Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 341676 |
| ensemblid | ENSG00000197168.14 |
| hgncid | 7748 |
| symbol | NEK5 |
| name | NIMA related kinase 5 |
| refseq_nuc | NM_001365552.1 |
| refseq_prot | NP_001352481.1 |
| ensembl_nuc | ENST00000684899.1 |
| ensembl_prot | ENSP00000509632.1 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 52033611 |
| end | 52129073 |
| strand | - |
| ver | v1.2 |
| region | chr13:52033611-52129073 |
| region5000 | chr13:52028611-52134073 |
| regionname0 | NEK5_chr13_52033611_52129073 |
| regionname5000 | NEK5_chr13_52028611_52134073 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 832 | 292 | 63 | 53 | 138 | 6 | 30 | 106 | NEK5_chr13_52028611_52134073 | NEK5 | MDKYD others(827): Show |
chr13 | 52028611 | 52134073 |
| a0002 | 0/0 | 832 | 31 | 1 | 13 | 10 | 4 | 3 | 6 | NEK5_chr13_52028611_52134073 | NEK5 | MDKYD others(827): Show |
chr13 | 52028611 | 52134073 |
| a0003 | 0/0 | 832 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | MDKYD others(827): Show |
chr13 | 52028611 | 52134073 |
| a0004 | 0/0 | 832 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | MDKYD others(827): Show |
chr13 | 52028611 | 52134073 |
| a0005 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | MDKYD others(827): Show |
chr13 | 52028611 | 52134073 |
| a0006 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | MDKYD others(827): Show |
chr13 | 52028611 | 52134073 |
| a0007 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | MDKYD others(827): Show |
chr13 | 52028611 | 52134073 |
| a0008 | 0/0 | 832 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | MDKYD others(827): Show |
chr13 | 52028611 | 52134073 |
| a0009 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | MDKYD others(827): Show |
chr13 | 52028611 | 52134073 |
| a0010 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | MDKYD others(827): Show |
chr13 | 52028611 | 52134073 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2496 | 276 | 58 | 51 | 133 | 6 | 26 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0001c0003 | 0/0 | 2496 | 9 | 1 | 1 | 4 | 0 | 3 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0001c0004 | 0/0 | 2496 | 3 | 3 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0001c0009 | 0/0 | 2496 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0001c0010 | 0/0 | 2496 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0001c0013 | 0/0 | 2496 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0001c0016 | 0/0 | 2496 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0002c0002 | 0/0 | 2496 | 31 | 1 | 13 | 10 | 4 | 3 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0003c0005 | 0/0 | 2496 | 3 | 2 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0004c0006 | 0/0 | 2496 | 2 | 1 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0005c0014 | 0/0 | 2496 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0006c0007 | 0/0 | 2496 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0007c0011 | 0/0 | 2496 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0008c0012 | 0/0 | 2496 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0009c0008 | 0/0 | 2496 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 | ||
| a0010c0015 | 0/0 | 2496 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATGGA others(2491): Show |
chr13 | 52028611 | 52134073 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5971 | 97 | 20 | 9 | 57 | 1 | 9 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0002 | 0/0 | 5974 | 59 | 5 | 13 | 33 | 3 | 5 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5969): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0003 | 0/0 | 5974 | 22 | 0 | 3 | 17 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5969): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0004 | 0/0 | 5971 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0006 | 0/0 | 5968 | 8 | 0 | 8 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5963): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0007 | 0/0 | 5975 | 7 | 1 | 0 | 4 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5970): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0008 | 0/0 | 5972 | 6 | 2 | 3 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5967): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0009 | 0/0 | 5972 | 4 | 1 | 0 | 2 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5967): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0011 | 0/0 | 5973 | 4 | 0 | 2 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5968): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0012 | 0/0 | 5970 | 4 | 4 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5965): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0014 | 0/0 | 5971 | 4 | 0 | 3 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0015 | 0/0 | 5972 | 4 | 1 | 0 | 3 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5967): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0016 | 0/0 | 5973 | 4 | 4 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5968): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0017 | 0/0 | 5970 | 3 | 0 | 0 | 2 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5965): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0018 | 0/1 | 5971 | 3 | 0 | 0 | 0 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0020 | 0/0 | 5975 | 3 | 0 | 1 | 1 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5970): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0021 | 0/0 | 5974 | 3 | 0 | 0 | 0 | 1 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5969): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0022 | 0/0 | 5971 | 3 | 3 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0023 | 0/0 | 5971 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0024 | 0/0 | 5971 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0025 | 0/0 | 5974 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5969): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0026 | 0/0 | 5970 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5965): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0028 | 0/0 | 5973 | 2 | 0 | 2 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5968): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0029 | 0/0 | 5975 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5970): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0030 | 0/0 | 5971 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0031 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5967): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0034 | 0/0 | 5973 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5968): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0035 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5967): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0036 | 0/0 | 5973 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5968): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0037 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5967): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0038 | 0/0 | 5969 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5964): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0039 | 0/0 | 5971 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0040 | 0/0 | 5970 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5965): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0041 | 0/0 | 5969 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5964): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0043 | 0/0 | 5969 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5964): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0044 | 0/0 | 5971 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0045 | 0/0 | 5971 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0046 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5967): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0047 | 0/0 | 5974 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5969): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0052 | 0/0 | 5971 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0053 | 0/0 | 5970 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5965): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0055 | 0/0 | 5974 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5969): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0056 | 0/0 | 5974 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5969): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0057 | 0/0 | 5973 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5968): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0058 | 0/0 | 5974 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5969): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0059 | 0/0 | 5975 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5970): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0060 | 0/0 | 5975 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5970): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0061 | 0/0 | 5974 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5969): Show |
