G | A | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.944+4433C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521057 | |||||||
| chr3:138521069 | C | T | 3 | a0002c0002t0002g0228 a0002c0002t0002g0229 a0002c0002t0002g0230 |
3 | NA18965.hp1 NA18975.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.944+4421G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521069 | |||||||
| chr3:138521221 | G | A | 2 | a0002c0002t0001g0204 a0004c0006t0005g0029 |
2 | HG00735.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.944+4269C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521221 | |||||||
| chr3:138521225 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+4265T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521225 | |||||||
| chr3:138521251 | G | A | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+4239C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521251 | |||||||
| chr3:138521344 | A | AC | 12 | a0001c0001t0001g0133 a0001c0001t0001g0148 a0001c0001t0001g0158 others(9): Show |
12 | HG01243.hp1 HG01516.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.944+4145dupG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521344 | |||||||
| chr3:138521349 | G | A | 2 | a0003c0003t0003g0104 a0003c0003t0003g0107 |
2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.944+4141C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521349 | |||||||
| chr3:138521367 | G | A | 1 | a0002c0002t0002g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.944+4123C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521367 | |||||||
| chr3:138521388 | A | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+4102T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521388 | |||||||
| chr3:138521401 | G | A | 1 | a0002c0002t0002g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.944+4089C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521401 | |||||||
| chr3:138521420 | G | A | 1 | a0003c0003t0003g0104 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.944+4070C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521420 | |||||||
| chr3:138521441 | G | A | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.944+4049C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521441 | |||||||
| chr3:138521492 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+3998A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521492 | |||||||
| chr3:138521535 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.944+3955G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521535 | |||||||
| chr3:138521570 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+3920C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521570 | |||||||
| chr3:138521577 | T | C | 182 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(179): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.944+3913A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521577 | |||||||
| chr3:138521578 | G | A | 1 | a0003c0003t0003g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.944+3912C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521578 | |||||||
| chr3:138521645 | C | T | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+3845G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521645 | |||||||
| chr3:138521649 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+3841G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521649 | |||||||
| chr3:138521657 | C | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.944+3833G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521657 | |||||||
| chr3:138521676 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.944+3814C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521676 | |||||||
| chr3:138521685 | C | T | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.944+3805G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521685 | |||||||
| chr3:138521694 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+3796G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521694 | |||||||
| chr3:138521771 | C | T | 1 | a0002c0002t0002g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.944+3719G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521771 | |||||||
| chr3:138521808 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+3682T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521808 | |||||||
| chr3:138521825 | C | T | 1 | a0002c0002t0002g0271 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.944+3665G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521825 | |||||||
| chr3:138522007 | C | T | 66 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(63): Show |
77 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.944+3483G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522007 | |||||||
| chr3:138522044 | G | A | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+3446C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522044 | |||||||
| chr3:138522091 | C | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+3399G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522091 | |||||||
| chr3:138522105 | C | T | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.944+3385G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522105 | |||||||
| chr3:138522117 | T | C | 180 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(177): Show |
199 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.944+3373A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522117 | |||||||
| chr3:138522294 | TA | T | 77 | a0001c0001t0001g0140 a0001c0001t0001g0283 a0002c0002t0002g0002 others(74): Show |
88 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.944+3195delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522294 | |||||||
| chr3:138522462 | T | C | 1 | a0002c0002t0002g0261 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.944+3028A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522462 | |||||||
| chr3:138522517 | C | T | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.944+2973G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522517 | |||||||
| chr3:138522518 | G | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+2972C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522518 | |||||||
| chr3:138522522 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+2968G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522522 | |||||||
| chr3:138522563 | A | G | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.944+2927T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522563 | |||||||
| chr3:138522578 | G | A | 80 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(77): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.944+2912C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522578 | |||||||
| chr3:138522602 | G | A | 1 | a0002c0002t0002g0275 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.944+2888C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522602 | |||||||
| chr3:138522681 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(81): Show |
96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.944+2809A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522681 | |||||||
| chr3:138522859 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+2631A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522859 | |||||||
| chr3:138522992 | G | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.944+2498C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522992 | |||||||
| chr3:138523099 | T | C | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.944+2391A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523099 | |||||||
| chr3:138523158 | T | C | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+2332A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523158 | |||||||
| chr3:138523174 | AC | A | 95 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(92): Show |
108 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.944+2315delG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523174 | |||||||
| chr3:138523176 | C | G | 2 | a0003c0005t0003g0057 a0003c0005t0003g0088 |
2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.944+2314G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523176 | |||||||
| chr3:138523379 | A | G | 1 | a0002c0002t0002g0271 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.944+2111T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523379 | |||||||
| chr3:138523442 | T | C | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.944+2048A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523442 | |||||||
| chr3:138523479 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.944+2011A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523479 | |||||||
| chr3:138523506 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+1984A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523506 | |||||||
| chr3:138523542 | T | C | 1 | a0002c0002t0002g0236 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.944+1948A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523542 | |||||||
| chr3:138523649 | C | G | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.944+1841G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523649 | |||||||
| chr3:138523664 | C | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+1826G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523664 | |||||||
| chr3:138523667 | G | T | 1 | a0002c0002t0002g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.944+1823C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523667 | |||||||
| chr3:138523671 | C | T | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.944+1819G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523671 | |||||||
| chr3:138523734 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+1756G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523734 | |||||||
| chr3:138523780 | G | A | 1 | a0003c0003t0003g0052 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.944+1710C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523780 | |||||||
| chr3:138523843 | C | A | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.944+1647G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523843 | |||||||
| chr3:138523849 | T | C | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.944+1641A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523849 | |||||||
| chr3:138523907 | G | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+1583C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523907 | |||||||
| chr3:138523908 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+1582G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523908 | |||||||
| chr3:138523975 | T | C | 1 | a0001c0004t0006g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.944+1515A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523975 | |||||||
| chr3:138524005 | T | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.944+1485A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524005 | |||||||
| chr3:138524026 | T | G | 182 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(179): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.944+1464A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524026 | |||||||
| chr3:138524028 | C | T | 181 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(178): Show |
198 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.944+1462G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524028 | |||||||
| chr3:138524034 | A | C | 182 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(179): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.944+1456T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524034 | |||||||
| chr3:138524077 | A | T | 184 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(181): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.944+1413T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524077 | |||||||
| chr3:138524135 | T | C | 1 | a0001c0001t0001g0016 | 2 | HG01255.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.944+1355A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524135 | |||||||
| chr3:138524207 | C | T | 1 | a0003c0003t0003g0033 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.944+1283G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524207 | |||||||
| chr3:138524388 | A | C | 95 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(92): Show |
108 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.944+1102T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524388 | |||||||
| chr3:138524591 | C | A | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.944+899G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524591 | |||||||
| chr3:138524600 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+890T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524600 | |||||||
| chr3:138524654 | C | T | 4 | a0003c0003t0003g0096 a0003c0003t0003g0097 a0003c0003t0003g0098 others(1): Show |
4 | HG01243.hp2 HG02559.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.944+836G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524654 | |||||||
| chr3:138524775 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+715T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524775 | |||||||
| chr3:138524797 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+693G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524797 | |||||||
| chr3:138524811 | T | C | 1 | a0002c0002t0002g0236 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.944+679A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524811 | |||||||
| chr3:138524953 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+537C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524953 | |||||||
| chr3:138525019 | G | A | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.944+471C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525019 | |||||||
| chr3:138525024 | A | T | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.944+466T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525024 | |||||||
| chr3:138525158 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.944+332C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525158 | |||||||
| chr3:138525184 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(81): Show |
96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.944+306A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525184 | |||||||
| chr3:138525270 | G | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+220C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525270 | |||||||
| chr3:138525303 | T | C | 1 | a0002c0002t0002g0228 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.944+187A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525303 | |||||||
| chr3:138525305 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+185G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525305 | |||||||
| chr3:138525334 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+156A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525334 | |||||||
| chr3:138525343 | A | C | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.944+147T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525343 | |||||||
| chr3:138525385 | G | A | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+105C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525385 | |||||||
| chr3:138525393 | A | G | 1 | a0002c0002t0002g0273 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.944+97T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525393 | |||||||
| chr3:138525599 | T | A | 1 | a0002c0002t0001g0204 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.870-35A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138525599 | |||||||
| chr3:138525670 | C | G | 1 | a0002c0002t0002g0219 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.870-106G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138525670 | |||||||
| chr3:138525699 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.870-135G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138525699 | |||||||
| chr3:138525770 | C | T | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.870-206G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138525770 | |||||||
| chr3:138525842 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.870-278T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138525842 | |||||||
| chr3:138525870 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.870-306G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138525870 | |||||||
| chr3:138526086 | G | C | 21 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(18): Show |
23 | HG00639.hp1 HG01071.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.870-522C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526086 | |||||||
| chr3:138526302 | C | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.870-738G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526302 | |||||||
| chr3:138526344 | G | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.870-780C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526344 | |||||||
| chr3:138526354 | G | A | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.870-790C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526354 | |||||||
| chr3:138526379 | GT | G | 161 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(158): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.870-816delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526379 | |||||||
| chr3:138526410 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.870-846A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526410 | |||||||
| chr3:138526452 | C | T | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.870-888G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526452 | |||||||
| chr3:138526749 | C | T | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.870-1185G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526749 | |||||||
| chr3:138526936 | T | C | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.870-1372A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526936 | |||||||
| chr3:138526982 | A | C | 80 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(77): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.870-1418T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526982 | |||||||
| chr3:138527011 | CA | C | 184 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(181): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.870-1448delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527011 | |||||||
| chr3:138527166 | TTTTTG | T | 3 | a0003c0003t0003g0010 a0003c0003t0003g0011 a0006c0009t0004g0216 |
5 | HG01175.hp1 HG01433.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.870-1607_870-1603d others(7): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527166 | |||||||
| chr3:138527187 | A | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(96): Show |
112 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.870-1623T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527187 | |||||||
| chr3:138527188 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.870-1624C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527188 | |||||||
| chr3:138527195 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.870-1631T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527195 | |||||||
| chr3:138527270 | A | ATCT | 180 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(177): Show |
199 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.870-1709_870-1707d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527270 | |||||||
| chr3:138527329 | A | AT | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(84): Show |
100 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.870-1766dupA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527329 | |||||||
| chr3:138527382 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.869+1817G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527382 | |||||||
| chr3:138527470 | G | A | 68 | a0001c0001t0001g0122 a0002c0002t0002g0002 a0002c0002t0002g0005 others(65): Show |
79 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.869+1729C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527470 | |||||||
| chr3:138527496 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.869+1703G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527496 | |||||||
| chr3:138527576 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0190 |
3 | NA18967.hp2 NA19002.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.869+1623G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527576 | |||||||
| chr3:138527600 | A | G | 1 | a0003c0003t0003g0041 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.869+1599T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527600 | |||||||
