Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 91754 |
| ensemblid | ENSG00000119638.14 |
| hgncid | 18591 |
| symbol | NEK9 |
| name | NIMA related kinase 9 |
| refseq_nuc | NM_033116.6 |
| refseq_prot | NP_149107.4 |
| ensembl_nuc | ENST00000238616.10 |
| ensembl_prot | ENSP00000238616.5 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 75079353 |
| end | 75127048 |
| strand | - |
| ver | v1.2 |
| region | chr14:75079353-75127048 |
| region5000 | chr14:75074353-75132048 |
| regionname0 | NEK9_chr14_75079353_75127048 |
| regionname5000 | NEK9_chr14_75074353_75132048 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 979 | 126 | 58 | 26 | 20 | 5 | 16 | 18 | NEK9_chr14_75074353_75132048 | NEK9 | MSVLG others(974): Show |
chr14 | 75074353 | 75132048 |
| a0002 | 0/1 | 979 | 127 | 22 | 24 | 57 | 7 | 16 | 44 | NEK9_chr14_75074353_75132048 | NEK9 | MSVLG others(974): Show |
chr14 | 75074353 | 75132048 |
| a0003 | 0/0 | 979 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | MSVLG others(974): Show |
chr14 | 75074353 | 75132048 |
| a0004 | 0/0 | 979 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | NEK9_chr14_75074353_75132048 | NEK9 | MSVLG others(974): Show |
chr14 | 75074353 | 75132048 |
| a0005 | 0/0 | 979 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | MSVLG others(974): Show |
chr14 | 75074353 | 75132048 |
| a0006 | 0/0 | 979 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | MSVLG others(974): Show |
chr14 | 75074353 | 75132048 |
| a0007 | 0/0 | 979 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | MSVLG others(974): Show |
chr14 | 75074353 | 75132048 |
| a0008 | 0/0 | 979 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | MSVLG others(974): Show |
chr14 | 75074353 | 75132048 |
| a0009 | 0/0 | 979 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | MSVLG others(974): Show |
chr14 | 75074353 | 75132048 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 2937 | 100 | 39 | 24 | 18 | 5 | 14 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0001c0003 | 0/0 | 2937 | 13 | 13 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0001c0004 | 1/0 | 2937 | 12 | 6 | 2 | 2 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0001c0011 | 0/0 | 2937 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0002c0001 | 0/1 | 2937 | 120 | 18 | 23 | 55 | 7 | 16 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0002c0009 | 0/0 | 2937 | 3 | 2 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0002c0013 | 0/0 | 2937 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0002c0014 | 0/0 | 2937 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0002c0016 | 0/0 | 2937 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0002c0018 | 0/0 | 2937 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0003c0005 | 0/0 | 2937 | 7 | 7 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0003c0010 | 0/0 | 2937 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0004c0006 | 0/0 | 2937 | 5 | 0 | 0 | 5 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0005c0007 | 0/0 | 2937 | 5 | 0 | 5 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0006c0008 | 0/0 | 2937 | 4 | 3 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0007c0012 | 0/0 | 2937 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0008c0017 | 0/0 | 2937 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 | ||
| a0009c0015 | 0/0 | 2937 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ATGTC others(2932): Show |
chr14 | 75074353 | 75132048 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002 | 0/0 | 8265 | 34 | 2 | 7 | 17 | 3 | 5 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0003 | 0/0 | 8265 | 30 | 13 | 11 | 0 | 1 | 5 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0004 | 0/0 | 8265 | 16 | 16 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0008 | 0/0 | 8265 | 5 | 1 | 2 | 0 | 0 | 2 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0017 | 0/0 | 8265 | 2 | 2 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0018 | 0/0 | 8265 | 2 | 2 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0019 | 0/0 | 8265 | 2 | 0 | 1 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0020 | 0/0 | 8265 | 2 | 0 | 2 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0022 | 0/0 | 8265 | 1 | 0 | 0 | 0 | 1 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0023 | 0/0 | 8265 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0034 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0035 | 0/0 | 8265 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0036 | 0/0 | 8265 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0037 | 0/0 | 8265 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0002t0040 | 0/0 | 8265 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0003t0007 | 0/0 | 8265 | 6 | 6 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0003t0010 | 0/0 | 8265 | 5 | 5 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0003t0025 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0001c0003t0042 | 0/0 | 8265 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0001c0004t0009 | 1/0 | 8278 | 6 | 3 | 2 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0001c0004t0014 | 0/0 | 8278 | 4 | 1 | 0 | 2 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0001c0004t0033 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0001c0004t0043 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0001c0011t0002 | 0/0 | 8265 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0002c0001t0001 | 0/0 | 8278 | 89 | 15 | 21 | 33 | 7 | 13 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0002c0001t0005 | 0/0 | 8278 | 12 | 0 | 0 | 12 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0002c0001t0006 | 0/0 | 8278 | 9 | 0 | 0 | 8 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0002c0001t0015 | 0/0 | 8278 | 2 | 0 | 2 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0002c0001t0021 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0002c0001t0024 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0002c0001t0026 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0002c0001t0027 | 0/0 | 8278 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0002c0001t0029 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0002c0001t0030 | 0/1 | 8274 | 1 | 0 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8269): Show |
chr14 | 75074353 | 75132048 |
| a0002c0001t0031 | 0/0 | 8290 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8285): Show |
chr14 | 75074353 | 75132048 |
| a0002c0001t0041 | 0/0 | 8278 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0002c0009t0012 | 0/0 | 8279 | 3 | 2 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8274): Show |
chr14 | 75074353 | 75132048 |
| a0002c0013t0012 | 0/0 | 8279 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8274): Show |
chr14 | 75074353 | 75132048 |
| a0002c0014t0038 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0002c0016t0001 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0002c0018t0006 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0003c0005t0011 | 0/0 | 8263 | 4 | 4 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8258): Show |
chr14 | 75074353 | 75132048 |
| a0003c0005t0016 | 0/0 | 8263 | 2 | 2 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8258): Show |
chr14 | 75074353 | 75132048 |
| a0003c0005t0032 | 0/0 | 8263 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8258): Show |
chr14 | 75074353 | 75132048 |
| a0003c0010t0011 | 0/0 | 8263 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8258): Show |
chr14 | 75074353 | 75132048 |
| a0004c0006t0002 | 0/0 | 8265 | 4 | 0 | 0 | 4 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0004c0006t0039 | 0/0 | 8265 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0005c0007t0001 | 0/0 | 8278 | 4 | 0 | 4 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0005c0007t0028 | 0/0 | 8278 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0006c0008t0013 | 0/0 | 8278 | 4 | 3 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0007c0012t0008 | 0/0 | 8265 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8260): Show |
chr14 | 75074353 | 75132048 |
| a0008c0017t0001 | 0/0 | 8278 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| a0009c0015t0001 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | ACCAT others(8273): Show |
chr14 | 75074353 | 75132048 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0004g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0008g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0008g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0008g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0008g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0017g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0017g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0018g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0018g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0019g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0019g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0020g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0022g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0023g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0034g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0035g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0036g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0037g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0002t0040g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0003t0007g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0003t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0003t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0003t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0003t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0003t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0003t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0003t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0003t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0003t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0003t0025g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0003t0042g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0004t0009g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0004t0009g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0004t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0004t0009g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0004t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0004t0014g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0004t0014g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0004t0014g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0004t0014g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0004t0033g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0004t0043g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0001c0011t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 3 | 2 | 2 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0002 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0005g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0005g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0015g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0015g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0021g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0024g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0026g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0027g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0029g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0030g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0031g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0001t0041g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0009t0012g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0009t0012g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0009t0012g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0013t0012g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0014t0038g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0016t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0002c0018t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0003c0005t0011g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0003c0005t0011g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0003c0005t0011g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0003c0005t0016g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0003c0005t0016g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0003c0005t0032g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0003c0010t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0004c0006t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0004c0006t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0004c0006t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0004c0006t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0004c0006t0039g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0005c0007t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0005c0007t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0005c0007t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0005c0007t0028g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0006c0008t0013g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0006c0008t0013g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0006c0008t0013g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0007c0012t0008g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0008c0017t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| a0009c0015t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0194 | EUR | GBR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0191 | EUR | GBR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00140 | hp1 | a0002 | c0001 | t0001 | g0002 | EUR | GBR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0157 | EUR | GBR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0019 | EUR | FIN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00280 | hp2 | a0002 | c0001 | t0001 | g0048 | EUR | FIN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0080 | EUR | FIN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00323 | hp2 | a0002 | c0001 | t0001 | g0001 | EUR | FIN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00423 | hp1 | a0002 | c0001 | t0001 | g0043 | EAS | CHS | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0222 | EAS | CHS | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0010 | EAS | CHS | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00544 | hp2 | a0002 | c0001 | t0001 | g0028 | EAS | CHS | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00558 | hp1 | a0002 | c0001 | t0006 | g0084 | EAS | CHS | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00558 | hp2 | a0002 | c0001 | t0005 | g0026 | EAS | CHS | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00621 | hp1 | a0002 | c0014 | t0038 | g0044 | EAS | CHS | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00621 | hp2 | a0004 | c0006 | t0002 | g0161 | EAS | CHS | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00639 | hp1 | a0007 | c0012 | t0008 | g0108 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0192 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00642 | hp1 | a0001 | c0002 | t0020 | g0013 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0168 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0137 | EAS | CHS | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0053 | EAS | CHS | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00735 | hp1 | a0001 | c0002 | t0020 | g0013 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00735 | hp2 | a0001 | c0002 | t0035 | g0167 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0058 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0023 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG00741 | hp2 | a0002 | c0001 | t0001 | g0204 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01070 | hp1 | a0002 | c0001 | t0015 | g0045 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0162 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01071 | hp1 | a0002 | c0001 | t0001 | g0050 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0165 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01081 | hp1 | a0001 | c0004 | t0009 | g0095 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01081 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0179 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01099 | hp2 | a0002 | c0001 | t0001 | g0227 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01109 | hp1 | a0002 | c0009 | t0012 | g0092 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0020 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01175 | hp1 | a0001 | c0002 | t0003 | g0023 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01175 | hp2 | a0001 | c0002 | t0003 | g0178 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0116 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01192 | hp2 | a0002 | c0001 | t0015 | g0046 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01243 | hp1 | a0006 | c0008 | t0013 | g0024 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | PUR | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01256 | hp1 | a0005 | c0007 | t0001 | g0059 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01256 | hp2 | a0001 | c0002 | t0019 | g0140 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0221 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0170 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0022 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01261 | hp2 | a0001 | c0002 | t0008 | g0109 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0214 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0184 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01358 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0169 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0041 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0042 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01496 | hp1 | a0001 | c0004 | t0009 | g0012 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01496 | hp2 | a0002 | c0001 | t0001 | g0047 | AMR | CLM | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0082 | EUR | IBS | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01515 | hp2 | a0002 | c0001 | t0001 | g0036 | EUR | IBS | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01884 | hp1 | a0006 | c0008 | t0013 | g0203 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01884 | hp2 | a0002 | c0001 | t0026 | g0218 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01891 | hp1 | a0002 | c0001 | t0001 | g0205 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01891 | hp2 | a0001 | c0002 | t0004 | g0003 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01928 | hp1 | a0002 | c0001 | t0001 | g0078 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01928 | hp2 | a0005 | c0007 | t0001 | g0007 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01943 | hp1 | a0005 | c0007 | t0028 | g0057 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0019 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01975 | hp2 | a0005 | c0007 | t0001 | g0081 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0063 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0223 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0230 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01981 | hp2 | a0001 | c0002 | t0008 | g0106 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0008 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG01993 | hp2 | a0008 | c0017 | t0001 | g0228 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02004 | hp1 | a0005 | c0007 | t0001 | g0007 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0005 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02015 | hp2 | a0001 | c0002 | t0034 | g0152 | EAS | KHV | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0175 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0180 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02056 | hp1 | a0002 | c0001 | t0006 | g0055 | EAS | KHV | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02056 | hp2 | a0002 | c0001 | t0005 | g0027 | EAS | KHV | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02145 | hp1 | a0001 | c0003 | t0007 | g0121 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0138 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0156 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02148 | hp2 | a0002 | c0001 | t0001 | g0051 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02165 | hp1 | a0002 | c0001 | t0006 | g0085 | EAS | CDX | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02165 | hp2 | a0002 | c0001 | t0005 | g0027 | EAS | CDX | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02257 | hp1 | a0001 | c0003 | t0007 | g0124 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0134 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0144 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02258 | hp2 | a0001 | c0002 | t0003 | g0022 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02280 | hp1 | a0002 | c0001 | t0001 | g0008 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02280 | hp2 | a0002 | c0001 | t0001 | g0200 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02293 | hp1 | a0002 | c0001 | t0001 | g0087 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02293 | hp2 | a0002 | c0001 | t0001 | g0079 | AMR | PEL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02451 | hp1 | a0001 | c0003 | t0007 | g0122 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02451 | hp2 | a0001 | c0002 | t0004 | g0145 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02572 | hp1 | a0002 | c0001 | t0001 | g0217 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02572 | hp2 | a0001 | c0002 | t0036 | g0118 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02615 | hp1 | a0001 | c0002 | t0018 | g0188 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02615 | hp2 | a0001 | c0002 | t0017 | g0164 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02622 | hp1 | a0003 | c0005 | t0011 | g0032 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02622 | hp2 | a0002 | c0016 | t0001 | g0215 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02630 | hp1 | a0006 | c0008 | t0013 | g0202 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02630 | hp2 | a0002 | c0001 | t0001 | g0209 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0003 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02647 | hp2 | a0001 | c0003 | t0010 | g0119 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02717 | hp1 | a0002 | c0001 | t0001 | g0210 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02717 | hp2 | a0002 | c0013 | t0012 | g0091 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02723 | hp1 | a0003 | c0005 | t0011 | g0035 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02723 | hp2 | a0001 | c0002 | t0004 | g0003 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02735 | hp2 | a0001 | c0002 | t0019 | g0141 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02818 | hp1 | a0001 | c0003 | t0010 | g0120 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02818 | hp2 | a0001 | c0002 | t0017 | g0166 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0102 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02886 | hp2 | a0006 | c0008 | t0013 | g0024 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02895 | hp1 | a0001 | c0002 | t0003 | g0182 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02895 | hp2 | a0002 | c0009 | t0012 | g0093 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02897 | hp1 | a0001 | c0002 | t0004 | g0189 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02897 | hp2 | a0001 | c0002 | t0003 | g0197 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02922 | hp1 | a0002 | c0001 | t0001 | g0025 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02922 | hp2 | a0001 | c0003 | t0010 | g0126 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0186 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02965 | hp2 | a0003 | c0005 | t0011 | g0006 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0131 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02970 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0142 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0181 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03017 | hp1 | a0001 | c0011 | t0002 | g0160 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03017 | hp2 | a0002 | c0001 | t0006 | g0064 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03041 | hp1 | a0001 | c0002 | t0023 | g0196 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03041 | hp2 | a0002 | c0009 | t0012 | g0094 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03098 | hp1 | a0001 | c0002 | t0040 | g0128 | AFR | MSL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03098 | hp2 | a0001 | c0004 | t0009 | g0096 | AFR | MSL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03130 | hp1 | a0001 | c0004 | t0009 | g0012 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03130 | hp2 | a0003 | c0005 | t0016 | g0034 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0016 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03139 | hp2 | a0003 | c0005 | t0016 | g0033 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03195 | hp1 | a0001 | c0004 | t0014 | g0103 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03195 | hp2 | a0001 | c0003 | t0025 | g0127 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0016 | AFR | MSL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03209 | hp2 | a0001 | c0003 | t0007 | g0015 | AFR | MSL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0147 | AFR | MSL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03453 | hp2 | a0002 | c0001 | t0001 | g0213 | AFR | MSL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0004 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0195 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03492 | hp1 | a0002 | c0001 | t0001 | g0004 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03492 | hp2 | a0001 | c0002 | t0003 | g0158 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0173 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03516 | hp2 | a0003 | c0005 | t0011 | g0006 | AFR | ESN | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03540 | hp1 | a0002 | c0001 | t0001 | g0025 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0129 | AFR | GWD | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0117 | AFR | MSL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0143 | AFR | MSL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03654 | hp1 | a0002 | c0001 | t0001 | g0004 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03654 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0018 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03669 | hp2 | a0002 | c0001 | t0001 | g0038 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0154 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03831 | hp1 | a0001 | c0002 | t0037 | g0185 | SAS | BEB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0076 | SAS | BEB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03834 | hp1 | a0001 | c0002 | t0008 | g0107 | SAS | BEB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0159 | SAS | BEB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0020 | SAS | BEB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03927 | hp2 | a0002 | c0001 | t0001 | g0072 | SAS | BEB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03942 | hp1 | a0001 | c0004 | t0014 | g0100 | SAS | BEB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03942 | hp2 | a0002 | c0001 | t0001 | g0065 | SAS | BEB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0060 | SAS | STU | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0153 | SAS | STU | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0133 | SAS | BEB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG04184 | hp2 | a0001 | c0002 | t0008 | g0113 | SAS | BEB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG04199 | hp1 | a0001 | c0002 | t0003 | g0183 | SAS | STU | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG04199 | hp2 | a0002 | c0001 | t0027 | g0049 | SAS | STU | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG04204 | hp1 | a0002 | c0001 | t0041 | g0069 | SAS | STU | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG04204 | hp2 | a0002 | c0001 | t0001 | g0201 | SAS | STU | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0077 | SAS | STU | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0139 | SAS | STU | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18522 | hp1 | a0001 | c0003 | t0007 | g0123 | AFR | YRI | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18522 | hp2 | a0003 | c0010 | t0011 | g0030 | AFR | YRI | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0114 | AFR | YRI | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18906 | hp2 | a0001 | c0004 | t0009 | g0098 | AFR | YRI | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18939 | hp1 | a0002 | c0001 | t0005 | g0026 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0088 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0207 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0074 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18952 | hp1 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18954 | hp1 | a0001 | c0004 | t0014 | g0104 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18957 | hp1 | a0002 | c0001 | t0006 | g0067 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18957 | hp2 | a0002 | c0001 | t0001 | g0068 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18960 | hp1 | a0002 | c0001 | t0005 | g0226 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18960 | hp2 | a0001 | c0004 | t0014 | g0105 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18961 | hp1 | a0002 | c0001 | t0005 | g0206 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18961 | hp2 | a0002 | c0001 | t0006 | g0090 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18965 | hp1 | a0004 | c0006 | t0002 | g0174 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18965 | hp2 | a0002 | c0001 | t0001 | g0039 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0061 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18969 | hp2 | a0002 | c0001 | t0005 | g0238 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18971 | hp1 | a0002 | c0001 | t0005 | g0232 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18971 | hp2 | a0002 | c0001 | t0001 | g0056 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18972 | hp1 | a0002 | c0001 | t0001 | g0052 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18972 | hp2 | a0002 | c0001 | t0001 | g0229 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18973 | hp1 | a0002 | c0001 | t0006 | g0199 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18973 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18979 | hp2 | a0002 | c0001 | t0001 | g0070 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18980 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18981 | hp1 | a0002 | c0001 | t0001 | g0083 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0062 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19003 | hp2 | a0002 | c0018 | t0006 | g0239 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19007 | hp1 | a0002 | c0001 | t0005 | g0073 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0208 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19009 | hp1 | a0002 | c0001 | t0001 | g0237 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19011 | hp1 | a0002 | c0001 | t0029 | g0066 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19011 | hp2 | a0002 | c0001 | t0024 | g0225 