Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 153241 |
| ensemblid | ENSG00000168944.17 |
| hgncid | 26690 |
| symbol | CEP120 |
| name | centrosomal protein 120 |
| refseq_nuc | NM_001375405.1 |
| refseq_prot | NP_001362334.1 |
| ensembl_nuc | ENST00000306467.10 |
| ensembl_prot | ENSP00000303058.6 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 123344892 |
| end | 123423403 |
| strand | - |
| ver | v1.2 |
| region | chr5:123344892-123423403 |
| region5000 | chr5:123339892-123428403 |
| regionname0 | CEP120_chr5_123344892_123423403 |
| regionname5000 | CEP120_chr5_123339892_123428403 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 986 | 167 | 52 | 38 | 53 | 8 | 14 | 43 | CEP120_chr5_123339892_123428403 | CEP120 | MVSKS others(981): Show |
chr5 | 123339892 | 123428403 |
| a0002 | 0/0 | 986 | 89 | 14 | 12 | 53 | 2 | 8 | 44 | CEP120_chr5_123339892_123428403 | CEP120 | MVSKS others(981): Show |
chr5 | 123339892 | 123428403 |
| a0003 | 0/0 | 986 | 74 | 13 | 11 | 42 | 1 | 7 | 32 | CEP120_chr5_123339892_123428403 | CEP120 | MVSKS others(981): Show |
chr5 | 123339892 | 123428403 |
| a0004 | 0/0 | 986 | 34 | 6 | 8 | 14 | 0 | 6 | 9 | CEP120_chr5_123339892_123428403 | CEP120 | MVSKS others(981): Show |
chr5 | 123339892 | 123428403 |
| a0005 | 0/0 | 986 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | MVSKS others(981): Show |
chr5 | 123339892 | 123428403 |
| a0006 | 0/0 | 986 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | MVSKS others(981): Show |
chr5 | 123339892 | 123428403 |
| a0007 | 0/0 | 986 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | MVSKS others(981): Show |
chr5 | 123339892 | 123428403 |
| a0008 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | MVSKS others(981): Show |
chr5 | 123339892 | 123428403 |
| a0009 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | MVSKS others(981): Show |
chr5 | 123339892 | 123428403 |
| a0010 | 0/0 | 986 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | MVSKS others(981): Show |
chr5 | 123339892 | 123428403 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2958 | 117 | 24 | 20 | 52 | 5 | 14 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0001c0005 | 0/0 | 2958 | 33 | 15 | 15 | 0 | 3 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0001c0006 | 0/0 | 2958 | 14 | 11 | 3 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0001c0011 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0001c0013 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0001c0016 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0002c0002 | 0/0 | 2958 | 82 | 13 | 12 | 47 | 2 | 8 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0002c0008 | 0/0 | 2958 | 4 | 0 | 0 | 4 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0002c0009 | 0/0 | 2958 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0002c0015 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0003c0003 | 0/0 | 2958 | 73 | 13 | 10 | 42 | 1 | 7 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0003c0018 | 0/0 | 2958 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0004c0004 | 0/0 | 2958 | 34 | 6 | 8 | 14 | 0 | 6 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0005c0007 | 0/0 | 2958 | 6 | 6 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0006c0010 | 0/0 | 2958 | 2 | 1 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0007c0014 | 0/0 | 2958 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0008c0017 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0009c0019 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 | ||
| a0010c0012 | 0/0 | 2958 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | ATGGT others(2953): Show |
chr5 | 123339892 | 123428403 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/1 | 4993 | 87 | 21 | 11 | 38 | 3 | 12 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0001t0004 | 0/0 | 4993 | 20 | 0 | 6 | 14 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0001t0006 | 0/0 | 4993 | 5 | 0 | 2 | 0 | 2 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0001t0007 | 0/0 | 4993 | 3 | 2 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0001t0011 | 0/0 | 4993 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0001t0012 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0005t0003 | 0/0 | 4993 | 13 | 9 | 2 | 0 | 2 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0005t0005 | 0/0 | 4993 | 20 | 6 | 13 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0006t0001 | 0/0 | 4993 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0006t0002 | 0/0 | 4993 | 8 | 6 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0006t0003 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0006t0008 | 0/0 | 4993 | 2 | 2 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0006t0009 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0006t0013 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0011t0002 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0013t0004 | 0/0 | 4993 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0001c0016t0002 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0002c0002t0001 | 0/0 | 4993 | 80 | 13 | 11 | 46 | 2 | 8 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0002c0002t0014 | 0/0 | 4993 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0002c0002t0018 | 0/0 | 4993 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0002c0008t0002 | 0/0 | 4993 | 4 | 0 | 0 | 4 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0002c0009t0001 | 0/0 | 4993 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0002c0009t0010 | 0/0 | 4993 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0002c0015t0001 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0003c0003t0001 | 0/0 | 4993 | 72 | 13 | 10 | 41 | 1 | 7 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0003c0003t0017 | 0/0 | 4993 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0003c0018t0001 | 0/0 | 4993 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0004c0004t0003 | 0/0 | 4993 | 34 | 6 | 8 | 14 | 0 | 6 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0005c0007t0003 | 0/0 | 4993 | 6 | 6 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0006c0010t0002 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0006c0010t0015 | 0/0 | 4993 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0007c0014t0005 | 0/0 | 4993 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0008c0017t0002 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0009c0019t0003 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| a0010c0012t0016 | 0/0 | 4993 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | GTTGT others(4988): Show |
chr5 | 123339892 | 123428403 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 8 | 0 | 3 | 2 | 0 | 3 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0008 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0231 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0006g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0006g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0007g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0011g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0001t0012g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0005t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0002g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0008g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0006t0013g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0011t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0013t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0001c0016t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0014g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0002t0018g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0008t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0008t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0008t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0008t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0009t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0009t0010g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0002c0015t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0002 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0003 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0003t0017g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0003c0018t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0004c0004t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0005c0007t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0005c0007t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0005c0007t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0005c0007t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0005c0007t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0005c0007t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0006c0010t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0006c0010t0015g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0007c0014t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0008c0017t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0009c0019t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| a0010c0012t0016g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0007 | c0014 | t0005 | g0075 | EUR | GBR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0282 | EUR | GBR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00280 | hp1 | a0003 | c0003 | t0001 | g0003 | EUR | FIN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0263 | EUR | FIN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0200 | EUR | FIN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00323 | hp2 | a0001 | c0005 | t0005 | g0070 | EUR | FIN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0133 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00438 | hp1 | a0002 | c0009 | t0010 | g0031 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0302 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00597 | hp1 | a0003 | c0003 | t0001 | g0139 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00609 | hp2 | a0004 | c0004 | t0003 | g0099 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00621 | hp2 | a0003 | c0003 | t0001 | g0293 | EAS | CHS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0198 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00642 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00733 | hp1 | a0004 | c0004 | t0003 | g0015 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00735 | hp1 | a0004 | c0004 | t0003 | g0054 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00738 | hp1 | a0001 | c0005 | t0005 | g0079 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00741 | hp1 | a0001 | c0005 | t0005 | g0004 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01069 | hp1 | a0001 | c0006 | t0002 | g0207 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0103 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01070 | hp2 | a0004 | c0004 | t0003 | g0043 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01071 | hp1 | a0001 | c0006 | t0002 | g0006 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01071 | hp2 | a0004 | c0004 | t0003 | g0042 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01074 | hp2 | a0001 | c0005 | t0005 | g0065 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01081 | hp1 | a0002 | c0002 | t0014 | g0124 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0248 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0129 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01099 | hp2 | a0003 | c0018 | t0001 | g0305 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01167 | hp1 | a0001 | c0005 | t0005 | g0004 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01167 | hp2 | a0004 | c0004 | t0003 | g0013 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01168 | hp2 | a0001 | c0005 | t0005 | g0063 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01169 | hp1 | a0001 | c0005 | t0005 | g0071 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01192 | hp1 | a0001 | c0005 | t0005 | g0074 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01192 | hp2 | a0004 | c0004 | t0003 | g0013 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01243 | hp1 | a0006 | c0010 | t0015 | g0032 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0146 | AMR | PUR | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01255 | hp1 | a0001 | c0005 | t0003 | g0090 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01255 | hp2 | a0001 | c0005 | t0003 | g0011 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01257 | hp1 | a0001 | c0006 | t0001 | g0102 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01257 | hp2 | a0001 | c0005 | t0005 | g0066 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01346 | hp1 | a0001 | c0005 | t0005 | g0073 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0272 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01361 | hp2 | a0001 | c0005 | t0005 | g0078 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01433 | hp1 | a0003 | c0003 | t0001 | g0306 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01496 | hp1 | a0001 | c0005 | t0005 | g0012 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0326 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0245 | EUR | IBS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01515 | hp2 | a0001 | c0005 | t0003 | g0011 | EUR | IBS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0029 | EUR | IBS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01517 | hp2 | a0001 | c0005 | t0003 | g0080 | EUR | IBS | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0184 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01891 | hp1 | a0004 | c0004 | t0003 | g0060 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0192 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0299 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01943 | hp2 | a0001 | c0005 | t0005 | g0012 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01952 | hp1 | a0004 | c0004 | t0003 | g0015 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0239 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0307 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01981 | hp1 | a0004 | c0004 | t0003 | g0046 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0298 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02004 | hp2 | a0001 | c0005 | t0005 | g0004 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02027 | hp2 | a0002 | c0002 | t0018 | g0329 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02040 | hp1 | a0004 | c0004 | t0003 | g0051 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02056 | hp2 | a0004 | c0004 | t0003 | g0050 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02071 | hp1 | a0003 | c0003 | t0001 | g0314 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02074 | hp2 | a0003 | c0003 | t0001 | g0100 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02080 | hp1 | a0003 | c0003 | t0001 | g0303 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0310 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02145 | hp1 | a0005 | c0007 | t0003 | g0086 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0193 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0308 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0178 | EAS | CDX | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CDX | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02257 | hp1 | a0001 | c0006 | t0002 | g0206 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02257 | hp2 | a0001 | c0005 | t0005 | g0035 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02258 | hp2 | a0001 | c0005 | t0003 | g0084 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02273 | hp1 | a0003 | c0003 | t0001 | g0183 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0254 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0318 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02280 | hp2 | a0004 | c0004 | t0003 | g0037 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02293 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0279 | AMR | PEL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02451 | hp1 | a0001 | c0006 | t0002 | g0006 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0327 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02523 | hp2 | a0004 | c0004 | t0003 | g0096 | EAS | KHV | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02572 | hp2 | a0003 | c0003 | t0001 | g0180 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02615 | hp1 | a0001 | c0005 | t0005 | g0077 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0196 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0320 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02647 | hp2 | a0001 | c0005 | t0003 | g0091 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0300 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0111 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0190 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0275 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02717 | hp2 | a0006 | c0010 | t0002 | g0202 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02723 | hp1 | a0005 | c0007 | t0003 | g0085 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02738 | hp1 | a0003 | c0003 | t0001 | g0188 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02809 | hp1 | a0004 | c0004 | t0003 | g0058 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02809 | hp2 | a0003 | c0003 | t0001 | g0182 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0153 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02818 | hp2 | a0001 | c0005 | t0003 | g0095 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02886 | hp1 | a0001 | c0005 | t0003 | g0081 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02896 | hp1 | a0001 | c0005 | t0003 | g0089 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0142 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02965 | hp2 | a0001 | c0005 | t0005 | g0069 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02970 | hp1 | a0008 | c0017 | t0002 | g0209 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02970 | hp2 | a0001 | c0005 | t0003 | g0324 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02976 | hp1 | a0001 | c0016 | t0002 | g0210 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02976 | hp2 | a0009 | c0019 | t0003 | g0107 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03017 | hp1 | a0001 | c0001 | t0011 | g0249 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0110 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03041 | hp1 | a0001 | c0006 | t0002 | g0205 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0316 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0328 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0185 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0187 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03130 | hp2 | a0002 | c0015 | t0001 | g0319 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03139 | hp1 | a0001 | c0005 | t0005 | g0067 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03195 | hp2 | a0001 | c0006 | t0013 | g0208 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0174 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03225 | hp1 | a0004 | c0004 | t0003 | g0057 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03239 | hp2 | a0004 | c0004 | t0003 | g0039 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03486 | hp1 | a0001 | c0006 | t0008 | g0010 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03486 | hp2 | a0005 | c0007 | t0003 | g0097 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03491 | hp1 | a0004 | c0004 | t0003 | g0044 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0017 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0017 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03516 | hp1 | a0001 | c0006 | t0003 | g0323 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | ESN | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03540 | hp2 | a0001 | c0006 | t0002 | g0204 | AFR | GWD | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0151 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03654 | hp2 | a0010 | c0012 | t0016 | g0068 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0117 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0121 | SAS | PJL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03834 | hp1 | a0001 | c0001 | t0006 | g0291 | SAS | BEB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | BEB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0201 | SAS | BEB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03942 | hp2 | a0004 | c0004 | t0003 | g0038 | SAS | BEB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04115 | hp1 | a0004 | c0004 | t0003 | g0056 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0280 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | BEB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04184 | hp2 | a0004 | c0004 | t0003 | g0036 | SAS | BEB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04199 | hp1 | a0004 | c0004 | t0003 | g0052 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0294 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04204 | hp1 | a0003 | c0003 | t0001 | g0002 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | STU | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18522 | hp1 | a0004 | c0004 | t0003 | g0059 | AFR | YRI | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18522 | hp2 | a0001 | c0011 | t0002 | g0203 | AFR | YRI | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18612 | hp1 | a0004 | c0004 | t0003 | g0053 | EAS | CHB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | CHB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0181 | AFR | YRI | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18906 | hp2 | a0001 | c0005 | t0003 | g0062 | AFR | YRI | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18939 | hp1 | a0003 | c0003 | t0001 | g0315 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18946 | hp1 | a0004 | c0004 | t0003 | g0045 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18949 | hp1 | a0001 | c0013 | t0004 | g0243 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18949 | hp2 | a0002 | c0008 | t0002 | g0217 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18950 | hp1 | a0002 | c0008 | t0002 | g0218 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18951 | hp2 | a0003 | c0003 | t0001 | g0311 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0137 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18953 | hp2 | a0004 | c0004 | t0003 | g0047 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18956 | hp1 | a0003 | c0003 | t0001 | g0313 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0195 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18963 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0176 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18966 | hp2 | a0002 | c0008 | t0002 | g0220 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18968 | hp1 | a0004 | c0004 | t0003 | g0040 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18972 | hp1 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18974 | hp2 | a0003 | c0003 | t0001 | g0022 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18977 | hp2 | a0003 | c0003 | t0001 | g0141 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18979 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18979 | hp2 | a0003 | c0003 | t0001 | g0173 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18981 | hp1 | a0003 | c0003 | t0001 | g0021 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18982 | hp1 | a0004 | c0004 | t0003 | g0048 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18988 | hp2 | a0003 | c0003 | t0001 | g0296 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18990 | hp2 | a0004 | c0004 | t0003 | g0093 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18991 | hp1 | a0004 | c0004 | t0003 | g0055 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18993 | hp2 | a0003 | c0003 | t0001 | g0312 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18994 | hp2 | a0003 | c0003 | t0001 | g0189 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0021 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19010 | hp2 | a0004 | c0004 | t0003 | g0061 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | LWK | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19030 | hp2 | a0001 | c0005 | t0003 | g0083 | AFR | LWK | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | LWK | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19043 | hp2 | a0005 | c0007 | t0003 | g0098 | AFR | LWK | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19054 | hp1 | a0004 | c0004 | t0003 | g0049 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19054 | hp2 | a0003 | c0003 | t0017 | g0177 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19059 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19059 | hp2 | a0003 | c0003 | t0001 | g0194 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0297 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19062 | hp2 | a0003 | c0003 | t0001 | g0020 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19065 | hp1 | a0003 | c0003 | t0001 | g0309 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19072 | hp1 | a0002 | c0008 | t0002 | g0219 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19079 | hp1 | a0003 | c0003 | t0001 | g0134 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0114 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19081 | hp1 | a0003 | c0003 | t0001 | g0179 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19083 | hp1 | a0003 | c0003 | t0001 | g0135 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19084 | hp2 | a0002 | c0009 | t0001 | g0125 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19085 | hp2 | a0003 | c0003 | t0001 | g0136 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19087 | hp1 | a0003 | c0003 | t0001 | g0022 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19090 | hp1 | a0003 | c0003 | t0001 | g0020 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA19091 | hp2 | a0004 | c0004 | t0003 | g0041 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20129 | hp1 | a0001 | c0006 | t0002 | g0325 | AFR | ASW | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20129 | hp2 | a0001 | c0006 | t0009 | g0030 | AFR | ASW | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0094 | EUR | TSI | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | TSI | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | GIH | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0186 | SAS | GIH | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG01123 | hp2 | a0003 | c0003 | t0001 | g0304 | AMR | CLM | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02109 | hp1 | a0001 | c0005 | t0005 | g0072 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02486 | hp1 | a0001 | c0005 | t0005 | g0076 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02486 | hp2 | a0005 | c0007 | t0003 | g0088 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG02559 | hp2 | a0001 | c0006 | t0008 | g0010 | AFR | ACB | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG03471 | hp2 | a0005 | c0007 | t0003 | g0087 | AFR | MSL | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG06807 | hp1 | a0001 | c0006 | t0002 | g0006 | AFR | USA | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| HG06807 | hp2 | a0003 | c0003 | t0001 | g0292 | AFR | USA | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18955 | hp1 | a0003 | c0003 | t0001 | g0301 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20300 | hp1 | a0004 | c0004 | t0003 | g0092 | AFR | USA | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA20300 | hp2 | a0001 | c0005 | t0003 | g0082 | AFR | USA | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA21309 | hp1 | a0003 | c0003 | t0001 | g0197 | AFR | LWK | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | LWK | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0231 | REF | REF | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0064 | REF | REF | CEP120_chr5_123339892_123428403 | CEP120 | chr5 | 123339892 | 123428403 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:123346640 | C | T | 2 | a0004 a0009 |
35 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
missense_variant | MODERATE | c.2840G>A | p.Arg947His | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 3245/4993 | 2840/2961 | 947/986 | chr5 | 123346640 | |||
| chr5:123350033 | C | G | 2 | a0003 a0010 |
75 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(72): Show |
missense_variant | MODERATE | c.2637G>C | p.Gln879His | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/20 | 3042/4993 | 2637/2961 | 879/986 | chr5 | 123350033 | |||
| chr5:123377399 | T | C | 1 | a0007 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.2333A>G | p.Glu778Gly | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/20 | 2738/4993 | 2333/2961 | 778/986 | chr5 | 123377399 | |||