| chr3:138527602 | A | G | 184 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(181): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.869+1597T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527602 | |||||||
| chr3:138527641 | C | A | 1 | a0001c0004t0004g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.869+1558G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527641 | |||||||
| chr3:138527690 | G | A | 1 | a0003c0003t0003g0067 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.869+1509C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527690 | |||||||
| chr3:138527694 | C | CA | 6 | a0001c0001t0001g0148 a0001c0001t0001g0278 a0004c0006t0005g0027 others(3): Show |
6 | HG00735.hp2 HG01175.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.869+1504dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527694 | |||||||
| chr3:138527694 | CA | C | 100 | a0001c0001t0001g0155 a0001c0001t0001g0163 a0001c0001t0001g0166 others(97): Show |
107 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.869+1504delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527694 | |||||||
| chr3:138527694 | CAA | C | 7 | a0002c0002t0002g0036 a0002c0002t0002g0228 a0003c0003t0001g0071 others(4): Show |
7 | HG01257.hp2 HG01891.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.869+1503_869+1504d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527694 | |||||||
| chr3:138527694 | CAAA | C | 68 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(65): Show |
79 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.869+1502_869+1504d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527694 | |||||||
| chr3:138527843 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.869+1356A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527843 | |||||||
| chr3:138527861 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.869+1338G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527861 | |||||||
| chr3:138528045 | G | GT | 10 | a0001c0001t0001g0117 a0001c0001t0001g0136 a0001c0001t0001g0138 others(7): Show |
10 | HG00673.hp1 HG01261.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.869+1153dupA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528045 | |||||||
| chr3:138528457 | G | A | 1 | a0002c0002t0002g0244 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.869+742C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528457 | |||||||
| chr3:138528541 | T | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.869+658A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528541 | |||||||
| chr3:138528629 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.869+570G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528629 | |||||||
| chr3:138528749 | TG | T | 180 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(177): Show |
199 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.869+449delC | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528749 | |||||||
| chr3:138528884 | C | T | 1 | a0003c0003t0003g0042 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.869+315G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528884 | |||||||
| chr3:138528954 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.869+245A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528954 | |||||||
| chr3:138528993 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.869+206C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528993 | |||||||
| chr3:138529012 | T | A | 182 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(179): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.869+187A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138529012 | |||||||
| chr3:138529079 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.869+120A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138529079 | |||||||
| chr3:138529167 | G | GA | 69 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(66): Show |
80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.869+31dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138529167 | |||||||
| chr3:138529336 | TTTA | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.780+36_780+38delTA others(1): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 9/17 | chr3 | 138529336 | |||||||
| chr3:138529599 | G | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.693-137C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138529599 | |||||||
| chr3:138529746 | A | T | 1 | a0004c0006t0005g0030 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.693-284T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138529746 | |||||||
| chr3:138529803 | C | G | 1 | a0002c0002t0002g0228 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.693-341G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138529803 | |||||||
| chr3:138529922 | T | C | 1 | a0003c0003t0003g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.693-460A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138529922 | |||||||
| chr3:138529943 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.693-481A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138529943 | |||||||
| chr3:138530032 | T | G | 1 | a0003c0003t0003g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.693-570A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530032 | |||||||
| chr3:138530153 | A | G | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.693-691T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530153 | |||||||
| chr3:138530226 | T | G | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.693-764A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530226 | |||||||
| chr3:138530416 | C | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.693-954G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530416 | |||||||
| chr3:138530506 | A | AAAC | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.693-1047_693-1045d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530506 | |||||||
| chr3:138530541 | T | C | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.693-1079A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530541 | |||||||
| chr3:138530684 | C | T | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.693-1222G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530684 | |||||||
| chr3:138530795 | A | G | 184 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(181): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.693-1333T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530795 | |||||||
| chr3:138531250 | T | G | 1 | a0002c0002t0002g0244 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.692+1264A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531250 | |||||||
| chr3:138531280 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.692+1234T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531280 | |||||||
| chr3:138531281 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.692+1233G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531281 | |||||||
| chr3:138531383 | A | G | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.692+1131T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531383 | |||||||
| chr3:138531472 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.692+1042C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531472 | |||||||
| chr3:138531591 | G | A | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.692+923C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531591 | |||||||
| chr3:138531683 | T | G | 1 | a0002c0002t0002g0261 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.692+831A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531683 | |||||||
| chr3:138531698 | C | CT | 10 | a0001c0001t0001g0115 a0001c0001t0001g0131 a0001c0001t0001g0154 others(7): Show |
10 | HG01069.hp1 HG01109.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.692+815dupA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531698 | |||||||
| chr3:138531698 | C | CTT | 74 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0066 others(71): Show |
80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.692+814_692+815dup others(2): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531698 | |||||||
| chr3:138531698 | CT | C | 67 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0002c0002t0002g0002 others(64): Show |
78 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.692+815delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531698 | |||||||
| chr3:138531732 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.692+782A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531732 | |||||||
| chr3:138531736 | G | A | 1 | a0002c0002t0001g0208 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.692+778C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531736 | |||||||
| chr3:138532054 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.692+460A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138532054 | |||||||
| chr3:138532156 | A | G | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.692+358T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138532156 | |||||||
| chr3:138532424 | T | C | 2 | a0003c0003t0003g0003 a0003c0003t0003g0076 |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.692+90A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138532424 | |||||||
| chr3:138532460 | G | T | 82 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(79): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.692+54C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138532460 | |||||||
| chr3:138532469 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.692+45T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138532469 | |||||||
| chr3:138532501 | G | C | 1 | a0004c0006t0005g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.692+13C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138532501 | |||||||
| chr3:138532605 | CGGTAT | C | 85 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(82): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.636-40_636-36delAT others(3): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138532605 | |||||||
| chr3:138532677 | A | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.636-107T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138532677 | |||||||
| chr3:138532914 | A | G | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.636-344T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138532914 | |||||||
| chr3:138532984 | A | G | 2 | a0003c0003t0003g0056 a0003c0003t0003g0058 |
2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.636-414T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138532984 | |||||||
| chr3:138533212 | C | T | 1 | a0003c0003t0003g0083 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.636-642G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533212 | |||||||
| chr3:138533326 | G | C | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.636-756C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533326 | |||||||
| chr3:138533368 | G | A | 82 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(79): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.636-798C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533368 | |||||||
| chr3:138533590 | C | T | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.636-1020G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533590 | |||||||
| chr3:138533672 | A | C | 1 | a0003c0005t0003g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.636-1102T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533672 | |||||||
| chr3:138533699 | G | C | 3 | a0003c0005t0003g0077 a0003c0005t0003g0078 a0003c0005t0003g0079 |
3 | HG02451.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.636-1129C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533699 | |||||||
| chr3:138533812 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.636-1242T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533812 | |||||||
| chr3:138533846 | G | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.636-1276C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533846 | |||||||
| chr3:138533909 | C | T | 59 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(56): Show |
68 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.636-1339G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533909 | |||||||
| chr3:138534020 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.636-1450C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534020 | |||||||
| chr3:138534079 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.636-1509G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534079 | |||||||
| chr3:138534336 | C | T | 1 | a0003c0003t0003g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.636-1766G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534336 | |||||||
| chr3:138534490 | G | T | 1 | a0001c0001t0001g0039 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.636-1920C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534490 | |||||||
| chr3:138534577 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.636-2007A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534577 | |||||||
| chr3:138534603 | T | C | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.636-2033A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534603 | |||||||
| chr3:138534613 | C | T | 1 | a0001c0004t0006g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.636-2043G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534613 | |||||||
| chr3:138534758 | T | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.636-2188A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534758 | |||||||
| chr3:138534773 | T | C | 95 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(92): Show |
108 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.636-2203A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534773 | |||||||
| chr3:138534785 | T | C | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.636-2215A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534785 | |||||||
| chr3:138534801 | C | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.636-2231G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534801 | |||||||
| chr3:138534867 | T | C | 1 | a0002c0002t0002g0261 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.636-2297A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534867 | |||||||
| chr3:138534969 | A | G | 1 | a0002c0002t0002g0237 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.635+2209T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534969 | |||||||
| chr3:138535163 | A | T | 1 | a0002c0002t0001g0194 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.635+2015T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535163 | |||||||
| chr3:138535192 | C | G | 1 | a0002c0012t0002g0269 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.635+1986G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535192 | |||||||
| chr3:138535276 | T | G | 1 | a0002c0002t0002g0268 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.635+1902A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535276 | |||||||
| chr3:138535436 | A | G | 184 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(181): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.635+1742T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535436 | |||||||
| chr3:138535528 | C | T | 1 | a0003c0003t0003g0043 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.635+1650G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535528 | |||||||
| chr3:138535529 | G | A | 7 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0036 others(4): Show |
9 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.635+1649C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535529 | |||||||
| chr3:138535795 | CTCT | C | 5 | a0001c0001t0001g0130 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG00140.hp2 HG01167.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+1380_635+1382d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535795 | |||||||
| chr3:138535808 | C | T | 1 | a0003c0003t0003g0069 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.635+1370G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535808 | |||||||
| chr3:138535852 | T | C | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.635+1326A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535852 | |||||||
| chr3:138535855 | C | T | 1 | a0006c0009t0004g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.635+1323G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535855 | |||||||
| chr3:138535876 | A | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+1302T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535876 | |||||||
| chr3:138536067 | T | A | 184 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(181): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.635+1111A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536067 | |||||||
| chr3:138536236 | T | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+942A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536236 | |||||||
| chr3:138536356 | C | T | 87 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0003c0003t0001g0025 others(84): Show |
93 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.635+822G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536356 | |||||||
| chr3:138536375 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+803T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536375 | |||||||
| chr3:138536498 | T | C | 2 | a0002c0002t0001g0193 a0002c0002t0001g0194 |
2 | HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.635+680A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536498 | |||||||
| chr3:138536538 | A | G | 2 | a0001c0004t0004g0214 a0001c0004t0004g0215 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.635+640T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536538 | |||||||
| chr3:138536540 | G | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+638C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536540 | |||||||
| chr3:138536563 | C | T | 161 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(158): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.635+615G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536563 | |||||||
| chr3:138536616 | T | G | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.635+562A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536616 | |||||||
| chr3:138536679 | G | A | 159 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0002g0002 others(156): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.635+499C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536679 | |||||||
| chr3:138536776 | T | C | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.635+402A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536776 | |||||||
| chr3:138536868 | C | T | 161 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0001c0004t0006g0028 others(158): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.635+310G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536868 | |||||||
| chr3:138536910 | T | C | 2 | a0003c0003t0003g0010 a0003c0003t0003g0011 |
4 | HG01175.hp1 HG01433.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.635+268A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536910 | |||||||
| chr3:138537001 | C | CA | 19 | a0001c0001t0001g0117 a0001c0001t0001g0132 a0001c0001t0001g0136 others(16): Show |
19 | HG00544.hp2 HG00735.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.635+176dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138537001 | |||||||
| chr3:138537001 | C | CAA | 120 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(117): Show |
135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.635+175_635+176dup others(2): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138537001 | |||||||
| chr3:138537001 | C | CAAA | 30 | a0002c0002t0002g0005 a0002c0002t0002g0024 a0002c0002t0002g0036 others(27): Show |
32 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.635+174_635+176dup others(3): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138537001 | |||||||
| chr3:138537061 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+117T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138537061 | |||||||
| chr3:138537139 | A | T | 2 | a0003c0003t0003g0106 a0003c0003t0003g0212 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.635+39T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138537139 | |||||||
| chr3:138537410 | G | A | 184 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(181): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.466-63C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537410 | |||||||