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19012 | hp1 | a0002 | c0001 | t0006 | g0037 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0130 | AFR | LWK | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19030 | hp2 | a0001 | c0002 | t0003 | g0136 | AFR | LWK | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19043 | hp1 | a0001 | c0002 | t0008 | g0110 | AFR | LWK | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19043 | hp2 | a0002 | c0001 | t0031 | g0236 | AFR | LWK | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19054 | hp2 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19062 | hp1 | a0002 | c0001 | t0001 | g0071 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19065 | hp1 | a0004 | c0006 | t0039 | g0101 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19065 | hp2 | a0002 | c0001 | t0005 | g0234 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19068 | hp2 | a0002 | c0001 | t0001 | g0054 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19074 | hp1 | a0002 | c0001 | t0005 | g0224 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19074 | hp2 | a0002 | c0001 | t0001 | g0086 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19075 | hp1 | a0004 | c0006 | t0002 | g0115 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19075 | hp2 | a0002 | c0001 | t0006 | g0089 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19077 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19078 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19080 | hp1 | a0004 | c0006 | t0002 | g0155 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19080 | hp2 | a0002 | c0001 | t0005 | g0233 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19084 | hp1 | a0002 | c0001 | t0001 | g0231 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0075 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19240 | hp1 | a0002 | c0001 | t0001 | g0219 | AFR | YRI | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA19240 | hp2 | a0003 | c0005 | t0032 | g0031 | AFR | YRI | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA20129 | hp1 | a0002 | c0001 | t0001 | g0002 | AFR | ASW | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA20129 | hp2 | a0001 | c0002 | t0003 | g0193 | AFR | ASW | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA20752 | hp1 | a0001 | c0002 | t0022 | g0151 | EUR | TSI | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0001 | EUR | TSI | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02109 | hp1 | a0001 | c0003 | t0042 | g0125 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02109 | hp2 | a0002 | c0001 | t0021 | g0029 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02486 | hp1 | a0001 | c0003 | t0010 | g0111 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02486 | hp2 | a0002 | c0001 | t0001 | g0212 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0146 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG02559 | hp2 | a0002 | c0001 | t0001 | g0216 | AFR | ACB | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03471 | hp1 | a0002 | c0001 | t0001 | g0211 | AFR | MSL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG03471 | hp2 | a0001 | c0002 | t0018 | g0187 | AFR | MSL | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG06807 | hp1 | a0001 | c0003 | t0007 | g0015 | AFR | USA | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| HG06807 | hp2 | a0001 | c0003 | t0010 | g0112 | AFR | USA | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18955 | hp1 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA20300 | hp1 | a0002 | c0001 | t0001 | g0220 | AFR | USA | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA20300 | hp2 | a0001 | c0004 | t0033 | g0099 | AFR | USA | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA21309 | hp1 | a0001 | c0004 | t0043 | g0240 | AFR | LWK | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| NA21309 | hp2 | a0009 | c0015 | t0001 | g0235 | AFR | LWK | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0030 | g0040 | REF | REF | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0009 | g0097 | REF | REF | NEK9_chr14_75074353_75132048 | NEK9 | chr14 | 75074353 | 75132048 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75084618 | T | G | 1 | a0006 | 4 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
missense_variant | MODERATE | c.2886A>C | p.Leu962Phe | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 3013/8278 | 2886/2940 | 962/979 | chr14 | 75084618 | |||
| chr14:75088559 | G | A | 1 | a0009 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2525C>T | p.Thr842Ile | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 20/22 | 2652/8278 | 2525/2940 | 842/979 | chr14 | 75088559 | |||
| chr14:75088602 | G | T | 1 | a0004 | 5 | HG00621.hp2 NA18965.hp1 NA19065.hp1 others(2): Show |
missense_variant | MODERATE | c.2482C>A | p.Pro828Thr | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 20/22 | 2609/8278 | 2482/2940 | 828/979 | chr14 | 75088602 | |||
| chr14:75091449 | C | T | 1 | a0005 | 5 | HG01256.hp1 HG01928.hp2 HG01943.hp1 others(2): Show |
missense_variant | MODERATE | c.2263G>A | p.Gly755Ser | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/22 | 2390/8278 | 2263/2940 | 755/979 | chr14 | 75091449 | |||
| chr14:75091460 | G | A | 1 | a0007 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.2252C>T | p.Pro751Leu | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/22 | 2379/8278 | 2252/2940 | 751/979 | chr14 | 75091460 | |||
| chr14:75091461 | G | A | 1 | a0008 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.2251C>T | p.Pro751Ser | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/22 | 2378/8278 | 2251/2940 | 751/979 | chr14 | 75091461 | |||
| chr14:75107384 | C | T | 5 | a0002 a0005 a0006 others(2): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
missense_variant | MODERATE | c.1286G>A | p.Arg429His | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 11/22 | 1413/8278 | 1286/2940 | 429/979 | chr14 | 75107384 | |||
| chr14:75126794 | C | G | 1 | a0003 | 8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
missense_variant | MODERATE | c.128G>C | p.Gly43Ala | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/22 | 255/8278 | 128/2940 | 43/979 | chr14 | 75126794 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75091342 | A | C | 1 | a0003c0010 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.2370T>G | p.Gly790Gly | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/22 | 2497/8278 | 2370/2940 | 790/979 | chr14 | 75091342 | |||
| chr14:75091441 | G | A | 1 | a0002c0016 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.2271C>T | p.Gly757Gly | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/22 | 2398/8278 | 2271/2940 | 757/979 | chr14 | 75091441 | |||
| chr14:75095423 | A | G | 1 | a0001c0011 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.2182T>C | p.Leu728Leu | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/22 | 2309/8278 | 2182/2940 | 728/979 | chr14 | 75095423 | |||
| chr14:75109817 | A | G | 1 | a0001c0003 | 13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
synonymous_variant | LOW | c.1050T>C | p.Tyr350Tyr | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/22 | 1177/8278 | 1050/2940 | 350/979 | chr14 | 75109817 | |||
| chr14:75124074 | C | T | 1 | a0002c0014 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.369G>A | p.Thr123Thr | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/22 | 496/8278 | 369/2940 | 123/979 | chr14 | 75124074 | |||
| chr14:75124080 | A | G | 1 | a0002c0013 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.363T>C | p.Asn121Asn | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/22 | 490/8278 | 363/2940 | 121/979 | chr14 | 75124080 | |||
| chr14:75124119 | G | A | 7 | a0002c0001 a0002c0014 a0002c0016 others(4): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
synonymous_variant | LOW | c.324C>T | p.His108His | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/22 | 451/8278 | 324/2940 | 108/979 | chr14 | 75124119 | |||
| chr14:75124143 | A | T | 7 | a0001c0002 a0001c0003 a0001c0011 others(4): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
synonymous_variant | LOW | c.300T>A | p.Ile100Ile | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/22 | 427/8278 | 300/2940 | 100/979 | chr14 | 75124143 | |||
| chr14:75126751 | G | A | 1 | a0002c0018 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.171C>T | p.Val57Val | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/22 | 298/8278 | 171/2940 | 57/979 | chr14 | 75126751 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75079387 | A | C | 4 | a0003c0005t0011 a0003c0005t0016 a0003c0005t0032 others(1): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5177T>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 5177 | chr14 | 75079387 | ||||||
| chr14:75079454 | A | T | 1 | a0001c0002t0035 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5110T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 5110 | chr14 | 75079454 | ||||||
| chr14:75079527 | C | T | 7 | a0001c0002t0002 a0001c0002t0019 a0001c0002t0034 others(4): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*5037G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 5037 | chr14 | 75079527 | ||||||
| chr14:75079547 | G | A | 51 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0004 others(48): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*5017C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 5017 | chr14 | 75079547 | ||||||
| chr14:75079699 | T | A | 1 | a0002c0001t0031 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4865A>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4865 | chr14 | 75079699 | ||||||
| chr14:75079701 | G | GCTATTTG others(5): Show |
1 | a0002c0001t0031 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4862_*4863insACCC others(8): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4862 | chr14 | 75079701 | ||||||
| chr14:75079703 | C | G | 1 | a0002c0001t0031 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4861G>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4861 | chr14 | 75079703 | ||||||
| chr14:75079704 | C | G | 1 | a0002c0001t0031 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4860G>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4860 | chr14 | 75079704 | ||||||
| chr14:75079705 | A | G | 1 | a0002c0001t0031 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4859T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4859 | chr14 | 75079705 | ||||||
| chr14:75079707 | C | T | 1 | a0002c0001t0031 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4857G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4857 | chr14 | 75079707 | ||||||
| chr14:75079708 | A | G | 1 | a0002c0001t0031 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4856T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4856 | chr14 | 75079708 | ||||||
| chr14:75079709 | A | T | 1 | a0002c0001t0031 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4855T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4855 | chr14 | 75079709 | ||||||
| chr14:75079710 | C | G | 1 | a0002c0001t0031 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4854G>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4854 | chr14 | 75079710 | ||||||
| chr14:75079711 | C | T | 1 | a0002c0001t0031 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4853G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4853 | chr14 | 75079711 | ||||||
| chr14:75079712 | C | T | 1 | a0002c0001t0031 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4852G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4852 | chr14 | 75079712 | ||||||
| chr14:75079714 | C | A | 1 | a0002c0001t0031 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4850G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4850 | chr14 | 75079714 | ||||||
| chr14:75079715 | A | T | 1 | a0002c0001t0031 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4849T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4849 | chr14 | 75079715 | ||||||
| chr14:75079853 | C | T | 19 | a0002c0001t0001 a0002c0001t0005 a0002c0001t0006 others(16): Show |
133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*4711G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4711 | chr14 | 75079853 | ||||||
| chr14:75079880 | C | T | 19 | a0002c0001t0001 a0002c0001t0005 a0002c0001t0006 others(16): Show |
133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*4684G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4684 | chr14 | 75079880 | ||||||
| chr14:75079975 | C | T | 1 | a0006c0008t0013 | 4 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4589G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4589 | chr14 | 75079975 | ||||||
| chr14:75080106 | C | T | 3 | a0001c0002t0008 a0001c0002t0020 a0007c0012t0008 |
8 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4458G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4458 | chr14 | 75080106 | ||||||
| chr14:75080113 | C | CA | 2 | a0002c0009t0012 a0002c0013t0012 |
4 | HG01109.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4450dupT | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4450 | chr14 | 75080113 | ||||||
| chr14:75080127 | C | G | 1 | a0006c0008t0013 | 4 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4437G>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4437 | chr14 | 75080127 | ||||||
| chr14:75080199 | G | A | 1 | a0003c0005t0032 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4365C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4365 | chr14 | 75080199 | ||||||
| chr14:75080222 | C | T | 2 | a0001c0002t0018 a0001c0002t0040 |
3 | HG02615.hp1 HG03098.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4342G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4342 | chr14 | 75080222 | ||||||
| chr14:75080249 | G | A | 19 | a0002c0001t0001 a0002c0001t0005 a0002c0001t0006 others(16): Show |
133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*4315C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4315 | chr14 | 75080249 | ||||||
| chr14:75080286 | C | T | 2 | a0001c0003t0007 a0001c0003t0042 |
7 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4278G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4278 | chr14 | 75080286 | ||||||
| chr14:75080329 | AAAAAAAA others(6): Show |
A | 25 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0004 others(22): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*4222_*4234delCTTT others(9): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4222 | chr14 | 75080329 | ||||||
| chr14:75080330 | AAAAAAAA others(5): Show |
A | 2 | a0001c0002t0034 a0001c0003t0025 |
2 | HG02015.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4222_*4233delCTTT others(8): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4222 | chr14 | 75080330 | ||||||
| chr14:75080342 | GAAAA | G | 20 | a0002c0001t0001 a0002c0001t0005 a0002c0001t0006 others(17): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*4218_*4221delTTTT | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4218 | chr14 | 75080342 | ||||||
| chr14:75080346 | A | G | 1 | a0002c0001t0029 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4218T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4218 | chr14 | 75080346 | ||||||
| chr14:75080388 | C | G | 2 | a0001c0004t0014 a0001c0004t0043 |
5 | HG03195.hp1 HG03942.hp1 NA18954.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4176G>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4176 | chr14 | 75080388 | ||||||
| chr14:75080455 | C | G | 51 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0004 others(48): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*4109G>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 4109 | chr14 | 75080455 | ||||||
| chr14:75080672 | C | T | 2 | a0002c0001t0006 a0002c0018t0006 |
10 | HG00558.hp1 HG02056.hp1 HG02165.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3892G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 3892 | chr14 | 75080672 | ||||||