| chr5:123378350 | T | C | 2 | a0006 a0008 |
3 | HG01243.hp1 HG02717.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.2182A>G | p.Ser728Gly | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/20 | 2587/4993 | 2182/2961 | 728/986 | chr5 | 123378350 | |||
| chr5:123383042 | G | C | 3 | a0002 a0003 a0009 |
164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
missense_variant | MODERATE | c.1804C>G | p.Leu602Val | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 12/20 | 2209/4993 | 1804/2961 | 602/986 | chr5 | 123383042 | |||
| chr5:123390074 | G | A | 1 | a0005 | 6 | HG02145.hp1 HG02486.hp2 HG02723.hp1 others(3): Show |
missense_variant | MODERATE | c.1105C>T | p.Pro369Ser | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/20 | 1510/4993 | 1105/2961 | 369/986 | chr5 | 123390074 | |||
| chr5:123412500 | T | C | 1 | a0006 | 2 | HG01243.hp1 HG02717.hp2 |
missense_variant | MODERATE | c.362A>G | p.Lys121Arg | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/20 | 767/4993 | 362/2961 | 121/986 | chr5 | 123412500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:123346636 | C | T | 1 | a0001c0013 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.2844G>A | p.Leu948Leu | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 3249/4993 | 2844/2961 | 948/986 | chr5 | 123346636 | |||
| chr5:123346654 | A | G | 16 | a0001c0005 a0001c0006 a0001c0011 others(13): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
synonymous_variant | LOW | c.2826T>C | p.Asp942Asp | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 3231/4993 | 2826/2961 | 942/986 | chr5 | 123346654 | |||
| chr5:123378345 | C | T | 1 | a0003c0018 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.2187G>A | p.Val729Val | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/20 | 2592/4993 | 2187/2961 | 729/986 | chr5 | 123378345 | |||
| chr5:123390105 | C | T | 1 | a0001c0016 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1074G>A | p.Glu358Glu | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/20 | 1479/4993 | 1074/2961 | 358/986 | chr5 | 123390105 | |||
| chr5:123391332 | G | A | 11 | a0001c0006 a0001c0011 a0001c0016 others(8): Show |
182 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(179): Show |
synonymous_variant | LOW | c.816C>T | p.His272His | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/20 | 1221/4993 | 816/2961 | 272/986 | chr5 | 123391332 | |||
| chr5:123412460 | G | A | 1 | a0002c0009 | 2 | HG00438.hp1 NA19084.hp2 |
synonymous_variant | LOW | c.402C>T | p.Thr134Thr | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/20 | 807/4993 | 402/2961 | 134/986 | chr5 | 123412460 | |||
| chr5:123418373 | C | T | 1 | a0001c0011 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.192G>A | p.Ala64Ala | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/20 | 597/4993 | 192/2961 | 64/986 | chr5 | 123418373 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:123344973 | T | G | 3 | a0001c0005t0005 a0007c0014t0005 a0010c0012t0016 |
22 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1546A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 1546 | chr5 | 123344973 | ||||||
| chr5:123344978 | A | G | 2 | a0001c0001t0004 a0001c0013t0004 |
21 | HG01433.hp2 HG01952.hp2 HG01975.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1541T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 1541 | chr5 | 123344978 | ||||||
| chr5:123345070 | C | A | 1 | a0001c0001t0011 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1449G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 1449 | chr5 | 123345070 | ||||||
| chr5:123345536 | G | C | 8 | a0001c0005t0003 a0001c0005t0005 a0001c0006t0003 others(5): Show |
77 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*983C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 983 | chr5 | 123345536 | ||||||
| chr5:123345585 | T | G | 11 | a0001c0006t0001 a0002c0002t0001 a0002c0002t0014 others(8): Show |
161 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*934A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 934 | chr5 | 123345585 | ||||||
| chr5:123345640 | T | C | 1 | a0001c0006t0008 | 2 | HG02559.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*879A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 879 | chr5 | 123345640 | ||||||
| chr5:123345726 | G | A | 1 | a0001c0001t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*793C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 793 | chr5 | 123345726 | ||||||
| chr5:123345762 | G | C | 1 | a0002c0002t0014 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*757C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 757 | chr5 | 123345762 | ||||||
| chr5:123345840 | A | T | 1 | a0001c0001t0006 | 5 | HG00280.hp2 HG01081.hp2 HG01346.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*679T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 679 | chr5 | 123345840 | ||||||
| chr5:123345977 | T | C | 1 | a0001c0006t0013 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*542A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 542 | chr5 | 123345977 | ||||||
| chr5:123346140 | C | T | 12 | a0001c0006t0001 a0001c0006t0008 a0001c0006t0009 others(9): Show |
163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*379G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 379 | chr5 | 123346140 | ||||||
| chr5:123346168 | T | C | 1 | a0003c0003t0017 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 351 | chr5 | 123346168 | ||||||
| chr5:123346272 | A | T | 2 | a0001c0006t0008 a0001c0006t0009 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*247T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 247 | chr5 | 123346272 | ||||||
| chr5:123346460 | T | G | 21 | a0001c0005t0003 a0001c0005t0005 a0001c0006t0001 others(18): Show |
241 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(238): Show |
3_prime_UTR_variant | MODIFIER | c.*59A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 20/20 | 59 | chr5 | 123346460 | ||||||
| chr5:123423029 | G | A | 1 | a0001c0001t0007 | 3 | HG01496.hp2 HG02451.hp2 HG03098.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-31C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/20 | chr5 | 123423029 | |||||||
| chr5:123423058 | C | G | 1 | a0002c0009t0010 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-60G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/20 | 60 | chr5 | 123423058 | ||||||
| chr5:123423275 | G | A | 1 | a0002c0002t0018 | 1 | HG02027.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-277C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/20 | chr5 | 123423275 | |||||||
| chr5:123423311 | C | T | 2 | a0001c0006t0008 a0001c0006t0009 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-313G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/20 | 313 | chr5 | 123423311 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:123347118 | G | A | 34 | a0001c0005t0003g0324 a0004c0004t0003g0013 a0004c0004t0003g0015 others(31): Show |
36 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.2727-365C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347118 | |||||||
| chr5:123347155 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2727-402T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347155 | |||||||
| chr5:123347178 | T | G | 1 | a0001c0006t0008g0010 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2727-425A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347178 | |||||||
| chr5:123347194 | G | T | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2727-441C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347194 | |||||||
| chr5:123347220 | C | T | 2 | a0001c0005t0005g0012 a0001c0005t0005g0072 |
3 | HG01496.hp1 HG01943.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2727-467G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347220 | |||||||
| chr5:123347255 | G | A | 1 | a0002c0002t0001g0104 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2727-502C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347255 | |||||||
| chr5:123347318 | A | T | 217 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(214): Show |
241 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.2727-565T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347318 | |||||||
| chr5:123347469 | C | G | 229 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(226): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2727-716G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347469 | |||||||
| chr5:123347771 | G | A | 1 | a0003c0003t0001g0173 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2727-1018C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347771 | |||||||
| chr5:123347793 | T | C | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2727-1040A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347793 | |||||||
| chr5:123347801 | C | T | 2 | a0003c0003t0001g0196 a0003c0003t0001g0197 |
2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2727-1048G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347801 | |||||||
| chr5:123347919 | GCC | G | 22 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(19): Show |
26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.2727-1168_2727-116 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347919 | |||||||
| chr5:123347977 | A | C | 144 | a0001c0006t0001g0102 a0002c0002t0001g0005 a0002c0002t0001g0016 others(141): Show |
161 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.2727-1224T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123347977 | |||||||
| chr5:123348139 | T | C | 1 | a0002c0002t0001g0126 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2727-1386A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348139 | |||||||
| chr5:123348302 | T | C | 146 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(143): Show |
164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.2727-1549A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348302 | |||||||
| chr5:123348315 | TATCTTTA others(152): Show |
T | 1 | a0002c0002t0001g0101 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2726+1470_2727-156 others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348315 | |||||||
| chr5:123348437 | A | G | 145 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(142): Show |
163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2726+1507T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348437 | |||||||
| chr5:123348480 | T | G | 1 | a0002c0002t0001g0101 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2726+1464A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348480 | |||||||
| chr5:123348526 | G | T | 11 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(8): Show |
13 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2726+1418C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348526 | |||||||
| chr5:123348551 | G | A | 228 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2726+1393C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348551 | |||||||
| chr5:123348651 | A | G | 1 | a0001c0001t0002g0283 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2726+1293T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348651 | |||||||
| chr5:123348652 | G | T | 1 | a0002c0002t0001g0101 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2726+1292C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348652 | |||||||
| chr5:123348681 | T | C | 1 | a0001c0001t0002g0283 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2726+1263A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348681 | |||||||
| chr5:123348870 | G | C | 217 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(214): Show |
241 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.2726+1074C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348870 | |||||||
| chr5:123348883 | A | G | 3 | a0002c0002t0001g0211 a0002c0002t0001g0212 a0002c0002t0001g0213 |
3 | HG02055.hp2 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2726+1061T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348883 | |||||||
| chr5:123348897 | G | A | 1 | a0002c0002t0018g0329 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2726+1047C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348897 | |||||||
| chr5:123348919 | T | C | 37 | a0001c0006t0001g0102 a0002c0002t0001g0005 a0002c0002t0001g0016 others(34): Show |
42 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.2726+1025A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123348919 | |||||||
| chr5:123349007 | T | C | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2726+937A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349007 | |||||||
| chr5:123349068 | C | T | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2726+876G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349068 | |||||||
| chr5:123349071 | C | T | 36 | a0001c0006t0001g0102 a0002c0002t0001g0005 a0002c0002t0001g0016 others(33): Show |
41 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.2726+873G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349071 | |||||||
| chr5:123349228 | C | T | 1 | a0001c0005t0003g0082 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2726+716G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349228 | |||||||
| chr5:123349383 | A | G | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2726+561T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349383 | |||||||
| chr5:123349434 | A | G | 146 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(143): Show |
164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.2726+510T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349434 | |||||||
| chr5:123349539 | A | C | 1 | a0002c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2726+405T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349539 | |||||||
| chr5:123349594 | T | A | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2726+350A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349594 | |||||||
| chr5:123349606 | A | G | 3 | a0002c0002t0001g0163 a0002c0002t0001g0168 a0002c0002t0001g0172 |
3 | NA18964.hp2 NA19059.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2726+338T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349606 | |||||||
| chr5:123349654 | T | C | 147 | a0001c0006t0001g0102 a0001c0006t0003g0323 a0001c0006t0008g0010 others(144): Show |
165 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2726+290A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349654 | |||||||
| chr5:123349662 | A | G | 9 | a0003c0003t0001g0114 a0003c0003t0001g0133 a0003c0003t0001g0134 others(6): Show |
9 | HG00423.hp1 HG00597.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.2726+282T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 19/19 | chr5 | 123349662 | |||||||
| chr5:123350212 | CT | C | 187 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(184): Show |
209 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.2581-124delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350212 | |||||||
| chr5:123350314 | A | T | 1 | a0001c0001t0004g0254 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2581-225T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350314 | |||||||
| chr5:123350405 | T | C | 36 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(33): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2581-316A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350405 | |||||||
| chr5:123350564 | A | T | 1 | a0002c0002t0001g0150 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2581-475T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350564 | |||||||
| chr5:123350575 | C | A | 1 | a0001c0005t0003g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2581-486G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350575 | |||||||
| chr5:123350578 | C | T | 1 | a0003c0018t0001g0305 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2581-489G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350578 | |||||||
| chr5:123350739 | C | G | 1 | a0001c0001t0002g0253 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2581-650G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350739 | |||||||
| chr5:123350821 | T | C | 2 | a0002c0002t0001g0200 a0002c0002t0001g0201 |
2 | HG00323.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2581-732A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350821 | |||||||
| chr5:123350903 | G | T | 8 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(5): Show |
10 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2581-814C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350903 | |||||||
| chr5:123350913 | C | G | 1 | a0002c0002t0001g0150 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2581-824G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350913 | |||||||
| chr5:123350982 | C | A | 7 | a0001c0005t0003g0081 a0001c0005t0003g0082 a0001c0005t0003g0083 others(4): Show |
7 | HG01255.hp1 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2581-893G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123350982 | |||||||
| chr5:123351131 | A | G | 4 | a0001c0001t0004g0233 a0001c0001t0004g0234 a0001c0001t0004g0235 others(1): Show |
4 | NA18941.hp1 NA18951.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.2581-1042T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351131 | |||||||
| chr5:123351211 | C | T | 4 | a0002c0002t0001g0094 a0002c0002t0001g0198 a0002c0002t0001g0200 others(1): Show |
4 | HG00323.hp1 HG00642.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.2581-1122G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351211 | |||||||
| chr5:123351222 | A | G | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2581-1133T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351222 | |||||||
| chr5:123351342 | C | G | 2 | a0006c0010t0002g0202 a0006c0010t0015g0032 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2581-1253G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351342 | |||||||
| chr5:123351379 | T | C | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2581-1290A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351379 | |||||||
| chr5:123351769 | TTC | T | 144 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(141): Show |
162 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2581-1682_2581-168 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351769 | |||||||
| chr5:123351925 | C | A | 8 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(5): Show |
10 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2581-1836G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123351925 | |||||||
| chr5:123352008 | A | G | 10 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2581-1919T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352008 | |||||||
| chr5:123352496 | A | G | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2581-2407T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352496 | |||||||
| chr5:123352540 | C | G | 146 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(143): Show |
164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.2581-2451G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352540 | |||||||
| chr5:123352623 | G | A | 1 | a0002c0002t0001g0121 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2581-2534C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352623 | |||||||
| chr5:123352722 | G | A | 1 | a0001c0001t0011g0249 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2581-2633C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352722 | |||||||
| chr5:123352731 | T | C | 228 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-2642A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352731 | |||||||
| chr5:123352894 | G | GATGCTAC others(5): Show |
229 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(226): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2581-2806_2581-280 others(16): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352894 | |||||||
| chr5:123352949 | T | C | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2581-2860A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123352949 | |||||||
| chr5:123353009 | G | C | 1 | a0004c0004t0003g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2581-2920C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353009 | |||||||
| chr5:123353016 | G | A | 1 | a0001c0001t0004g0025 | 2 | NA18994.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2581-2927C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353016 | |||||||
| chr5:123353033 | C | T | 229 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(226): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2581-2944G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353033 | |||||||
| chr5:123353052 | A | C | 4 | a0001c0001t0002g0014 a0001c0001t0002g0247 a0001c0001t0002g0280 others(1): Show |
5 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.2581-2963T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353052 | |||||||
| chr5:123353094 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2581-3005A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353094 | |||||||
| chr5:123353175 | A | C | 2 | a0002c0002t0001g0166 a0002c0002t0001g0170 |
2 | NA19006.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2581-3086T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353175 | |||||||
| chr5:123353276 | G | T | 1 | a0001c0005t0003g0089 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2581-3187C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353276 | |||||||
| chr5:123353410 | C | A | 1 | a0001c0001t0004g0274 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2581-3321G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353410 | |||||||
| chr5:123353410 | C | T | 2 | a0002c0002t0001g0153 a0002c0002t0001g0169 |
2 | HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2581-3321G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353410 | |||||||
| chr5:123353520 | G | A | 1 | a0002c0002t0001g0172 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2581-3431C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353520 | |||||||
| chr5:123353521 | T | G | 1 | a0002c0002t0001g0172 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2581-3432A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353521 | |||||||
| chr5:123353521 | T | TAAG | 227 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(224): Show |
253 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.2581-3435_2581-343 others(7): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353521 | |||||||
| chr5:123353727 | C | T | 228 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-3638G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353727 | |||||||
| chr5:123353790 | A | G | 229 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(226): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2581-3701T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123353790 | |||||||
| chr5:123354086 | A | G | 13 | a0001c0005t0003g0081 a0001c0005t0003g0082 a0001c0005t0003g0083 others(10): Show |
13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2581-3997T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354086 | |||||||
| chr5:123354300 | G | A | 1 | a0001c0001t0002g0264 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2581-4211C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354300 | |||||||
| chr5:123354361 | T | C | 1 | a0002c0008t0002g0219 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2581-4272A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354361 | |||||||
| chr5:123354435 | T | C | 1 | a0003c0003t0001g0320 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2581-4346A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354435 | |||||||
| chr5:123354629 | C | A | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2581-4540G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354629 | |||||||
| chr5:123354667 | G | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0228 a0001c0001t0002g0289 |
4 | NA18990.hp1 NA19009.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.2581-4578C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354667 | |||||||
| chr5:123354693 | T | C | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2581-4604A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354693 | |||||||
| chr5:123354736 | A | G | 1 | a0002c0002t0001g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2581-4647T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354736 | |||||||
| chr5:123354775 | GT | G | 228 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-4687delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354775 | |||||||
| chr5:123354785 | T | A | 9 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(6): Show |
11 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2581-4696A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354785 | |||||||
| chr5:123354868 | T | G | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2581-4779A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354868 | |||||||
| chr5:123354881 | C | A | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2581-4792G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354881 | |||||||
| chr5:123354891 | C | T | 13 | a0001c0005t0003g0081 a0001c0005t0003g0082 a0001c0005t0003g0083 others(10): Show |
13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2581-4802G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354891 | |||||||
| chr5:123354892 | G | A | 1 | a0004c0004t0003g0049 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2581-4803C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354892 | |||||||
| chr5:123354915 | C | T | 1 | a0001c0006t0002g0325 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2581-4826G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354915 | |||||||
| chr5:123354957 | C | A | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2581-4868G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123354957 | |||||||
| chr5:123355027 | C | A | 13 | a0001c0005t0003g0081 a0001c0005t0003g0082 a0001c0005t0003g0083 others(10): Show |
13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2581-4938G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355027 | |||||||
| chr5:123355122 | T | C | 1 | a0001c0001t0004g0250 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2581-5033A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355122 | |||||||
| chr5:123355195 | T | C | 227 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(224): Show |
253 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.2581-5106A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355195 | |||||||
| chr5:123355247 | C | T | 2 | a0003c0003t0001g0196 a0003c0003t0001g0197 |
2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2581-5158G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355247 | |||||||
| chr5:123355284 | C | A | 5 | a0002c0002t0001g0146 a0002c0002t0001g0149 a0002c0002t0001g0150 others(2): Show |
5 | HG01243.hp2 HG02622.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2581-5195G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355284 | |||||||
| chr5:123355306 | G | T | 13 | a0001c0001t0002g0232 a0001c0006t0002g0006 a0001c0006t0002g0204 others(10): Show |
15 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2581-5217C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355306 | |||||||
| chr5:123355308 | G | A | 2 | a0004c0004t0003g0059 a0004c0004t0003g0060 |
2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2581-5219C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355308 | |||||||
| chr5:123355334 | A | T | 1 | a0001c0001t0002g0246 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2581-5245T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355334 | |||||||
| chr5:123355471 | C | T | 7 | a0001c0016t0002g0210 a0002c0002t0001g0018 a0002c0002t0001g0101 others(4): Show |
8 | HG00597.hp2 HG02080.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.2581-5382G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355471 | |||||||
| chr5:123355520 | G | A | 228 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-5431C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355520 | |||||||
| chr5:123355561 | T | G | 48 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(45): Show |
54 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.2581-5472A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355561 | |||||||
| chr5:123355574 | T | C | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2581-5485A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355574 | |||||||
| chr5:123355874 | T | A | 216 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(213): Show |
240 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.2581-5785A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355874 | |||||||
| chr5:123355876 | A | G | 228 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-5787T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355876 | |||||||
| chr5:123355892 | G | A | 228 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-5803C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355892 | |||||||