| chr3:138537458 | C | T | 1 | a0003c0003t0003g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.466-111G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537458 | |||||||
| chr3:138537536 | A | G | 3 | a0002c0002t0002g0223 a0002c0002t0002g0253 a0002c0002t0002g0254 |
3 | NA19054.hp2 NA19063.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.466-189T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537536 | |||||||
| chr3:138537582 | G | A | 161 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0001c0004t0006g0028 others(158): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.466-235C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537582 | |||||||
| chr3:138537583 | T | C | 1 | a0002c0002t0002g0251 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.466-236A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537583 | |||||||
| chr3:138537656 | G | A | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-309C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537656 | |||||||
| chr3:138537927 | G | C | 1 | a0002c0002t0002g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.466-580C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537927 | |||||||
| chr3:138537928 | A | C | 1 | a0002c0002t0002g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.466-581T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537928 | |||||||
| chr3:138537929 | T | C | 1 | a0002c0002t0002g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.466-582A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537929 | |||||||
| chr3:138538112 | G | A | 1 | a0003c0003t0001g0191 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.466-765C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538112 | |||||||
| chr3:138538165 | T | C | 184 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(181): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.466-818A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538165 | |||||||
| chr3:138538168 | A | G | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.466-821T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538168 | |||||||
| chr3:138538173 | A | C | 14 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(11): Show |
16 | HG00738.hp2 HG02257.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.466-826T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538173 | |||||||
| chr3:138538208 | A | G | 1 | a0002c0002t0001g0197 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.466-861T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538208 | |||||||
| chr3:138538391 | A | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-1044T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538391 | |||||||
| chr3:138538482 | C | A | 1 | a0001c0001t0001g0163 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.466-1135G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538482 | |||||||
| chr3:138538686 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.466-1339C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538686 | |||||||
| chr3:138538695 | T | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-1348A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538695 | |||||||
| chr3:138539021 | G | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-1674C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138539021 | |||||||
| chr3:138539170 | G | A | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-1823C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138539170 | |||||||
| chr3:138539496 | A | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-2149T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138539496 | |||||||
| chr3:138539554 | G | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-2207C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138539554 | |||||||
| chr3:138539676 | C | A | 1 | a0002c0002t0001g0204 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.466-2329G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138539676 | |||||||
| chr3:138539699 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-2352A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138539699 | |||||||
| chr3:138540004 | A | G | 1 | a0002c0002t0002g0228 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.466-2657T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540004 | |||||||
| chr3:138540065 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0128 a0001c0001t0001g0187 others(5): Show |
10 | HG00735.hp2 HG01123.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.466-2718C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540065 | |||||||
| chr3:138540095 | G | A | 2 | a0001c0004t0004g0214 a0001c0004t0004g0215 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.466-2748C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540095 | |||||||
| chr3:138540223 | G | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-2876C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540223 | |||||||
| chr3:138540228 | C | T | 1 | a0003c0003t0003g0092 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.466-2881G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540228 | |||||||
| chr3:138540304 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.466-2957C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540304 | |||||||
| chr3:138540412 | A | AC | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-3066dupG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540412 | |||||||
| chr3:138540466 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.466-3119T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540466 | |||||||
| chr3:138540480 | T | TA | 18 | a0001c0001t0001g0039 a0001c0001t0001g0127 a0001c0001t0001g0131 others(15): Show |
18 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.466-3134dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540480 | |||||||
| chr3:138540480 | TAA | T | 154 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0002g0002 others(151): Show |
171 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.466-3135_466-3134d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540480 | |||||||
| chr3:138540609 | G | T | 82 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(79): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.466-3262C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540609 | |||||||
| chr3:138540707 | G | A | 2 | a0003c0003t0003g0093 a0003c0003t0003g0094 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.466-3360C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540707 | |||||||
| chr3:138540892 | C | A | 2 | a0003c0003t0003g0056 a0003c0003t0003g0058 |
2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.466-3545G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540892 | |||||||
| chr3:138540962 | C | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-3615G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540962 | |||||||
| chr3:138540975 | A | G | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-3628T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540975 | |||||||
| chr3:138541196 | C | T | 12 | a0003c0003t0003g0033 a0003c0003t0003g0040 a0003c0003t0003g0041 others(9): Show |
12 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.466-3849G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541196 | |||||||
| chr3:138541394 | G | A | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.466-4047C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541394 | |||||||
| chr3:138541430 | G | GA | 82 | a0001c0001t0001g0158 a0003c0003t0001g0025 a0003c0003t0001g0026 others(79): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.466-4084dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541430 | |||||||
| chr3:138541430 | GA | G | 74 | a0001c0001t0001g0133 a0002c0002t0001g0206 a0002c0002t0002g0002 others(71): Show |
85 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.466-4084delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541430 | |||||||
| chr3:138541625 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.466-4278A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541625 | |||||||
| chr3:138541636 | G | T | 28 | a0003c0003t0003g0009 a0003c0003t0003g0049 a0003c0003t0003g0051 others(25): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.466-4289C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541636 | |||||||
| chr3:138541941 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-4594T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541941 | |||||||
| chr3:138542108 | G | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-4761C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542108 | |||||||
| chr3:138542446 | G | A | 80 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(77): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.466-5099C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542446 | |||||||
| chr3:138542576 | G | C | 1 | a0002c0002t0002g0236 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.466-5229C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542576 | |||||||
| chr3:138542583 | G | A | 1 | a0003c0003t0001g0059 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.466-5236C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542583 | |||||||
| chr3:138542720 | C | T | 2 | a0003c0003t0003g0093 a0003c0003t0003g0094 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.466-5373G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542720 | |||||||
| chr3:138542739 | G | A | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.466-5392C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542739 | |||||||
| chr3:138542965 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.466-5618C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542965 | |||||||
| chr3:138542974 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.466-5627C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542974 | |||||||
| chr3:138543085 | G | T | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.466-5738C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543085 | |||||||
| chr3:138543251 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-5904T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543251 | |||||||
| chr3:138543398 | C | T | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-6051G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543398 | |||||||
| chr3:138543610 | C | G | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-6263G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543610 | |||||||
| chr3:138543629 | T | C | 82 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(79): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.466-6282A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543629 | |||||||
| chr3:138543636 | C | A | 1 | a0002c0002t0002g0275 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.466-6289G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543636 | |||||||
| chr3:138543696 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-6349A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543696 | |||||||
| chr3:138543839 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-6492A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543839 | |||||||
| chr3:138543972 | G | A | 74 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0002g0002 others(71): Show |
85 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.466-6625C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543972 | |||||||
| chr3:138543989 | T | TCTATTTA others(477): Show |
2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-6643_466-6642i others(486): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543989 | |||||||
| chr3:138544110 | A | G | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-6763T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544110 | |||||||
| chr3:138544133 | C | T | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-6786G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544133 | |||||||
| chr3:138544225 | A | AAAAAAAA others(475): Show |
2 | a0001c0004t0006g0031 a0004c0006t0005g0027 |
2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.466-6879_466-6878i others(484): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544225 | |||||||
| chr3:138544233 | A | G | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.466-6886T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544233 | |||||||
| chr3:138544307 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.466-6960G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544307 | |||||||
| chr3:138544357 | C | CAAAAAAA others(483): Show |
1 | a0001c0004t0006g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.466-7011_466-7010i others(492): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544357 | |||||||
| chr3:138544357 | CA | C | 176 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(173): Show |
195 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.466-7011delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544357 | |||||||
| chr3:138544507 | G | C | 1 | a0004c0006t0005g0030 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.466-7160C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544507 | |||||||
| chr3:138544509 | G | GTGTA | 84 | a0001c0001t0001g0111 a0001c0001t0001g0165 a0001c0001t0001g0278 others(81): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.466-7166_466-7163d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544509 | |||||||
| chr3:138544509 | G | GTGTATGT others(1): Show |
5 | a0003c0003t0003g0038 a0003c0003t0003g0063 a0003c0003t0003g0064 others(2): Show |
5 | HG01496.hp1 HG02622.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-7170_466-7163d others(10): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544509 | |||||||
| chr3:138544509 | G | GTGTATGT others(5): Show |
2 | a0003c0003t0003g0093 a0003c0003t0003g0094 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.466-7174_466-7163d others(14): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544509 | |||||||
| chr3:138544509 | GTGTA | G | 4 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0005c0010t0004g0022 others(1): Show |
4 | HG01243.hp1 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-7166_466-7163d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544509 | |||||||
| chr3:138544537 | A | G | 2 | a0002c0002t0002g0240 a0002c0002t0002g0241 |
2 | NA18949.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.466-7190T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544537 | |||||||
| chr3:138544804 | G | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-7457C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544804 | |||||||
| chr3:138544873 | G | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-7526C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544873 | |||||||
| chr3:138544883 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.466-7536G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544883 | |||||||
| chr3:138544888 | G | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-7541C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544888 | |||||||
| chr3:138544899 | C | T | 1 | a0003c0003t0003g0043 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.466-7552G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544899 | |||||||
| chr3:138545018 | C | A | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.466-7671G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545018 | |||||||
| chr3:138545048 | G | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-7701C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545048 | |||||||
| chr3:138545184 | C | T | 1 | a0002c0002t0002g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.466-7837G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545184 | |||||||
| chr3:138545205 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02698.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.466-7858A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545205 | |||||||
| chr3:138545653 | T | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-8306A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545653 | |||||||
| chr3:138545815 | T | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-8468A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545815 | |||||||
| chr3:138545914 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-8567A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545914 | |||||||
| chr3:138545948 | C | T | 1 | a0002c0002t0002g0236 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.466-8601G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545948 | |||||||
| chr3:138546042 | T | G | 2 | a0003c0003t0003g0010 a0003c0003t0003g0011 |
4 | HG01175.hp1 HG01433.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-8695A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546042 | |||||||
| chr3:138546134 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.466-8787G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546134 | |||||||
| chr3:138546259 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-8912G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546259 | |||||||
| chr3:138546348 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.466-9001A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546348 | |||||||
| chr3:138546549 | G | A | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-9202C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546549 | |||||||
| chr3:138546578 | G | A | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-9231C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546578 | |||||||
| chr3:138546593 | A | G | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-9246T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546593 | |||||||
| chr3:138546610 | G | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-9263C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546610 | |||||||
| chr3:138546612 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-9265T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546612 | |||||||
| chr3:138546738 | G | A | 7 | a0002c0002t0002g0002 a0002c0002t0002g0223 a0002c0002t0002g0246 others(4): Show |
10 | NA18950.hp1 NA19007.hp1 NA19054.hp2 others(7): Show |
intron_variant | MODIFIER | c.466-9391C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546738 | |||||||
| chr3:138546765 | T | TA | 91 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(88): Show |
104 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.466-9419dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546765 | |||||||
| chr3:138546828 | G | T | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-9481C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546828 | |||||||
| chr3:138546864 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-9517T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546864 | |||||||
| chr3:138546897 | G | A | 2 | a0003c0003t0003g0093 a0003c0003t0003g0094 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.466-9550C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546897 | |||||||
| chr3:138547016 | AAATGAAA others(12): Show |
A | 3 | a0001c0001t0001g0281 a0002c0002t0001g0195 a0002c0002t0001g0196 |
3 | HG02647.hp2 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.466-9688_466-9670d others(21): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547016 | |||||||
| chr3:138547142 | G | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(280): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.466-9795C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547142 | |||||||
| chr3:138547146 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(280): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.466-9799T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547146 | |||||||
| chr3:138547336 | T | C | 2 | a0003c0003t0003g0068 a0003c0003t0003g0070 |
2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.466-9989A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547336 | |||||||
| chr3:138547754 | G | A | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.466-10407C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547754 | |||||||
| chr3:138547793 | G | A | 91 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(88): Show |
104 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.466-10446C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547793 | |||||||
| chr3:138547861 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.466-10514A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547861 | |||||||
| chr3:138547922 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.466-10575G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547922 | |||||||