chr13 | 52028611 | 52134073 |
| a0001c0001t0062 | 0/0 | 5974 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5969): Show |
chr13 | 52028611 | 52134073 |
| a0001c0003t0010 | 0/0 | 5971 | 5 | 1 | 1 | 0 | 0 | 3 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0003t0013 | 0/0 | 5970 | 4 | 0 | 0 | 4 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5965): Show |
chr13 | 52028611 | 52134073 |
| a0001c0004t0019 | 0/0 | 5970 | 3 | 3 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5965): Show |
chr13 | 52028611 | 52134073 |
| a0001c0009t0001 | 0/0 | 5971 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0010t0048 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5967): Show |
chr13 | 52028611 | 52134073 |
| a0001c0013t0001 | 0/0 | 5971 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0001c0016t0001 | 0/0 | 5971 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0002c0002t0004 | 0/0 | 5971 | 16 | 0 | 5 | 9 | 1 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0002c0002t0005 | 0/0 | 5971 | 10 | 0 | 6 | 0 | 3 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0002c0002t0032 | 0/0 | 5972 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5967): Show |
chr13 | 52028611 | 52134073 |
| a0002c0002t0033 | 0/0 | 5970 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5965): Show |
chr13 | 52028611 | 52134073 |
| a0002c0002t0049 | 0/0 | 5972 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5967): Show |
chr13 | 52028611 | 52134073 |
| a0002c0002t0050 | 0/0 | 5971 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0002c0002t0051 | 0/0 | 5970 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5965): Show |
chr13 | 52028611 | 52134073 |
| a0003c0005t0027 | 0/0 | 5971 | 2 | 1 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0003c0005t0054 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5967): Show |
chr13 | 52028611 | 52134073 |
| a0004c0006t0002 | 0/0 | 5974 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5969): Show |
chr13 | 52028611 | 52134073 |
| a0004c0006t0011 | 0/0 | 5973 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5968): Show |
chr13 | 52028611 | 52134073 |
| a0005c0014t0004 | 0/0 | 5971 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0006c0007t0001 | 0/0 | 5971 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0007c0011t0042 | 0/0 | 5961 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5956): Show |
chr13 | 52028611 | 52134073 |
| a0008c0012t0001 | 0/0 | 5971 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| a0009c0008t0009 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5967): Show |
chr13 | 52028611 | 52134073 |
| a0010c0015t0001 | 0/0 | 5971 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | ATCCT others(5966): Show |
chr13 | 52028611 | 52134073 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0006g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0006g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0006g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0007g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0007g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0007g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0007g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0008g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0008g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0009g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0009g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0009g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0011g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0011g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0011g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0011g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0012g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0012g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0012g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0014g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0014g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0014g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0014g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0015g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0015g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0015g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0015g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0016g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0016g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0016g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0016g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0017g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0017g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0017g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0018g0016 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0018g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0018g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0020g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0020g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0020g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0021g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0021g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0021g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0022g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0022g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0022g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0023g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0023g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0024g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0024g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0025g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0025g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0026g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0028g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0028g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0029g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0029g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0030g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0031g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0034g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0035g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0036g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0037g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0038g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0039g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0040g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0041g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0043g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0044g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0045g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0046g