| chr5:123355920 | G | T | 1 | a0001c0005t0003g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2581-5831C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355920 | |||||||
| chr5:123355971 | G | A | 1 | a0002c0002t0001g0094 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2581-5882C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355971 | |||||||
| chr5:123355995 | T | A | 1 | a0003c0003t0001g0294 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2581-5906A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123355995 | |||||||
| chr5:123356028 | A | G | 98 | a0002c0002t0001g0295 a0003c0003t0001g0002 a0003c0003t0001g0003 others(95): Show |
111 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.2581-5939T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356028 | |||||||
| chr5:123356143 | G | C | 228 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-6054C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356143 | |||||||
| chr5:123356332 | C | G | 1 | a0002c0002t0001g0094 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2581-6243G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356332 | |||||||
| chr5:123356386 | C | T | 145 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(142): Show |
163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2581-6297G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356386 | |||||||
| chr5:123356563 | T | C | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2581-6474A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356563 | |||||||
| chr5:123356612 | AATTTGTC | A | 144 | a0001c0006t0001g0102 a0002c0002t0001g0005 a0002c0002t0001g0016 others(141): Show |
161 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.2581-6530_2581-652 others(11): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356612 | |||||||
| chr5:123356660 | A | G | 228 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2581-6571T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356660 | |||||||
| chr5:123356691 | A | C | 229 | a0001c0001t0002g0251 a0001c0005t0003g0011 a0001c0005t0003g0062 others(226): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2581-6602T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356691 | |||||||
| chr5:123356959 | G | GT | 177 | a0001c0006t0001g0102 a0002c0002t0001g0005 a0002c0002t0001g0016 others(174): Show |
196 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.2581-6871dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123356959 | |||||||
| chr5:123357092 | G | C | 36 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(33): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2581-7003C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357092 | |||||||
| chr5:123357507 | T | C | 1 | a0001c0001t0004g0267 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2580+6989A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357507 | |||||||
| chr5:123357592 | AAAACCCT others(8): Show |
A | 1 | a0001c0005t0005g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2580+6889_2580+690 others(19): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357592 | |||||||
| chr5:123357641 | A | G | 8 | a0003c0003t0001g0114 a0003c0003t0001g0133 a0003c0003t0001g0134 others(5): Show |
8 | HG00423.hp1 HG00597.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2580+6855T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357641 | |||||||
| chr5:123357653 | T | G | 1 | a0009c0019t0003g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2580+6843A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357653 | |||||||
| chr5:123357762 | G | A | 228 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2580+6734C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357762 | |||||||
| chr5:123357863 | ACATCTGA others(7): Show |
A | 4 | a0003c0003t0001g0180 a0003c0003t0001g0181 a0003c0003t0001g0182 others(1): Show |
4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2580+6619_2580+663 others(18): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357863 | |||||||
| chr5:123357880 | A | G | 4 | a0003c0003t0001g0180 a0003c0003t0001g0181 a0003c0003t0001g0182 others(1): Show |
4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2580+6616T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357880 | |||||||
| chr5:123357883 | A | G | 228 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2580+6613T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357883 | |||||||
| chr5:123357914 | A | G | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2580+6582T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123357914 | |||||||
| chr5:123358092 | T | C | 228 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2580+6404A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358092 | |||||||
| chr5:123358156 | A | G | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2580+6340T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358156 | |||||||
| chr5:123358173 | A | ACTT | 6 | a0005c0007t0003g0085 a0005c0007t0003g0086 a0005c0007t0003g0087 others(3): Show |
6 | HG02145.hp1 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2580+6320_2580+632 others(7): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358173 | |||||||
| chr5:123358207 | A | G | 228 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.2580+6289T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358207 | |||||||
| chr5:123358355 | A | G | 5 | a0002c0002t0001g0156 a0002c0002t0001g0158 a0002c0002t0001g0159 others(2): Show |
5 | NA18944.hp2 NA18948.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.2580+6141T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358355 | |||||||
| chr5:123358368 | G | C | 42 | a0001c0006t0001g0102 a0002c0002t0001g0005 a0002c0002t0001g0016 others(39): Show |
47 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.2580+6128C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358368 | |||||||
| chr5:123358694 | T | TCA | 226 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(223): Show |
252 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.2580+5800_2580+580 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358694 | |||||||
| chr5:123358717 | G | A | 1 | a0002c0002t0001g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2580+5779C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358717 | |||||||
| chr5:123358856 | C | T | 1 | a0001c0001t0006g0245 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2580+5640G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358856 | |||||||
| chr5:123358907 | T | G | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2580+5589A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358907 | |||||||
| chr5:123358983 | A | G | 1 | a0001c0001t0002g0278 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2580+5513T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123358983 | |||||||
| chr5:123359072 | G | C | 229 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(226): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2580+5424C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123359072 | |||||||
| chr5:123359337 | A | G | 229 | a0001c0001t0002g0277 a0001c0005t0003g0011 a0001c0005t0003g0062 others(226): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2580+5159T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123359337 | |||||||
| chr5:123359396 | T | G | 2 | a0002c0002t0001g0174 a0002c0002t0001g0175 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2580+5100A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123359396 | |||||||
| chr5:123359480 | T | G | 1 | a0001c0001t0002g0255 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2580+5016A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123359480 | |||||||
| chr5:123359536 | A | T | 2 | a0003c0003t0001g0196 a0003c0003t0001g0197 |
2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2580+4960T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123359536 | |||||||
| chr5:123360105 | T | G | 1 | a0001c0001t0002g0230 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2580+4391A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360105 | |||||||
| chr5:123360129 | CACAA | C | 34 | a0001c0006t0001g0102 a0002c0002t0001g0005 a0002c0002t0001g0016 others(31): Show |
39 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.2580+4363_2580+436 others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360129 | |||||||
| chr5:123360296 | C | T | 2 | a0003c0003t0001g0196 a0003c0003t0001g0197 |
2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2580+4200G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360296 | |||||||
| chr5:123360387 | A | G | 1 | a0002c0002t0001g0118 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2580+4109T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360387 | |||||||
| chr5:123360605 | C | G | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2580+3891G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360605 | |||||||
| chr5:123360653 | G | GCAAGAGG others(12): Show |
144 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(141): Show |
162 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2580+3824_2580+384 others(23): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360653 | |||||||
| chr5:123360673 | A | C | 230 | a0001c0001t0002g0251 a0001c0001t0002g0322 a0001c0005t0003g0011 others(227): Show |
256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.2580+3823T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360673 | |||||||
| chr5:123360697 | G | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2580+3799C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360697 | |||||||
| chr5:123360774 | G | C | 34 | a0001c0001t0002g0251 a0001c0005t0003g0324 a0004c0004t0003g0013 others(31): Show |
36 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.2580+3722C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360774 | |||||||
| chr5:123360780 | C | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2580+3716G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360780 | |||||||
| chr5:123360811 | C | G | 3 | a0001c0001t0002g0215 a0001c0001t0002g0244 a0001c0001t0002g0278 |
3 | NA18968.hp2 NA18977.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2580+3685G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360811 | |||||||
| chr5:123360812 | T | TAC | 4 | a0002c0002t0001g0113 a0002c0002t0001g0128 a0002c0002t0001g0138 others(1): Show |
4 | NA18969.hp1 NA18987.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.2580+3682_2580+368 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360812 | |||||||
| chr5:123360859 | G | A | 3 | a0002c0002t0001g0112 a0002c0009t0001g0125 a0002c0009t0010g0031 |
3 | HG00438.hp1 NA18984.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2580+3637C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360859 | |||||||
| chr5:123360900 | A | G | 2 | a0001c0005t0003g0011 a0001c0005t0003g0080 |
3 | HG01255.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2580+3596T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360900 | |||||||
| chr5:123360940 | A | G | 1 | a0002c0002t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2580+3556T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123360940 | |||||||
| chr5:123361031 | A | ATAAT | 233 | a0001c0001t0002g0251 a0001c0005t0003g0011 a0001c0005t0003g0062 others(230): Show |
259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2580+3461_2580+346 others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361031 | |||||||
| chr5:123361049 | A | G | 233 | a0001c0001t0002g0251 a0001c0005t0003g0011 a0001c0005t0003g0062 others(230): Show |
259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2580+3447T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361049 | |||||||
| chr5:123361188 | G | T | 230 | a0001c0001t0002g0251 a0001c0001t0002g0322 a0001c0005t0003g0011 others(227): Show |
256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.2580+3308C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361188 | |||||||
| chr5:123361281 | G | A | 2 | a0002c0002t0001g0143 a0002c0002t0001g0144 |
2 | NA18960.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.2580+3215C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361281 | |||||||
| chr5:123361315 | T | C | 36 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(33): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2580+3181A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361315 | |||||||
| chr5:123361416 | G | C | 1 | a0002c0002t0001g0164 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2580+3080C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361416 | |||||||
| chr5:123361601 | C | G | 36 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(33): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2580+2895G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361601 | |||||||
| chr5:123361737 | C | T | 22 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(19): Show |
26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.2580+2759G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361737 | |||||||
| chr5:123361764 | G | A | 35 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(32): Show |
39 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2580+2732C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123361764 | |||||||
| chr5:123362198 | T | C | 3 | a0003c0003t0001g0003 a0003c0003t0001g0300 a0003c0003t0001g0304 |
6 | HG00280.hp1 HG00642.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.2580+2298A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362198 | |||||||
| chr5:123362299 | G | A | 1 | a0002c0002t0001g0295 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2580+2197C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362299 | |||||||
| chr5:123362438 | A | T | 1 | a0001c0005t0005g0069 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2580+2058T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362438 | |||||||
| chr5:123362661 | A | C | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2580+1835T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362661 | |||||||
| chr5:123362673 | G | A | 222 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(219): Show |
246 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.2580+1823C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362673 | |||||||
| chr5:123362695 | C | T | 233 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(230): Show |
259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2580+1801G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362695 | |||||||
| chr5:123362839 | A | G | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2580+1657T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362839 | |||||||
| chr5:123362944 | T | A | 1 | a0001c0005t0003g0324 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2580+1552A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123362944 | |||||||
| chr5:123363001 | T | A | 35 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(32): Show |
39 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2580+1495A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363001 | |||||||
| chr5:123363075 | C | T | 1 | a0001c0001t0002g0283 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2580+1421G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363075 | |||||||
| chr5:123363227 | A | G | 1 | a0003c0003t0001g0186 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2580+1269T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363227 | |||||||
| chr5:123363228 | T | C | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2580+1268A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363228 | |||||||
| chr5:123363422 | C | T | 1 | a0001c0005t0005g0067 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2580+1074G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363422 | |||||||
| chr5:123363491 | G | A | 1 | a0002c0002t0001g0129 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2580+1005C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363491 | |||||||
| chr5:123363504 | C | CTA | 182 | a0001c0001t0002g0251 a0001c0006t0001g0102 a0002c0002t0001g0005 others(179): Show |
201 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.2580+990_2580+991d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363504 | |||||||
| chr5:123363583 | T | G | 1 | a0001c0001t0012g0275 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2580+913A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363583 | |||||||
| chr5:123363643 | C | G | 1 | a0001c0001t0002g0236 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2580+853G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363643 | |||||||
| chr5:123363731 | T | C | 233 | a0001c0001t0002g0251 a0001c0005t0003g0011 a0001c0005t0003g0062 others(230): Show |
259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2580+765A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363731 | |||||||
| chr5:123363795 | T | C | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2580+701A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363795 | |||||||
| chr5:123363909 | T | C | 2 | a0003c0003t0001g0180 a0003c0003t0001g0181 |
2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2580+587A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123363909 | |||||||
| chr5:123364118 | T | G | 68 | a0002c0002t0001g0118 a0002c0002t0001g0295 a0002c0008t0002g0217 others(65): Show |
79 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.2580+378A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 18/19 | chr5 | 123364118 | |||||||
| chr5:123364684 | A | G | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2482-90T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123364684 | |||||||
| chr5:123364709 | C | T | 1 | a0002c0002t0001g0157 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2482-115G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123364709 | |||||||
| chr5:123364929 | C | A | 1 | a0001c0001t0002g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2482-335G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123364929 | |||||||
| chr5:123364962 | T | C | 151 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(148): Show |
169 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.2482-368A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123364962 | |||||||
| chr5:123365112 | T | C | 3 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0192 |
3 | HG01884.hp2 HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2482-518A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123365112 | |||||||
| chr5:123365234 | G | GA | 233 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(230): Show |
259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2482-641dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123365234 | |||||||
| chr5:123365540 | A | G | 23 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(20): Show |
27 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.2482-946T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123365540 | |||||||
| chr5:123365579 | T | G | 2 | a0004c0004t0003g0057 a0004c0004t0003g0058 |
2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2482-985A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123365579 | |||||||
| chr5:123365822 | T | G | 2 | a0002c0002t0001g0200 a0002c0002t0001g0201 |
2 | HG00323.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2482-1228A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123365822 | |||||||
| chr5:123365867 | T | C | 233 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(230): Show |
259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2482-1273A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123365867 | |||||||
| chr5:123366005 | TCACACTA others(8): Show |
T | 232 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(229): Show |
258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.2482-1426_2482-141 others(19): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366005 | |||||||
| chr5:123366317 | A | G | 76 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(73): Show |
84 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.2482-1723T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366317 | |||||||
| chr5:123366471 | G | A | 2 | a0001c0001t0002g0238 a0001c0001t0002g0322 |
2 | HG03654.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2482-1877C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366471 | |||||||
| chr5:123366600 | T | C | 233 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(230): Show |
259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2482-2006A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366600 | |||||||
| chr5:123366644 | A | G | 230 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(227): Show |
256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.2482-2050T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366644 | |||||||
| chr5:123366880 | G | T | 17 | a0001c0005t0005g0004 a0001c0005t0005g0012 a0001c0005t0005g0035 others(14): Show |
20 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.2482-2286C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366880 | |||||||
| chr5:123366881 | A | T | 17 | a0001c0005t0005g0004 a0001c0005t0005g0012 a0001c0005t0005g0035 others(14): Show |
20 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.2482-2287T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366881 | |||||||
| chr5:123366882 | A | G | 17 | a0001c0005t0005g0004 a0001c0005t0005g0012 a0001c0005t0005g0035 others(14): Show |
20 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.2482-2288T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366882 | |||||||
| chr5:123366883 | A | T | 17 | a0001c0005t0005g0004 a0001c0005t0005g0012 a0001c0005t0005g0035 others(14): Show |
20 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.2482-2289T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123366883 | |||||||
| chr5:123367068 | T | G | 232 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(229): Show |
258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.2482-2474A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367068 | |||||||
| chr5:123367072 | T | G | 156 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(153): Show |
174 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.2482-2478A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367072 | |||||||
| chr5:123367214 | C | T | 2 | a0003c0003t0001g0196 a0003c0003t0001g0197 |
2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2482-2620G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367214 | |||||||
| chr5:123367227 | A | C | 1 | a0001c0001t0004g0233 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2482-2633T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367227 | |||||||
| chr5:123367264 | T | G | 8 | a0001c0006t0008g0010 a0001c0006t0009g0030 a0005c0007t0003g0085 others(5): Show |
9 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2482-2670A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367264 | |||||||
| chr5:123367315 | A | G | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2482-2721T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367315 | |||||||
| chr5:123367332 | C | A | 221 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(218): Show |
245 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.2482-2738G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367332 | |||||||
| chr5:123367414 | A | ATATG | 3 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0192 |
3 | HG01884.hp2 HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2482-2824_2482-282 others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367414 | |||||||
| chr5:123367535 | C | T | 5 | a0001c0006t0002g0006 a0001c0006t0002g0206 a0001c0006t0002g0207 others(2): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2482-2941G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367535 | |||||||
| chr5:123367578 | A | C | 232 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(229): Show |
258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.2482-2984T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367578 | |||||||
| chr5:123367866 | T | G | 5 | a0002c0002t0001g0156 a0002c0002t0001g0158 a0002c0002t0001g0159 others(2): Show |
5 | NA18944.hp2 NA18948.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.2482-3272A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367866 | |||||||
| chr5:123367890 | G | A | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2482-3296C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367890 | |||||||
| chr5:123367903 | T | G | 2 | a0003c0003t0001g0180 a0003c0003t0001g0181 |
2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2482-3309A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123367903 | |||||||
| chr5:123368326 | A | T | 222 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(219): Show |
246 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.2482-3732T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368326 | |||||||
| chr5:123368375 | T | C | 1 | a0002c0002t0001g0165 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2482-3781A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368375 | |||||||
| chr5:123368428 | G | A | 33 | a0001c0005t0003g0324 a0004c0004t0003g0013 a0004c0004t0003g0015 others(30): Show |
35 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2482-3834C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368428 | |||||||
| chr5:123368431 | T | C | 1 | a0001c0005t0005g0078 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2482-3837A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368431 | |||||||
| chr5:123368445 | A | G | 1 | a0003c0003t0001g0189 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2482-3851T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368445 | |||||||
| chr5:123368648 | G | T | 28 | a0004c0004t0003g0013 a0004c0004t0003g0015 a0004c0004t0003g0036 others(25): Show |
30 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.2481+4002C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368648 | |||||||
| chr5:123368732 | A | G | 232 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(229): Show |
258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.2481+3918T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368732 | |||||||
| chr5:123368858 | A | G | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2481+3792T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368858 | |||||||
| chr5:123368955 | C | T | 221 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(218): Show |
245 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.2481+3695G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123368955 | |||||||
| chr5:123369236 | A | G | 1 | a0002c0002t0018g0329 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2481+3414T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369236 | |||||||
| chr5:123369416 | A | G | 231 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(228): Show |
257 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.2481+3234T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369416 | |||||||
| chr5:123369550 | C | T | 33 | a0001c0005t0003g0324 a0004c0004t0003g0013 a0004c0004t0003g0015 others(30): Show |
35 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2481+3100G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369550 | |||||||
| chr5:123369627 | A | G | 230 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(227): Show |
256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.2481+3023T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369627 | |||||||
| chr5:123369637 | T | C | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2481+3013A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369637 | |||||||
| chr5:123369687 | T | C | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2963A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369687 | |||||||
| chr5:123369690 | T | A | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2960A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369690 | |||||||
| chr5:123369693 | A | T | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2957T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369693 | |||||||
| chr5:123369703 | C | G | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2947G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369703 | |||||||
| chr5:123369704 | C | G | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2946G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369704 | |||||||
| chr5:123369709 | C | G | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2941G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369709 | |||||||
| chr5:123369710 | C | G | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2940G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369710 | |||||||
| chr5:123369716 | A | T | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2934T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369716 | |||||||