| chr3:138548044 | A | G | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-10697T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548044 | |||||||
| chr3:138548055 | A | C | 2 | a0003c0003t0003g0113 a0003c0003t0003g0114 |
2 | NA18957.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.466-10708T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548055 | |||||||
| chr3:138548063 | T | C | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.466-10716A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548063 | |||||||
| chr3:138548202 | G | C | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.466-10855C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548202 | |||||||
| chr3:138548251 | T | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-10904A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548251 | |||||||
| chr3:138548388 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-11041G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548388 | |||||||
| chr3:138548632 | C | T | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.466-11285G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548632 | |||||||
| chr3:138548695 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.466-11348A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548695 | |||||||
| chr3:138548931 | A | G | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-11584T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548931 | |||||||
| chr3:138548963 | T | C | 184 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(181): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.466-11616A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548963 | |||||||
| chr3:138549051 | G | A | 1 | a0003c0003t0001g0026 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.466-11704C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549051 | |||||||
| chr3:138549231 | T | C | 1 | a0002c0002t0002g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.466-11884A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549231 | |||||||
| chr3:138549303 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.466-11956C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549303 | |||||||
| chr3:138549304 | C | G | 1 | a0001c0001t0001g0039 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.466-11957G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549304 | |||||||
| chr3:138549305 | A | C | 1 | a0001c0001t0001g0039 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.466-11958T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549305 | |||||||
| chr3:138549363 | C | T | 1 | a0003c0003t0003g0040 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.466-12016G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549363 | |||||||
| chr3:138549364 | G | A | 1 | a0003c0003t0003g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.466-12017C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549364 | |||||||
| chr3:138549367 | T | C | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-12020A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549367 | |||||||
| chr3:138549588 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-12241G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549588 | |||||||
| chr3:138549590 | C | T | 10 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0137 others(7): Show |
10 | HG00544.hp2 HG02071.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.466-12243G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549590 | |||||||
| chr3:138549649 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-12302T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549649 | |||||||
| chr3:138549673 | G | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.466-12326C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549673 | |||||||
| chr3:138549696 | C | T | 28 | a0003c0003t0003g0009 a0003c0003t0003g0049 a0003c0003t0003g0051 others(25): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.466-12349G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549696 | |||||||
| chr3:138549697 | G | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-12350C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549697 | |||||||
| chr3:138549709 | C | T | 82 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(79): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.466-12362G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549709 | |||||||
| chr3:138549719 | A | T | 182 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0001c0004t0006g0028 others(179): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.466-12372T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549719 | |||||||
| chr3:138549820 | T | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02083.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.466-12473A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549820 | |||||||
| chr3:138549874 | G | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-12527C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549874 | |||||||
| chr3:138549949 | T | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-12602A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549949 | |||||||
| chr3:138550041 | G | A | 1 | a0003c0003t0003g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.466-12694C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138550041 | |||||||
| chr3:138550151 | C | T | 91 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(88): Show |
104 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.466-12804G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138550151 | |||||||
| chr3:138550161 | C | A | 5 | a0002c0002t0002g0005 a0002c0002t0002g0218 a0002c0002t0002g0219 others(2): Show |
7 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.466-12814G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138550161 | |||||||
| chr3:138550390 | T | A | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-13043A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138550390 | |||||||
| chr3:138550485 | T | A | 1 | a0003c0003t0003g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.466-13138A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138550485 | |||||||
| chr3:138550609 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-13262G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138550609 | |||||||
| chr3:138551180 | A | T | 2 | a0001c0004t0004g0214 a0001c0004t0004g0215 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.466-13833T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551180 | |||||||
| chr3:138551313 | G | A | 82 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(79): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.466-13966C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551313 | |||||||
| chr3:138551557 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.466-14210G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551557 | |||||||
| chr3:138551574 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0153 |
2 | NA18941.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.466-14227G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551574 | |||||||
| chr3:138551702 | C | T | 3 | a0003c0003t0003g0042 a0003c0003t0003g0046 a0003c0003t0003g0047 |
3 | HG00621.hp1 HG00673.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.466-14355G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551702 | |||||||
| chr3:138551758 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.466-14411T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551758 | |||||||
| chr3:138551758 | AT | A | 93 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0002c0002t0002g0005 others(90): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.466-14412delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551758 | |||||||
| chr3:138551759 | T | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
208 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.466-14412A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551759 | |||||||
| chr3:138551760 | A | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-14413T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551760 | |||||||
| chr3:138551760 | A | T | 5 | a0001c0001t0001g0115 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
5 | HG02027.hp2 HG02040.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-14413T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551760 | |||||||
| chr3:138551761 | A | T | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.466-14414T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551761 | |||||||
| chr3:138551764 | T | A | 12 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0002c0002t0002g0232 others(9): Show |
12 | HG00323.hp2 HG00735.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.466-14417A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551764 | |||||||
| chr3:138551764 | T | C | 172 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(169): Show |
191 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.466-14417A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551764 | |||||||
| chr3:138551769 | C | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-14422G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551769 | |||||||
| chr3:138551796 | T | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-14449A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551796 | |||||||
| chr3:138551877 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-14530A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551877 | |||||||
| chr3:138551985 | T | G | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-14638A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551985 | |||||||
| chr3:138552312 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-14965G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552312 | |||||||
| chr3:138552357 | C | A | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.466-15010G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552357 | |||||||
| chr3:138552447 | T | G | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-15100A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552447 | |||||||
| chr3:138552483 | A | T | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.466-15136T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552483 | |||||||
| chr3:138552511 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.466-15164G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552511 | |||||||
| chr3:138552535 | T | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-15188A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552535 | |||||||
| chr3:138552608 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-15261G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552608 | |||||||
| chr3:138552925 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-15578G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552925 | |||||||
| chr3:138552938 | G | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-15591C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552938 | |||||||
| chr3:138553052 | A | G | 3 | a0002c0002t0002g0232 a0002c0002t0002g0248 a0002c0002t0002g0268 |
3 | NA18612.hp2 NA18969.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.466-15705T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553052 | |||||||
| chr3:138553053 | C | T | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.466-15706G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553053 | |||||||
| chr3:138553207 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.466-15860G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553207 | |||||||
| chr3:138553290 | T | G | 59 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(56): Show |
68 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.466-15943A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553290 | |||||||
| chr3:138553341 | G | A | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.466-15994C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553341 | |||||||
| chr3:138553352 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-16005A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553352 | |||||||
| chr3:138553353 | G | A | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.466-16006C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553353 | |||||||
| chr3:138553379 | C | A | 1 | a0002c0002t0002g0247 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.466-16032G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553379 | |||||||
| chr3:138553487 | C | CA | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(118): Show |
140 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.466-16141dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553487 | |||||||
| chr3:138553544 | A | AAAG | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-16200_466-1619 others(7): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553544 | |||||||
| chr3:138553745 | C | T | 95 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(92): Show |
108 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.466-16398G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553745 | |||||||
| chr3:138553783 | T | A | 1 | a0001c0001t0001g0137 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.466-16436A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553783 | |||||||
| chr3:138554169 | C | G | 1 | a0003c0003t0003g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.465+16149G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554169 | |||||||
| chr3:138554200 | G | GA | 13 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0166 others(10): Show |
13 | HG00280.hp2 HG01109.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.465+16117dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554200 | |||||||
| chr3:138554200 | GA | G | 30 | a0001c0001t0001g0013 a0001c0001t0001g0122 a0001c0001t0001g0133 others(27): Show |
33 | HG00738.hp2 HG01123.hp2 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.465+16117delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554200 | |||||||
| chr3:138554292 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+16026G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554292 | |||||||
| chr3:138554523 | G | A | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.465+15795C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554523 | |||||||
| chr3:138554645 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(201): Show |
230 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.465+15673A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554645 | |||||||
| chr3:138554827 | T | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+15491A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554827 | |||||||
| chr3:138554872 | G | C | 2 | a0003c0003t0003g0098 a0003c0003t0003g0099 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.465+15446C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554872 | |||||||
| chr3:138554935 | T | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+15383A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554935 | |||||||
| chr3:138554969 | T | C | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+15349A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554969 | |||||||
| chr3:138554998 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+15320A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554998 | |||||||
| chr3:138555060 | C | T | 1 | a0002c0002t0002g0259 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.465+15258G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555060 | |||||||
| chr3:138555156 | G | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+15162C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555156 | |||||||
| chr3:138555180 | G | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+15138C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555180 | |||||||
| chr3:138555193 | G | A | 1 | a0003c0003t0003g0070 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.465+15125C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555193 | |||||||
| chr3:138555248 | C | CAAAA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(93): Show |
109 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.465+15066_465+1506 others(8): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555248 | |||||||
| chr3:138555248 | C | CAAAAA | 44 | a0001c0001t0001g0137 a0001c0001t0001g0168 a0001c0001t0001g0170 others(41): Show |
48 | HG00738.hp2 HG01123.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.465+15065_465+1506 others(9): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555248 | |||||||
| chr3:138555248 | C | CAAAAAA | 57 | a0001c0004t0004g0215 a0002c0002t0002g0002 a0002c0002t0002g0006 others(54): Show |
66 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.465+15064_465+1506 others(10): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555248 | |||||||
| chr3:138555375 | T | G | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.465+14943A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555375 | |||||||
| chr3:138555673 | A | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+14645T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555673 | |||||||
| chr3:138555709 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+14609T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555709 | |||||||
| chr3:138555910 | C | T | 1 | a0003c0003t0001g0059 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.465+14408G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555910 | |||||||
| chr3:138556013 | G | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.465+14305C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556013 | |||||||
| chr3:138556043 | G | C | 1 | a0002c0002t0002g0245 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.465+14275C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556043 | |||||||
| chr3:138556069 | C | T | 95 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(92): Show |
108 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.465+14249G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556069 | |||||||
| chr3:138556121 | A | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+14197T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556121 | |||||||
| chr3:138556137 | T | C | 1 | a0003c0003t0003g0046 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.465+14181A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556137 | |||||||
| chr3:138556288 | C | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+14030G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556288 | |||||||
| chr3:138556308 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+14010A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556308 | |||||||
| chr3:138556414 | G | C | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+13904C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556414 | |||||||
| chr3:138556527 | C | CA | 17 | a0003c0003t0001g0025 a0003c0003t0001g0026 a0003c0003t0001g0059 others(14): Show |
17 | HG00621.hp1 HG00639.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.465+13790dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556527 | |||||||
| chr3:138556527 | CA | C | 94 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0170 others(91): Show |
107 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.465+13790delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556527 | |||||||
| chr3:138556527 | CAA | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+13789_465+1379 others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556527 | |||||||
| chr3:138556584 | G | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+13734C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556584 | |||||||
| chr3:138556617 | C | T | 2 | a0002c0002t0002g0237 a0004c0006t0005g0027 |
2 | HG06807.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.465+13701G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556617 | |||||||
| chr3:138556635 | G | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+13683C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556635 | |||||||
| chr3:138556649 | G | A | 1 | a0003c0003t0003g0065 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.465+13669C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556649 | |||||||
| chr3:138556717 | C | G | 4 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0005c0010t0004g0022 others(1): Show |
4 | HG01243.hp1 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+13601G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556717 | |||||||