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0047g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0052g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0053g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0055g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0056g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0057g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0058g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0059g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0060g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0061g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0001t0062g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0003t0010g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0003t0010g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0003t0010g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0003t0010g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0003t0010g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0003t0013g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0003t0013g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0003t0013g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0003t0013g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0004t0019g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0004t0019g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0004t0019g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0009t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0010t0048g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0013t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0001c0016t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0005g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0005g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0005g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0032g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0033g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0049g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0050g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0002c0002t0051g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0003c0005t0027g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0003c0005t0027g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0003c0005t0054g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0004c0006t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0004c0006t0011g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0005c0014t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0006c0007t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0007c0011t0042g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0008c0012t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0009c0008t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| a0010c0015t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0222 | EUR | GBR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00099 | hp2 | a0002 | c0002 | t0005 | g0069 | EUR | GBR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00323 | hp1 | a0002 | c0002 | t0004 | g0180 | EUR | FIN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00323 | hp2 | a0001 | c0001 | t0021 | g0226 | EUR | FIN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00408 | hp2 | a0002 | c0002 | t0004 | g0184 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00544 | hp1 | a0001 | c0003 | t0013 | g0024 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00621 | hp1 | a0002 | c0002 | t0049 | g0189 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00639 | hp1 | a0004 | c0006 | t0011 | g0207 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0270 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00642 | hp2 | a0002 | c0002 | t0005 | g0067 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00733 | hp1 | a0001 | c0001 | t0014 | g0293 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00733 | hp2 | a0002 | c0002 | t0004 | g0183 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00738 | hp1 | a0002 | c0002 | t0005 | g0074 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01074 | hp2 | a0002 | c0002 | t0050 | g0317 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01081 | hp1 | a0002 | c0002 | t0004 | g0181 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0064 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01099 | hp1 | a0002 | c0002 | t0005 | g0075 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01099 | hp2 | a0001 | c0003 | t0010 | g0020 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0063 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01167 | hp1 | a0002 | c0002 | t0005 | g0065 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01168 | hp1 | a0002 | c0002 | t0005 | g0066 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01169 | hp1 | a0002 | c0002 | t0033 | g0076 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0096 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01192 | hp1 | a0003 | c0005 | t0027 | g0318 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01243 | hp1 | a0001 | c0001 | t0036 | g0035 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01243 | hp2 | a0001 | c0001 | t0052 | g0315 | AMR | PUR | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0030 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01255 | hp2 | a0001 | c0009 | t0001 | g0042 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0028 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01256 | hp2 | a0001 | c0001 | t0028 | g0278 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01257 | hp1 | a0001 | c0001 | t0053 | g0294 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01258 | hp1 | a0001 | c0001 | t0028 | g0204 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01258 | hp2 | a0001 | c0001 | t0014 | g0295 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01261 | hp2 | a0002 | c0002 | t0004 | g0179 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01346 | hp2 | a0001 | c0001 | t0020 | g0308 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01358 | hp1 | a0002 | c0002 | t0004 | g0182 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01361 | hp1 | a0001 | c0001 | t0014 | g0296 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0027 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01516 | hp1 | a0002 | c0002 | t0005 | g0072 | EUR | IBS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01516 | hp2 | a0001 | c0001 | t0039 | g0145 | EUR | IBS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0267 | EUR | IBS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01517 | hp2 | a0002 | c0002 | t0005 | g0073 | EUR | IBS | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01891 | hp1 | a0001 | c0001 | t0012 | g0039 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01891 | hp2 | a0002 | c0002 | t0051 | g0316 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0032 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01943 | hp1 | a0001 | c0001 | t0040 | g0091 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01943 | hp2 | a0001 | c0001 | t0011 | g0205 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01952 | hp1 | a0001 | c0001 | t0011 | g0240 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0029 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0257 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01993 | hp1 | a0001 | c0001 | t0058 | g0284 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0256 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0044 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02055 | hp2 | a0004 | c0006 | t0002 | g0208 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02071 | hp2 | a0001 | c0001 | t0007 | g0238 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02074 | hp1 | a0001 | c0001 | t0015 | g0197 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02132 | hp2 | a0002 | c0002 | t0004 | g0190 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02135 | hp1 | a0002 | c0002 | t0004 | g0177 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02135 | hp2 | a0001 | c0001 | t0015 | g0230 | EAS | KHV | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | CDX | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02165 | hp1 | a0001 | c0001 | t0062 | g0275 | EAS | CDX | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0003 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02257 | hp2 | a0001 | c0001 | t0016 | g0304 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02258 | hp1 | a0001 | c0004 | t0019 | g0298 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02273 | hp1 | a0001 | c0001 | t0006 | g0031 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0288 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02280 | hp1 | a0005 | c0014 | t0004 | g0297 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02280 | hp2 | a0001 | c0001 | t0047 | g0194 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02293 | hp2 | a0002 | c0002 | t0004 | g0188 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02300 | hp2 | a0001 | c0001 | t0055 | g0249 | AMR | PEL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02451 | hp1 | a0001 | c0001 | t0022 | g0311 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02451 | hp2 | a0001 | c0001 | t0031 | g0054 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02572 | hp2 | a0003 | c0005 | t0054 | g0320 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02602 | hp1 | a0002 | c0002 | t0032 | g0068 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02602 | hp2 | a0001 | c0001 | t0021 | g0227 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02615 | hp1 | a0001 | c0001 | t0043 | g0037 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02615 | hp2 | a0001 | c0001 | t0023 | g0014 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02622 | hp2 | a0001 | c0001 | t0023 | g0015 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0193 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02717 | hp1 | a0006 | c0007 | t0001 | g0055 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0309 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02738 | hp1 | a0001 | c0001 | t0009 | g0150 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02738 | hp2 | a0002 | c0002 | t0004 | g0191 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02809 | hp2 | a0001 | c0001 | t0024 | g0078 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02886 | hp1 | a0007 | c0011 | t0042 | g0040 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02895 | hp1 | a0001 | c0001 | t0016 | g0301 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02896 | hp1 | a0001 | c0010 | t0048 | g0290 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02896 | hp2 | a0001 | c0001 | t0025 | g0062 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02897 | hp1 | a0001 | c0001 | t0016 | g0305 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02897 | hp2 | a0001 | c0001 | t0046 | g0060 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02965 | hp2 | a0003 | c0005 | t0027 | g0319 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0034 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02970 | hp2 | a0001 | c0001 | t0012 | g0038 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03017 | hp1 | a0001 | c0001 | t0044 | g0019 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03017 | hp2 | a0001 | c0003 | t0010 | g0023 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03041 | hp2 | a0001 | c0001 | t0025 | g0061 | AFR | GWD | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03130 | hp1 | a0001 | c0004 | t0019 | g0300 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03139 | hp2 | a0001 | c0004 | t0019 | g0299 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03209 | hp1 | a0001 | c0001 | t0041 | g0085 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03209 | hp2 | a0001 | c0001 | t0030 | g0045 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03225 | hp2 | a0001 | c0001 | t0022 | g0310 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03239 | hp2 | a0002 | c0002 | t0005 | g0070 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03486 | hp1 | a0001 | c0001 | t0024 | g0036 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03486 | hp2 | a0001 | c0001 | t0037 | g0128 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03490 | hp1 | a0001 | c0001 | t0018 | g0017 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03491 | hp1 | a0008 | c0012 | t0001 | g0101 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03654 | hp2 | a0001 | c0001 | t0018 | g0018 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03688 | hp1 | a0001 | c0003 | t0010 | g0022 | SAS | STU | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0232 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03710 | hp1 | a0001 | c0001 | t0020 | g0223 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03710 | hp2 | a0001 | c0013 | t0001 | g0133 | SAS | PJL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | BEB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03831 | hp2 | a0001 | c0001 | t0017 | g0104 | SAS | BEB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG04115 | hp1 | a0001 | c0001 | t0021 | g0285 | SAS | STU | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0202 | SAS | STU | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | CHB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18906 | hp1 | a0009 | c0008 | t0009 | g0153 | AFR | YRI | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | YRI | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18941 | hp2 | a0002 | c0002 | t0004 | g0185 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18964 | hp2 | a0001 | c0001 | t0017 | g0314 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18965 | hp2 | a0001 | c0001 | t0009 | g0120 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18968 | hp1 | a0001 | c0001 | t0011 | g0306 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18970 | hp1 | a0002 | c0002 | t0004 | g0178 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18972 | hp1 | a0001 | c0001 | t0034 | g0136 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18972 | hp2 | a0001 | c0001 | t0057 | g0279 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18973 | hp1 | a0001 | c0001 | t0007 | g0245 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18974 | hp2 | a0001 | c0016 | t0001 | g0170 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18984 | hp2 | a0002 | c0002 | t0004 | g0187 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18985 | hp2 | a0001 | c0001 | t0060 | g0280 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18991 | hp1 | a0002 | c0002 | t0004 | g0186 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18994 | hp1 | a0001 | c0001 | t0008 | g0106 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18994 | hp2 | a0001 | c0003 | t0013 | g0025 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18999 | hp1 | a0002 | c0002 | t0004 | g0176 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19002 | hp1 | a0001 | c0001 | t0011 | g0224 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19009 | hp1 | a0001 | c0001 | t0029 | g0258 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19009 | hp2 | a0001 | c0001 | t0045 | g0094 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19030 | hp1 | a0010 | c0015 | t0001 | g0056 | AFR | LWK | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0052 | AFR | LWK | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19055 | hp2 | a0002 | c0002 | t0004 | g0175 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19060 | hp1 | a0001 | c0001 | t0029 | g0252 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19063 | hp1 | a0001 | c0001 | t0007 | g0242 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19065 | hp1 | a0001 | c0001 | t0020 | g0277 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19068 | hp1 | a0001 | c0001 | t0014 | g0286 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19075 | hp1 | a0001 | c0001 | t0056 | g0282 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19075 | hp2 | a0001 | c0001 | t0017 | g0129 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19080 | hp1 | a0001 | c0003 | t0013 | g0026 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19082 | hp1 | a0001 | c0001 | t0007 | g0239 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19082 | hp2 | a0001 | c0003 | t0013 | g0021 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19087 | hp1 | a0001 | c0001 | t0015 | g0273 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19087 | hp2 | a0001 | c0001 | t0009 | g0089 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19089 | hp2 | a0001 | c0001 | t0038 | g0119 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19091 | hp1 | a0001 | c0001 | t0059 | g0261 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19240 | hp1 | a0001 | c0001 | t0026 | g0013 | AFR | YRI | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA19240 | hp2 | a0001 | c0001 | t0022 | g0312 | AFR | YRI | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | ASW | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ASW | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0201 | EUR | TSI | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA20905 | hp1 | a0001 | c0003 | t0010 | g0174 | SAS | GIH | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | GIH | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG01123 | hp2 | a0002 | c0002 | t0005 | g0071 | AMR | CLM | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02109 | hp2 | a0001 | c0001 | t0012 | g0003 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG02486 | hp2 | a0001 | c0001 | t0061 | g0302 | AFR | ACB | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG06807 | hp1 | a0001 | c0003 | t0010 | g0173 | AFR | USA | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | USA | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA20300 | hp1 | a0001 | c0001 | t0035 | g0127 | AFR | USA | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA20300 | hp2 | a0001 | c0001 | t0026 | g0013 | AFR | USA | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA21309 | hp1 | a0001 | c0001 | t0016 | g0303 | AFR | LWK | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| NA21309 | hp2 | a0001 | c0001 | t0015 | g0200 | AFR | LWK | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0018 | g0016 | REF | REF | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0082 | REF | REF | NEK5_chr13_52028611_52134073 | NEK5 | chr13 | 52028611 | 52134073 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52050158 | G | T | 1 | a0005 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.2174C>A | p.Ser725Tyr | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/24 | 2309/5971 | 2174/2499 | 725/832 | chr13 | 52050158 | |||
| chr13:52076143 | C | A | 2 | a0003 a0007 |
4 | HG01192.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1573G>T | p.Asp525Tyr | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 18/24 | 1708/5971 | 1573/2499 | 525/832 | chr13 | 52076143 | |||
| chr13:52086336 | G | A | 1 | a0004 | 2 | HG00639.hp1 HG02055.hp2 |
missense_variant | MODERATE | c.1420C>T | p.Arg474Cys | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/24 | 1555/5971 | 1420/2499 | 474/832 | chr13 | 52086336 | |||
| chr13:52087340 | G | C | 1 | a0008 | 1 | HG03491.hp1 | missense_variant&splice_region_variant | MODERATE | c.1390C>G | p.Gln464Glu | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/24 | 1525/5971 | 1390/2499 | 464/832 | chr13 | 52087340 | |||
| chr13:52099768 | G | T | 1 | a0009 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.1001C>A | p.Pro334Gln | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/24 | 1136/5971 | 1001/2499 | 334/832 | chr13 | 52099768 | |||
| chr13:52102139 | T | G | 2 | a0002 a0005 |
32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
missense_variant | MODERATE | c.763A>C | p.Lys255Gln | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 10/24 | 898/5971 | 763/2499 | 255/832 | chr13 | 52102139 | |||
| chr13:52102204 | T | C | 1 | a0003 | 3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
missense_variant | MODERATE | c.698A>G | p.His233Arg | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 10/24 | 833/5971 | 698/2499 | 233/832 | chr13 | 52102204 | |||
| chr13:52110356 | C | T | 1 | a0006 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.451G>A | p.Ala151Thr | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/24 | 586/5971 | 451/2499 | 151/832 | chr13 | 52110356 | |||
| chr13:52119376 | T | C | 1 | a0010 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.157A>G | p.Ile53Val | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/24 | 292/5971 | 157/2499 | 53/832 | chr13 | 52119376 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52065581 | C | T | 1 | a0001c0010 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.1878G>A | p.Val626Val | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/24 | 2013/5971 | 1878/2499 | 626/832 | chr13 | 52065581 | |||
| chr13:52065599 | C | T | 1 | a0001c0009 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.1860G>A | p.Thr620Thr | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/24 | 1995/5971 | 1860/2499 | 620/832 | chr13 | 52065599 | |||
| chr13:52093092 | G | A | 1 | a0001c0003 | 9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
synonymous_variant | LOW | c.1170C>T | p.Tyr390Tyr | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/24 | 1305/5971 | 1170/2499 | 390/832 | chr13 | 52093092 | |||
| chr13:52099833 | T | C | 1 | a0001c0013 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.936A>G | p.Pro312Pro | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/24 | 1071/5971 | 936/2499 | 312/832 | chr13 | 52099833 | |||
| chr13:52101943 | C | T | 1 | a0001c0004 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.882G>A | p.Lys294Lys | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/24 | 1017/5971 | 882/2499 | 294/832 | chr13 | 52101943 | |||
| chr13:52127450 | C | A | 1 | a0001c0016 | 1 | NA18974.hp2 | synonymous_variant | LOW | c.33G>T | p.Gly11Gly | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/24 | 168/5971 | 33/2499 | 11/832 | chr13 | 52127450 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52033618 | T | C | 1 | a0001c0001t0035 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3330A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 3330 | chr13 | 52033618 | ||||||
| chr13:52033730 | A | T | 40 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(37): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*3218T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 3218 | chr13 | 52033730 | ||||||
| chr13:52034169 | A | T | 2 | a0002c0002t0050 a0002c0002t0051 |
2 | HG01074.hp2 HG01891.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2779T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2779 | chr13 | 52034169 | ||||||
| chr13:52034348 | A | G | 1 | a0001c0001t0044 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2600T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2600 | chr13 | 52034348 | ||||||
| chr13:52034436 | T | C | 1 | a0007c0011t0042 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2512A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2512 | chr13 | 52034436 | ||||||
| chr13:52034504 | C | CT | 13 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0012 others(10): Show |
28 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2443dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2443 | chr13 | 52034504 | ||||||
| chr13:52034504 | C | T | 1 | a0001c0001t0024 | 2 | HG02809.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2444G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2444 | chr13 | 52034504 | ||||||
| chr13:52034504 | CT | C | 5 | a0001c0001t0011 a0001c0001t0038 a0001c0001t0053 others(2): Show |