| chr5:123369719 | T | A | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2931A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369719 | |||||||
| chr5:123369722 | G | A | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2928C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369722 | |||||||
| chr5:123369749 | T | A | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+2901A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369749 | |||||||
| chr5:123369753 | T | C | 4 | a0002c0002t0001g0018 a0002c0002t0001g0116 a0002c0002t0001g0121 others(1): Show |
5 | HG00597.hp2 HG02080.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.2481+2897A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369753 | |||||||
| chr5:123369841 | C | T | 69 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(66): Show |
75 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.2481+2809G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369841 | |||||||
| chr5:123369922 | A | G | 8 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(5): Show |
10 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2481+2728T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123369922 | |||||||
| chr5:123370043 | C | A | 218 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(215): Show |
241 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.2481+2607G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370043 | |||||||
| chr5:123370177 | G | C | 1 | a0001c0001t0002g0287 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2481+2473C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370177 | |||||||
| chr5:123370471 | C | T | 2 | a0001c0001t0002g0261 a0001c0001t0002g0270 |
2 | HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2481+2179G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370471 | |||||||
| chr5:123370471 | CTTTG | C | 15 | a0001c0005t0005g0004 a0001c0005t0005g0012 a0001c0005t0005g0035 others(12): Show |
18 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.2481+2175_2481+217 others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370471 | |||||||
| chr5:123370609 | C | A | 1 | a0002c0002t0001g0160 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2481+2041G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370609 | |||||||
| chr5:123370671 | A | ATG | 13 | a0001c0005t0003g0081 a0001c0005t0003g0082 a0001c0005t0003g0083 others(10): Show |
13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2481+1977_2481+197 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370671 | |||||||
| chr5:123370677 | G | GTA | 10 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2481+1972_2481+197 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370677 | |||||||
| chr5:123370685 | G | A | 2 | a0004c0004t0003g0057 a0004c0004t0003g0058 |
2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2481+1965C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370685 | |||||||
| chr5:123370685 | G | GTA | 205 | a0001c0005t0003g0062 a0001c0005t0003g0095 a0001c0005t0003g0324 others(202): Show |
228 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.2481+1963_2481+196 others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370685 | |||||||
| chr5:123370685 | G | GTATA | 2 | a0001c0005t0003g0011 a0001c0005t0003g0080 |
3 | HG01255.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2481+1961_2481+196 others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370685 | |||||||
| chr5:123370750 | A | ATATATAT others(13): Show |
2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2481+1880_2481+189 others(24): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123370750 | |||||||
| chr5:123371055 | T | C | 1 | a0001c0001t0002g0287 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2481+1595A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371055 | |||||||
| chr5:123371193 | T | C | 1 | a0001c0005t0003g0090 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2481+1457A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371193 | |||||||
| chr5:123371231 | G | C | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2481+1419C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371231 | |||||||
| chr5:123371239 | G | T | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2481+1411C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371239 | |||||||
| chr5:123371428 | A | C | 1 | a0002c0002t0001g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2481+1222T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371428 | |||||||
| chr5:123371441 | C | T | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2481+1209G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371441 | |||||||
| chr5:123371510 | T | G | 4 | a0004c0004t0003g0057 a0004c0004t0003g0058 a0004c0004t0003g0059 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2481+1140A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371510 | |||||||
| chr5:123371754 | C | T | 1 | a0001c0005t0005g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2481+896G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371754 | |||||||
| chr5:123371814 | A | C | 1 | a0002c0002t0001g0162 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2481+836T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123371814 | |||||||
| chr5:123372002 | A | G | 1 | a0002c0002t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2481+648T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372002 | |||||||
| chr5:123372029 | T | C | 1 | a0003c0003t0001g0181 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2481+621A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372029 | |||||||
| chr5:123372190 | C | G | 13 | a0001c0005t0003g0081 a0001c0005t0003g0082 a0001c0005t0003g0083 others(10): Show |
13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2481+460G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372190 | |||||||
| chr5:123372192 | C | T | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2481+458G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372192 | |||||||
| chr5:123372296 | G | A | 2 | a0006c0010t0002g0202 a0006c0010t0015g0032 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2481+354C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372296 | |||||||
| chr5:123372301 | C | T | 1 | a0001c0001t0002g0014 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2481+349G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372301 | |||||||
| chr5:123372321 | C | T | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2481+329G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372321 | |||||||
| chr5:123372510 | G | A | 1 | a0002c0002t0001g0295 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2481+140C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372510 | |||||||
| chr5:123372579 | T | A | 4 | a0004c0004t0003g0057 a0004c0004t0003g0058 a0004c0004t0003g0059 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2481+71A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372579 | |||||||
| chr5:123372583 | C | T | 1 | a0001c0005t0003g0324 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2481+67G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 17/19 | chr5 | 123372583 | |||||||
| chr5:123372780 | A | T | 1 | a0003c0003t0001g0135 | 1 | NA19083.hp1 | splice_region_variant&intron_variant | LOW | c.2359-8T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123372780 | |||||||
| chr5:123372903 | A | C | 2 | a0002c0002t0001g0155 a0002c0002t0001g0167 |
2 | NA18967.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2359-131T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123372903 | |||||||
| chr5:123373124 | A | C | 1 | a0001c0001t0002g0029 | 2 | HG01109.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2359-352T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373124 | |||||||
| chr5:123373137 | G | C | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2359-365C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373137 | |||||||
| chr5:123373228 | G | A | 4 | a0003c0003t0001g0296 a0003c0003t0001g0302 a0003c0003t0001g0303 others(1): Show |
4 | HG00558.hp2 HG02071.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2359-456C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373228 | |||||||
| chr5:123373428 | G | C | 1 | a0001c0005t0003g0082 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2359-656C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373428 | |||||||
| chr5:123373559 | A | G | 1 | a0002c0002t0001g0119 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2359-787T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373559 | |||||||
| chr5:123373633 | A | T | 148 | a0001c0006t0001g0102 a0002c0002t0001g0005 a0002c0002t0001g0016 others(145): Show |
165 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2359-861T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373633 | |||||||
| chr5:123373665 | T | C | 1 | a0001c0005t0003g0082 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2359-893A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373665 | |||||||
| chr5:123373668 | C | T | 13 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0214 others(10): Show |
15 | HG01496.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2359-896G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373668 | |||||||
| chr5:123373678 | T | C | 1 | a0003c0003t0001g0186 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2359-906A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373678 | |||||||
| chr5:123373703 | C | T | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2359-931G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373703 | |||||||
| chr5:123373728 | C | T | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2359-956G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373728 | |||||||
| chr5:123373740 | A | G | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2359-968T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373740 | |||||||
| chr5:123373935 | C | T | 163 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(160): Show |
183 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.2359-1163G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123373935 | |||||||
| chr5:123374476 | A | G | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2359-1704T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123374476 | |||||||
| chr5:123374556 | T | G | 199 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(196): Show |
223 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.2359-1784A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123374556 | |||||||
| chr5:123374732 | T | C | 1 | a0002c0002t0001g0129 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2359-1960A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123374732 | |||||||
| chr5:123375054 | A | T | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2359-2282T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375054 | |||||||
| chr5:123375154 | G | A | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2358+2220C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375154 | |||||||
| chr5:123375330 | C | CT | 36 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(33): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2358+2043dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375330 | |||||||
| chr5:123375341 | G | A | 36 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(33): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2358+2033C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375341 | |||||||
| chr5:123375474 | C | T | 33 | a0001c0005t0003g0324 a0004c0004t0003g0013 a0004c0004t0003g0015 others(30): Show |
35 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2358+1900G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375474 | |||||||
| chr5:123375582 | G | A | 3 | a0006c0010t0002g0202 a0006c0010t0015g0032 a0008c0017t0002g0209 |
3 | HG01243.hp1 HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2358+1792C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375582 | |||||||
| chr5:123375588 | GTTGGGAT others(1): Show |
G | 150 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(147): Show |
168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2358+1778_2358+178 others(12): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375588 | |||||||
| chr5:123375597 | A | G | 150 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(147): Show |
168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2358+1777T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375597 | |||||||
| chr5:123375790 | T | C | 2 | a0001c0005t0003g0081 a0001c0005t0003g0083 |
2 | HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2358+1584A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375790 | |||||||
| chr5:123375947 | T | C | 23 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(20): Show |
27 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.2358+1427A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375947 | |||||||
| chr5:123375993 | C | CT | 38 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(35): Show |
43 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.2358+1380dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123375993 | |||||||
| chr5:123376070 | A | G | 2 | a0002c0002t0001g0110 a0002c0002t0001g0117 |
2 | HG03017.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2358+1304T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376070 | |||||||
| chr5:123376075 | C | G | 1 | a0008c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2358+1299G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376075 | |||||||
| chr5:123376076 | C | T | 1 | a0009c0019t0003g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2358+1298G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376076 | |||||||
| chr5:123376095 | C | A | 1 | a0005c0007t0003g0088 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2358+1279G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376095 | |||||||
| chr5:123376147 | C | T | 163 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(160): Show |
183 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.2358+1227G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376147 | |||||||
| chr5:123376152 | T | A | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2358+1222A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376152 | |||||||
| chr5:123376452 | T | C | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2358+922A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376452 | |||||||
| chr5:123376462 | T | C | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2358+912A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376462 | |||||||
| chr5:123376549 | C | T | 1 | a0003c0003t0001g0304 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2358+825G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376549 | |||||||
| chr5:123376597 | G | A | 1 | a0003c0003t0001g0315 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2358+777C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376597 | |||||||
| chr5:123376694 | G | A | 1 | a0001c0001t0002g0278 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2358+680C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376694 | |||||||
| chr5:123376825 | G | C | 199 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(196): Show |
223 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.2358+549C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376825 | |||||||
| chr5:123376869 | G | A | 33 | a0001c0005t0003g0324 a0004c0004t0003g0013 a0004c0004t0003g0015 others(30): Show |
35 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2358+505C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376869 | |||||||
| chr5:123376874 | G | A | 2 | a0001c0006t0002g0204 a0001c0006t0002g0205 |
2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2358+500C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376874 | |||||||
| chr5:123376903 | C | G | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2358+471G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123376903 | |||||||
| chr5:123377019 | G | T | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2358+355C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123377019 | |||||||
| chr5:123377354 | T | C | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2358+20A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123377354 | |||||||
| chr5:123377360 | G | A | 1 | a0001c0001t0002g0318 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2358+14C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 16/19 | chr5 | 123377360 | |||||||
| chr5:123377545 | A | C | 1 | a0001c0005t0003g0090 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2197-10T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/19 | chr5 | 123377545 | |||||||
| chr5:123377951 | C | T | 2 | a0002c0002t0001g0116 a0002c0002t0001g0123 |
2 | HG00597.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.2196+385G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/19 | chr5 | 123377951 | |||||||
| chr5:123378145 | TA | T | 150 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(147): Show |
168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2196+190delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/19 | chr5 | 123378145 | |||||||
| chr5:123378243 | G | A | 1 | a0008c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2196+93C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/19 | chr5 | 123378243 | |||||||
| chr5:123378295 | C | T | 45 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(42): Show |
51 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.2196+41G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 15/19 | chr5 | 123378295 | |||||||
| chr5:123378440 | T | TA | 15 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(12): Show |
17 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2104-13dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378440 | |||||||
| chr5:123378440 | TA | T | 6 | a0001c0005t0003g0324 a0002c0002t0001g0155 a0004c0004t0003g0057 others(3): Show |
6 | HG01891.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2104-13delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378440 | |||||||
| chr5:123378440 | TAAAAAA | T | 38 | a0001c0006t0001g0102 a0002c0002t0001g0005 a0002c0002t0001g0016 others(35): Show |
43 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2104-18_2104-13del others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378440 | |||||||
| chr5:123378498 | C | A | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2104-70G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378498 | |||||||
| chr5:123378528 | G | C | 2 | a0002c0002t0001g0212 a0002c0002t0001g0213 |
2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.2104-100C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378528 | |||||||
| chr5:123378562 | G | T | 1 | a0001c0013t0004g0243 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2104-134C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378562 | |||||||
| chr5:123378647 | A | G | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2104-219T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378647 | |||||||
| chr5:123378772 | T | A | 1 | a0003c0003t0001g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2104-344A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378772 | |||||||
| chr5:123378783 | A | C | 110 | a0002c0002t0001g0019 a0002c0002t0001g0094 a0002c0002t0001g0115 others(107): Show |
122 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.2104-355T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378783 | |||||||
| chr5:123378798 | G | C | 2 | a0002c0002t0001g0200 a0002c0002t0001g0201 |
2 | HG00323.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2104-370C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123378798 | |||||||
| chr5:123379036 | A | C | 5 | a0002c0002t0001g0094 a0002c0002t0001g0198 a0002c0002t0001g0199 others(2): Show |
5 | HG00323.hp1 HG00642.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.2104-608T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379036 | |||||||
| chr5:123379044 | A | T | 1 | a0004c0004t0003g0057 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2104-616T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379044 | |||||||
| chr5:123379096 | C | G | 1 | a0004c0004t0003g0038 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2104-668G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379096 | |||||||
| chr5:123379149 | G | A | 39 | a0002c0002t0001g0019 a0002c0002t0001g0094 a0002c0002t0001g0115 others(36): Show |
40 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.2104-721C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379149 | |||||||
| chr5:123379278 | A | G | 199 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(196): Show |
223 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.2104-850T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379278 | |||||||
| chr5:123379300 | C | T | 1 | a0002c0008t0002g0217 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2104-872G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379300 | |||||||
| chr5:123379377 | T | A | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2104-949A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379377 | |||||||
| chr5:123379386 | T | C | 1 | a0003c0003t0001g0297 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2104-958A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379386 | |||||||
| chr5:123379416 | T | C | 3 | a0006c0010t0002g0202 a0006c0010t0015g0032 a0008c0017t0002g0209 |
3 | HG01243.hp1 HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2104-988A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379416 | |||||||
| chr5:123379420 | A | C | 1 | a0005c0007t0003g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2104-992T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379420 | |||||||
| chr5:123379445 | A | G | 15 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0034 others(12): Show |
17 | HG01496.hp2 HG02258.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2104-1017T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379445 | |||||||
| chr5:123379542 | A | G | 1 | a0001c0005t0005g0063 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2104-1114T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379542 | |||||||
| chr5:123379724 | A | G | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2104-1296T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379724 | |||||||
| chr5:123379781 | C | G | 1 | a0003c0003t0001g0301 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2104-1353G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123379781 | |||||||
| chr5:123380212 | CT | C | 7 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0216 others(4): Show |
9 | NA18944.hp1 NA18946.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.2104-1785delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123380212 | |||||||
| chr5:123380228 | C | T | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2104-1800G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123380228 | |||||||
| chr5:123380670 | A | G | 2 | a0001c0001t0002g0225 a0001c0001t0002g0242 |
2 | HG02074.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2103+1441T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123380670 | |||||||
| chr5:123381028 | A | AAGTT | 32 | a0001c0005t0003g0324 a0004c0004t0003g0013 a0004c0004t0003g0015 others(29): Show |
34 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.2103+1079_2103+108 others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381028 | |||||||
| chr5:123381103 | T | C | 36 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(33): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2103+1008A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381103 | |||||||
| chr5:123381125 | C | A | 229 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(226): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.2103+986G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381125 | |||||||
| chr5:123381197 | A | G | 13 | a0001c0005t0003g0081 a0001c0005t0003g0082 a0001c0005t0003g0083 others(10): Show |
13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2103+914T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381197 | |||||||
| chr5:123381221 | A | C | 162 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(159): Show |
182 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.2103+890T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381221 | |||||||
| chr5:123381377 | A | AGGAGCAC others(1): Show |
162 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(159): Show |
182 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.2103+726_2103+733d others(10): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381377 | |||||||
| chr5:123381607 | T | C | 26 | a0004c0004t0003g0013 a0004c0004t0003g0015 a0004c0004t0003g0036 others(23): Show |
28 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.2103+504A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381607 | |||||||
| chr5:123381742 | T | C | 1 | a0001c0001t0002g0276 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2103+369A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381742 | |||||||
| chr5:123381758 | C | T | 1 | a0001c0001t0002g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2103+353G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381758 | |||||||
| chr5:123381766 | T | C | 150 | a0001c0001t0002g0276 a0001c0006t0001g0102 a0001c0006t0008g0010 others(147): Show |
168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2103+345A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381766 | |||||||
| chr5:123381767 | AT | A | 151 | a0001c0001t0002g0276 a0001c0006t0001g0102 a0001c0006t0008g0010 others(148): Show |
169 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.2103+343delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381767 | |||||||
| chr5:123381820 | T | A | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2103+291A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381820 | |||||||
| chr5:123381969 | C | G | 1 | a0001c0005t0003g0090 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2103+142G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123381969 | |||||||
| chr5:123382046 | C | T | 5 | a0002c0002t0001g0112 a0002c0002t0001g0212 a0002c0002t0001g0213 others(2): Show |
5 | HG00438.hp1 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2103+65G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 14/19 | chr5 | 123382046 | |||||||
| chr5:123382226 | G | T | 2 | a0001c0001t0002g0280 a0001c0001t0002g0281 |
2 | HG01123.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2014-26C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382226 | |||||||
| chr5:123382263 | T | C | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2014-63A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382263 | |||||||
| chr5:123382324 | C | A | 16 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0034 others(13): Show |
18 | HG01496.hp2 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.2014-124G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382324 | |||||||
| chr5:123382325 | T | TA | 26 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(23): Show |
30 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.2014-126dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382325 | |||||||
| chr5:123382325 | TA | T | 46 | a0001c0001t0002g0241 a0001c0001t0002g0316 a0001c0001t0004g0233 others(43): Show |
51 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.2014-126delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382325 | |||||||
| chr5:123382326 | A | T | 1 | a0001c0001t0002g0033 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2014-126T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382326 | |||||||
| chr5:123382350 | G | T | 149 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(146): Show |
167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.2014-150C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382350 | |||||||
| chr5:123382354 | C | A | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2014-154G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382354 | |||||||
| chr5:123382442 | A | G | 32 | a0001c0005t0003g0324 a0004c0004t0003g0013 a0004c0004t0003g0015 others(29): Show |
34 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.2014-242T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382442 | |||||||
| chr5:123382545 | G | A | 4 | a0004c0004t0003g0048 a0004c0004t0003g0049 a0004c0004t0003g0055 others(1): Show |
4 | NA18982.hp1 NA18990.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.2013+192C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382545 | |||||||
| chr5:123382647 | C | T | 36 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(33): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2013+90G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382647 | |||||||
| chr5:123382654 | T | C | 4 | a0002c0008t0002g0217 a0002c0008t0002g0218 a0002c0008t0002g0219 others(1): Show |