| chr3:138556728 | G | A | 95 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(92): Show |
108 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.465+13590C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556728 | |||||||
| chr3:138556776 | G | T | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.465+13542C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556776 | |||||||
| chr3:138556780 | T | C | 2 | a0003c0003t0003g0093 a0003c0003t0003g0094 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.465+13538A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556780 | |||||||
| chr3:138556797 | G | A | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+13521C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556797 | |||||||
| chr3:138556865 | G | A | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.465+13453C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556865 | |||||||
| chr3:138556969 | T | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.465+13349A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556969 | |||||||
| chr3:138556985 | G | A | 95 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(92): Show |
108 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.465+13333C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556985 | |||||||
| chr3:138557036 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+13282T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557036 | |||||||
| chr3:138557043 | C | T | 1 | a0002c0002t0002g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.465+13275G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557043 | |||||||
| chr3:138557049 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+13269A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557049 | |||||||
| chr3:138557100 | C | T | 1 | a0002c0002t0002g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.465+13218G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557100 | |||||||
| chr3:138557120 | T | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+13198A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557120 | |||||||
| chr3:138557141 | A | G | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.465+13177T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557141 | |||||||
| chr3:138557201 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+13117T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557201 | |||||||
| chr3:138557209 | G | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+13109C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557209 | |||||||
| chr3:138557291 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.465+13027G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557291 | |||||||
| chr3:138557313 | TACAA | T | 9 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0003c0003t0003g0049 others(6): Show |
9 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.465+13001_465+1300 others(8): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557313 | |||||||
| chr3:138557354 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+12964A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557354 | |||||||
| chr3:138557428 | G | T | 2 | a0003c0003t0001g0066 a0003c0003t0001g0191 |
2 | HG01071.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.465+12890C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557428 | |||||||
| chr3:138557435 | T | C | 1 | a0002c0002t0002g0230 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.465+12883A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557435 | |||||||
| chr3:138557440 | G | T | 1 | a0003c0003t0003g0041 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.465+12878C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557440 | |||||||
| chr3:138557576 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+12742A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557576 | |||||||
| chr3:138557644 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.465+12674A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557644 | |||||||
| chr3:138557669 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.465+12649T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557669 | |||||||
| chr3:138557699 | T | C | 77 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(74): Show |
89 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.465+12619A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557699 | |||||||
| chr3:138557712 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.465+12606T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557712 | |||||||
| chr3:138557843 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.465+12475C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557843 | |||||||
| chr3:138557873 | T | C | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.465+12445A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557873 | |||||||
| chr3:138557970 | A | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+12348T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557970 | |||||||
| chr3:138558018 | T | C | 1 | a0006c0009t0004g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.465+12300A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558018 | |||||||
| chr3:138558106 | T | C | 1 | a0002c0002t0002g0258 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.465+12212A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558106 | |||||||
| chr3:138558124 | C | T | 1 | a0002c0002t0002g0231 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.465+12194G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558124 | |||||||
| chr3:138558139 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.465+12179G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558139 | |||||||
| chr3:138558167 | C | A | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+12151G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558167 | |||||||
| chr3:138558274 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
120 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.465+12044G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558274 | |||||||
| chr3:138558275 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.465+12043T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558275 | |||||||
| chr3:138558329 | C | T | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+11989G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558329 | |||||||
| chr3:138558360 | G | A | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+11958C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558360 | |||||||
| chr3:138558388 | T | C | 1 | a0003c0003t0003g0053 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.465+11930A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558388 | |||||||
| chr3:138558510 | T | C | 3 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 |
3 | HG02615.hp2 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+11808A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558510 | |||||||
| chr3:138558608 | T | C | 1 | a0002c0002t0001g0194 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.465+11710A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558608 | |||||||
| chr3:138558848 | C | T | 1 | a0001c0004t0004g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.465+11470G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558848 | |||||||
| chr3:138559069 | T | C | 1 | a0002c0002t0001g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.465+11249A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559069 | |||||||
| chr3:138559086 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA18975.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.465+11232G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559086 | |||||||
| chr3:138559159 | C | T | 12 | a0003c0003t0001g0026 a0003c0003t0003g0009 a0003c0003t0003g0060 others(9): Show |
13 | HG00140.hp1 HG00735.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.465+11159G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559159 | |||||||
| chr3:138559202 | G | A | 1 | a0002c0002t0002g0260 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.465+11116C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559202 | |||||||
| chr3:138559364 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(194): Show |
223 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.465+10954C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559364 | |||||||
| chr3:138559377 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+10941A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559377 | |||||||
| chr3:138559378 | G | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+10940C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559378 | |||||||
| chr3:138559413 | G | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+10905C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559413 | |||||||
| chr3:138559487 | C | T | 11 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(8): Show |
11 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.465+10831G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559487 | |||||||
| chr3:138559632 | G | A | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+10686C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559632 | |||||||
| chr3:138559656 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.465+10662G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559656 | |||||||
| chr3:138560112 | C | T | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+10206G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560112 | |||||||
| chr3:138560143 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | NA18945.hp1 NA18975.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.465+10175G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560143 | |||||||
| chr3:138560218 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02083.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.465+10100C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560218 | |||||||
| chr3:138560338 | T | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+9980A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560338 | |||||||
| chr3:138560373 | G | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+9945C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560373 | |||||||
| chr3:138560473 | G | GT | 14 | a0001c0001t0001g0115 a0001c0001t0001g0122 a0001c0001t0001g0134 others(11): Show |
14 | HG01099.hp2 HG01243.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.465+9844dupA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560473 | |||||||
| chr3:138560473 | G | T | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.465+9845C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560473 | |||||||
| chr3:138560567 | AGGTCTG | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+9745_465+9750d others(8): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560567 | |||||||
| chr3:138560708 | G | A | 91 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(88): Show |
104 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.465+9610C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560708 | |||||||
| chr3:138560944 | G | A | 2 | a0003c0003t0003g0075 a0003c0003t0003g0090 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.465+9374C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560944 | |||||||
| chr3:138560960 | G | T | 1 | a0001c0001t0001g0133 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.465+9358C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560960 | |||||||
| chr3:138560973 | G | A | 1 | a0002c0002t0001g0206 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.465+9345C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560973 | |||||||
| chr3:138560986 | G | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+9332C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560986 | |||||||
| chr3:138561015 | C | G | 1 | a0002c0002t0001g0201 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.465+9303G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561015 | |||||||
| chr3:138561032 | G | A | 8 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(5): Show |
8 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.465+9286C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561032 | |||||||
| chr3:138561046 | G | A | 1 | a0003c0003t0003g0096 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.465+9272C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561046 | |||||||
| chr3:138561136 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.465+9182C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561136 | |||||||
| chr3:138561171 | G | A | 1 | a0002c0002t0002g0239 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.465+9147C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561171 | |||||||
| chr3:138561376 | C | T | 1 | a0002c0002t0002g0239 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.465+8942G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561376 | |||||||
| chr3:138561401 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.465+8917C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561401 | |||||||
| chr3:138561826 | A | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.465+8492T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561826 | |||||||
| chr3:138561852 | G | A | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.465+8466C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561852 | |||||||
| chr3:138561896 | C | T | 1 | a0003c0003t0003g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.465+8422G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561896 | |||||||
| chr3:138561968 | A | G | 1 | a0003c0003t0003g0100 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.465+8350T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561968 | |||||||
| chr3:138562002 | G | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.465+8316C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562002 | |||||||
| chr3:138562022 | CA | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(184): Show |
210 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.465+8295delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562022 | |||||||
| chr3:138562074 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.465+8244G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562074 | |||||||
| chr3:138562075 | C | T | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.465+8243G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562075 | |||||||
| chr3:138562163 | T | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+8155A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562163 | |||||||
| chr3:138562242 | A | C | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.465+8076T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562242 | |||||||
| chr3:138562321 | T | C | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.465+7997A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562321 | |||||||
| chr3:138562326 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.465+7992C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562326 | |||||||
| chr3:138562332 | C | T | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+7986G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562332 | |||||||
| chr3:138562344 | G | GA | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+7973dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562344 | |||||||
| chr3:138562361 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+7957G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562361 | |||||||
| chr3:138562434 | A | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(83): Show |
99 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.465+7884T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562434 | |||||||
| chr3:138562449 | C | A | 4 | a0002c0002t0002g0236 a0002c0002t0002g0256 a0002c0002t0002g0257 others(1): Show |
4 | HG00408.hp2 HG02074.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+7869G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562449 | |||||||
| chr3:138562497 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.465+7821G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562497 | |||||||
| chr3:138562522 | C | T | 1 | a0002c0002t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.465+7796G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562522 | |||||||
| chr3:138562742 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.465+7576G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562742 | |||||||
| chr3:138562933 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.465+7385A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562933 | |||||||
| chr3:138563029 | CA | C | 6 | a0001c0001t0001g0217 a0001c0004t0006g0028 a0001c0004t0006g0031 others(3): Show |
6 | HG00280.hp1 HG00735.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.465+7288delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563029 | |||||||
| chr3:138563062 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.465+7256A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563062 | |||||||
| chr3:138563080 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.465+7238T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563080 | |||||||
| chr3:138563135 | G | GCAA | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+7180_465+7182d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563135 | |||||||
| chr3:138563254 | G | A | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.465+7064C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563254 | |||||||
| chr3:138563350 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.465+6968G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563350 | |||||||
| chr3:138563601 | G | A | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+6717C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563601 | |||||||
| chr3:138563634 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+6684C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563634 | |||||||
| chr3:138563649 | T | C | 3 | a0003c0003t0003g0097 a0003c0003t0003g0098 a0003c0003t0003g0099 |
3 | HG01243.hp2 HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.465+6669A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563649 | |||||||
| chr3:138563655 | C | A | 2 | a0001c0004t0004g0214 a0001c0004t0004g0215 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+6663G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563655 | |||||||
| chr3:138563726 | G | A | 1 | a0002c0002t0002g0271 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.465+6592C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563726 | |||||||
| chr3:138563764 | A | AC | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+6553dupG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563764 | |||||||
| chr3:138563764 | A | G | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+6554T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563764 | |||||||
| chr3:138563778 | T | C | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+6540A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563778 | |||||||
| chr3:138563789 | A | G | 1 | a0002c0002t0002g0259 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.465+6529T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563789 | |||||||
| chr3:138563809 | A | T | 15 | a0002c0002t0002g0006 a0002c0002t0002g0020 a0002c0002t0002g0228 others(12): Show |
18 | HG01346.hp1 HG01884.hp1 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.465+6509T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563809 | |||||||
| chr3:138563857 | T | C | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+6461A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563857 | |||||||
| chr3:138564104 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.465+6214A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564104 | |||||||
| chr3:138564310 | C | T | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.465+6008G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564310 | |||||||
| chr3:138564428 | C | G | 1 | a0002c0002t0002g0261 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.465+5890G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564428 | |||||||
| chr3:138564501 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(97): Show |
113 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.465+5817C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564501 | |||||||
| chr3:138564617 | T | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+5701A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564617 | |||||||