8 | HG00639.hp1 HG01257.hp1 HG01891.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2443delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2443 | chr13 | 52034504 | ||||||
| chr13:52034564 | A | G | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(20): Show |
128 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*2384T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2384 | chr13 | 52034564 | ||||||
| chr13:52034659 | T | C | 2 | a0001c0001t0016 a0001c0001t0061 |
5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2289A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2289 | chr13 | 52034659 | ||||||
| chr13:52034695 | C | CT | 5 | a0001c0001t0016 a0001c0001t0036 a0001c0001t0037 others(2): Show |
8 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2252dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2252 | chr13 | 52034695 | ||||||
| chr13:52034695 | C | CTT | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(14): Show |
112 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2251_*2252dupAA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2252 | chr13 | 52034695 | ||||||
| chr13:52034695 | CT | C | 4 | a0001c0001t0017 a0001c0001t0038 a0001c0001t0041 others(1): Show |
9 | HG00544.hp1 HG03209.hp1 HG03831.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2252delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2252 | chr13 | 52034695 | ||||||
| chr13:52034799 | A | T | 1 | a0001c0001t0021 | 3 | HG00323.hp2 HG02602.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2149T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2149 | chr13 | 52034799 | ||||||
| chr13:52034881 | C | CT | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(19): Show |
120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*2066dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2066 | chr13 | 52034881 | ||||||
| chr13:52034881 | C | CTT | 4 | a0001c0001t0020 a0001c0001t0056 a0001c0001t0057 others(1): Show |
6 | HG01346.hp2 HG03710.hp1 NA18972.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2065_*2066dupAA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2066 | chr13 | 52034881 | ||||||
| chr13:52034881 | CT | C | 8 | a0001c0001t0006 a0001c0001t0026 a0001c0001t0039 others(5): Show |
18 | HG01109.hp1 HG01169.hp1 HG01243.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2066delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2066 | chr13 | 52034881 | ||||||
| chr13:52034881 | CTTTTTTT others(3): Show |
C | 1 | a0007c0011t0042 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2057_*2066delAAAA others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 2057 | chr13 | 52034881 | ||||||
| chr13:52034993 | A | G | 1 | a0001c0001t0022 | 3 | HG02451.hp1 HG03225.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1955T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1955 | chr13 | 52034993 | ||||||
| chr13:52035057 | G | T | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(32): Show |
165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*1891C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1891 | chr13 | 52035057 | ||||||
| chr13:52035067 | AAG | A | 2 | a0001c0001t0012 a0001c0001t0043 |
5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1879_*1880delCT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1879 | chr13 | 52035067 | ||||||
| chr13:52035072 | T | C | 4 | a0001c0001t0003 a0001c0001t0029 a0001c0001t0055 others(1): Show |
26 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1876A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1876 | chr13 | 52035072 | ||||||
| chr13:52035142 | T | C | 2 | a0003c0005t0027 a0003c0005t0054 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1806A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1806 | chr13 | 52035142 | ||||||
| chr13:52035240 | A | C | 1 | a0001c0001t0031 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1708T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1708 | chr13 | 52035240 | ||||||
| chr13:52035247 | AAT | A | 1 | a0001c0001t0006 | 8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1699_*1700delAT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1699 | chr13 | 52035247 | ||||||
| chr13:52035268 | G | A | 1 | a0001c0004t0019 | 3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1680C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1680 | chr13 | 52035268 | ||||||
| chr13:52035304 | A | T | 1 | a0001c0001t0055 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1644T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1644 | chr13 | 52035304 | ||||||
| chr13:52035431 | C | A | 2 | a0001c0001t0018 a0001c0001t0044 |
3 | HG03017.hp1 HG03490.hp1 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1517G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1517 | chr13 | 52035431 | ||||||
| chr13:52035540 | T | C | 1 | a0001c0001t0045 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1408A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1408 | chr13 | 52035540 | ||||||
| chr13:52035579 | T | A | 1 | a0001c0001t0060 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1369A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1369 | chr13 | 52035579 | ||||||
| chr13:52035779 | T | C | 21 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(18): Show |
119 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1169A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 1169 | chr13 | 52035779 | ||||||
| chr13:52036047 | C | CA | 2 | a0001c0001t0016 a0001c0001t0061 |
5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*900dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 900 | chr13 | 52036047 | ||||||
| chr13:52036656 | C | T | 1 | a0001c0001t0047 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*292G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 292 | chr13 | 52036656 | ||||||
| chr13:52036787 | T | C | 1 | a0001c0001t0062 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*161A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 161 | chr13 | 52036787 | ||||||
| chr13:52036792 | A | G | 1 | a0001c0001t0030 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*156T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 24/24 | 156 | chr13 | 52036792 | ||||||
| chr13:52127501 | T | G | 38 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(35): Show |
174 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
5_prime_UTR_variant | MODIFIER | c.-19A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/24 | 19 | chr13 | 52127501 | ||||||
| chr13:52127646 | T | C | 38 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(35): Show |
174 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
5_prime_UTR_variant | MODIFIER | c.-74A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 2/24 | 164 | chr13 | 52127646 | ||||||
| chr13:52127647 | T | C | 1 | a0001c0001t0022 | 3 | HG02451.hp1 HG03225.hp2 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-75A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 2/24 | 165 | chr13 | 52127647 | ||||||
| chr13:52129061 | G | T | 1 | a0001c0001t0023 | 2 | HG02615.hp2 HG02622.hp2 |
5_prime_UTR_variant | MODIFIER | c.-123C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/24 | 1579 | chr13 | 52129061 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52037550 | C | G | 4 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 others(1): Show |
4 | HG01192.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2229-332G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037550 | |||||||
| chr13:52037671 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0008g0034 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2229-453G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037671 | |||||||
| chr13:52037694 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2229-476G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037694 | |||||||
| chr13:52037705 | C | T | 1 | a0001c0001t0002g0241 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2229-487G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037705 | |||||||