| chr14:75080694 | G | A | 1 | a0001c0002t0019 | 2 | HG01256.hp2 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3870C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 3870 | chr14 | 75080694 | ||||||
| chr14:75080726 | C | T | 1 | a0001c0002t0036 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3838G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 3838 | chr14 | 75080726 | ||||||
| chr14:75080786 | G | A | 1 | a0001c0002t0020 | 2 | HG00642.hp1 HG00735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3778C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 3778 | chr14 | 75080786 | ||||||
| chr14:75080941 | A | T | 1 | a0005c0007t0028 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3623T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 3623 | chr14 | 75080941 | ||||||
| chr14:75081040 | T | C | 19 | a0002c0001t0001 a0002c0001t0005 a0002c0001t0006 others(16): Show |
133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*3524A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 3524 | chr14 | 75081040 | ||||||
| chr14:75081235 | C | T | 1 | a0002c0001t0027 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3329G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 3329 | chr14 | 75081235 | ||||||
| chr14:75081244 | C | T | 1 | a0001c0002t0017 | 2 | HG02615.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3320G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 3320 | chr14 | 75081244 | ||||||
| chr14:75081682 | T | G | 1 | a0001c0002t0004 | 16 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2882A>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 2882 | chr14 | 75081682 | ||||||
| chr14:75081878 | C | T | 1 | a0002c0001t0026 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2686G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 2686 | chr14 | 75081878 | ||||||
| chr14:75082053 | T | C | 21 | a0002c0001t0001 a0002c0001t0005 a0002c0001t0006 others(18): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*2511A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 2511 | chr14 | 75082053 | ||||||
| chr14:75082228 | G | A | 1 | a0001c0002t0036 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2336C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 2336 | chr14 | 75082228 | ||||||
| chr14:75082241 | T | G | 1 | a0002c0001t0005 | 12 | HG00558.hp2 HG02056.hp2 HG02165.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2323A>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 2323 | chr14 | 75082241 | ||||||
| chr14:75082244 | G | C | 1 | a0001c0002t0037 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2320C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 2320 | chr14 | 75082244 | ||||||
| chr14:75082589 | G | C | 3 | a0003c0005t0011 a0003c0005t0032 a0003c0010t0011 |
6 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1975C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 1975 | chr14 | 75082589 | ||||||
| chr14:75082667 | T | C | 21 | a0002c0001t0001 a0002c0001t0005 a0002c0001t0006 others(18): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1897A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 1897 | chr14 | 75082667 | ||||||
| chr14:75083028 | G | A | 1 | a0004c0006t0039 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1536C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 1536 | chr14 | 75083028 | ||||||
| chr14:75083033 | C | G | 1 | a0001c0004t0033 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1531G>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 1531 | chr14 | 75083033 | ||||||
| chr14:75083099 | C | T | 1 | a0001c0004t0033 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1465G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 1465 | chr14 | 75083099 | ||||||
| chr14:75083432 | T | C | 1 | a0001c0002t0040 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1132A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 1132 | chr14 | 75083432 | ||||||
| chr14:75083556 | A | G | 1 | a0002c0001t0015 | 2 | HG01070.hp1 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1008T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 1008 | chr14 | 75083556 | ||||||
| chr14:75083821 | CCA | C | 4 | a0003c0005t0011 a0003c0005t0016 a0003c0005t0032 others(1): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*741_*742delTG | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 741 | chr14 | 75083821 | ||||||
| chr14:75083881 | G | T | 20 | a0002c0001t0001 a0002c0001t0005 a0002c0001t0006 others(17): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*683C>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 683 | chr14 | 75083881 | ||||||
| chr14:75083888 | C | T | 4 | a0001c0003t0007 a0001c0003t0010 a0001c0003t0025 others(1): Show |
13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*676G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 676 | chr14 | 75083888 | ||||||
| chr14:75084126 | T | C | 1 | a0002c0001t0041 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*438A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 438 | chr14 | 75084126 | ||||||
| chr14:75084160 | G | A | 1 | a0001c0003t0042 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*404C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 404 | chr14 | 75084160 | ||||||
| chr14:75084240 | C | T | 1 | a0002c0001t0024 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*324G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 324 | chr14 | 75084240 | ||||||
| chr14:75084351 | C | G | 1 | a0001c0002t0023 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*213G>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 213 | chr14 | 75084351 | ||||||
| chr14:75084364 | A | G | 1 | a0001c0002t0022 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 200 | chr14 | 75084364 | ||||||
| chr14:75084551 | C | T | 51 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0004 others(48): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*13G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 22/22 | 13 | chr14 | 75084551 | ||||||
| chr14:75126975 | C | A | 1 | a0001c0004t0043 | 1 | NA21309.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-54G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/22 | chr14 | 75126975 | |||||||
| chr14:75126991 | C | T | 1 | a0002c0001t0021 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/22 | 70 | chr14 | 75126991 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75084739 | A | C | 234 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(231): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.2818-53T>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75084739 | |||||||
| chr14:75084826 | C | T | 1 | a0002c0001t0001g0043 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2818-140G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75084826 | |||||||
| chr14:75085204 | C | T | 1 | a0001c0002t0002g0163 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2818-518G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75085204 | |||||||
| chr14:75085406 | A | G | 1 | a0002c0001t0029g0066 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2818-720T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75085406 | |||||||
| chr14:75085416 | A | G | 1 | a0002c0001t0024g0225 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2818-730T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75085416 | |||||||
| chr14:75085782 | T | C | 1 | a0004c0006t0039g0101 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2818-1096A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75085782 | |||||||
| chr14:75085855 | A | G | 1 | a0001c0004t0033g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2817+1163T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75085855 | |||||||
| chr14:75086187 | AAAAAAT | A | 126 | a0001c0004t0014g0100 a0001c0004t0014g0103 a0001c0004t0014g0104 others(123): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.2817+825_2817+830d others(8): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75086187 | |||||||
| chr14:75086187 | AAAAAATA others(5): Show |
A | 1 | a0002c0001t0001g0209 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2817+819_2817+830d others(14): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75086187 | |||||||
| chr14:75086234 | A | T | 1 | a0001c0003t0010g0111 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2817+784T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75086234 | |||||||
| chr14:75086264 | T | C | 3 | a0001c0002t0003g0014 a0001c0002t0003g0117 a0001c0002t0003g0186 |
4 | HG01243.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2817+754A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75086264 | |||||||
| chr14:75086336 | T | A | 1 | a0001c0002t0002g0175 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2817+682A>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75086336 | |||||||
| chr14:75086543 | A | G | 2 | a0002c0001t0006g0055 a0002c0001t0006g0084 |
2 | HG00558.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2817+475T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75086543 | |||||||
| chr14:75086626 | G | A | 1 | a0001c0002t0037g0185 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2817+392C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75086626 | |||||||
| chr14:75086634 | G | A | 4 | a0002c0009t0012g0092 a0002c0009t0012g0093 a0002c0009t0012g0094 others(1): Show |
4 | HG01109.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2817+384C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75086634 | |||||||
| chr14:75086678 | C | T | 1 | a0001c0002t0036g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2817+340G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75086678 | |||||||
| chr14:75086723 | C | T | 2 | a0002c0001t0001g0058 a0002c0001t0001g0080 |
2 | HG00323.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.2817+295G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75086723 | |||||||
| chr14:75086952 | T | C | 233 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(230): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.2817+66A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 21/21 | chr14 | 75086952 | |||||||
| chr14:75087293 | A | G | 4 | a0002c0001t0001g0052 a0002c0001t0001g0086 a0002c0001t0001g0087 others(1): Show |
4 | HG02293.hp1 NA18972.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2605-63T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 20/21 | chr14 | 75087293 | |||||||
| chr14:75087497 | T | C | 1 | a0001c0002t0002g0139 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2605-267A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 20/21 | chr14 | 75087497 | |||||||
| chr14:75087638 | G | A | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2605-408C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 20/21 | chr14 | 75087638 | |||||||
| chr14:75087658 | G | C | 107 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(104): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.2605-428C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 20/21 | chr14 | 75087658 | |||||||
| chr14:75088036 | G | A | 1 | a0002c0001t0001g0010 | 2 | HG00544.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.2604+444C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 20/21 | chr14 | 75088036 | |||||||
| chr14:75088048 | A | G | 1 | a0002c0001t0029g0066 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2604+432T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 20/21 | chr14 | 75088048 | |||||||
| chr14:75088658 | G | T | 1 | a0001c0002t0002g0198 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2443-17C>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75088658 | |||||||
| chr14:75088787 | C | A | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2443-146G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75088787 | |||||||
| chr14:75088887 | C | T | 14 | a0001c0002t0003g0182 a0001c0002t0003g0197 a0001c0003t0007g0015 others(11): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2443-246G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75088887 | |||||||
| chr14:75088900 | C | T | 1 | a0002c0014t0038g0044 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2443-259G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75088900 | |||||||
| chr14:75088921 | G | A | 114 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(111): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2443-280C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75088921 | |||||||
| chr14:75088933 | A | T | 114 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(111): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2443-292T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75088933 | |||||||
| chr14:75088968 | C | T | 4 | a0002c0009t0012g0092 a0002c0009t0012g0093 a0002c0009t0012g0094 others(1): Show |
4 | HG01109.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2443-327G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75088968 | |||||||
| chr14:75089173 | C | A | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2443-532G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75089173 | |||||||
| chr14:75089352 | C | A | 4 | a0002c0009t0012g0092 a0002c0009t0012g0093 a0002c0009t0012g0094 others(1): Show |
4 | HG01109.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2443-711G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75089352 | |||||||
| chr14:75089370 | A | T | 2 | a0002c0001t0001g0209 a0009c0015t0001g0235 |
2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2443-729T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75089370 | |||||||
| chr14:75089522 | C | T | 1 | a0006c0008t0013g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2443-881G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75089522 | |||||||
| chr14:75089574 | C | T | 1 | a0001c0004t0009g0096 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2443-933G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75089574 | |||||||
| chr14:75089580 | G | A | 1 | a0002c0001t0001g0070 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2443-939C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75089580 | |||||||
| chr14:75089592 | G | C | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2443-951C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75089592 | |||||||
| chr14:75089598 | C | T | 2 | a0002c0001t0001g0009 a0002c0001t0001g0083 |
3 | NA18954.hp2 NA18981.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2443-957G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75089598 | |||||||
| chr14:75089668 | T | C | 81 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(78): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.2443-1027A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75089668 | |||||||
| chr14:75089702 | A | ATT | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2443-1063_2443-106 others(6): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75089702 | |||||||
| chr14:75089722 | C | T | 110 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(107): Show |
133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.2443-1081G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75089722 | |||||||
| chr14:75089723 | G | A | 114 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(111): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.2443-1082C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75089723 | |||||||
| chr14:75089921 | T | C | 1 | a0001c0002t0003g0184 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2443-1280A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75089921 | |||||||
| chr14:75090151 | A | T | 232 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(229): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2442+1119T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75090151 | |||||||
| chr14:75090277 | CT | C | 7 | a0001c0002t0003g0179 a0001c0004t0014g0100 a0001c0004t0014g0103 others(4): Show |