| chr3:138564687 | C | T | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+5631G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564687 | |||||||
| chr3:138564824 | A | C | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.465+5494T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564824 | |||||||
| chr3:138565149 | G | A | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+5169C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565149 | |||||||
| chr3:138565208 | A | C | 1 | a0002c0002t0002g0268 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.465+5110T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565208 | |||||||
| chr3:138565220 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.465+5098A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565220 | |||||||
| chr3:138565266 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+5052A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565266 | |||||||
| chr3:138565518 | C | T | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.465+4800G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565518 | |||||||
| chr3:138565528 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+4790C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565528 | |||||||
| chr3:138565555 | C | T | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.465+4763G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565555 | |||||||
| chr3:138565670 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.465+4648G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565670 | |||||||
| chr3:138565721 | C | G | 1 | a0002c0002t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.465+4597G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565721 | |||||||
| chr3:138565733 | C | T | 2 | a0002c0002t0002g0260 a0002c0002t0002g0264 |
2 | HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.465+4585G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565733 | |||||||
| chr3:138565749 | G | A | 2 | a0001c0004t0004g0214 a0001c0004t0004g0215 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+4569C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565749 | |||||||
| chr3:138565874 | A | G | 1 | a0002c0002t0002g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.465+4444T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565874 | |||||||
| chr3:138565921 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.465+4397G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565921 | |||||||
| chr3:138565922 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.465+4396G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565922 | |||||||
| chr3:138566060 | C | T | 7 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0036 others(4): Show |
9 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.465+4258G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566060 | |||||||
| chr3:138566153 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.465+4165C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566153 | |||||||
| chr3:138566184 | C | T | 1 | a0001c0004t0004g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.465+4134G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566184 | |||||||
| chr3:138566220 | T | A | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+4098A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566220 | |||||||
| chr3:138566278 | A | G | 1 | a0001c0004t0006g0031 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.465+4040T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566278 | |||||||
| chr3:138566373 | T | C | 1 | a0003c0003t0003g0038 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.465+3945A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566373 | |||||||
| chr3:138566379 | C | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+3939G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566379 | |||||||
| chr3:138566379 | C | T | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+3939G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566379 | |||||||
| chr3:138566493 | C | T | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+3825G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566493 | |||||||
| chr3:138566601 | G | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+3717C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566601 | |||||||
| chr3:138566681 | G | A | 2 | a0001c0004t0004g0214 a0001c0004t0004g0215 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+3637C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566681 | |||||||
| chr3:138566803 | G | GTA | 65 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(62): Show |
75 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.465+3513_465+3514d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566803 | |||||||
| chr3:138566803 | G | GTATA | 2 | a0002c0002t0002g0021 a0002c0002t0002g0259 |
3 | HG00544.hp1 NA19012.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.465+3511_465+3514d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566803 | |||||||
| chr3:138566803 | GTA | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+3513_465+3514d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566803 | |||||||
| chr3:138566815 | A | C | 1 | a0003c0003t0003g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.465+3503T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566815 | |||||||
| chr3:138566820 | A | T | 14 | a0002c0002t0002g0006 a0002c0002t0002g0020 a0003c0003t0003g0033 others(11): Show |
17 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.465+3498T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566820 | |||||||
| chr3:138567060 | A | T | 2 | a0003c0003t0003g0049 a0003c0003t0003g0080 |
2 | NA18986.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.465+3258T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567060 | |||||||
| chr3:138567199 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.465+3119A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567199 | |||||||
| chr3:138567338 | T | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+2980A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567338 | |||||||
| chr3:138567576 | G | A | 1 | a0006c0009t0004g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.465+2742C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567576 | |||||||
| chr3:138567619 | T | C | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.465+2699A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567619 | |||||||
| chr3:138567633 | C | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+2685G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567633 | |||||||
| chr3:138567867 | T | C | 1 | a0003c0003t0003g0094 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.465+2451A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567867 | |||||||
| chr3:138567888 | G | A | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.465+2430C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567888 | |||||||
| chr3:138567983 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+2335C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567983 | |||||||
| chr3:138567985 | C | T | 1 | a0002c0002t0002g0238 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.465+2333G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567985 | |||||||
| chr3:138567999 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.465+2319A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567999 | |||||||
| chr3:138568058 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+2260G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568058 | |||||||
| chr3:138568230 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.465+2088G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568230 | |||||||
| chr3:138568427 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.465+1891A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568427 | |||||||
| chr3:138568703 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG00408.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.465+1615C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568703 | |||||||
| chr3:138568836 | G | A | 5 | a0001c0004t0004g0108 a0001c0004t0004g0109 a0001c0004t0004g0214 others(2): Show |
5 | HG02258.hp1 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+1482C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568836 | |||||||
| chr3:138568843 | G | A | 1 | a0002c0002t0002g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.465+1475C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568843 | |||||||
| chr3:138568889 | G | A | 1 | a0003c0003t0003g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.465+1429C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568889 | |||||||
| chr3:138568994 | C | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(198): Show |
227 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.465+1324G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568994 | |||||||
| chr3:138568994 | C | CA | 6 | a0003c0003t0003g0003 a0003c0003t0003g0076 a0003c0003t0003g0096 others(3): Show |
8 | HG01243.hp2 HG02559.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.465+1323dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568994 | |||||||
| chr3:138568995 | A | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(188): Show |
217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.465+1323T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568995 | |||||||
| chr3:138568996 | A | C | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.465+1322T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568996 | |||||||
| chr3:138569000 | A | C | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.465+1318T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569000 | |||||||
| chr3:138569009 | A | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+1309T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569009 | |||||||
| chr3:138569101 | A | C | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.465+1217T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569101 | |||||||
| chr3:138569171 | C | T | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.465+1147G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569171 | |||||||
| chr3:138569279 | C | G | 1 | a0002c0002t0002g0237 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.465+1039G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569279 | |||||||
| chr3:138569282 | G | T | 1 | a0002c0002t0001g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.465+1036C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569282 | |||||||
| chr3:138569283 | C | T | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+1035G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569283 | |||||||
| chr3:138569482 | A | C | 2 | a0001c0001t0001g0111 a0001c0011t0001g0110 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.465+836T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569482 | |||||||
| chr3:138569530 | A | C | 1 | a0002c0002t0002g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.465+788T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569530 | |||||||
| chr3:138569633 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+685G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569633 | |||||||
| chr3:138569729 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+589C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569729 | |||||||
| chr3:138569737 | A | G | 1 | a0002c0002t0002g0236 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.465+581T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569737 | |||||||
| chr3:138569758 | C | T | 1 | a0006c0009t0004g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.465+560G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569758 | |||||||
| chr3:138569962 | G | A | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.465+356C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569962 | |||||||
| chr3:138569980 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.465+338G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569980 | |||||||
| chr3:138570224 | A | G | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+94T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138570224 | |||||||
| chr3:138570574 | T | C | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.285-76A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 5/17 | chr3 | 138570574 | |||||||
| chr3:138570778 | T | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(277): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.284+256A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 5/17 | chr3 | 138570778 | |||||||
| chr3:138570787 | C | G | 2 | a0003c0003t0003g0093 a0003c0003t0003g0094 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.284+247G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 5/17 | chr3 | 138570787 | |||||||
| chr3:138571189 | A | AAAAATAA others(1801): Show |
2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.161-33_161-32insGT others(1806): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 4/17 | chr3 | 138571189 | |||||||
| chr3:138571220 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.160+46T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 4/17 | chr3 | 138571220 | |||||||
| chr3:138571594 | G | C | 1 | a0003c0003t0003g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.70-238C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571594 | |||||||
| chr3:138571647 | A | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70-291T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571647 | |||||||
| chr3:138571740 | T | TAAAGA | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.70-389_70-385dupTC others(3): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571740 | |||||||
| chr3:138571766 | C | A | 1 | a0002c0002t0001g0194 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.70-410G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571766 | |||||||
| chr3:138571820 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.70-464G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571820 | |||||||
| chr3:138571836 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.70-480G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571836 | |||||||
| chr3:138571905 | A | G | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.70-549T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571905 | |||||||
| chr3:138571935 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(98): Show |
114 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.70-579G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571935 | |||||||
| chr3:138572069 | C | CA | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.70-714_70-713insT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572069 | |||||||
| chr3:138572200 | G | A | 2 | a0002c0002t0002g0260 a0002c0002t0002g0264 |
2 | HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.69+659C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572200 | |||||||
| chr3:138572216 | G | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(98): Show |
114 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.69+643C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572216 | |||||||
| chr3:138572310 | C | T | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.69+549G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572310 | |||||||
| chr3:138572369 | C | G | 1 | a0003c0003t0003g0085 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.69+490G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572369 | |||||||
| chr3:138572370 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG00673.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.69+489C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572370 | |||||||
| chr3:138572392 | A | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.69+467T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572392 | |||||||
| chr3:138572395 | T | C | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.69+464A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572395 | |||||||
| chr3:138572515 | A | G | 1 | a0004c0006t0005g0030 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.69+344T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572515 | |||||||
| chr3:138572531 | C | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.69+328G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572531 | |||||||
| chr3:138572664 | G | A | 3 | a0002c0002t0002g0261 a0002c0002t0002g0262 a0002c0002t0002g0263 |
3 | NA18994.hp2 NA19062.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.69+195C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572664 | |||||||
| chr3:138572690 | T | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0126 a0001c0001t0001g0178 |
4 | HG01256.hp2 HG01258.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+169A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572690 | |||||||
| chr3:138572706 | T | C | 1 | a0003c0003t0003g0085 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.69+153A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572706 | |||||||
| chr3:138572727 | T | C | 69 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(66): Show |
80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.69+132A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572727 | |||||||
| chr3:138572976 | T | C | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5-44A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138572976 | |||||||
| chr3:138573091 | G | C | 1 | a0006c0009t0004g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-5-159C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573091 | |||||||
| chr3:138573142 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-5-210T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573142 | |||||||
| chr3:138573205 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-273G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573205 | |||||||
| chr3:138573207 | C | T | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-275G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573207 | |||||||
| chr3:138573309 | A | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-377T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573309 | |||||||
| chr3:138573380 | T | TA | 16 | a0001c0001t0001g0179 a0002c0002t0002g0032 a0003c0003t0003g0049 others(13): Show |
16 | HG01243.hp2 HG01255.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5-449dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573380 | |||||||
| chr3:138573420 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-5-488G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573420 | |||||||
| chr3:138573561 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-629A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573561 | |||||||
| chr3:138574025 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-5-1093C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574025 | |||||||
| chr3:138574118 | C | T | 1 | a0003c0003t0003g0033 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-5-1186G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574118 | |||||||
| chr3:138574122 | C | T | 1 | a0002c0002t0002g0235 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-5-1190G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574122 | |||||||
| chr3:138574141 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-1209A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574141 | |||||||
| chr3:138574168 | G | A | 69 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(66): Show |
80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-5-1236C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574168 | |||||||
| chr3:138574194 | A | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0128 a0001c0001t0001g0187 |
5 | HG01123.hp1 HG01257.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-1262T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574194 | |||||||
| chr3:138574200 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(97): Show |
113 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-5-1268A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574200 | |||||||
| chr3:138574246 | C | T | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-5-1314G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574246 | |||||||
| chr3:138574247 | G | A | 3 | a0002c0002t0002g0228 a0002c0002t0002g0229 a0002c0002t0002g0230 |
3 | NA18965.hp1 NA18975.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-5-1315C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574247 | |||||||