4 | NA18949.hp2 NA18950.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2013+83A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 13/19 | chr5 | 123382654 | |||||||
| chr5:123382934 | T | C | 1 | a0001c0005t0003g0324 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1861-45A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 12/19 | chr5 | 123382934 | |||||||
| chr5:123383200 | A | G | 1 | a0001c0001t0002g0280 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1764-118T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123383200 | |||||||
| chr5:123383502 | T | C | 1 | a0003c0003t0001g0303 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1764-420A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123383502 | |||||||
| chr5:123383612 | T | C | 1 | a0001c0001t0002g0222 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1764-530A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123383612 | |||||||
| chr5:123383633 | T | C | 1 | a0004c0004t0003g0052 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1764-551A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123383633 | |||||||
| chr5:123383848 | C | A | 2 | a0001c0006t0002g0204 a0001c0006t0002g0205 |
2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1764-766G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123383848 | |||||||
| chr5:123383988 | T | A | 149 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(146): Show |
167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1764-906A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123383988 | |||||||
| chr5:123384253 | T | C | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1763+698A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384253 | |||||||
| chr5:123384287 | CTTGT | C | 145 | a0001c0006t0001g0102 a0002c0002t0001g0005 a0002c0002t0001g0016 others(142): Show |
161 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1763+660_1763+663d others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384287 | |||||||
| chr5:123384290 | G | C | 2 | a0002c0002t0001g0017 a0002c0002t0001g0104 |
3 | HG00735.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1763+661C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384290 | |||||||
| chr5:123384292 | T | C | 2 | a0002c0002t0001g0017 a0002c0002t0001g0104 |
3 | HG00735.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1763+659A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384292 | |||||||
| chr5:123384293 | TCTC | T | 2 | a0002c0002t0001g0017 a0002c0002t0001g0104 |
3 | HG00735.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1763+655_1763+657d others(5): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384293 | |||||||
| chr5:123384326 | G | A | 147 | a0001c0006t0001g0102 a0002c0002t0001g0005 a0002c0002t0001g0016 others(144): Show |
164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1763+625C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384326 | |||||||
| chr5:123384423 | A | T | 1 | a0001c0001t0002g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1763+528T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384423 | |||||||
| chr5:123384431 | G | A | 1 | a0008c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1763+520C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384431 | |||||||
| chr5:123384613 | A | G | 4 | a0002c0002t0001g0094 a0002c0002t0001g0198 a0002c0002t0001g0200 others(1): Show |
4 | HG00323.hp1 HG00642.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1763+338T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384613 | |||||||
| chr5:123384639 | A | C | 1 | a0001c0001t0002g0288 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1763+312T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 11/19 | chr5 | 123384639 | |||||||
| chr5:123385229 | T | A | 149 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(146): Show |
167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1581-96A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385229 | |||||||
| chr5:123385252 | G | A | 1 | a0002c0002t0001g0126 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1581-119C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385252 | |||||||
| chr5:123385394 | C | T | 68 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(65): Show |
74 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.1581-261G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385394 | |||||||
| chr5:123385559 | G | T | 69 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(66): Show |
75 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1581-426C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385559 | |||||||
| chr5:123385619 | GT | G | 159 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0205 others(156): Show |
179 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1581-487delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385619 | |||||||
| chr5:123385692 | C | T | 162 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(159): Show |
182 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1581-559G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385692 | |||||||
| chr5:123385862 | C | T | 2 | a0001c0005t0003g0011 a0001c0005t0003g0080 |
3 | HG01255.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1580+656G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385862 | |||||||
| chr5:123385984 | G | A | 2 | a0002c0002t0001g0110 a0002c0002t0001g0117 |
2 | HG03017.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1580+534C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123385984 | |||||||
| chr5:123386042 | G | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1580+476C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386042 | |||||||
| chr5:123386111 | G | A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1580+407C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386111 | |||||||
| chr5:123386124 | A | C | 3 | a0002c0002t0001g0211 a0002c0002t0001g0212 a0002c0002t0001g0213 |
3 | HG02055.hp2 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1580+394T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386124 | |||||||
| chr5:123386158 | A | C | 10 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1580+360T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386158 | |||||||
| chr5:123386179 | T | C | 1 | a0001c0005t0005g0063 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1580+339A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386179 | |||||||
| chr5:123386200 | T | G | 2 | a0003c0003t0001g0022 a0003c0003t0001g0195 |
3 | NA18959.hp1 NA18974.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1580+318A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386200 | |||||||
| chr5:123386306 | G | A | 1 | a0004c0004t0003g0013 | 2 | HG01167.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1580+212C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 10/19 | chr5 | 123386306 | |||||||
| chr5:123386673 | AT | A | 53 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0207 others(50): Show |
61 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(58): Show |
splice_region_variant&intron_variant | LOW | c.1431-7delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386673 | |||||||
| chr5:123386674 | T | A | 6 | a0001c0006t0002g0204 a0001c0006t0002g0205 a0001c0006t0002g0206 others(3): Show |
6 | HG02257.hp1 HG02970.hp1 HG03041.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1431-7A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386674 | |||||||
| chr5:123386675 | T | A | 4 | a0001c0006t0002g0006 a0001c0006t0002g0207 a0001c0006t0013g0208 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1431-8A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386675 | |||||||
| chr5:123386675 | T | TA | 4 | a0002c0002t0001g0151 a0002c0002t0001g0157 a0002c0002t0001g0162 others(1): Show |
4 | HG03579.hp2 NA18939.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1431-9_1431-8insT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386675 | |||||||
| chr5:123386675 | TTA | T | 3 | a0001c0006t0003g0323 a0002c0002t0001g0103 a0008c0017t0002g0209 |
3 | HG01070.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1431-10_1431-9delT others(1): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386675 | |||||||
| chr5:123386676 | T | A | 105 | a0001c0006t0002g0204 a0001c0006t0002g0205 a0001c0006t0002g0206 others(102): Show |
117 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1431-9A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386676 | |||||||
| chr5:123386676 | T | TA | 10 | a0001c0005t0003g0324 a0001c0005t0005g0063 a0001c0005t0005g0071 others(7): Show |
10 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1431-10dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386676 | |||||||
| chr5:123386676 | T | TAA | 54 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(51): Show |
60 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.1431-11_1431-10dup others(2): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386676 | |||||||
| chr5:123386678 | A | T | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1431-11T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386678 | |||||||
| chr5:123386874 | C | T | 147 | a0001c0006t0001g0102 a0002c0002t0001g0005 a0002c0002t0001g0016 others(144): Show |
164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1431-207G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386874 | |||||||
| chr5:123386900 | T | C | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1431-233A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123386900 | |||||||
| chr5:123387243 | C | G | 2 | a0004c0004t0003g0057 a0004c0004t0003g0058 |
2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1431-576G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387243 | |||||||
| chr5:123387464 | G | C | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1431-797C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387464 | |||||||
| chr5:123387570 | G | T | 149 | a0001c0006t0001g0102 a0001c0006t0008g0010 a0001c0006t0009g0030 others(146): Show |
167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1430+862C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387570 | |||||||
| chr5:123387784 | C | T | 1 | a0003c0003t0001g0300 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1430+648G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387784 | |||||||
| chr5:123387788 | C | G | 2 | a0002c0002t0001g0111 a0002c0002t0014g0124 |
2 | HG01081.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1430+644G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387788 | |||||||
| chr5:123387899 | C | T | 162 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(159): Show |
182 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1430+533G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387899 | |||||||
| chr5:123387992 | A | G | 1 | a0001c0005t0005g0079 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1430+440T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123387992 | |||||||
| chr5:123388013 | CTTTTTGA others(49): Show |
C | 162 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(159): Show |
182 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1430+363_1430+418d others(58): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123388013 | |||||||
| chr5:123388258 | T | C | 1 | a0001c0005t0003g0082 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1430+174A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123388258 | |||||||
| chr5:123388316 | C | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1430+116G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 9/19 | chr5 | 123388316 | |||||||
| chr5:123388730 | T | C | 8 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0001g0157 others(5): Show |
8 | NA18939.hp2 NA18960.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.1256-124A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123388730 | |||||||
| chr5:123388752 | A | G | 70 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0011 others(67): Show |
76 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1256-146T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123388752 | |||||||
| chr5:123388804 | T | C | 3 | a0002c0002t0001g0211 a0002c0002t0001g0212 a0002c0002t0001g0213 |
3 | HG02055.hp2 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1256-198A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123388804 | |||||||
| chr5:123388850 | G | A | 4 | a0002c0002t0001g0005 a0002c0002t0001g0130 a0002c0002t0001g0131 others(1): Show |
6 | HG02027.hp1 NA18950.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.1256-244C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123388850 | |||||||
| chr5:123388944 | A | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1256-338T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123388944 | |||||||
| chr5:123388973 | C | A | 148 | a0001c0006t0008g0010 a0001c0006t0009g0030 a0002c0002t0001g0005 others(145): Show |
166 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1256-367G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123388973 | |||||||
| chr5:123389258 | G | A | 1 | a0001c0001t0002g0278 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1256-652C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389258 | |||||||
| chr5:123389291 | CAACTGTT others(7): Show |
C | 2 | a0003c0003t0001g0183 a0003c0003t0001g0193 |
2 | HG02145.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1255+619_1255+632d others(16): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389291 | |||||||
| chr5:123389358 | T | C | 1 | a0002c0002t0001g0170 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1255+566A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389358 | |||||||
| chr5:123389394 | G | C | 4 | a0002c0008t0002g0217 a0002c0008t0002g0218 a0002c0008t0002g0219 others(1): Show |
4 | NA18949.hp2 NA18950.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255+530C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389394 | |||||||
| chr5:123389536 | T | C | 4 | a0001c0001t0004g0009 a0001c0001t0004g0239 a0001c0001t0004g0254 others(1): Show |
6 | HG01433.hp2 HG01952.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255+388A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389536 | |||||||
| chr5:123389562 | G | A | 2 | a0004c0004t0003g0042 a0004c0004t0003g0043 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1255+362C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389562 | |||||||
| chr5:123389563 | C | T | 148 | a0001c0006t0008g0010 a0001c0006t0009g0030 a0002c0002t0001g0005 others(145): Show |
166 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1255+361G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389563 | |||||||
| chr5:123389741 | C | G | 70 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0011 others(67): Show |
76 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1255+183G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389741 | |||||||
| chr5:123389751 | C | T | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1255+173G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389751 | |||||||
| chr5:123389803 | T | C | 34 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0324 others(31): Show |
36 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1255+121A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389803 | |||||||
| chr5:123389884 | A | G | 1 | a0003c0003t0001g0183 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1255+40T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 8/19 | chr5 | 123389884 | |||||||
| chr5:123390159 | T | C | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1039-19A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123390159 | |||||||
| chr5:123390520 | C | T | 1 | a0001c0005t0003g0324 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1039-380G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123390520 | |||||||
| chr5:123390700 | C | T | 1 | a0002c0002t0001g0117 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1038+410G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123390700 | |||||||
| chr5:123390856 | G | A | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1038+254C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123390856 | |||||||
| chr5:123390877 | T | C | 1 | a0003c0003t0001g0137 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1038+233A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123390877 | |||||||
| chr5:123390973 | G | A | 1 | a0002c0002t0001g0138 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1038+137C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123390973 | |||||||
| chr5:123391089 | T | C | 36 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(33): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1038+21A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 7/19 | chr5 | 123391089 | |||||||
| chr5:123391381 | C | T | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.811-44G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391381 | |||||||
| chr5:123391444 | T | A | 324 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(321): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.811-107A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391444 | |||||||
| chr5:123391477 | G | T | 230 | a0001c0001t0002g0322 a0001c0005t0003g0011 a0001c0005t0003g0062 others(227): Show |
256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.811-140C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391477 | |||||||
| chr5:123391501 | C | G | 2 | a0002c0002t0001g0116 a0002c0002t0001g0123 |
2 | HG00597.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.811-164G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391501 | |||||||
| chr5:123391536 | A | T | 4 | a0001c0006t0002g0006 a0001c0006t0002g0207 a0001c0006t0013g0208 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.811-199T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391536 | |||||||
| chr5:123391602 | CTTCTTT | C | 149 | a0001c0006t0008g0010 a0001c0006t0009g0030 a0002c0002t0001g0005 others(146): Show |
167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.811-271_811-266del others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391602 | |||||||
| chr5:123391904 | G | A | 232 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0322 others(229): Show |
258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.811-567C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123391904 | |||||||
| chr5:123392066 | T | C | 1 | a0003c0003t0001g0298 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.811-729A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392066 | |||||||
| chr5:123392125 | T | C | 164 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(161): Show |
185 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.811-788A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392125 | |||||||
| chr5:123392208 | T | C | 1 | a0001c0001t0002g0281 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.811-871A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392208 | |||||||
| chr5:123392234 | G | A | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.811-897C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392234 | |||||||
| chr5:123392267 | C | T | 232 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0322 others(229): Show |
258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.811-930G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392267 | |||||||
| chr5:123392431 | C | T | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.810+869G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392431 | |||||||
| chr5:123392567 | C | G | 231 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0011 others(228): Show |
257 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.810+733G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392567 | |||||||
| chr5:123392654 | G | A | 2 | a0002c0002t0001g0166 a0002c0002t0001g0170 |
2 | NA19006.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.810+646C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392654 | |||||||
| chr5:123392715 | G | A | 1 | a0001c0001t0007g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.810+585C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392715 | |||||||
| chr5:123392718 | C | T | 1 | a0004c0004t0003g0050 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.810+582G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392718 | |||||||
| chr5:123392747 | T | G | 2 | a0002c0002t0001g0174 a0002c0002t0001g0175 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.810+553A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392747 | |||||||
| chr5:123392911 | G | A | 1 | a0007c0014t0005g0075 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.810+389C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123392911 | |||||||
| chr5:123393219 | C | T | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.810+81G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 6/19 | chr5 | 123393219 | |||||||
| chr5:123393531 | C | T | 5 | a0002c0002t0001g0156 a0002c0002t0001g0158 a0002c0002t0001g0159 others(2): Show |
5 | NA18944.hp2 NA18948.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.613-34G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393531 | |||||||
| chr5:123393536 | T | A | 70 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0011 others(67): Show |
76 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.613-39A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393536 | |||||||
| chr5:123393615 | C | T | 2 | a0003c0003t0001g0182 a0003c0003t0001g0187 |
2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.613-118G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393615 | |||||||
| chr5:123393675 | AAGAGTCG others(4): Show |
A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.613-189_613-179del others(11): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393675 | |||||||
| chr5:123393682 | G | A | 230 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0011 others(227): Show |
256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.613-185C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393682 | |||||||
| chr5:123393701 | T | C | 1 | a0002c0002t0001g0108 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.613-204A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393701 | |||||||
| chr5:123393735 | T | C | 1 | a0002c0002t0018g0329 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.613-238A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393735 | |||||||
| chr5:123393985 | G | T | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.613-488C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123393985 | |||||||
| chr5:123394014 | T | G | 13 | a0001c0005t0003g0081 a0001c0005t0003g0082 a0001c0005t0003g0083 others(10): Show |
13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.613-517A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394014 | |||||||
| chr5:123394245 | T | C | 1 | a0008c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.613-748A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394245 | |||||||
| chr5:123394304 | C | T | 232 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0322 others(229): Show |
258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.613-807G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394304 | |||||||
| chr5:123394348 | A | G | 10 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.613-851T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394348 | |||||||
| chr5:123394394 | C | T | 2 | a0004c0004t0003g0042 a0004c0004t0003g0043 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.613-897G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394394 | |||||||
| chr5:123394602 | C | T | 1 | a0002c0002t0001g0122 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.613-1105G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394602 | |||||||
| chr5:123394616 | A | G | 1 | a0002c0002t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.613-1119T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394616 | |||||||
| chr5:123394669 | A | G | 10 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.613-1172T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394669 | |||||||
| chr5:123394875 | T | C | 1 | a0003c0003t0001g0300 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.613-1378A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394875 | |||||||
| chr5:123394917 | C | A | 3 | a0003c0003t0001g0186 a0003c0003t0001g0188 a0003c0003t0001g0190 |
3 | HG02698.hp2 HG02738.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.613-1420G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394917 | |||||||
| chr5:123394935 | G | A | 40 | a0002c0002t0001g0005 a0002c0002t0001g0016 a0002c0002t0001g0017 others(37): Show |
45 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.613-1438C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394935 | |||||||
| chr5:123394957 | G | T | 148 | a0001c0006t0008g0010 a0001c0006t0009g0030 a0002c0002t0001g0005 others(145): Show |
166 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.613-1460C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394957 | |||||||
| chr5:123394959 | C | G | 17 | a0001c0005t0005g0004 a0001c0005t0005g0012 a0001c0005t0005g0035 others(14): Show |
20 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.613-1462G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123394959 | |||||||
| chr5:123395163 | G | A | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.613-1666C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395163 | |||||||
| chr5:123395190 | C | A | 6 | a0001c0006t0002g0006 a0001c0006t0002g0206 a0001c0006t0002g0207 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.613-1693G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395190 | |||||||
| chr5:123395228 | C | T | 231 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0322 others(228): Show |
257 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.613-1731G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395228 | |||||||
| chr5:123395290 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.613-1793C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395290 | |||||||
| chr5:123395292 | C | G | 1 | a0001c0001t0002g0268 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.613-1795G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395292 | |||||||
| chr5:123395311 | A | G | 11 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(8): Show |
13 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.613-1814T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395311 | |||||||
| chr5:123395470 | C | G | 11 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(8): Show |
13 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.613-1973G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395470 | |||||||
| chr5:123395508 | C | G | 1 | a0002c0002t0001g0157 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.613-2011G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395508 | |||||||
| chr5:123395534 | C | T | 1 | a0001c0006t0002g0325 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.613-2037G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395534 | |||||||
| chr5:123395585 | G | A | 1 | a0005c0007t0003g0085 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.613-2088C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395585 | |||||||
| chr5:123395681 | C | CT | 12 | a0001c0001t0002g0265 a0004c0004t0003g0013 a0004c0004t0003g0036 others(9): Show |
13 | HG01167.hp2 HG01192.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.613-2185dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395681 | |||||||
| chr5:123395681 | CT | C | 15 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(12): Show |
17 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.613-2185delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395681 | |||||||
| chr5:123395681 | CTT | C | 143 | a0001c0006t0003g0323 a0001c0006t0008g0010 a0001c0016t0002g0210 others(140): Show |
161 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.613-2186_613-2185d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395681 | |||||||
| chr5:123395702 | G | T | 1 | a0001c0001t0004g0239 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.613-2205C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395702 | |||||||
| chr5:123395708 | T | A | 11 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(8): Show |
13 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.613-2211A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395708 | |||||||
| chr5:123395708 | T | G | 150 | a0001c0006t0003g0323 a0001c0006t0008g0010 a0001c0006t0009g0030 others(147): Show |
168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.613-2211A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395708 | |||||||
| chr5:123395712 | T | C | 231 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0011 others(228): Show |