7 | HG01099.hp1 HG01099.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2442+992delA | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 19/21 | chr14 | 75090277 | |||||||
| chr14:75091528 | A | C | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2234-50T>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75091528 | |||||||
| chr14:75091951 | G | A | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2234-473C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75091951 | |||||||
| chr14:75092045 | T | C | 1 | a0002c0001t0001g0208 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2234-567A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75092045 | |||||||
| chr14:75092208 | G | C | 1 | a0001c0002t0002g0191 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2234-730C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75092208 | |||||||
| chr14:75092272 | A | AT | 110 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(107): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.2234-795dupA | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75092272 | |||||||
| chr14:75092272 | A | ATTT | 6 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(3): Show |
7 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2234-797_2234-795d others(5): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75092272 | |||||||
| chr14:75092329 | C | T | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2234-851G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75092329 | |||||||
| chr14:75092945 | T | C | 1 | a0001c0002t0036g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2234-1467A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75092945 | |||||||
| chr14:75093260 | T | C | 113 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(110): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.2234-1782A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75093260 | |||||||
| chr14:75093263 | T | C | 1 | a0002c0001t0001g0074 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2234-1785A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75093263 | |||||||
| chr14:75093493 | G | A | 1 | a0001c0002t0034g0152 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2233+1879C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75093493 | |||||||
| chr14:75093612 | C | A | 1 | a0001c0002t0036g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2233+1760G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75093612 | |||||||
| chr14:75094449 | C | T | 109 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(106): Show |
132 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.2233+923G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75094449 | |||||||
| chr14:75094542 | T | G | 6 | a0001c0003t0007g0015 a0001c0003t0007g0121 a0001c0003t0007g0122 others(3): Show |
7 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2233+830A>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75094542 | |||||||
| chr14:75094617 | T | C | 1 | a0002c0001t0031g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2233+755A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75094617 | |||||||
| chr14:75094652 | T | C | 13 | a0001c0002t0004g0003 a0001c0002t0004g0016 a0001c0002t0004g0114 others(10): Show |
16 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.2233+720A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75094652 | |||||||
| chr14:75094915 | T | G | 1 | a0001c0004t0033g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2233+457A>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75094915 | |||||||
| chr14:75094990 | G | C | 1 | a0002c0001t0001g0214 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2233+382C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75094990 | |||||||
| chr14:75095125 | T | C | 1 | a0001c0002t0003g0178 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2233+247A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75095125 | |||||||
| chr14:75095168 | A | C | 114 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(111): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.2233+204T>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75095168 | |||||||
| chr14:75095325 | G | C | 1 | a0002c0001t0006g0199 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2233+47C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 18/21 | chr14 | 75095325 | |||||||
| chr14:75095513 | T | C | 1 | a0002c0001t0005g0226 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2174-82A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75095513 | |||||||
| chr14:75095777 | C | T | 1 | a0001c0002t0023g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2174-346G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75095777 | |||||||
| chr14:75095959 | G | T | 1 | a0001c0002t0002g0133 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2174-528C>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75095959 | |||||||
| chr14:75096073 | G | A | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2174-642C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096073 | |||||||
| chr14:75096197 | C | T | 114 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(111): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2174-766G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096197 | |||||||
| chr14:75096232 | G | A | 1 | a0002c0001t0001g0201 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2174-801C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096232 | |||||||
| chr14:75096248 | G | C | 1 | a0002c0001t0006g0064 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2174-817C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096248 | |||||||
| chr14:75096270 | T | C | 1 | a0002c0016t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2173+830A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096270 | |||||||
| chr14:75096276 | CAA | C | 23 | a0001c0004t0033g0099 a0002c0001t0001g0039 a0002c0001t0001g0053 others(20): Show |
24 | HG00673.hp2 HG00738.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.2173+822_2173+823d others(4): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096276 | |||||||
| chr14:75096276 | CAAA | C | 108 | a0001c0002t0003g0014 a0001c0002t0003g0117 a0001c0002t0003g0162 others(105): Show |
132 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.2173+821_2173+823d others(5): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096276 | |||||||
| chr14:75096276 | CAAAA | C | 98 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(95): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.2173+820_2173+823d others(6): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096276 | |||||||
| chr14:75096300 | AAGCTTCT others(94): Show |
A | 1 | a0002c0016t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2173+699_2173+799d others(2): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096300 | |||||||
| chr14:75096404 | C | A | 1 | a0002c0016t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2173+696G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096404 | |||||||
| chr14:75096408 | G | A | 1 | a0002c0016t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2173+692C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096408 | |||||||
| chr14:75096409 | T | A | 1 | a0002c0016t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2173+691A>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096409 | |||||||
| chr14:75096422 | G | A | 1 | a0002c0016t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2173+678C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096422 | |||||||
| chr14:75096433 | T | A | 1 | a0002c0016t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2173+667A>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096433 | |||||||
| chr14:75096436 | T | A | 1 | a0002c0016t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2173+664A>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096436 | |||||||
| chr14:75096437 | T | A | 1 | a0002c0016t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2173+663A>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096437 | |||||||
| chr14:75096438 | T | A | 1 | a0002c0016t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2173+662A>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096438 | |||||||
| chr14:75096685 | T | A | 1 | a0002c0001t0001g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2173+415A>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096685 | |||||||
| chr14:75096766 | C | T | 81 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(78): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.2173+334G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096766 | |||||||
| chr14:75096829 | C | CA | 112 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(109): Show |
135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.2173+270dupT | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096829 | |||||||
| chr14:75096950 | C | T | 6 | a0002c0001t0005g0026 a0002c0001t0005g0073 a0002c0001t0005g0206 others(3): Show |
7 | HG00558.hp2 NA18939.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.2173+150G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 17/21 | chr14 | 75096950 | |||||||
| chr14:75097373 | T | C | 1 | a0001c0002t0002g0172 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2003-103A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75097373 | |||||||
| chr14:75097781 | T | G | 1 | a0001c0002t0002g0157 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2003-511A>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75097781 | |||||||
| chr14:75097814 | C | T | 5 | a0001c0003t0010g0112 a0001c0003t0010g0119 a0001c0003t0010g0120 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2003-544G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75097814 | |||||||
| chr14:75097956 | G | T | 110 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(107): Show |
133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.2003-686C>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75097956 | |||||||
| chr14:75098023 | G | A | 7 | a0001c0002t0008g0106 a0001c0002t0008g0107 a0001c0002t0008g0109 others(4): Show |
8 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2003-753C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75098023 | |||||||
| chr14:75098119 | A | G | 2 | a0001c0002t0002g0017 a0001c0002t0002g0163 |
3 | NA18979.hp1 NA19062.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2003-849T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75098119 | |||||||
| chr14:75098337 | G | A | 1 | a0001c0002t0003g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2003-1067C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75098337 | |||||||
| chr14:75098352 | T | C | 9 | a0002c0001t0001g0005 a0002c0001t0001g0028 a0002c0001t0001g0221 others(6): Show |
12 | HG00423.hp2 HG00544.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.2003-1082A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75098352 | |||||||
| chr14:75098523 | A | G | 233 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(230): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.2003-1253T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75098523 | |||||||
| chr14:75098834 | T | C | 1 | a0001c0004t0033g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2003-1564A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75098834 | |||||||
| chr14:75098857 | A | G | 3 | a0001c0002t0003g0014 a0001c0002t0003g0117 a0001c0002t0003g0186 |
4 | HG01243.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003-1587T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75098857 | |||||||
| chr14:75098972 | T | C | 1 | a0001c0002t0036g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2003-1702A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75098972 | |||||||
| chr14:75099177 | TGGCTG | T | 2 | a0001c0004t0009g0012 a0001c0004t0009g0098 |
3 | HG01496.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2002+1810_2002+181 others(9): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75099177 | |||||||
| chr14:75099506 | G | A | 110 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(107): Show |
133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.2002+1486C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75099506 | |||||||
| chr14:75099707 | G | A | 84 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(81): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.2002+1285C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75099707 | |||||||
| chr14:75099741 | C | T | 1 | a0002c0014t0038g0044 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2002+1251G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75099741 | |||||||
| chr14:75099760 | C | T | 11 | a0001c0002t0003g0014 a0001c0002t0003g0117 a0001c0002t0003g0186 others(8): Show |
13 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.2002+1232G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75099760 | |||||||
| chr14:75099782 | C | CA | 200 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(197): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2002+1209dupT | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75099782 | |||||||
| chr14:75099872 | T | C | 1 | a0002c0001t0006g0085 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2002+1120A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75099872 | |||||||
| chr14:75100053 | C | T | 1 | a0002c0001t0001g0221 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2002+939G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100053 | |||||||
| chr14:75100066 | T | C | 5 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(2): Show |
6 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2002+926A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100066 | |||||||
| chr14:75100085 | C | T | 3 | a0002c0001t0001g0237 a0002c0009t0012g0092 a0002c0009t0012g0093 |
3 | HG01109.hp1 HG02895.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2002+907G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100085 | |||||||
| chr14:75100128 | C | CA | 30 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0135 others(27): Show |
33 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.2002+863dupT | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | C | CAA | 27 | a0001c0002t0002g0019 a0001c0002t0002g0116 a0001c0002t0002g0132 others(24): Show |
31 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2002+862_2002+863d others(4): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | C | CAAA | 15 | a0001c0002t0002g0139 a0001c0002t0002g0153 a0001c0002t0002g0175 others(12): Show |
16 | HG00735.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2002+861_2002+863d others(5): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | C | CAAAA | 5 | a0001c0002t0003g0184 a0001c0002t0004g0003 a0001c0002t0004g0130 others(2): Show |
7 | HG01346.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002+860_2002+863d others(6): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | C | CAAAAAAA others(5): Show |
1 | a0001c0002t0002g0168 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2002+852_2002+863d others(14): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | C | CAAAAAAA others(6): Show |
2 | a0001c0002t0002g0134 a0001c0002t0002g0169 |
2 | HG01358.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2002+851_2002+863d others(15): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | C | CAAAAAAA others(10): Show |
1 | a0001c0002t0002g0170 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2002+847_2002+863d others(19): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CA | C | 6 | a0001c0002t0040g0128 a0001c0003t0007g0121 a0001c0003t0007g0122 others(3): Show |
6 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2002+863delT | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAA | C | 7 | a0001c0002t0003g0117 a0001c0003t0007g0015 a0001c0003t0007g0123 others(4): Show |