| chr3:138574411 | G | A | 1 | a0003c0003t0003g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-5-1479C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574411 | |||||||
| chr3:138574431 | C | T | 5 | a0002c0002t0002g0005 a0002c0002t0002g0218 a0002c0002t0002g0219 others(2): Show |
7 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-1499G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574431 | |||||||
| chr3:138574449 | T | C | 69 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(66): Show |
80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-5-1517A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574449 | |||||||
| chr3:138574518 | T | C | 1 | a0003c0003t0003g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-5-1586A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574518 | |||||||
| chr3:138574558 | T | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-1626A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574558 | |||||||
| chr3:138574564 | T | C | 1 | a0002c0002t0002g0264 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-5-1632A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574564 | |||||||
| chr3:138574656 | C | T | 58 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(55): Show |
67 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-5-1724G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574656 | |||||||
| chr3:138574660 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-1728C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574660 | |||||||
| chr3:138574895 | A | G | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-5-1963T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574895 | |||||||
| chr3:138574898 | G | A | 3 | a0003c0005t0003g0057 a0003c0005t0003g0087 a0003c0005t0003g0088 |
3 | HG02280.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-5-1966C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574898 | |||||||
| chr3:138574987 | A | C | 1 | a0003c0003t0003g0042 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-5-2055T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574987 | |||||||
| chr3:138575080 | C | G | 1 | a0003c0005t0003g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-5-2148G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575080 | |||||||
| chr3:138575090 | T | C | 1 | a0002c0002t0002g0006 | 3 | HG02735.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-5-2158A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575090 | |||||||
| chr3:138575107 | G | T | 1 | a0003c0003t0003g0056 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-5-2175C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575107 | |||||||
| chr3:138575264 | G | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-2332C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575264 | |||||||
| chr3:138575304 | A | T | 13 | a0001c0001t0001g0111 a0001c0001t0001g0276 a0001c0001t0001g0277 others(10): Show |
13 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5-2372T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575304 | |||||||
| chr3:138575383 | C | T | 2 | a0003c0003t0003g0053 a0005c0010t0004g0022 |
2 | HG01243.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-5-2451G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575383 | |||||||
| chr3:138575393 | A | G | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-2461T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575393 | |||||||
| chr3:138575471 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(201): Show |
230 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.-5-2539G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575471 | |||||||
| chr3:138575473 | G | C | 2 | a0003c0003t0003g0093 a0003c0003t0003g0094 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-5-2541C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575473 | |||||||
| chr3:138575474 | T | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(201): Show |
230 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.-5-2542A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575474 | |||||||
| chr3:138575494 | T | G | 281 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(278): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.-5-2562A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575494 | |||||||
| chr3:138575499 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-2567C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575499 | |||||||
| chr3:138575513 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-2581G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575513 | |||||||
| chr3:138575529 | A | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-2597T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575529 | |||||||
| chr3:138575565 | G | C | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-2633C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575565 | |||||||
| chr3:138575620 | G | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0126 |
3 | HG01256.hp2 HG01258.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-5-2688C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575620 | |||||||
| chr3:138575944 | G | A | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5-3012C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575944 | |||||||
| chr3:138575975 | C | G | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5-3043G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575975 | |||||||
| chr3:138575975 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-3043G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575975 | |||||||
| chr3:138575976 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-3044T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575976 | |||||||
| chr3:138576216 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-3284C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576216 | |||||||
| chr3:138576287 | G | C | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-3355C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576287 | |||||||
| chr3:138576332 | G | A | 2 | a0002c0002t0002g0021 a0002c0002t0002g0234 |
3 | HG00544.hp1 HG00558.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-5-3400C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576332 | |||||||
| chr3:138576416 | C | T | 1 | a0004c0006t0005g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-5-3484G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576416 | |||||||
| chr3:138576419 | G | A | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-3487C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576419 | |||||||
| chr3:138576501 | T | G | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-3569A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576501 | |||||||
| chr3:138576684 | T | C | 1 | a0003c0003t0003g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-5-3752A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576684 | |||||||
| chr3:138576711 | T | A | 1 | a0006c0009t0004g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-5-3779A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576711 | |||||||
| chr3:138576770 | G | A | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-3838C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576770 | |||||||
| chr3:138576773 | A | C | 1 | a0003c0003t0003g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-5-3841T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576773 | |||||||
| chr3:138576808 | C | G | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-5-3876G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576808 | |||||||
| chr3:138576852 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-5-3920T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576852 | |||||||
| chr3:138577036 | T | A | 1 | a0002c0002t0001g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-5-4104A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577036 | |||||||
| chr3:138577167 | G | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(275): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.-5-4235C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577167 | |||||||
| chr3:138577193 | C | T | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5-4261G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577193 | |||||||
| chr3:138577194 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(194): Show |
223 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.-5-4262C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577194 | |||||||
| chr3:138577201 | G | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02698.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-5-4269C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577201 | |||||||
| chr3:138577208 | T | G | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5-4276A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577208 | |||||||
| chr3:138577233 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(201): Show |
230 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.-5-4301C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577233 | |||||||
| chr3:138577357 | T | TA | 2 | a0002c0002t0002g0007 a0002c0002t0002g0273 |
4 | HG02040.hp1 NA18942.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-4426dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577357 | |||||||
| chr3:138577419 | C | A | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5-4487G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577419 | |||||||
| chr3:138577421 | G | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG00408.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-5-4489C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577421 | |||||||
| chr3:138577580 | G | A | 2 | a0001c0004t0004g0214 a0001c0004t0004g0215 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-4648C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577580 | |||||||
| chr3:138577596 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-5-4664G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577596 | |||||||
| chr3:138577664 | T | A | 26 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0002c0002t0001g0018 others(23): Show |
28 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-4732A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577664 | |||||||
| chr3:138577778 | T | A | 1 | a0002c0002t0002g0274 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-5-4846A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577778 | |||||||
| chr3:138578037 | C | T | 3 | a0003c0003t0003g0097 a0003c0003t0003g0098 a0003c0003t0003g0099 |
3 | HG01243.hp2 HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-5-5105G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578037 | |||||||
| chr3:138578046 | A | G | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG01175.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-5-5114T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578046 | |||||||
| chr3:138578126 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(97): Show |
113 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-5-5194G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578126 | |||||||
| chr3:138578272 | C | T | 3 | a0004c0006t0005g0027 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-5340G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578272 | |||||||
| chr3:138578564 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-5632G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578564 | |||||||
| chr3:138578642 | A | T | 59 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(56): Show |
68 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.-5-5710T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578642 | |||||||
| chr3:138578718 | C | A | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-5-5786G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578718 | |||||||
| chr3:138578719 | A | C | 2 | a0001c0004t0004g0108 a0001c0004t0004g0109 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-5-5787T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578719 | |||||||
| chr3:138578844 | G | A | 1 | a0003c0003t0003g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-5-5912C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578844 | |||||||
| chr3:138578899 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-5-5967G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578899 | |||||||
| chr3:138579089 | G | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-6157C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579089 | |||||||
| chr3:138579140 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-5-6208A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579140 | |||||||
| chr3:138579167 | C | A | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5-6235G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579167 | |||||||
| chr3:138579235 | C | T | 69 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(66): Show |
80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-5-6303G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579235 | |||||||
| chr3:138579396 | C | T | 2 | a0001c0004t0004g0214 a0001c0004t0004g0215 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-6464G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579396 | |||||||
| chr3:138579513 | C | T | 1 | a0003c0003t0003g0041 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-5-6581G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579513 | |||||||
| chr3:138579535 | A | G | 1 | a0002c0002t0002g0268 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-5-6603T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579535 | |||||||
| chr3:138579741 | T | C | 3 | a0003c0003t0003g0097 a0003c0003t0003g0098 a0003c0003t0003g0099 |
3 | HG01243.hp2 HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-5-6809A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579741 | |||||||
| chr3:138579771 | C | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-6839G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579771 | |||||||
| chr3:138579847 | T | C | 1 | a0003c0003t0003g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-5-6915A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579847 | |||||||
| chr3:138580195 | T | C | 1 | a0003c0003t0003g0033 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-5-7263A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580195 | |||||||
| chr3:138580267 | C | T | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5-7335G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580267 | |||||||
| chr3:138580382 | A | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-5-7450T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580382 | |||||||
| chr3:138580413 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-7481G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580413 | |||||||
| chr3:138580421 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-7489G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580421 | |||||||
| chr3:138580450 | T | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-5-7518A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580450 | |||||||
| chr3:138580725 | T | C | 1 | a0006c0009t0004g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-5-7793A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580725 | |||||||
| chr3:138580795 | C | G | 7 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0036 others(4): Show |
9 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-7863G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580795 | |||||||
| chr3:138580881 | T | C | 1 | a0001c0001t0001g0017 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-5-7949A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580881 | |||||||
| chr3:138580914 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-7982A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580914 | |||||||
| chr3:138580990 | A | C | 1 | a0003c0003t0003g0040 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-5-8058T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580990 | |||||||
| chr3:138581001 | C | T | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5-8069G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581001 | |||||||
| chr3:138581154 | G | A | 2 | a0003c0003t0003g0091 a0005c0010t0004g0022 |
2 | HG01243.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-5-8222C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581154 | |||||||
| chr3:138581215 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(194): Show |
223 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.-5-8283C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581215 | |||||||
| chr3:138581239 | G | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.-5-8307C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581239 | |||||||
| chr3:138581281 | CA | C | 7 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0002c0002t0002g0234 others(4): Show |
7 | HG00558.hp2 HG00735.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-8350delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581281 | |||||||
| chr3:138581301 | G | A | 1 | a0002c0002t0002g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-5-8369C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581301 | |||||||
| chr3:138581395 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-8463T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581395 | |||||||
| chr3:138581489 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-8557A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581489 | |||||||
| chr3:138581576 | G | C | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-8644C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581576 | |||||||
| chr3:138581628 | G | A | 1 | a0002c0002t0002g0230 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-5-8696C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581628 | |||||||
| chr3:138581694 | C | CA | 23 | a0001c0001t0001g0276 a0002c0002t0001g0018 a0002c0002t0001g0019 others(20): Show |
25 | HG00735.hp1 HG01123.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.-5-8763dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581694 | |||||||
| chr3:138581694 | CA | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(161): Show |
188 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.-5-8763delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581694 | |||||||
| chr3:138581694 | CAA | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0123 a0001c0004t0004g0214 others(4): Show |
7 | HG03195.hp2 HG03516.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5-8764_-5-8763del others(2): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581694 | |||||||
| chr3:138581719 | T | A | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-8787A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581719 | |||||||
| chr3:138581827 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-8895A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581827 | |||||||
| chr3:138581893 | A | T | 1 | a0001c0001t0001g0278 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-5-8961T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581893 | |||||||
| chr3:138581927 | A | C | 95 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0002c0002t0001g0018 others(92): Show |
108 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.-5-8995T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581927 | |||||||
| chr3:138581993 | A | C | 1 | a0002c0002t0002g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-5-9061T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581993 | |||||||
| chr3:138582011 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-5-9079C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582011 | |||||||
| chr3:138582132 | C | T | 2 | a0002c0002t0001g0197 a0002c0002t0001g0198 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-5-9200G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582132 | |||||||
| chr3:138582193 | T | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-9261A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582193 | |||||||
| chr3:138582365 | G | A | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-9433C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582365 | |||||||
| chr3:138582409 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+9445G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582409 | |||||||
| chr3:138582472 | A | AAAAAATT | 91 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(88): Show |