| chr13:52037816 | G | A | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2229-598C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037816 | |||||||
| chr13:52037922 | C | CA | 18 | a0001c0001t0002g0007 a0001c0001t0002g0195 a0001c0001t0002g0255 others(15): Show |
20 | HG01106.hp2 HG01109.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2229-705dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037922 | |||||||
| chr13:52037922 | C | CAA | 104 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0171 others(101): Show |
109 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.2229-706_2229-705d others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52037922 | |||||||
| chr13:52038054 | A | G | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2229-836T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038054 | |||||||
| chr13:52038170 | C | CAAAAAAT others(1): Show |
35 | a0001c0001t0004g0270 a0001c0001t0026g0013 a0001c0001t0052g0315 others(32): Show |
36 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.2229-960_2229-953d others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038170 | |||||||
| chr13:52038488 | G | T | 1 | a0010c0015t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2229-1270C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038488 | |||||||
| chr13:52038531 | T | C | 1 | a0001c0001t0015g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2229-1313A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038531 | |||||||
| chr13:52038592 | C | T | 1 | a0001c0001t0037g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2229-1374G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038592 | |||||||
| chr13:52038823 | C | T | 35 | a0001c0001t0004g0270 a0001c0001t0026g0013 a0001c0001t0052g0315 others(32): Show |
36 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.2229-1605G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038823 | |||||||
| chr13:52038824 | T | TA | 2 | a0001c0001t0026g0013 a0001c0001t0052g0315 |
3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2229-1607_2229-160 others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038824 | |||||||
| chr13:52038825 | G | A | 35 | a0001c0001t0004g0270 a0001c0001t0026g0013 a0001c0001t0052g0315 others(32): Show |
36 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.2229-1607C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038825 | |||||||
| chr13:52038825 | G | GA | 34 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0001g0088 others(31): Show |
36 | HG00544.hp2 HG00609.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.2229-1608dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038825 | |||||||
| chr13:52038825 | G | GAAA | 7 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0173 others(4): Show |
7 | HG00544.hp1 HG01099.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2229-1610_2229-160 others(7): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038825 | |||||||
| chr13:52038825 | G | GAAAA | 95 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0171 others(92): Show |
100 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.2229-1611_2229-160 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038825 | |||||||
| chr13:52038825 | G | GAAAAA | 18 | a0001c0001t0002g0007 a0001c0001t0002g0195 a0001c0001t0002g0215 others(15): Show |
19 | HG01106.hp2 HG01358.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2229-1612_2229-160 others(9): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038825 | |||||||
| chr13:52038826 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0008g0096 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2229-1608T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038826 | |||||||
| chr13:52038839 | A | C | 33 | a0001c0001t0004g0270 a0002c0002t0004g0175 a0002c0002t0004g0176 others(30): Show |
33 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.2229-1621T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52038839 | |||||||
| chr13:52039079 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2229-1861G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039079 | |||||||
| chr13:52039138 | G | A | 158 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(155): Show |
165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2229-1920C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039138 | |||||||
| chr13:52039201 | G | A | 33 | a0001c0001t0004g0270 a0002c0002t0004g0175 a0002c0002t0004g0176 others(30): Show |
33 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.2229-1983C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039201 | |||||||
| chr13:52039516 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2229-2298A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039516 | |||||||
| chr13:52039823 | T | TATAATTT others(12): Show |
1 | a0001c0001t0001g0148 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2229-2606_2229-260 others(23): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039823 | |||||||
| chr13:52039879 | C | T | 2 | a0001c0001t0031g0054 a0010c0015t0001g0056 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2229-2661G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039879 | |||||||
| chr13:52039982 | G | A | 4 | a0001c0001t0012g0003 a0001c0001t0012g0038 a0001c0001t0012g0039 others(1): Show |
5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2229-2764C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039982 | |||||||
| chr13:52039996 | T | A | 1 | a0001c0001t0002g0220 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2229-2778A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52039996 | |||||||
| chr13:52040081 | C | CT | 12 | a0001c0001t0001g0048 a0001c0001t0001g0131 a0001c0001t0001g0164 others(9): Show |
12 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2229-2864dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040081 | |||||||
| chr13:52040081 | CT | C | 26 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0081 others(23): Show |
28 | HG01069.hp1 HG01081.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.2229-2864delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040081 | |||||||
| chr13:52040081 | CTT | C | 116 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(113): Show |
122 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.2229-2865_2229-286 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040081 | |||||||
| chr13:52040081 | CTTT | C | 9 | a0001c0001t0002g0209 a0001c0001t0002g0237 a0001c0001t0015g0230 others(6): Show |
9 | HG00642.hp2 HG01167.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.2229-2866_2229-286 others(7): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040081 | |||||||
| chr13:52040081 | CTTTT | C | 30 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(27): Show |
31 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.2229-2867_2229-286 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040081 | |||||||
| chr13:52040532 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2229-3314A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040532 | |||||||
| chr13:52040662 | A | G | 114 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(111): Show |
120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2229-3444T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040662 | |||||||
| chr13:52040815 | G | A | 114 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(111): Show |
120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2229-3597C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52040815 | |||||||
| chr13:52041076 | C | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(314): Show |
331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.2229-3858G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041076 | |||||||
| chr13:52041080 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2229-3862T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041080 | |||||||
| chr13:52041438 | A | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0049 |