9 | HG01496.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2002+862_2002+863d others(4): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAAA | C | 5 | a0001c0002t0003g0014 a0001c0002t0003g0186 a0001c0003t0010g0120 others(2): Show |
6 | HG01243.hp2 HG02486.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2002+861_2002+863d others(5): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAAAA | C | 10 | a0002c0001t0001g0028 a0002c0001t0001g0204 a0002c0001t0001g0205 others(7): Show |
11 | HG00544.hp2 HG00741.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2002+860_2002+863d others(6): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAAAAA | C | 52 | a0002c0001t0001g0004 a0002c0001t0001g0005 a0002c0001t0001g0011 others(49): Show |
61 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.2002+859_2002+863d others(7): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAAAAAA | C | 45 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0008 others(42): Show |
58 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.2002+858_2002+863d others(8): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAAAAAAA others(3): Show |
C | 2 | a0001c0002t0036g0118 a0002c0001t0006g0055 |
2 | HG02056.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2002+854_2002+863d others(12): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAAAAAAA others(4): Show |
C | 1 | a0002c0001t0006g0084 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2002+853_2002+863d others(13): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0004g0131 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2002+850_2002+863d others(16): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAAAAAAA others(8): Show |
C | 2 | a0001c0002t0004g0147 a0001c0004t0033g0099 |
2 | HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2002+849_2002+863d others(17): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAAAAAAA others(9): Show |
C | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2002+848_2002+863d others(18): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAAAAAAA others(10): Show |
C | 1 | a0001c0002t0003g0158 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2002+847_2002+863d others(19): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAAAAAAA others(11): Show |
C | 1 | a0001c0002t0003g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2002+846_2002+863d others(20): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAAAAAAA others(13): Show |
C | 1 | a0001c0002t0004g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2002+844_2002+863d others(22): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100128 | CAAAAAAA others(14): Show |
C | 1 | a0002c0001t0026g0218 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2002+843_2002+863d others(23): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100128 | |||||||
| chr14:75100161 | A | C | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2002+831T>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100161 | |||||||
| chr14:75100212 | C | T | 84 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(81): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.2002+780G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100212 | |||||||
| chr14:75100360 | C | T | 4 | a0001c0002t0002g0157 a0001c0004t0014g0103 a0001c0004t0014g0104 others(1): Show |
4 | HG00140.hp2 HG03195.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2002+632G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100360 | |||||||
| chr14:75100475 | C | T | 114 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(111): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2002+517G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100475 | |||||||
| chr14:75100596 | AG | A | 3 | a0002c0001t0001g0200 a0002c0001t0001g0209 a0009c0015t0001g0235 |
3 | HG02280.hp2 HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2002+395delC | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100596 | |||||||
| chr14:75100826 | G | C | 5 | a0001c0004t0014g0100 a0001c0004t0014g0103 a0001c0004t0014g0104 others(2): Show |
5 | HG03195.hp1 HG03942.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.2002+166C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | 75100826 | |||||||
| chr14:75101435 | A | G | 114 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(111): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1840+222T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 15/21 | chr14 | 75101435 | |||||||
| chr14:75101796 | A | G | 5 | a0001c0004t0014g0100 a0001c0004t0014g0103 a0001c0004t0014g0104 others(2): Show |
5 | HG03195.hp1 HG03942.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1732-31T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75101796 | |||||||
| chr14:75101883 | A | C | 1 | a0001c0004t0014g0104 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1732-118T>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75101883 | |||||||
| chr14:75102255 | CTCATT | C | 5 | a0001c0004t0014g0100 a0001c0004t0014g0103 a0001c0004t0014g0104 others(2): Show |
5 | HG03195.hp1 HG03942.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1732-495_1732-491d others(7): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75102255 | |||||||
| chr14:75102308 | A | G | 5 | a0001c0004t0014g0100 a0001c0004t0014g0103 a0001c0004t0014g0104 others(2): Show |
5 | HG03195.hp1 HG03942.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1732-543T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75102308 | |||||||
| chr14:75102387 | G | A | 114 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(111): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1732-622C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75102387 | |||||||
| chr14:75102409 | G | A | 2 | a0001c0002t0004g0131 a0001c0002t0004g0144 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1732-644C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75102409 | |||||||
| chr14:75102457 | C | T | 1 | a0001c0002t0002g0156 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1732-692G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75102457 | |||||||
| chr14:75102496 | C | T | 1 | a0005c0007t0001g0059 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1732-731G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75102496 | |||||||
| chr14:75102513 | G | GT | 120 | a0001c0002t0040g0128 a0001c0003t0007g0121 a0001c0003t0007g0122 others(117): Show |
143 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1732-749dupA | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75102513 | |||||||
| chr14:75102643 | T | C | 222 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(219): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1732-878A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75102643 | |||||||
| chr14:75102677 | A | G | 2 | a0001c0002t0002g0137 a0001c0002t0002g0150 |
2 | HG00673.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1732-912T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75102677 | |||||||
| chr14:75102748 | A | G | 4 | a0002c0001t0001g0210 a0002c0001t0001g0211 a0002c0001t0001g0212 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1732-983T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75102748 | |||||||
| chr14:75102856 | C | T | 12 | a0001c0003t0007g0015 a0001c0003t0007g0121 a0001c0003t0007g0122 others(9): Show |
13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1731+986G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75102856 | |||||||
| chr14:75102880 | C | A | 114 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(111): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1731+962G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75102880 | |||||||
| chr14:75102959 | C | T | 2 | a0002c0001t0006g0055 a0002c0001t0006g0084 |
2 | HG00558.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.1731+883G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75102959 | |||||||
| chr14:75103063 | G | A | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1731+779C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75103063 | |||||||
| chr14:75103151 | C | A | 1 | a0001c0002t0004g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1731+691G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75103151 | |||||||
| chr14:75103193 | TA | T | 7 | a0001c0002t0018g0187 a0001c0002t0019g0140 a0002c0001t0001g0080 others(4): Show |
7 | HG00323.hp1 HG01256.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1731+648delT | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75103193 | |||||||
| chr14:75103590 | C | T | 107 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(104): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1731+252G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75103590 | |||||||
| chr14:75103825 | C | A | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1731+17G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75103825 | |||||||
| chr14:75103825 | C | T | 4 | a0002c0009t0012g0092 a0002c0009t0012g0093 a0002c0009t0012g0094 others(1): Show |
4 | HG01109.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1731+17G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 14/21 | chr14 | 75103825 | |||||||
| chr14:75104041 | C | T | 1 | a0001c0004t0043g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1576-44G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104041 | |||||||
| chr14:75104126 | A | G | 2 | a0001c0004t0009g0012 a0001c0004t0009g0098 |
3 | HG01496.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1576-129T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104126 | |||||||
| chr14:75104167 | C | CT | 3 | a0001c0002t0002g0153 a0001c0002t0003g0154 a0001c0002t0004g0003 |
5 | HG01891.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1576-171dupA | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104167 | |||||||
| chr14:75104167 | CT | C | 114 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(111): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1576-171delA | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104167 | |||||||
| chr14:75104220 | A | G | 9 | a0002c0001t0001g0068 a0002c0001t0006g0037 a0002c0001t0006g0055 others(6): Show |
9 | HG00558.hp1 HG02056.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-223T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104220 | |||||||
| chr14:75104250 | T | C | 1 | a0001c0002t0036g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1576-253A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104250 | |||||||
| chr14:75104304 | G | A | 2 | a0001c0002t0002g0176 a0001c0002t0002g0177 |
2 | NA19009.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1576-307C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104304 | |||||||
| chr14:75104323 | G | A | 114 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(111): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1576-326C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104323 | |||||||
| chr14:75104420 | C | A | 1 | a0001c0004t0014g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1576-423G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104420 | |||||||
| chr14:75104488 | C | CT | 108 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(105): Show |
131 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1576-492dupA | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104488 | |||||||
| chr14:75104507 | A | G | 1 | a0002c0001t0029g0066 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1576-510T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104507 | |||||||
| chr14:75104586 | G | C | 1 | a0002c0001t0001g0075 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1576-589C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104586 | |||||||
| chr14:75104644 | A | G | 1 | a0002c0001t0001g0036 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1576-647T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104644 | |||||||
| chr14:75104867 | C | T | 1 | a0002c0001t0001g0065 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1576-870G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104867 | |||||||
| chr14:75104923 | A | G | 1 | a0002c0001t0001g0222 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1576-926T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75104923 | |||||||
| chr14:75105215 | G | A | 1 | a0001c0002t0040g0128 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1575+735C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75105215 | |||||||
| chr14:75105453 | C | T | 1 | a0002c0001t0001g0048 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1575+497G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75105453 | |||||||
| chr14:75105472 | G | A | 2 | a0002c0001t0001g0205 a0002c0001t0031g0236 |
2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1575+478C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75105472 | |||||||
| chr14:75105562 | G | A | 65 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(62): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1575+388C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75105562 | |||||||
| chr14:75105615 | G | A | 1 | a0002c0001t0001g0207 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1575+335C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75105615 | |||||||
| chr14:75105716 | G | T | 107 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(104): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.1575+234C>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75105716 | |||||||
| chr14:75105752 | C | G | 1 | a0001c0003t0010g0126 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1575+198G>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75105752 | |||||||
| chr14:75105856 | T | C | 233 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(230): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1575+94A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75105856 | |||||||
| chr14:75105892 | T | C | 5 | a0001c0002t0002g0021 a0001c0002t0002g0135 a0001c0002t0002g0171 others(2): Show |
6 | NA18955.hp2 NA18981.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.1575+58A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 13/21 | chr14 | 75105892 | |||||||
| chr14:75106121 | C | T | 1 | a0002c0001t0001g0080 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1529-125G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 12/21 | chr14 | 75106121 | |||||||
| chr14:75106184 | C | T | 1 | a0001c0002t0020g0013 | 2 | HG00642.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1529-188G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 12/21 | chr14 | 75106184 | |||||||
| chr14:75106348 | G | C | 1 | a0001c0002t0003g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1528+154C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 12/21 | chr14 | 75106348 | |||||||
| chr14:75106361 | G | GA | 11 | a0001c0004t0014g0100 a0002c0001t0001g0050 a0002c0001t0001g0063 others(8): Show |
11 | HG00621.hp1 HG01071.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1528+140dupT | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 12/21 | chr14 | 75106361 | |||||||
| chr14:75106361 | GA | G | 106 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(103): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.1528+140delT | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 12/21 | chr14 | 75106361 | |||||||
| chr14:75106764 | T | C | 1 | a0001c0002t0023g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1328-62A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 11/21 | chr14 | 75106764 | |||||||
| chr14:75106822 | T | C | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1328-120A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 11/21 | chr14 | 75106822 | |||||||
| chr14:75107013 | T | C | 1 | a0001c0002t0002g0116 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1328-311A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 11/21 | chr14 | 75107013 | |||||||