104 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.-6+9375_-6+9381dup others(7): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582472 | |||||||
| chr3:138582494 | A | G | 2 | a0002c0002t0001g0195 a0002c0002t0001g0196 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-6+9360T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582494 | |||||||
| chr3:138582599 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+9255T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582599 | |||||||
| chr3:138582770 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+9084T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582770 | |||||||
| chr3:138582773 | A | AAAAT | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+9077_-6+9080dup others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582773 | |||||||
| chr3:138582906 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-6+8948T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582906 | |||||||
| chr3:138582912 | C | T | 1 | a0002c0002t0002g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-6+8942G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582912 | |||||||
| chr3:138582987 | A | G | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
4 | HG00639.hp2 HG02735.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+8867T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582987 | |||||||
| chr3:138583179 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-6+8675T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583179 | |||||||
| chr3:138583349 | T | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+8505A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583349 | |||||||
| chr3:138583641 | GT | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+8212delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583641 | |||||||
| chr3:138583692 | AG | A | 90 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(87): Show |
103 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.-6+8161delC | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583692 | |||||||
| chr3:138583694 | G | C | 90 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(87): Show |
103 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.-6+8160C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583694 | |||||||
| chr3:138583737 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+8117T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583737 | |||||||
| chr3:138583798 | C | T | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.-6+8056G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583798 | |||||||
| chr3:138583973 | GAAC | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+7878_-6+7880del others(3): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583973 | |||||||
| chr3:138584236 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-6+7618A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584236 | |||||||
| chr3:138584281 | G | C | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-6+7573C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584281 | |||||||
| chr3:138584333 | C | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
116 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-6+7521G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584333 | |||||||
| chr3:138584456 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-6+7398G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584456 | |||||||
| chr3:138584461 | C | CA | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(112): Show |
129 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-6+7392dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584461 | |||||||
| chr3:138584478 | A | G | 3 | a0002c0002t0002g0006 a0002c0002t0002g0020 a0002c0002t0002g0231 |
6 | HG02735.hp2 HG03490.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+7376T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584478 | |||||||
| chr3:138584529 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+7325A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584529 | |||||||
| chr3:138584722 | A | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+7132T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584722 | |||||||
| chr3:138584782 | G | T | 3 | a0002c0002t0002g0228 a0002c0002t0002g0229 a0002c0002t0002g0230 |
3 | NA18965.hp1 NA18975.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-6+7072C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584782 | |||||||
| chr3:138584907 | A | C | 5 | a0002c0002t0002g0222 a0002c0002t0002g0224 a0002c0002t0002g0225 others(2): Show |
5 | HG02071.hp1 NA18747.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+6947T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584907 | |||||||
| chr3:138585122 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-6+6732G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585122 | |||||||
| chr3:138585256 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(98): Show |
114 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-6+6598T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585256 | |||||||
| chr3:138585356 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
116 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-6+6498T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585356 | |||||||
| chr3:138585397 | C | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-6+6457G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585397 | |||||||
| chr3:138585458 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-6+6396A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585458 | |||||||
| chr3:138585830 | T | C | 4 | a0003c0003t0003g0096 a0003c0003t0003g0097 a0003c0003t0003g0098 others(1): Show |
4 | HG01243.hp2 HG02559.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+6024A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585830 | |||||||
| chr3:138585833 | A | G | 2 | a0002c0002t0002g0035 a0002c0002t0002g0036 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-6+6021T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585833 | |||||||
| chr3:138586005 | C | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+5849G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586005 | |||||||
| chr3:138586260 | C | T | 24 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0003c0003t0003g0012 others(21): Show |
25 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.-6+5594G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586260 | |||||||
| chr3:138586345 | A | T | 1 | a0002c0002t0002g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-6+5509T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586345 | |||||||
| chr3:138586511 | T | A | 10 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(7): Show |
10 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-6+5343A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586511 | |||||||
| chr3:138586511 | T | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(90): Show |
106 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.-6+5343A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586511 | |||||||
| chr3:138586560 | T | C | 20 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(17): Show |
22 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.-6+5294A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586560 | |||||||
| chr3:138586650 | C | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+5204G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586650 | |||||||
| chr3:138586675 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-6+5179C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586675 | |||||||
| chr3:138586905 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+4949T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586905 | |||||||
| chr3:138587059 | C | G | 3 | a0002c0002t0001g0018 a0002c0002t0001g0193 a0002c0002t0001g0194 |
4 | HG02257.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+4795G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587059 | |||||||
| chr3:138587290 | TA | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-6+4563delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587290 | |||||||
| chr3:138587321 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+4533A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587321 | |||||||
| chr3:138587471 | T | A | 1 | a0006c0009t0004g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-6+4383A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587471 | |||||||
| chr3:138587474 | A | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-6+4380T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587474 | |||||||
| chr3:138587524 | T | C | 10 | a0003c0003t0003g0012 a0003c0003t0003g0038 a0003c0003t0003g0100 others(7): Show |
11 | HG01167.hp1 HG01169.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6+4330A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587524 | |||||||
| chr3:138587578 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+4276T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587578 | |||||||
| chr3:138587620 | C | CAAAAAAA others(3): Show |
118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(115): Show |
133 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-6+4233_-6+4234ins others(10): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587620 | |||||||
| chr3:138587620 | C | CAAAAAAA others(4): Show |
84 | a0001c0001t0001g0190 a0001c0004t0006g0028 a0001c0004t0006g0031 others(81): Show |
95 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.-6+4233_-6+4234ins others(11): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587620 | |||||||
| chr3:138588016 | A | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-6+3838T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588016 | |||||||
| chr3:138588056 | G | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+3798C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588056 | |||||||
| chr3:138588192 | C | T | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-6+3662G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588192 | |||||||
| chr3:138588296 | G | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+3558C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588296 | |||||||
| chr3:138588357 | T | C | 2 | a0002c0002t0002g0265 a0002c0002t0002g0267 |
2 | HG01884.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-6+3497A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588357 | |||||||
| chr3:138588360 | G | C | 1 | a0002c0002t0002g0268 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-6+3494C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588360 | |||||||
| chr3:138588549 | C | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.-6+3305G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588549 | |||||||
| chr3:138588688 | G | C | 1 | a0001c0001t0001g0286 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-6+3166C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588688 | |||||||
| chr3:138588789 | G | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+3065C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588789 | |||||||
| chr3:138588811 | C | A | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.-6+3043G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588811 | |||||||
| chr3:138588846 | G | C | 1 | a0002c0002t0002g0032 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-6+3008C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588846 | |||||||
| chr3:138589093 | G | C | 1 | a0003c0003t0003g0112 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-6+2761C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589093 | |||||||
| chr3:138589100 | T | C | 2 | a0003c0003t0003g0113 a0003c0003t0003g0114 |
2 | NA18957.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-6+2754A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589100 | |||||||
| chr3:138589207 | A | T | 2 | a0001c0004t0006g0028 a0001c0004t0006g0031 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-6+2647T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589207 | |||||||
| chr3:138589337 | T | A | 69 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(66): Show |
80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-6+2517A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589337 | |||||||
| chr3:138589371 | T | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(96): Show |
112 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-6+2483A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589371 | |||||||
| chr3:138589491 | GA | G | 7 | a0001c0001t0001g0039 a0001c0004t0006g0028 a0001c0004t0006g0031 others(4): Show |
7 | HG00735.hp2 HG01496.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+2362delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589491 | |||||||
| chr3:138589536 | T | C | 1 | a0003c0003t0001g0191 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-6+2318A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589536 | |||||||
| chr3:138589807 | C | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+2047G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589807 | |||||||
| chr3:138589825 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+2029G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589825 | |||||||
| chr3:138590024 | G | C | 91 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(88): Show |
104 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.-6+1830C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590024 | |||||||
| chr3:138590122 | C | CA | 6 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0003c0003t0001g0026 others(3): Show |
6 | HG00735.hp2 HG01168.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+1731dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590122 | |||||||
| chr3:138590155 | T | C | 1 | a0001c0004t0006g0031 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-6+1699A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590155 | |||||||
| chr3:138590215 | G | A | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-6+1639C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590215 | |||||||
| chr3:138590246 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+1608A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590246 | |||||||
| chr3:138590327 | A | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+1527T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590327 | |||||||
| chr3:138590534 | C | T | 1 | a0002c0002t0001g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-6+1320G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590534 | |||||||
| chr3:138590646 | T | TA | 68 | a0001c0001t0001g0192 a0002c0002t0002g0002 a0002c0002t0002g0005 others(65): Show |
79 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-6+1207dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590646 | |||||||
| chr3:138590712 | G | A | 3 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0006c0009t0004g0216 |
3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-6+1142C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590712 | |||||||
| chr3:138590767 | T | C | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+1087A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590767 | |||||||
| chr3:138590816 | T | C | 7 | a0002c0002t0002g0007 a0002c0002t0002g0270 a0002c0002t0002g0271 others(4): Show |
9 | HG02040.hp1 HG02129.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-6+1038A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590816 | |||||||
| chr3:138590823 | T | TA | 21 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0193 others(18): Show |
23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.-6+1030dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590823 | |||||||
| chr3:138590882 | A | T | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-6+972T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590882 | |||||||
| chr3:138591013 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-6+841G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138591013 | |||||||
| chr3:138591217 | C | A | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+637G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138591217 | |||||||
| chr3:138591365 | A | AT | 70 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0006 others(67): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.-6+488dupA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138591365 | |||||||
| chr3:138591691 | C | T | 1 | a0003c0003t0003g0033 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-6+163G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138591691 | |||||||
| chr3:138591851 | T | C | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | splice_region_variant&intron_variant | LOW | c.-6+3A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138591851 | |||||||
| chr3:138592034 | A | G | 1 | a0002c0002t0002g0032 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-108-78T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592034 | |||||||
| chr3:138592126 | C | T | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-108-170G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592126 | |||||||
| chr3:138592359 | T | C | 2 | a0002c0002t0001g0019 a0002c0002t0001g0211 |
3 | HG02572.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-108-403A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592359 | |||||||
| chr3:138592372 | A | G | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-108-416T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592372 | |||||||
| chr3:138592518 | C | G | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-108-562G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592518 | |||||||
| chr3:138592522 | C | A | 1 | a0003c0003t0003g0212 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-108-566G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592522 | |||||||
| chr3:138592547 | TGGGGGTA others(7): Show |
T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-108-605_-108-592d others(16): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592547 | |||||||
| chr3:138592577 | A | G | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-108-621T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592577 | |||||||
| chr3:138592717 | G | A | 1 | a0003c0003t0003g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-108-761C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592717 | |||||||
| chr3:138593228 | T | C | 4 | a0001c0004t0004g0214 a0001c0004t0004g0215 a0004c0006t0005g0027 others(1): Show |
4 | HG03195.hp2 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+970A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593228 | |||||||
| chr3:138593239 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-109+959A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593239 | |||||||
| chr3:138593245 | CAG | C | 5 | a0002c0002t0002g0005 a0002c0002t0002g0218 a0002c0002t0002g0219 others(2): Show |
7 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+951_-109+952d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593245 | |||||||
| chr3:138593289 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+909G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593289 | |||||||
| chr3:138593291 | C | T | 5 | a0001c0004t0006g0028 a0001c0004t0006g0031 a0004c0006t0005g0027 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+907G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593291 | |||||||
| chr3:138593388 | A | T | 1 | a0004c0006t0005g0027 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-109+810T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593388 | |||||||
| chr3:138593442 | C | T | 2 | a0003c0003t0001g0025 a0003c0003t0001g0026 |
2 | HG01168.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-109+756G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593442 | |||||||
| chr3:138593825 | T | G | 58 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0007 others(55): Show |
67 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-109+373A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593825 | |||||||
| chr3:138593916 | G | T | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+282C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593916 | |||||||
| chr3:138594051 | G | A | 11 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(8): Show |
11 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.-109+147C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138594051 | |||||||
| chr3:138594184 | C | T | 1 | a0005c0010t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-109+14G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138594184 |