257 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.613-2215A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395712 | |||||||
| chr5:123395753 | C | T | 1 | a0003c0003t0001g0320 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.613-2256G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395753 | |||||||
| chr5:123395872 | T | A | 1 | a0001c0011t0002g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.613-2375A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395872 | |||||||
| chr5:123395874 | G | C | 148 | a0001c0006t0008g0010 a0001c0006t0009g0030 a0002c0002t0001g0005 others(145): Show |
166 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.613-2377C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395874 | |||||||
| chr5:123395924 | C | T | 3 | a0001c0001t0002g0259 a0004c0004t0003g0057 a0004c0004t0003g0058 |
3 | HG02809.hp1 HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.613-2427G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395924 | |||||||
| chr5:123395989 | C | CT | 35 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0238 others(32): Show |
36 | HG00609.hp2 HG01070.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.613-2493dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395989 | |||||||
| chr5:123395989 | CT | C | 111 | a0001c0001t0002g0264 a0001c0005t0005g0070 a0001c0006t0002g0006 others(108): Show |
125 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.613-2493delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123395989 | |||||||
| chr5:123396020 | G | A | 1 | a0003c0003t0001g0139 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.613-2523C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396020 | |||||||
| chr5:123396120 | A | C | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.613-2623T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396120 | |||||||
| chr5:123396196 | C | T | 34 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0324 others(31): Show |
36 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.613-2699G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396196 | |||||||
| chr5:123396202 | T | C | 1 | a0001c0006t0008g0010 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.613-2705A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396202 | |||||||
| chr5:123396217 | T | C | 1 | a0001c0001t0002g0228 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.613-2720A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396217 | |||||||
| chr5:123396227 | C | CT | 2 | a0001c0005t0005g0012 a0001c0005t0005g0072 |
3 | HG01496.hp1 HG01943.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.613-2731dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396227 | |||||||
| chr5:123396342 | T | G | 1 | a0001c0005t0003g0324 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.612+2794A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396342 | |||||||
| chr5:123396355 | C | T | 5 | a0001c0006t0002g0006 a0001c0006t0002g0206 a0001c0006t0002g0207 others(2): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+2781G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396355 | |||||||
| chr5:123396356 | T | G | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.612+2780A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396356 | |||||||
| chr5:123396409 | C | A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.612+2727G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396409 | |||||||
| chr5:123396416 | C | A | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.612+2720G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396416 | |||||||
| chr5:123396435 | T | C | 2 | a0004c0004t0003g0040 a0004c0004t0003g0041 |
2 | NA18968.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.612+2701A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396435 | |||||||
| chr5:123396472 | T | G | 2 | a0001c0006t0002g0204 a0001c0006t0002g0205 |
2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.612+2664A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396472 | |||||||
| chr5:123396542 | T | C | 232 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0322 others(229): Show |
258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.612+2594A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396542 | |||||||
| chr5:123396587 | T | C | 1 | a0003c0003t0001g0299 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.612+2549A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396587 | |||||||
| chr5:123396648 | G | A | 7 | a0004c0004t0003g0015 a0004c0004t0003g0042 a0004c0004t0003g0043 others(4): Show |
8 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+2488C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396648 | |||||||
| chr5:123396879 | A | C | 2 | a0002c0002t0001g0174 a0002c0002t0001g0175 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.612+2257T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123396879 | |||||||
| chr5:123397012 | T | C | 13 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(10): Show |
15 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.612+2124A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397012 | |||||||
| chr5:123397325 | A | C | 11 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(8): Show |
13 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.612+1811T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397325 | |||||||
| chr5:123397379 | A | G | 1 | a0003c0003t0001g0193 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.612+1757T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397379 | |||||||
| chr5:123397623 | G | A | 146 | a0002c0002t0001g0005 a0002c0002t0001g0016 a0002c0002t0001g0017 others(143): Show |
163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.612+1513C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397623 | |||||||
| chr5:123397701 | G | C | 148 | a0001c0006t0008g0010 a0001c0006t0009g0030 a0002c0002t0001g0005 others(145): Show |
166 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.612+1435C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397701 | |||||||
| chr5:123397789 | A | C | 1 | a0004c0004t0003g0051 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.612+1347T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397789 | |||||||
| chr5:123397839 | C | T | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.612+1297G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397839 | |||||||
| chr5:123397862 | T | C | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.612+1274A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123397862 | |||||||
| chr5:123398009 | T | C | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.612+1127A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398009 | |||||||
| chr5:123398187 | A | G | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.612+949T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398187 | |||||||
| chr5:123398311 | G | T | 148 | a0001c0006t0008g0010 a0001c0006t0009g0030 a0002c0002t0001g0005 others(145): Show |
166 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.612+825C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398311 | |||||||
| chr5:123398364 | G | T | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.612+772C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398364 | |||||||
| chr5:123398393 | T | C | 1 | a0001c0001t0004g0226 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.612+743A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398393 | |||||||
| chr5:123398514 | T | A | 1 | a0001c0001t0002g0264 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.612+622A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398514 | |||||||
| chr5:123398598 | C | G | 1 | a0001c0005t0005g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.612+538G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398598 | |||||||
| chr5:123398621 | T | G | 1 | a0004c0004t0003g0044 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.612+515A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398621 | |||||||
| chr5:123398824 | C | G | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.612+312G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398824 | |||||||
| chr5:123398967 | T | C | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.612+169A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123398967 | |||||||
| chr5:123399030 | T | TA | 160 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(157): Show |
180 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.612+105dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 5/19 | chr5 | 123399030 | |||||||
| chr5:123399758 | A | T | 36 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(33): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.464-474T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123399758 | |||||||
| chr5:123399812 | C | T | 2 | a0001c0001t0002g0236 a0001c0001t0002g0237 |
2 | HG02735.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.464-528G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123399812 | |||||||
| chr5:123399980 | T | C | 1 | a0001c0001t0002g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.464-696A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123399980 | |||||||
| chr5:123400048 | G | A | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.464-764C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400048 | |||||||
| chr5:123400056 | A | T | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-772T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400056 | |||||||
| chr5:123400172 | G | A | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.464-888C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400172 | |||||||
| chr5:123400263 | A | G | 1 | a0004c0004t0003g0046 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.464-979T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400263 | |||||||
| chr5:123400274 | T | C | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.464-990A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400274 | |||||||
| chr5:123400275 | C | A | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.464-991G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400275 | |||||||
| chr5:123400275 | C | T | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.464-991G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400275 | |||||||
| chr5:123400402 | G | A | 2 | a0001c0001t0002g0255 a0001c0001t0002g0282 |
2 | HG00140.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.464-1118C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400402 | |||||||
| chr5:123400450 | T | C | 1 | a0002c0002t0001g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.464-1166A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400450 | |||||||
| chr5:123400595 | A | G | 10 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.464-1311T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400595 | |||||||
| chr5:123400659 | C | CT | 189 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0026 others(186): Show |
210 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.464-1376dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400659 | |||||||
| chr5:123400659 | C | CTT | 6 | a0002c0002t0018g0329 a0003c0003t0001g0021 a0003c0003t0001g0135 others(3): Show |
7 | HG02027.hp2 HG02145.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.464-1377_464-1376d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400659 | |||||||
| chr5:123400704 | C | CA | 38 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0288 others(35): Show |
40 | HG00609.hp2 HG00621.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.464-1421dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400704 | |||||||
| chr5:123400704 | CA | C | 163 | a0001c0001t0002g0265 a0001c0001t0004g0025 a0001c0001t0004g0233 others(160): Show |
184 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.464-1421delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400704 | |||||||
| chr5:123400708 | A | G | 1 | a0008c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.464-1424T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400708 | |||||||
| chr5:123400885 | G | C | 149 | a0001c0006t0008g0010 a0001c0006t0009g0030 a0002c0002t0001g0005 others(146): Show |
167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.464-1601C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400885 | |||||||
| chr5:123400941 | G | A | 13 | a0001c0005t0003g0081 a0001c0005t0003g0082 a0001c0005t0003g0083 others(10): Show |
13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.464-1657C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400941 | |||||||
| chr5:123400966 | G | A | 12 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(9): Show |
14 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.464-1682C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400966 | |||||||
| chr5:123400973 | G | A | 149 | a0001c0006t0008g0010 a0001c0006t0009g0030 a0002c0002t0001g0005 others(146): Show |
167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.464-1689C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400973 | |||||||
| chr5:123400974 | A | ATCT | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-1693_464-1691d others(5): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400974 | |||||||
| chr5:123400998 | T | G | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-1714A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123400998 | |||||||
| chr5:123401088 | T | C | 1 | a0001c0006t0009g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.464-1804A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401088 | |||||||
| chr5:123401133 | G | A | 1 | a0003c0003t0001g0100 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.464-1849C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401133 | |||||||
| chr5:123401154 | C | T | 4 | a0002c0008t0002g0217 a0002c0008t0002g0218 a0002c0008t0002g0219 others(1): Show |
4 | NA18949.hp2 NA18950.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-1870G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401154 | |||||||
| chr5:123401206 | C | T | 9 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(6): Show |
11 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.464-1922G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401206 | |||||||
| chr5:123401208 | T | C | 1 | a0002c0002t0001g0144 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.464-1924A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401208 | |||||||
| chr5:123401229 | C | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-1945G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401229 | |||||||
| chr5:123401230 | G | A | 1 | a0003c0003t0001g0179 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.464-1946C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401230 | |||||||
| chr5:123401234 | C | T | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.464-1950G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401234 | |||||||
| chr5:123401259 | C | T | 1 | a0003c0003t0001g0292 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.464-1975G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401259 | |||||||
| chr5:123401278 | G | A | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-1994C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401278 | |||||||
| chr5:123401359 | C | T | 2 | a0002c0002t0001g0109 a0009c0019t0003g0107 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.464-2075G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401359 | |||||||
| chr5:123401455 | A | G | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-2171T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401455 | |||||||
| chr5:123401475 | G | A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-2191C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401475 | |||||||
| chr5:123401476 | C | A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-2192G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401476 | |||||||
| chr5:123401514 | C | T | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-2230G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401514 | |||||||
| chr5:123401563 | G | A | 36 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(33): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.464-2279C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401563 | |||||||
| chr5:123401705 | C | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-2421G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401705 | |||||||
| chr5:123401728 | A | C | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-2444T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401728 | |||||||
| chr5:123401745 | CA | C | 233 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0322 others(230): Show |
259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.464-2462delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401745 | |||||||
| chr5:123401804 | C | T | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-2520G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401804 | |||||||
| chr5:123401898 | C | T | 1 | a0001c0001t0002g0232 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.464-2614G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401898 | |||||||
| chr5:123401916 | T | C | 2 | a0003c0003t0001g0188 a0003c0003t0001g0190 |
2 | HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.464-2632A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123401916 | |||||||
| chr5:123402007 | C | T | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.464-2723G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402007 | |||||||
| chr5:123402016 | G | T | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.464-2732C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402016 | |||||||
| chr5:123402097 | C | T | 3 | a0003c0003t0001g0180 a0003c0003t0001g0181 a0006c0010t0015g0032 |
3 | HG01243.hp1 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.464-2813G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402097 | |||||||
| chr5:123402149 | C | T | 35 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0324 others(32): Show |
37 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.464-2865G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402149 | |||||||
| chr5:123402183 | C | T | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-2899G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402183 | |||||||
| chr5:123402330 | C | A | 233 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0322 others(230): Show |
259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.464-3046G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402330 | |||||||
| chr5:123402367 | C | A | 37 | a0002c0002t0001g0005 a0002c0002t0001g0016 a0002c0002t0001g0017 others(34): Show |
42 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.464-3083G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402367 | |||||||
| chr5:123402382 | A | G | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-3098T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402382 | |||||||
| chr5:123402502 | C | A | 1 | a0004c0004t0003g0052 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.464-3218G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402502 | |||||||
| chr5:123402507 | A | C | 23 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(20): Show |
27 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.464-3223T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402507 | |||||||
| chr5:123402522 | C | T | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.464-3238G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402522 | |||||||
| chr5:123402529 | C | T | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.464-3245G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402529 | |||||||
| chr5:123402585 | C | G | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-3301G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402585 | |||||||
| chr5:123402628 | G | A | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-3344C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402628 | |||||||
| chr5:123402886 | T | C | 11 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(8): Show |
13 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.464-3602A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402886 | |||||||
| chr5:123402988 | T | C | 233 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0322 others(230): Show |
259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.464-3704A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123402988 | |||||||
| chr5:123403446 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-4162C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403446 | |||||||
| chr5:123403516 | T | G | 13 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(10): Show |
15 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.464-4232A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403516 | |||||||
| chr5:123403522 | G | T | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-4238C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403522 | |||||||
| chr5:123403548 | T | C | 34 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0324 others(31): Show |
36 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.464-4264A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403548 | |||||||
| chr5:123403650 | C | G | 1 | a0003c0003t0001g0293 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.464-4366G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403650 | |||||||
| chr5:123403727 | G | C | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-4443C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403727 | |||||||
| chr5:123403809 | C | T | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.464-4525G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403809 | |||||||
| chr5:123403816 | G | A | 8 | a0002c0008t0002g0217 a0002c0008t0002g0218 a0002c0008t0002g0219 others(5): Show |
10 | NA18949.hp2 NA18950.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.464-4532C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123403816 | |||||||
| chr5:123404041 | A | G | 146 | a0002c0002t0001g0005 a0002c0002t0001g0016 a0002c0002t0001g0017 others(143): Show |
163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.464-4757T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404041 | |||||||
| chr5:123404042 | A | T | 1 | a0002c0002t0001g0126 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.464-4758T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404042 | |||||||
| chr5:123404060 | G | A | 1 | a0002c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.464-4776C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404060 | |||||||
| chr5:123404112 | G | C | 1 | a0001c0001t0002g0223 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.464-4828C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404112 | |||||||
| chr5:123404138 | A | C | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.464-4854T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404138 | |||||||
| chr5:123404138 | A | T | 2 | a0001c0006t0002g0204 a0001c0006t0002g0205 |
2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.464-4854T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404138 | |||||||
| chr5:123404165 | T | TCATAA | 160 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(157): Show |
180 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.464-4882_464-4881i others(7): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404165 | |||||||
| chr5:123404257 | C | G | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-4973G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404257 | |||||||
| chr5:123404299 | C | G | 23 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(20): Show |
27 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.464-5015G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404299 | |||||||
| chr5:123404300 | G | T | 161 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.464-5016C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404300 | |||||||
| chr5:123404327 | C | T | 1 | a0001c0005t0003g0090 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.464-5043G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404327 | |||||||
| chr5:123404507 | G | A | 5 | a0004c0004t0003g0050 a0005c0007t0003g0085 a0005c0007t0003g0086 others(2): Show |
5 | HG02056.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-5223C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404507 | |||||||
| chr5:123404837 | T | C | 1 | a0004c0004t0003g0061 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.464-5553A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404837 | |||||||
| chr5:123404876 | C | A | 1 | a0003c0003t0001g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.464-5592G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404876 | |||||||
| chr5:123404992 | T | C | 6 | a0002c0002t0001g0016 a0002c0002t0001g0017 a0002c0002t0001g0103 others(3): Show |
8 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.464-5708A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123404992 | |||||||
| chr5:123405012 | C | G | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.464-5728G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405012 | |||||||
| chr5:123405079 | A | C | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.464-5795T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405079 | |||||||
| chr5:123405094 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.464-5810A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405094 | |||||||
| chr5:123405227 | G | T | 71 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0011 others(68): Show |
77 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.464-5943C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405227 | |||||||
| chr5:123405239 | G | A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-5955C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405239 | |||||||
| chr5:123405251 | G | C | 1 | a0004c0004t0003g0045 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.464-5967C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405251 | |||||||
| chr5:123405431 | T | C | 1 | a0002c0002t0001g0106 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.464-6147A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405431 | |||||||
| chr5:123405492 | T | A | 28 | a0002c0002t0001g0019 a0002c0002t0001g0094 a0002c0002t0001g0143 others(25): Show |
29 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.464-6208A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405492 | |||||||
| chr5:123405650 | T | C | 157 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(154): Show |
177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.464-6366A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405650 | |||||||
| chr5:123405717 | T | C | 157 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(154): Show |
177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.464-6433A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405717 | |||||||
| chr5:123405889 | G | A | 3 | a0002c0002t0001g0111 a0002c0002t0001g0122 a0002c0002t0014g0124 |
3 | HG01081.hp1 HG01981.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.463+6510C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123405889 | |||||||
| chr5:123406052 | C | T | 142 | a0002c0002t0001g0005 a0002c0002t0001g0016 a0002c0002t0001g0017 others(139): Show |
159 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.463+6347G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406052 | |||||||
| chr5:123406059 | G | A | 2 | a0002c0002t0001g0122 a0003c0003t0001g0300 |
2 | HG01981.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.463+6340C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406059 | |||||||
| chr5:123406060 | A | T | 1 | a0002c0002t0001g0122 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.463+6339T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406060 | |||||||
| chr5:123406061 | A | T | 1 | a0002c0002t0001g0122 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.463+6338T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406061 | |||||||
| chr5:123406062 | T | C | 1 | a0002c0002t0001g0122 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.463+6337A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406062 | |||||||
| chr5:123406069 | G | A | 2 | a0004c0004t0003g0059 a0004c0004t0003g0060 |
2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.463+6330C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406069 | |||||||
| chr5:123406178 | GA | G | 229 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0322 others(226): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.463+6220delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406178 | |||||||
| chr5:123406227 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.463+6172T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406227 | |||||||
| chr5:123406393 | C | CA | 156 | a0001c0001t0004g0226 a0001c0006t0002g0006 a0001c0006t0002g0204 others(153): Show |