| chr14:75107061 | T | C | 233 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(230): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1327+282A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 11/21 | chr14 | 75107061 | |||||||
| chr14:75108064 | A | C | 1 | a0001c0004t0043g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1183-577T>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108064 | |||||||
| chr14:75108086 | G | A | 1 | a0001c0004t0043g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1183-599C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108086 | |||||||
| chr14:75108125 | C | CT | 6 | a0001c0002t0002g0153 a0001c0004t0014g0103 a0001c0004t0014g0104 others(3): Show |
6 | HG01981.hp1 HG03195.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.1183-639dupA | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108125 | |||||||
| chr14:75108227 | C | A | 1 | a0001c0004t0033g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1183-740G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108227 | |||||||
| chr14:75108274 | G | A | 3 | a0002c0001t0001g0004 a0002c0001t0001g0204 a0002c0001t0001g0214 |
5 | HG00741.hp2 HG01346.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1183-787C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108274 | |||||||
| chr14:75108282 | G | A | 1 | a0002c0001t0001g0076 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1183-795C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108282 | |||||||
| chr14:75108514 | C | CGT | 8 | a0001c0004t0014g0100 a0001c0004t0014g0103 a0001c0004t0014g0104 others(5): Show |
8 | HG01109.hp1 HG02717.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1183-1029_1183-102 others(6): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108514 | |||||||
| chr14:75108514 | CGT | C | 107 | a0001c0002t0003g0014 a0001c0002t0003g0117 a0001c0002t0003g0186 others(104): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1183-1029_1183-102 others(6): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108514 | |||||||
| chr14:75108514 | CGTGT | C | 8 | a0001c0003t0010g0119 a0001c0003t0010g0120 a0001c0003t0010g0126 others(5): Show |
9 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183-1031_1183-102 others(8): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108514 | |||||||
| chr14:75108514 | CGTGTGT | C | 3 | a0001c0004t0009g0098 a0002c0001t0001g0205 a0002c0001t0031g0236 |
3 | HG01891.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1183-1033_1183-102 others(10): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108514 | |||||||
| chr14:75108514 | CGTGTGTG others(9): Show |
C | 84 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(81): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.1183-1043_1183-102 others(20): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108514 | |||||||
| chr14:75108520 | T | C | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1183-1033A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108520 | |||||||
| chr14:75108522 | T | C | 1 | a0002c0018t0006g0239 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1183-1035A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108522 | |||||||
| chr14:75108561 | A | T | 1 | a0001c0004t0014g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1183-1074T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108561 | |||||||
| chr14:75108563 | T | A | 25 | a0001c0002t0002g0132 a0001c0002t0002g0137 a0001c0002t0002g0150 others(22): Show |
26 | HG00673.hp1 HG01109.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1183-1076A>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108563 | |||||||
| chr14:75108593 | C | T | 2 | a0001c0002t0008g0106 a0001c0002t0020g0013 |
3 | HG00642.hp1 HG00735.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1182+1092G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108593 | |||||||
| chr14:75108640 | C | T | 3 | a0006c0008t0013g0024 a0006c0008t0013g0202 a0006c0008t0013g0203 |
4 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+1045G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108640 | |||||||
| chr14:75108942 | A | G | 1 | a0001c0003t0007g0122 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1182+743T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75108942 | |||||||
| chr14:75109015 | C | T | 1 | a0001c0003t0007g0121 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1182+670G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75109015 | |||||||
| chr14:75109163 | A | G | 1 | a0002c0001t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1182+522T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75109163 | |||||||
| chr14:75109199 | G | A | 1 | a0001c0002t0002g0139 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1182+486C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 10/21 | chr14 | 75109199 | |||||||
| chr14:75109956 | GAGA | G | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.990-82_990-80delTC others(1): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 9/21 | chr14 | 75109956 | |||||||
| chr14:75110627 | G | A | 3 | a0001c0004t0014g0103 a0001c0004t0014g0104 a0001c0004t0014g0105 |
3 | HG03195.hp1 NA18954.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.939-256C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75110627 | |||||||
| chr14:75110670 | T | C | 5 | a0001c0004t0014g0100 a0001c0004t0014g0103 a0001c0004t0014g0104 others(2): Show |
5 | HG03195.hp1 HG03942.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.939-299A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75110670 | |||||||
| chr14:75110714 | G | T | 1 | a0001c0002t0034g0152 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.939-343C>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75110714 | |||||||
| chr14:75111079 | A | G | 1 | a0001c0002t0002g0191 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.939-708T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75111079 | |||||||
| chr14:75111092 | C | T | 1 | a0003c0005t0016g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.939-721G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75111092 | |||||||
| chr14:75111354 | A | T | 1 | a0001c0002t0022g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.939-983T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75111354 | |||||||
| chr14:75111457 | A | T | 1 | a0001c0002t0002g0150 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.939-1086T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75111457 | |||||||
| chr14:75111487 | T | C | 3 | a0001c0002t0003g0023 a0001c0002t0003g0182 a0001c0002t0003g0197 |
4 | HG00741.hp1 HG01175.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.939-1116A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75111487 | |||||||
| chr14:75111579 | G | T | 4 | a0001c0002t0002g0132 a0001c0002t0002g0148 a0001c0002t0002g0149 others(1): Show |
4 | NA18980.hp1 NA19003.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.939-1208C>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75111579 | |||||||
| chr14:75111777 | G | A | 3 | a0006c0008t0013g0024 a0006c0008t0013g0202 a0006c0008t0013g0203 |
4 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.939-1406C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75111777 | |||||||
| chr14:75111810 | A | G | 234 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(231): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.939-1439T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75111810 | |||||||
| chr14:75112164 | A | AATTAGGG others(30): Show |
1 | a0002c0001t0006g0089 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.938+1138_938+1174d others(39): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75112164 | |||||||
| chr14:75112522 | C | T | 1 | a0001c0004t0043g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.938+817G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75112522 | |||||||
| chr14:75112713 | C | T | 110 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(107): Show |
133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.938+626G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75112713 | |||||||
| chr14:75112798 | G | A | 1 | a0002c0001t0001g0229 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.938+541C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75112798 | |||||||
| chr14:75112872 | C | A | 1 | a0002c0001t0001g0230 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.938+467G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75112872 | |||||||
| chr14:75112881 | G | A | 234 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(231): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.938+458C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75112881 | |||||||
| chr14:75112921 | G | A | 1 | a0001c0002t0004g0147 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.938+418C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75112921 | |||||||
| chr14:75112940 | A | G | 107 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(104): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.938+399T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75112940 | |||||||
| chr14:75112979 | C | T | 2 | a0002c0001t0015g0045 a0002c0001t0015g0046 |
2 | HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.938+360G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75112979 | |||||||
| chr14:75113098 | C | A | 3 | a0001c0002t0003g0023 a0001c0002t0003g0182 a0001c0002t0003g0197 |
4 | HG00741.hp1 HG01175.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.938+241G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 8/21 | chr14 | 75113098 | |||||||
| chr14:75113449 | G | A | 234 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(231): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.874-46C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 7/21 | chr14 | 75113449 | |||||||
| chr14:75113455 | G | A | 1 | a0002c0001t0001g0231 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.874-52C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 7/21 | chr14 | 75113455 | |||||||
| chr14:75113830 | A | C | 1 | a0002c0001t0001g0220 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.873+373T>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 7/21 | chr14 | 75113830 | |||||||
| chr14:75113947 | TA | T | 234 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(231): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.873+255delT | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 7/21 | chr14 | 75113947 | |||||||
| chr14:75113956 | G | A | 2 | a0001c0002t0002g0176 a0001c0002t0002g0177 |
2 | NA19009.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.873+247C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 7/21 | chr14 | 75113956 | |||||||
| chr14:75114579 | A | G | 4 | a0002c0009t0012g0092 a0002c0009t0012g0093 a0002c0009t0012g0094 others(1): Show |
4 | HG01109.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.763-266T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75114579 | |||||||
| chr14:75114902 | A | G | 1 | a0001c0002t0003g0178 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.763-589T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75114902 | |||||||
| chr14:75114999 | A | G | 219 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(216): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.763-686T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75114999 | |||||||
| chr14:75115010 | C | T | 232 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(229): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.763-697G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115010 | |||||||
| chr14:75115054 | TAC | T | 13 | a0001c0002t0004g0003 a0001c0002t0004g0016 a0001c0002t0004g0114 others(10): Show |
16 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.763-743_763-742del others(2): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115054 | |||||||
| chr14:75115056 | CACACACG others(51): Show |
C | 2 | a0001c0002t0019g0140 a0001c0002t0019g0141 |
2 | HG01256.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.763-801_763-744del others(58): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115056 | |||||||
| chr14:75115062 | CGT | C | 110 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(107): Show |
133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.763-751_763-750del others(2): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115062 | |||||||
| chr14:75115082 | C | T | 1 | a0002c0001t0001g0209 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.763-769G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115082 | |||||||
| chr14:75115084 | T | C | 7 | a0001c0002t0008g0106 a0001c0002t0008g0107 a0001c0002t0008g0109 others(4): Show |
8 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.763-771A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115084 | |||||||
| chr14:75115087 | G | C | 2 | a0002c0009t0012g0092 a0002c0009t0012g0093 |
2 | HG01109.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.763-774C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115087 | |||||||
| chr14:75115113 | G | A | 105 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(102): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.763-800C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115113 | |||||||
| chr14:75115114 | T | TAC | 101 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(98): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.763-803_763-802dup others(2): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115114 | |||||||
| chr14:75115114 | T | TACAC | 122 | a0001c0002t0003g0014 a0001c0002t0003g0117 a0001c0002t0003g0186 others(119): Show |
146 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.763-805_763-802dup others(4): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115114 | |||||||
| chr14:75115114 | T | TACACAC | 5 | a0001c0002t0036g0118 a0002c0009t0012g0092 a0002c0009t0012g0093 others(2): Show |
5 | HG01109.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.763-807_763-802dup others(6): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115114 | |||||||
| chr14:75115363 | C | T | 107 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(104): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.763-1050G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115363 | |||||||
| chr14:75115406 | C | T | 4 | a0002c0009t0012g0092 a0002c0009t0012g0093 a0002c0009t0012g0094 others(1): Show |
4 | HG01109.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.763-1093G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115406 | |||||||
| chr14:75115482 | C | A | 4 | a0001c0003t0010g0119 a0001c0003t0010g0120 a0001c0003t0010g0126 others(1): Show |
4 | HG02647.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.763-1169G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75115482 | |||||||
| chr14:75116038 | T | G | 1 | a0001c0002t0003g0183 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.762+1157A>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75116038 | |||||||
| chr14:75116179 | T | C | 1 | a0001c0004t0043g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.762+1016A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75116179 | |||||||
| chr14:75116565 | T | C | 107 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(104): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.762+630A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75116565 | |||||||
| chr14:75116911 | C | T | 1 | a0002c0009t0012g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.762+284G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75116911 | |||||||
| chr14:75116914 | C | A | 1 | a0001c0004t0033g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.762+281G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75116914 | |||||||
| chr14:75116929 | C | T | 234 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(231): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.762+266G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75116929 | |||||||
| chr14:75116940 | G | A | 1 | a0002c0001t0026g0218 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.762+255C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75116940 | |||||||
| chr14:75116988 | C | T | 1 | a0001c0003t0010g0120 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.762+207G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75116988 | |||||||
| chr14:75117121 | G | A | 26 | a0002c0001t0001g0005 a0002c0001t0001g0028 a0002c0001t0001g0201 others(23): Show |
31 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.762+74C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 6/21 | chr14 | 75117121 | |||||||
| chr14:75117505 | C | A | 1 | a0001c0002t0003g0184 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.631-179G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75117505 | |||||||
| chr14:75117558 | G | C | 4 | a0002c0009t0012g0092 a0002c0009t0012g0093 a0002c0009t0012g0094 others(1): Show |
4 | HG01109.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-232C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75117558 | |||||||
| chr14:75117685 | C | G | 6 | a0001c0003t0007g0015 a0001c0003t0007g0121 a0001c0003t0007g0122 others(3): Show |
7 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.631-359G>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75117685 | |||||||
| chr14:75117804 | C | T | 84 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(81): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.631-478G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75117804 | |||||||
| chr14:75117922 | T | C | 1 | a0002c0001t0021g0029 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.631-596A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75117922 | |||||||
| chr14:75118025 | A | T | 1 | a0001c0003t0010g0120 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.631-699T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75118025 | |||||||
| chr14:75118164 | C | T | 114 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(111): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.630+666G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75118164 | |||||||
| chr14:75118206 | T | A | 8 | a0001c0002t0008g0106 a0001c0002t0008g0107 a0001c0002t0008g0109 others(5): Show |
9 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.630+624A>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75118206 | |||||||
| chr14:75118248 | T | C | 1 | a0001c0004t0033g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.630+582A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75118248 | |||||||
| chr14:75118263 | G | A | 1 | a0002c0001t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.630+567C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75118263 | |||||||
| chr14:75118433 | T | C | 1 | a0003c0005t0016g0033 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.630+397A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75118433 | |||||||
| chr14:75118568 | C | G | 1 | a0001c0004t0014g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.630+262G>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75118568 | |||||||
| chr14:75118595 | G | A | 1 | a0001c0004t0043g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.630+235C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75118595 | |||||||
| chr14:75118595 | G | C | 2 | a0002c0001t0001g0208 a0002c0001t0005g0232 |
2 | NA18971.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.630+235C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75118595 | |||||||
| chr14:75118602 | G | A | 26 | a0002c0001t0001g0005 a0002c0001t0001g0028 a0002c0001t0001g0201 others(23): Show |
31 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.630+228C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 5/21 | chr14 | 75118602 | |||||||
| chr14:75119204 | C | T | 4 | a0002c0009t0012g0092 a0002c0009t0012g0093 a0002c0009t0012g0094 others(1): Show |
4 | HG01109.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-269G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 4/21 | chr14 | 75119204 | |||||||
| chr14:75119223 | G | C | 1 | a0002c0001t0001g0078 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.525-288C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 4/21 | chr14 | 75119223 | |||||||
| chr14:75119266 | T | C | 1 | a0002c0001t0005g0233 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.525-331A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 4/21 | chr14 | 75119266 | |||||||
| chr14:75119350 | C | A | 5 | a0001c0004t0014g0100 a0001c0004t0014g0103 a0001c0004t0014g0104 others(2): Show |
5 | HG03195.hp1 HG03942.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.525-415G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 4/21 | chr14 | 75119350 | |||||||
| chr14:75119357 | T | C | 1 | a0001c0004t0033g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.525-422A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 4/21 | chr14 | 75119357 | |||||||
| chr14:75119585 | C | A | 114 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(111): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.525-650G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 4/21 | chr14 | 75119585 | |||||||
| chr14:75119919 | C | T | 233 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(230): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.524+591G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 4/21 | chr14 | 75119919 | |||||||
| chr14:75120311 | A | G | 12 | a0002c0001t0001g0008 a0002c0001t0001g0042 a0002c0001t0001g0051 others(9): Show |
14 | HG00323.hp1 HG00738.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.524+199T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 4/21 | chr14 | 75120311 | |||||||
| chr14:75120460 | G | C | 2 | a0002c0009t0012g0092 a0002c0009t0012g0093 |
2 | HG01109.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.524+50C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 4/21 | chr14 | 75120460 | |||||||
| chr14:75120468 | T | C | 1 | a0001c0004t0043g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.524+42A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 4/21 | chr14 | 75120468 | |||||||
| chr14:75120502 | C | T | 1 | a0002c0001t0005g0238 | 1 | NA18969.hp2 | splice_region_variant&intron_variant | LOW | c.524+8G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 4/21 | chr14 | 75120502 | |||||||
| chr14:75120636 | T | C | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.454-56A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 3/21 | chr14 | 75120636 | |||||||
| chr14:75120648 | T | C | 233 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(230): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.454-68A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 3/21 | chr14 | 75120648 | |||||||
| chr14:75120749 | A | G | 2 | a0002c0001t0001g0025 a0002c0001t0001g0213 |
3 | HG02922.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.454-169T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 3/21 | chr14 | 75120749 | |||||||
| chr14:75121617 | G | A | 11 | a0001c0002t0003g0014 a0001c0002t0003g0117 a0001c0002t0003g0186 others(8): Show |
13 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-443C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75121617 | |||||||
| chr14:75121734 | C | T | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.398-560G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75121734 | |||||||
| chr14:75121736 | A | C | 1 | a0001c0004t0043g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.398-562T>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75121736 | |||||||
| chr14:75121894 | C | T | 1 | a0004c0006t0039g0101 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.398-720G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75121894 | |||||||
| chr14:75122121 | A | G | 114 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(111): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.398-947T>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75122121 | |||||||
| chr14:75122492 | G | C | 114 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(111): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.398-1318C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75122492 | |||||||
| chr14:75122581 | T | C | 114 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(111): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.398-1407A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75122581 | |||||||
| chr14:75122582 | G | A | 12 | a0001c0003t0007g0015 a0001c0003t0007g0121 a0001c0003t0007g0122 others(9): Show |
13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-1408C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75122582 | |||||||
| chr14:75122608 | G | A | 1 | a0001c0002t0040g0128 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.398-1434C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75122608 | |||||||
| chr14:75122694 | C | G | 1 | a0002c0001t0001g0056 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.397+1352G>C | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75122694 | |||||||
| chr14:75122789 | C | CT | 95 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(92): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.397+1256dupA | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75122789 | |||||||
| chr14:75122789 | C | CTT | 34 | a0001c0002t0002g0132 a0001c0002t0002g0133 a0001c0002t0002g0134 others(31): Show |
37 | HG00639.hp1 HG00642.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.397+1255_397+1256d others(4): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75122789 | |||||||
| chr14:75122853 | C | T | 234 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(231): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.397+1193G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75122853 | |||||||
| chr14:75123026 | C | T | 107 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(104): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.397+1020G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75123026 | |||||||
| chr14:75123175 | C | T | 81 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(78): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.397+871G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75123175 | |||||||
| chr14:75123180 | C | T | 81 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(78): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.397+866G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75123180 | |||||||
| chr14:75123198 | C | T | 1 | a0001c0004t0033g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.397+848G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75123198 | |||||||
| chr14:75123404 | CAAA | C | 4 | a0002c0001t0001g0002 a0002c0001t0001g0048 a0002c0001t0001g0050 others(1): Show |
7 | HG00140.hp1 HG00280.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.397+639_397+641del others(3): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75123404 | |||||||
| chr14:75123410 | A | T | 106 | a0002c0001t0001g0001 a0002c0001t0001g0004 a0002c0001t0001g0005 others(103): Show |
126 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.397+636T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75123410 | |||||||
| chr14:75123413 | T | A | 1 | a0001c0004t0014g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.397+633A>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75123413 | |||||||
| chr14:75123428 | A | T | 7 | a0002c0001t0001g0002 a0002c0001t0001g0047 a0002c0001t0001g0048 others(4): Show |
10 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.397+618T>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75123428 | |||||||
| chr14:75123637 | G | A | 81 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(78): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.397+409C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75123637 | |||||||
| chr14:75123770 | C | A | 1 | a0006c0008t0013g0203 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.397+276G>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75123770 | |||||||
| chr14:75124019 | G | A | 5 | a0001c0004t0014g0100 a0001c0004t0014g0103 a0001c0004t0014g0104 others(2): Show |
5 | HG03195.hp1 HG03942.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+27C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 2/21 | chr14 | 75124019 | |||||||
| chr14:75124260 | T | C | 1 | a0002c0001t0005g0234 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.220-37A>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75124260 | |||||||
| chr14:75124368 | G | A | 114 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(111): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.220-145C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75124368 | |||||||
| chr14:75124545 | AT | A | 3 | a0001c0004t0014g0103 a0001c0004t0014g0104 a0001c0004t0014g0105 |
3 | HG03195.hp1 NA18954.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.220-323delA | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75124545 | |||||||
| chr14:75124698 | G | A | 234 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(231): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.220-475C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75124698 | |||||||
| chr14:75124713 | TTTG | T | 7 | a0003c0005t0011g0006 a0003c0005t0011g0032 a0003c0005t0011g0035 others(4): Show |
8 | HG02622.hp1 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.220-493_220-491del others(3): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75124713 | |||||||
| chr14:75124775 | C | CT | 13 | a0001c0002t0002g0116 a0001c0002t0004g0114 a0001c0002t0008g0106 others(10): Show |
14 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-553dupA | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75124775 | |||||||
| chr14:75124775 | CT | C | 108 | a0001c0002t0002g0190 a0001c0002t0002g0191 a0001c0002t0002g0198 others(105): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.220-553delA | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75124775 | |||||||
| chr14:75124775 | CTT | C | 14 | a0002c0001t0001g0041 a0002c0001t0001g0042 a0002c0001t0001g0079 others(11): Show |
14 | HG00323.hp1 HG00558.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-554_220-553del others(2): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75124775 | |||||||
| chr14:75124938 | A | AT | 100 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(97): Show |
123 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.220-716dupA | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75124938 | |||||||
| chr14:75124938 | A | ATT | 11 | a0002c0001t0001g0036 a0002c0001t0001g0038 a0002c0001t0001g0039 others(8): Show |
11 | HG01109.hp1 HG01433.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-717_220-716dup others(2): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75124938 | |||||||
| chr14:75124938 | AT | A | 112 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(109): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.220-716delA | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75124938 | |||||||
| chr14:75125043 | G | A | 2 | a0002c0001t0006g0089 a0002c0001t0006g0090 |
2 | NA18961.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.220-820C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75125043 | |||||||
| chr14:75125780 | G | C | 110 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0004 others(107): Show |
133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.219+923C>G | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75125780 | |||||||
| chr14:75126321 | G | A | 1 | a0002c0018t0006g0239 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.219+382C>T | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75126321 | |||||||
| chr14:75126449 | C | T | 62 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0008 others(59): Show |
76 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.219+254G>A | NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 1/21 | chr14 | 75126449 |