176 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.463+6005dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406393 | |||||||
| chr5:123406479 | C | T | 3 | a0002c0002t0001g0112 a0002c0009t0001g0125 a0002c0009t0010g0031 |
3 | HG00438.hp1 NA18984.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.463+5920G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406479 | |||||||
| chr5:123406482 | GA | G | 157 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(154): Show |
177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.463+5916delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406482 | |||||||
| chr5:123406586 | G | GA | 150 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0206 others(147): Show |
169 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.463+5812dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406586 | |||||||
| chr5:123406586 | G | GAA | 6 | a0001c0006t0002g0205 a0001c0006t0008g0010 a0001c0006t0009g0030 others(3): Show |
7 | HG01975.hp2 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.463+5811_463+5812d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406586 | |||||||
| chr5:123406586 | GA | G | 35 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0230 others(32): Show |
37 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.463+5812delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406586 | |||||||
| chr5:123406647 | G | A | 37 | a0002c0002t0001g0005 a0002c0002t0001g0016 a0002c0002t0001g0017 others(34): Show |
42 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.463+5752C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406647 | |||||||
| chr5:123406684 | AG | A | 9 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(6): Show |
11 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.463+5714delC | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406684 | |||||||
| chr5:123406818 | A | G | 1 | a0002c0002t0001g0131 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.463+5581T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406818 | |||||||
| chr5:123406852 | G | A | 157 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(154): Show |
177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.463+5547C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406852 | |||||||
| chr5:123406908 | T | G | 72 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0322 others(69): Show |
78 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.463+5491A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406908 | |||||||
| chr5:123406961 | G | A | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.463+5438C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123406961 | |||||||
| chr5:123407105 | T | TA | 142 | a0001c0001t0002g0227 a0001c0006t0003g0323 a0001c0006t0009g0030 others(139): Show |
159 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.463+5293dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407105 | |||||||
| chr5:123407105 | T | TAA | 14 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(11): Show |
16 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.463+5292_463+5293d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407105 | |||||||
| chr5:123407113 | A | C | 1 | a0001c0001t0002g0264 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.463+5286T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407113 | |||||||
| chr5:123407120 | C | A | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.463+5279G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407120 | |||||||
| chr5:123407276 | G | A | 2 | a0002c0002t0001g0174 a0002c0002t0001g0175 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.463+5123C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407276 | |||||||
| chr5:123407370 | C | T | 1 | a0001c0005t0003g0090 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.463+5029G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407370 | |||||||
| chr5:123407548 | C | T | 142 | a0002c0002t0001g0005 a0002c0002t0001g0016 a0002c0002t0001g0017 others(139): Show |
159 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.463+4851G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407548 | |||||||
| chr5:123407631 | A | T | 157 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(154): Show |
177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.463+4768T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407631 | |||||||
| chr5:123407683 | T | C | 11 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(8): Show |
13 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.463+4716A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123407683 | |||||||
| chr5:123408035 | G | C | 156 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(153): Show |
176 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.463+4364C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408035 | |||||||
| chr5:123408225 | G | A | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.463+4174C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408225 | |||||||
| chr5:123408311 | C | A | 156 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(153): Show |
176 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.463+4088G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408311 | |||||||
| chr5:123408433 | T | C | 1 | a0002c0002t0001g0017 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.463+3966A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408433 | |||||||
| chr5:123408454 | C | T | 1 | a0002c0002t0018g0329 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.463+3945G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408454 | |||||||
| chr5:123408484 | T | C | 64 | a0002c0002t0001g0138 a0002c0002t0001g0172 a0002c0002t0001g0295 others(61): Show |
75 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.463+3915A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408484 | |||||||
| chr5:123408525 | T | C | 6 | a0005c0007t0003g0085 a0005c0007t0003g0086 a0005c0007t0003g0087 others(3): Show |
6 | HG02145.hp1 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.463+3874A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408525 | |||||||
| chr5:123408542 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3857T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408542 | |||||||
| chr5:123408548 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3851T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408548 | |||||||
| chr5:123408551 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3848T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408551 | |||||||
| chr5:123408568 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3831T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408568 | |||||||
| chr5:123408579 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3820T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408579 | |||||||
| chr5:123408585 | T | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3814A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408585 | |||||||
| chr5:123408588 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3811T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408588 | |||||||
| chr5:123408589 | T | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3810A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408589 | |||||||
| chr5:123408590 | A | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3809T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408590 | |||||||
| chr5:123408608 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3791T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408608 | |||||||
| chr5:123408609 | G | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3790C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408609 | |||||||
| chr5:123408611 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3788T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408611 | |||||||
| chr5:123408621 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3778T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408621 | |||||||
| chr5:123408623 | A | T | 36 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0324 others(33): Show |
38 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.463+3776T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408623 | |||||||
| chr5:123408628 | A | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3771T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408628 | |||||||
| chr5:123408629 | T | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3770A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408629 | |||||||
| chr5:123408631 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3768T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408631 | |||||||
| chr5:123408632 | C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3767G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408632 | |||||||
| chr5:123408632 | C | T | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.463+3767G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408632 | |||||||
| chr5:123408636 | C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3763G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408636 | |||||||
| chr5:123408637 | C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3762G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408637 | |||||||
| chr5:123408638 | C | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3761G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408638 | |||||||
| chr5:123408639 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3760T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408639 | |||||||
| chr5:123408640 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3759T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408640 | |||||||
| chr5:123408641 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3758T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408641 | |||||||
| chr5:123408642 | C | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3757G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408642 | |||||||
| chr5:123408643 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3756T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408643 | |||||||
| chr5:123408647 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3752T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408647 | |||||||
| chr5:123408650 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3749T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408650 | |||||||
| chr5:123408651 | C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3748G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408651 | |||||||
| chr5:123408652 | C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3747G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408652 | |||||||
| chr5:123408677 | C | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3722G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408677 | |||||||
| chr5:123408685 | C | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3714G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408685 | |||||||
| chr5:123408686 | A | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3713T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408686 | |||||||
| chr5:123408691 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3708T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408691 | |||||||
| chr5:123408692 | G | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3707C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408692 | |||||||
| chr5:123408696 | G | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3703C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408696 | |||||||
| chr5:123408697 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3702T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408697 | |||||||
| chr5:123408699 | A | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3700T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408699 | |||||||
| chr5:123408702 | A | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3697T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408702 | |||||||
| chr5:123408711 | C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3688G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408711 | |||||||
| chr5:123408764 | C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3635G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408764 | |||||||
| chr5:123408768 | GAGGCCAG others(49): Show |
G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3575_463+3630d others(58): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408768 | |||||||
| chr5:123408826 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3573T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408826 | |||||||
| chr5:123408828 | C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3571G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408828 | |||||||
| chr5:123408832 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3567T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408832 | |||||||
| chr5:123408836 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3563T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408836 | |||||||
| chr5:123408841 | C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3558G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408841 | |||||||
| chr5:123408850 | C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3549G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408850 | |||||||
| chr5:123408858 | C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3541G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408858 | |||||||
| chr5:123408900 | C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3499G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408900 | |||||||
| chr5:123408910 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3489T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408910 | |||||||
| chr5:123408929 | G | A | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.463+3470C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408929 | |||||||
| chr5:123408958 | G | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3441C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408958 | |||||||
| chr5:123408961 | C | CGTGTGTA others(31): Show |
1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3437_463+3438i others(40): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408961 | |||||||
| chr5:123408962 | T | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3437A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408962 | |||||||
| chr5:123408965 | G | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3434C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408965 | |||||||
| chr5:123408968 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3431T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408968 | |||||||
| chr5:123408984 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3415T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408984 | |||||||
| chr5:123408988 | C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3411G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123408988 | |||||||
| chr5:123409112 | C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3287G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409112 | |||||||
| chr5:123409130 | A | C | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.463+3269T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409130 | |||||||
| chr5:123409141 | T | C | 1 | a0001c0005t0003g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.463+3258A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409141 | |||||||
| chr5:123409231 | C | A | 3 | a0003c0003t0001g0302 a0003c0003t0001g0303 a0003c0003t0001g0314 |
3 | HG00558.hp2 HG02071.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.463+3168G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409231 | |||||||
| chr5:123409297 | A | G | 1 | a0001c0001t0006g0263 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.463+3102T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409297 | |||||||
| chr5:123409311 | A | C | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3088T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409311 | |||||||
| chr5:123409313 | C | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3086G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409313 | |||||||
| chr5:123409317 | C | T | 40 | a0002c0002t0001g0005 a0002c0002t0001g0016 a0002c0002t0001g0017 others(37): Show |
45 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.463+3082G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409317 | |||||||
| chr5:123409324 | C | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3075G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409324 | |||||||
| chr5:123409328 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3071T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409328 | |||||||
| chr5:123409335 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3064T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409335 | |||||||
| chr5:123409336 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3063T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409336 | |||||||
| chr5:123409339 | C | A | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3060G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409339 | |||||||
| chr5:123409340 | C | G | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3059G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409340 | |||||||
| chr5:123409364 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.463+3035T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409364 | |||||||
| chr5:123409563 | A | C | 1 | a0002c0002t0001g0199 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.463+2836T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409563 | |||||||
| chr5:123409597 | T | C | 157 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(154): Show |
177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.463+2802A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409597 | |||||||
| chr5:123409693 | C | T | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.463+2706G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409693 | |||||||
| chr5:123409712 | C | A | 1 | a0001c0001t0006g0291 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.463+2687G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409712 | |||||||
| chr5:123409762 | G | A | 157 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(154): Show |
177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.463+2637C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409762 | |||||||
| chr5:123409779 | G | A | 1 | a0004c0004t0003g0046 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.463+2620C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409779 | |||||||
| chr5:123409938 | A | T | 1 | a0002c0002t0001g0130 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.463+2461T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409938 | |||||||
| chr5:123409953 | C | G | 6 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0004c0004t0003g0057 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.463+2446G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409953 | |||||||
| chr5:123409971 | C | CA | 12 | a0001c0001t0002g0229 a0001c0001t0002g0256 a0001c0001t0002g0280 others(9): Show |
12 | HG00140.hp2 HG01123.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.463+2427dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409971 | |||||||
| chr5:123409971 | CA | C | 30 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(27): Show |
34 | HG00140.hp1 HG00323.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.463+2427delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409971 | |||||||
| chr5:123409989 | A | ACCAC | 39 | a0002c0002t0001g0005 a0002c0002t0001g0016 a0002c0002t0001g0017 others(36): Show |
44 | HG00438.hp1 HG00639.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.463+2409_463+2410i others(6): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409989 | |||||||
| chr5:123409989 | A | ACCACAC | 54 | a0002c0002t0001g0127 a0002c0002t0001g0138 a0002c0002t0001g0146 others(51): Show |
63 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.463+2409_463+2410i others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409989 | |||||||
| chr5:123409989 | A | ACCACACA others(1): Show |
32 | a0002c0002t0001g0019 a0002c0002t0001g0094 a0002c0002t0001g0143 others(29): Show |
33 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.463+2409_463+2410i others(10): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409989 | |||||||
| chr5:123409989 | A | ACCACACA others(3): Show |
1 | a0003c0003t0001g0178 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.463+2409_463+2410i others(12): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409989 | |||||||
| chr5:123409991 | A | C | 147 | a0001c0005t0005g0079 a0001c0006t0008g0010 a0001c0006t0009g0030 others(144): Show |
165 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.463+2408T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409991 | |||||||
| chr5:123409992 | C | A | 131 | a0001c0001t0002g0283 a0001c0001t0002g0284 a0001c0006t0002g0207 others(128): Show |
146 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.463+2407G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409992 | |||||||
| chr5:123409992 | C | CA | 3 | a0001c0005t0005g0079 a0001c0006t0008g0010 a0005c0007t0003g0086 |
4 | HG00738.hp1 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+2406_463+2407i others(3): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409992 | |||||||
| chr5:123409992 | C | CACACA | 3 | a0002c0002t0001g0123 a0002c0002t0001g0126 a0002c0002t0001g0130 |
3 | HG00597.hp2 NA18972.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.463+2406_463+2407i others(7): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409992 | |||||||
| chr5:123409992 | C | CACACACA | 10 | a0001c0006t0009g0030 a0003c0003t0001g0021 a0003c0003t0001g0022 others(7): Show |
12 | HG01123.hp2 HG01891.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.463+2406_463+2407i others(9): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409992 | |||||||
| chr5:123409992 | C | CACACACA others(2): Show |
3 | a0002c0002t0001g0169 a0002c0002t0001g0201 a0003c0003t0001g0308 |
3 | HG02148.hp2 HG03453.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.463+2406_463+2407i others(11): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409992 | |||||||
| chr5:123409992 | C | CCA | 8 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(5): Show |
10 | HG01071.hp1 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.463+2405_463+2406d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123409992 | |||||||
| chr5:123410039 | A | G | 229 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0322 others(226): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.463+2360T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410039 | |||||||
| chr5:123410130 | C | T | 1 | a0005c0007t0003g0085 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.463+2269G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410130 | |||||||
| chr5:123410188 | T | C | 1 | a0003c0003t0001g0309 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.463+2211A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410188 | |||||||
| chr5:123410325 | T | C | 1 | a0001c0001t0002g0258 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.463+2074A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410325 | |||||||
| chr5:123410372 | G | T | 1 | a0001c0006t0002g0325 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.463+2027C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410372 | |||||||
| chr5:123410458 | A | G | 157 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(154): Show |
177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.463+1941T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410458 | |||||||
| chr5:123410470 | T | A | 23 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(20): Show |
27 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.463+1929A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410470 | |||||||
| chr5:123410470 | T | C | 1 | a0001c0001t0002g0257 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.463+1929A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410470 | |||||||
| chr5:123410834 | C | T | 229 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0322 others(226): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.463+1565G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410834 | |||||||
| chr5:123410969 | A | G | 9 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(6): Show |
11 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.463+1430T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123410969 | |||||||
| chr5:123411177 | C | A | 141 | a0002c0002t0001g0005 a0002c0002t0001g0016 a0002c0002t0001g0017 others(138): Show |
158 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.463+1222G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411177 | |||||||
| chr5:123411247 | C | A | 72 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0011 others(69): Show |
78 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.463+1152G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411247 | |||||||
| chr5:123411274 | T | C | 1 | a0001c0005t0005g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.463+1125A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411274 | |||||||
| chr5:123411280 | A | T | 1 | a0002c0002t0001g0148 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.463+1119T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411280 | |||||||
| chr5:123411283 | G | A | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.463+1116C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411283 | |||||||
| chr5:123411301 | C | A | 156 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(153): Show |
176 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.463+1098G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411301 | |||||||
| chr5:123411373 | T | C | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.463+1026A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411373 | |||||||
| chr5:123411389 | C | A | 2 | a0001c0006t0002g0204 a0001c0006t0002g0205 |
2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.463+1010G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411389 | |||||||
| chr5:123411634 | A | G | 1 | a0008c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.463+765T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411634 | |||||||
| chr5:123411683 | T | C | 2 | a0006c0010t0002g0202 a0006c0010t0015g0032 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.463+716A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411683 | |||||||
| chr5:123411698 | A | T | 1 | a0001c0005t0003g0089 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.463+701T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123411698 | |||||||
| chr5:123412046 | T | C | 4 | a0005c0007t0003g0085 a0005c0007t0003g0086 a0005c0007t0003g0087 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+353A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123412046 | |||||||
| chr5:123412072 | G | A | 3 | a0002c0002t0001g0211 a0002c0002t0001g0212 a0002c0002t0001g0213 |
3 | HG02055.hp2 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.463+327C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123412072 | |||||||
| chr5:123412151 | A | G | 6 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0004c0004t0003g0057 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.463+248T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123412151 | |||||||
| chr5:123412361 | A | T | 8 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(5): Show |
10 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.463+38T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 4/19 | chr5 | 123412361 | |||||||
| chr5:123412595 | T | C | 2 | a0001c0001t0002g0258 a0001c0001t0002g0285 |
2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.322-55A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123412595 | |||||||
| chr5:123412611 | A | G | 7 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0216 others(4): Show |
9 | NA18944.hp1 NA18946.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.322-71T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123412611 | |||||||
| chr5:123412655 | A | AT | 38 | a0002c0002t0001g0019 a0002c0002t0001g0094 a0002c0002t0001g0143 others(35): Show |
39 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.322-116dupA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123412655 | |||||||
| chr5:123412901 | T | C | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.322-361A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123412901 | |||||||
| chr5:123412913 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.322-373G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123412913 | |||||||
| chr5:123412978 | T | C | 3 | a0001c0001t0002g0027 a0001c0001t0002g0259 a0001c0001t0002g0260 |
4 | HG00639.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.322-438A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123412978 | |||||||
| chr5:123413032 | C | G | 36 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 others(33): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.322-492G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413032 | |||||||
| chr5:123413180 | G | C | 1 | a0001c0016t0002g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.322-640C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413180 | |||||||
| chr5:123413248 | A | C | 1 | a0001c0005t0003g0324 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.322-708T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413248 | |||||||
| chr5:123413265 | C | A | 1 | a0001c0001t0002g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.322-725G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413265 | |||||||
| chr5:123413270 | C | A | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.322-730G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413270 | |||||||
| chr5:123413358 | C | T | 15 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(12): Show |
17 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.322-818G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413358 | |||||||
| chr5:123413469 | C | T | 1 | a0002c0002t0001g0199 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.322-929G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413469 | |||||||
| chr5:123413605 | C | A | 228 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0011 others(225): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.322-1065G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413605 | |||||||
| chr5:123413914 | C | G | 144 | a0001c0006t0008g0010 a0001c0006t0009g0030 a0002c0002t0001g0005 others(141): Show |
162 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.322-1374G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413914 | |||||||
| chr5:123413947 | G | A | 1 | a0003c0003t0001g0190 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.322-1407C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123413947 | |||||||
| chr5:123414084 | C | G | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.322-1544G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414084 | |||||||
| chr5:123414149 | T | A | 1 | a0004c0004t0003g0051 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.322-1609A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414149 | |||||||
| chr5:123414233 | G | C | 2 | a0004c0004t0003g0057 a0004c0004t0003g0058 |
2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.322-1693C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414233 | |||||||
| chr5:123414409 | T | G | 1 | a0003c0003t0001g0310 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.321+1601A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414409 | |||||||
| chr5:123414480 | G | A | 1 | a0003c0003t0001g0179 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.321+1530C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414480 | |||||||
| chr5:123414527 | T | C | 99 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(96): Show |
120 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.321+1483A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414527 | |||||||
| chr5:123414538 | A | G | 1 | a0003c0003t0001g0133 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.321+1472T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414538 | |||||||
| chr5:123414674 | C | T | 35 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0324 others(32): Show |
37 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.321+1336G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414674 | |||||||
| chr5:123414688 | C | T | 1 | a0008c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.321+1322G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414688 | |||||||
| chr5:123414694 | C | T | 35 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0324 others(32): Show |
37 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.321+1316G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414694 | |||||||
| chr5:123414739 | G | A | 3 | a0003c0003t0001g0311 a0003c0003t0001g0312 a0003c0003t0001g0315 |
3 | NA18939.hp1 NA18951.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.321+1271C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414739 | |||||||
| chr5:123414832 | C | G | 18 | a0002c0002t0001g0138 a0002c0002t0001g0172 a0003c0003t0001g0020 others(15): Show |
19 | HG00423.hp1 HG00597.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.321+1178G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414832 | |||||||
| chr5:123414840 | C | T | 1 | a0002c0002t0001g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.321+1170G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414840 | |||||||
| chr5:123414896 | C | T | 2 | a0004c0004t0003g0057 a0004c0004t0003g0058 |
2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.321+1114G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414896 | |||||||
| chr5:123414971 | C | CA | 9 | a0001c0001t0002g0286 a0001c0005t0005g0072 a0001c0005t0005g0073 others(6): Show |
9 | HG00140.hp1 HG00738.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.321+1038dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | |||||||
| chr5:123414971 | C | CAAAAAAA others(3): Show |
1 | a0001c0006t0002g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.321+1029_321+1038d others(12): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | |||||||
| chr5:123414971 | C | CAAAAAAA others(4): Show |
3 | a0001c0006t0002g0006 a0001c0006t0002g0207 a0001c0011t0002g0203 |
5 | HG01069.hp1 HG01071.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+1028_321+1038d others(13): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | |||||||
| chr5:123414971 | C | CAAAAAAA others(5): Show |
2 | a0001c0006t0013g0208 a0006c0010t0002g0202 |
2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.321+1027_321+1038d others(14): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | |||||||
| chr5:123414971 | C | CAAAAAAA others(12): Show |
1 | a0008c0017t0002g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.321+1020_321+1038d others(21): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | |||||||
| chr5:123414971 | CA | C | 79 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0023 others(76): Show |
98 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.321+1038delT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | |||||||
| chr5:123414971 | CAA | C | 11 | a0001c0001t0002g0033 a0004c0004t0003g0036 a0004c0004t0003g0052 others(8): Show |
11 | HG00735.hp1 HG01891.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.321+1037_321+1038d others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | |||||||
| chr5:123414971 | CAAA | C | 25 | a0001c0001t0002g0034 a0001c0005t0003g0324 a0002c0002t0001g0094 others(22): Show |
27 | HG00609.hp2 HG00733.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.321+1036_321+1038d others(5): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | |||||||
| chr5:123414971 | CAAAAAA | C | 15 | a0001c0006t0002g0204 a0001c0006t0002g0205 a0001c0006t0008g0010 others(12): Show |
16 | HG01891.hp2 HG02055.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+1033_321+1038d others(8): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | |||||||
| chr5:123414971 | CAAAAAAA | C | 126 | a0001c0006t0002g0325 a0002c0002t0001g0005 a0002c0002t0001g0016 others(123): Show |
143 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.321+1032_321+1038d others(9): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123414971 | |||||||
| chr5:123415020 | G | A | 143 | a0001c0006t0008g0010 a0001c0006t0009g0030 a0002c0002t0001g0005 others(140): Show |
161 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.321+990C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415020 | |||||||
| chr5:123415153 | T | C | 101 | a0002c0002t0001g0019 a0002c0002t0001g0138 a0002c0002t0001g0143 others(98): Show |
113 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.321+857A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415153 | |||||||
| chr5:123415172 | A | G | 1 | a0001c0001t0004g0226 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.321+838T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415172 | |||||||
| chr5:123415173 | G | C | 156 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(153): Show |
176 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.321+837C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415173 | |||||||
| chr5:123415212 | A | T | 1 | a0002c0002t0001g0172 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.321+798T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415212 | |||||||
| chr5:123415278 | A | C | 157 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(154): Show |
177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.321+732T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415278 | |||||||
| chr5:123415352 | G | C | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.321+658C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415352 | |||||||
| chr5:123415431 | C | T | 2 | a0002c0002t0001g0174 a0002c0002t0001g0175 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.321+579G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415431 | |||||||
| chr5:123415458 | G | A | 1 | a0002c0002t0001g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.321+552C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415458 | |||||||
| chr5:123415466 | C | T | 3 | a0001c0005t0003g0011 a0001c0005t0003g0062 a0001c0005t0003g0080 |
4 | HG01255.hp2 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+544G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415466 | |||||||
| chr5:123415761 | C | T | 28 | a0004c0004t0003g0013 a0004c0004t0003g0015 a0004c0004t0003g0036 others(25): Show |
30 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.321+249G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415761 | |||||||
| chr5:123415809 | T | C | 1 | a0005c0007t0003g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.321+201A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415809 | |||||||
| chr5:123415829 | G | A | 1 | a0003c0003t0001g0141 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.321+181C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415829 | |||||||
| chr5:123415864 | T | A | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.321+146A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415864 | |||||||
| chr5:123415969 | T | A | 1 | a0004c0004t0003g0015 | 2 | HG00733.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.321+41A>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415969 | |||||||
| chr5:123415985 | T | C | 2 | a0001c0001t0002g0287 a0001c0001t0002g0288 |
2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.321+25A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 3/19 | chr5 | 123415985 | |||||||
| chr5:123416234 | G | A | 1 | a0003c0003t0001g0193 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.207-110C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416234 | |||||||
| chr5:123416400 | A | G | 1 | a0002c0002t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.207-276T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416400 | |||||||
| chr5:123416436 | T | C | 1 | a0004c0004t0003g0061 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.207-312A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416436 | |||||||
| chr5:123416526 | G | A | 1 | a0001c0001t0002g0289 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.207-402C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416526 | |||||||
| chr5:123416602 | AT | A | 7 | a0002c0002t0001g0016 a0002c0002t0001g0017 a0002c0002t0001g0103 others(4): Show |
9 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.207-479delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416602 | |||||||
| chr5:123416661 | C | T | 1 | a0002c0008t0002g0217 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.207-537G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416661 | |||||||
| chr5:123416916 | C | T | 1 | a0002c0009t0010g0031 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.207-792G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416916 | |||||||
| chr5:123416936 | G | T | 36 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0005t0003g0324 others(33): Show |
38 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.207-812C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123416936 | |||||||
| chr5:123417014 | T | C | 11 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(8): Show |
13 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.207-890A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417014 | |||||||
| chr5:123417173 | A | G | 1 | a0004c0004t0003g0036 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.207-1049T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417173 | |||||||
| chr5:123417250 | A | G | 4 | a0001c0001t0002g0316 a0001c0001t0002g0317 a0001c0001t0002g0318 others(1): Show |
4 | HG02280.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.206+1109T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417250 | |||||||
| chr5:123417296 | CT | C | 101 | a0002c0002t0001g0019 a0002c0002t0001g0138 a0002c0002t0001g0143 others(98): Show |
113 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.206+1062delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417296 | |||||||
| chr5:123417467 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.206+892T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417467 | |||||||
| chr5:123417727 | C | T | 1 | a0002c0002t0001g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.206+632G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417727 | |||||||
| chr5:123417886 | A | C | 159 | a0001c0001t0002g0225 a0001c0006t0001g0102 a0001c0006t0002g0006 others(156): Show |
179 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.206+473T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123417886 | |||||||
| chr5:123418175 | G | T | 4 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(1): Show |
4 | HG00558.hp1 NA18982.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.206+184C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123418175 | |||||||
| chr5:123418224 | T | TCTTA | 158 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(155): Show |
178 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.206+134_206+135ins others(4): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 2/19 | chr5 | 123418224 | |||||||
| chr5:123418588 | T | C | 2 | a0003c0003t0001g0022 a0003c0003t0001g0195 |
3 | NA18959.hp1 NA18974.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.50-73A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418588 | |||||||
| chr5:123418599 | GT | G | 7 | a0001c0005t0003g0080 a0002c0002t0001g0108 a0002c0002t0001g0109 others(4): Show |
7 | HG01243.hp2 HG01517.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-85delA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418599 | |||||||
| chr5:123418599 | GTT | G | 148 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(145): Show |
168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.50-86_50-85delAA | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418599 | |||||||
| chr5:123418625 | C | A | 13 | a0001c0005t0003g0081 a0001c0005t0003g0082 a0001c0005t0003g0083 others(10): Show |
13 | HG01255.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.50-110G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418625 | |||||||
| chr5:123418699 | C | T | 2 | a0002c0002t0001g0143 a0002c0002t0001g0144 |
2 | NA18960.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.50-184G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418699 | |||||||
| chr5:123418722 | A | G | 161 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(158): Show |
181 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.50-207T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418722 | |||||||
| chr5:123418732 | G | T | 7 | a0001c0006t0001g0102 a0002c0002t0001g0016 a0002c0002t0001g0017 others(4): Show |
9 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.50-217C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418732 | |||||||
| chr5:123418877 | C | A | 1 | a0001c0001t0002g0029 | 2 | HG01109.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.50-362G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418877 | |||||||
| chr5:123418919 | T | C | 42 | a0001c0006t0001g0102 a0001c0016t0002g0210 a0002c0002t0001g0005 others(39): Show |
47 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-404A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123418919 | |||||||
| chr5:123419066 | C | T | 1 | a0001c0001t0002g0216 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.50-551G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419066 | |||||||
| chr5:123419346 | A | C | 1 | a0001c0001t0002g0215 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.50-831T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419346 | |||||||
| chr5:123419347 | G | A | 1 | a0001c0005t0005g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.50-832C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419347 | |||||||
| chr5:123419375 | G | A | 12 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(9): Show |
14 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.50-860C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419375 | |||||||
| chr5:123419527 | A | G | 159 | a0001c0001t0002g0214 a0001c0006t0001g0102 a0001c0006t0002g0006 others(156): Show |
179 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.50-1012T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419527 | |||||||
| chr5:123419533 | A | C | 1 | a0001c0005t0005g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.50-1018T>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419533 | |||||||
| chr5:123419548 | A | G | 1 | a0002c0002t0001g0101 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.50-1033T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419548 | |||||||
| chr5:123419553 | C | CA | 7 | a0001c0001t0002g0290 a0001c0006t0003g0323 a0003c0003t0001g0292 others(4): Show |
8 | HG01167.hp2 HG01192.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-1039dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419553 | |||||||
| chr5:123419553 | C | CAA | 102 | a0001c0006t0001g0102 a0001c0016t0002g0210 a0002c0002t0001g0005 others(99): Show |
117 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.50-1040_50-1039dup others(2): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419553 | |||||||
| chr5:123419553 | C | CAAA | 5 | a0002c0002t0001g0132 a0003c0003t0001g0022 a0003c0003t0001g0194 others(2): Show |
6 | NA18939.hp1 NA18950.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-1041_50-1039dup others(3): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419553 | |||||||
| chr5:123419555 | A | AAC | 35 | a0002c0002t0001g0019 a0002c0002t0001g0094 a0002c0002t0001g0143 others(32): Show |
36 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.50-1041_50-1040ins others(2): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419555 | |||||||
| chr5:123419556 | A | AC | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.50-1042_50-1041ins others(1): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419556 | |||||||
| chr5:123419558 | A | AC | 10 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-1044_50-1043ins others(1): Show |
CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419558 | |||||||
| chr5:123419640 | G | A | 95 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0023 others(92): Show |
115 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.50-1125C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419640 | |||||||
| chr5:123419658 | T | G | 97 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(94): Show |
118 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.50-1143A>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419658 | |||||||
| chr5:123419708 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.50-1193A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419708 | |||||||
| chr5:123419782 | C | T | 158 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(155): Show |
178 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.50-1267G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419782 | |||||||
| chr5:123419868 | C | T | 157 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(154): Show |
177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.50-1353G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419868 | |||||||
| chr5:123419912 | G | A | 158 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(155): Show |
178 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.50-1397C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419912 | |||||||
| chr5:123419915 | T | C | 1 | a0001c0005t0003g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.50-1400A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419915 | |||||||
| chr5:123419945 | G | T | 1 | a0002c0002t0001g0130 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.50-1430C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123419945 | |||||||
| chr5:123420135 | T | C | 2 | a0003c0003t0001g0196 a0003c0003t0001g0197 |
2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.50-1620A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420135 | |||||||
| chr5:123420434 | T | C | 1 | a0002c0015t0001g0319 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.50-1919A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420434 | |||||||
| chr5:123420567 | G | A | 1 | a0001c0001t0002g0322 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50-2052C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420567 | |||||||
| chr5:123420771 | T | C | 1 | a0004c0004t0003g0096 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.49+2179A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420771 | |||||||
| chr5:123420943 | T | C | 1 | a0001c0006t0008g0010 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.49+2007A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420943 | |||||||
| chr5:123420952 | T | C | 11 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(8): Show |
13 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+1998A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420952 | |||||||
| chr5:123420966 | G | A | 4 | a0002c0002t0001g0005 a0002c0002t0001g0130 a0002c0002t0001g0131 others(1): Show |
6 | HG02027.hp1 NA18950.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+1984C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420966 | |||||||
| chr5:123420966 | G | C | 4 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(1): Show |
4 | HG00323.hp1 HG00642.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+1984C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123420966 | |||||||
| chr5:123421295 | C | T | 1 | a0001c0006t0008g0010 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.49+1655G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421295 | |||||||
| chr5:123421484 | C | A | 1 | a0001c0001t0006g0291 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.49+1466G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421484 | |||||||
| chr5:123421548 | T | C | 2 | a0005c0007t0003g0097 a0005c0007t0003g0098 |
2 | HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.49+1402A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421548 | |||||||
| chr5:123421573 | T | C | 1 | a0006c0010t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.49+1377A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421573 | |||||||
| chr5:123421591 | C | A | 10 | a0001c0006t0002g0006 a0001c0006t0002g0204 a0001c0006t0002g0205 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+1359G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421591 | |||||||
| chr5:123421743 | T | C | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.49+1207A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421743 | |||||||
| chr5:123421752 | A | G | 254 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0023 others(251): Show |
294 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.49+1198T>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421752 | |||||||
| chr5:123421752 | A | T | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.49+1198T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421752 | |||||||
| chr5:123421847 | C | A | 1 | a0002c0002t0018g0329 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.49+1103G>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421847 | |||||||
| chr5:123421907 | T | C | 3 | a0002c0002t0001g0211 a0002c0002t0001g0212 a0002c0002t0001g0213 |
3 | HG02055.hp2 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.49+1043A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421907 | |||||||
| chr5:123421962 | G | A | 1 | a0004c0004t0003g0015 | 2 | HG00733.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.49+988C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123421962 | |||||||
| chr5:123422024 | C | T | 157 | a0001c0006t0001g0102 a0001c0006t0002g0006 a0001c0006t0002g0204 others(154): Show |
177 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.49+926G>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422024 | |||||||
| chr5:123422179 | G | A | 26 | a0002c0002t0001g0295 a0003c0003t0001g0002 a0003c0003t0001g0003 others(23): Show |
34 | HG00280.hp1 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.49+771C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422179 | |||||||
| chr5:123422195 | G | C | 1 | a0004c0004t0003g0099 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.49+755C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422195 | |||||||
| chr5:123422217 | C | G | 1 | a0003c0003t0001g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.49+733G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422217 | |||||||
| chr5:123422326 | C | G | 1 | a0003c0003t0001g0100 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.49+624G>C | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422326 | |||||||
| chr5:123422438 | T | TA | 4 | a0001c0001t0002g0316 a0001c0001t0002g0317 a0001c0001t0002g0318 others(1): Show |
4 | HG02280.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+511dupT | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422438 | |||||||
| chr5:123422458 | A | T | 9 | a0002c0002t0001g0138 a0003c0003t0001g0133 a0003c0003t0001g0134 others(6): Show |
9 | HG00423.hp1 HG00597.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+492T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422458 | |||||||
| chr5:123422473 | A | T | 38 | a0001c0006t0001g0102 a0002c0002t0001g0005 a0002c0002t0001g0016 others(35): Show |
43 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.49+477T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422473 | |||||||
| chr5:123422551 | G | A | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.49+399C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422551 | |||||||
| chr5:123422574 | G | C | 254 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0023 others(251): Show |
294 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.49+376C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422574 | |||||||
| chr5:123422674 | G | C | 2 | a0001c0006t0008g0010 a0001c0006t0009g0030 |
3 | HG02559.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.49+276C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422674 | |||||||
| chr5:123422719 | G | A | 1 | a0003c0003t0001g0320 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49+231C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422719 | |||||||
| chr5:123422756 | T | C | 2 | a0001c0001t0002g0321 a0001c0001t0002g0322 |
2 | NA18967.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.49+194A>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422756 | |||||||
| chr5:123422793 | G | T | 1 | a0006c0010t0015g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.49+157C>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422793 | |||||||
| chr5:123422860 | G | C | 1 | a0001c0006t0003g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.49+90C>G | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422860 | |||||||
| chr5:123422869 | G | A | 2 | a0001c0005t0003g0324 a0001c0006t0002g0325 |
2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.49+81C>T | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422869 | |||||||
| chr5:123422920 | A | T | 1 | a0002c0002t0001g0117 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.49+30T>A | CEP120 | ENSG00000168944.17 | transcript | ENST00000306467.10 | protein_coding | 1/19 | chr5 | 123422920 |