2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2229-4220T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041438 | |||||||
| chr13:52041726 | C | A | 1 | a0001c0001t0011g0205 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2229-4508G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041726 | |||||||
| chr13:52041728 | C | CA | 55 | a0001c0001t0001g0080 a0001c0001t0001g0092 a0001c0001t0001g0097 others(52): Show |
56 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.2229-4511dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | |||||||
| chr13:52041728 | C | CAA | 13 | a0001c0001t0001g0108 a0001c0001t0002g0203 a0001c0001t0002g0225 others(10): Show |
14 | HG01192.hp2 HG01243.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.2229-4512_2229-451 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | |||||||
| chr13:52041728 | C | CAAA | 91 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(88): Show |
97 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.2229-4513_2229-451 others(7): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | |||||||
| chr13:52041728 | C | CAAAA | 20 | a0001c0001t0002g0215 a0001c0001t0002g0221 a0001c0001t0002g0222 others(17): Show |
20 | HG00099.hp1 HG01261.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.2229-4514_2229-451 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | |||||||
| chr13:52041728 | C | CAAAAAAA others(3): Show |
3 | a0001c0004t0019g0299 a0001c0004t0019g0300 a0001c0010t0048g0290 |
3 | HG02896.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2229-4520_2229-451 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | |||||||
| chr13:52041728 | C | CAAAAAAA others(4): Show |
1 | a0001c0004t0019g0298 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2229-4521_2229-451 others(15): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | |||||||
| chr13:52041728 | CA | C | 11 | a0001c0001t0001g0112 a0001c0001t0001g0116 a0001c0001t0001g0131 others(8): Show |
12 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2229-4511delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | |||||||
| chr13:52041728 | CAA | C | 9 | a0001c0001t0001g0155 a0001c0001t0061g0302 a0001c0003t0010g0022 others(6): Show |
9 | HG00544.hp1 HG02486.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2229-4512_2229-451 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041728 | |||||||
| chr13:52041771 | AAAG | A | 4 | a0001c0001t0012g0003 a0001c0001t0012g0038 a0001c0001t0012g0039 others(1): Show |
5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2229-4556_2229-455 others(7): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041771 | |||||||
| chr13:52041825 | A | C | 1 | a0001c0001t0006g0030 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2229-4607T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041825 | |||||||
| chr13:52041830 | A | C | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2229-4612T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041830 | |||||||
| chr13:52041854 | T | C | 1 | a0001c0001t0038g0119 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2229-4636A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041854 | |||||||
| chr13:52041975 | A | T | 1 | a0001c0001t0003g0217 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2229-4757T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041975 | |||||||
| chr13:52041999 | T | C | 1 | a0009c0008t0009g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2229-4781A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52041999 | |||||||
| chr13:52042098 | T | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2229-4880A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042098 | |||||||
| chr13:52042292 | C | T | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2229-5074G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042292 | |||||||
| chr13:52042349 | G | A | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2229-5131C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042349 | |||||||
| chr13:52042373 | T | C | 2 | a0001c0001t0002g0291 a0001c0001t0002g0292 |
2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.2229-5155A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042373 | |||||||
| chr13:52042440 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2229-5222T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042440 | |||||||
| chr13:52042470 | CA | C | 114 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(111): Show |
120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2229-5253delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042470 | |||||||
| chr13:52042566 | T | C | 1 | a0001c0001t0034g0136 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2229-5348A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042566 | |||||||
| chr13:52042835 | G | A | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2229-5617C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042835 | |||||||
| chr13:52042921 | A | C | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2229-5703T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52042921 | |||||||
| chr13:52043071 | G | T | 30 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(27): Show |
30 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.2229-5853C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043071 | |||||||
| chr13:52043261 | G | A | 3 | a0001c0001t0012g0038 a0001c0001t0015g0200 a0001c0001t0043g0037 |
3 | HG02615.hp1 HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2229-6043C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043261 | |||||||
| chr13:52043536 | C | CA | 14 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0002g0255 others(11): Show |
14 | HG00544.hp1 HG01099.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2229-6319dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043536 | |||||||
| chr13:52043546 | AAAAAAGA others(3): Show |
A | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2229-6338_2229-632 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043546 | |||||||
| chr13:52043548 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2229-6330T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043548 | |||||||
| chr13:52043563 | A | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0169 a0001c0001t0017g0104 |
3 | HG02735.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2229-6345T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043563 | |||||||
| chr13:52043573 | GA | G | 7 | a0001c0001t0002g0009 a0001c0001t0002g0231 a0001c0001t0002g0235 others(4): Show |
8 | HG02071.hp2 NA18942.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.2229-6356delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043573 | |||||||
| chr13:52043925 | T | C | 2 | a0001c0003t0010g0173 a0001c0003t0010g0174 |
2 | HG06807.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2228+6179A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52043925 | |||||||
| chr13:52044054 | G | A | 34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.2228+6050C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044054 | |||||||
| chr13:52044075 | G | A | 165 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(162): Show |
173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.2228+6029C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044075 | |||||||
| chr13:52044274 | C | A | 4 | a0001c0001t0002g0010 a0001c0001t0002g0253 a0001c0001t0007g0239 others(1): Show |
5 | NA18969.hp1 NA18983.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.2228+5830G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044274 | |||||||
| chr13:52044366 | C | T | 2 | a0001c0001t0002g0243 a0001c0001t0002g0287 |
2 | HG02083.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2228+5738G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044366 | |||||||
| chr13:52044440 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2228+5664A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044440 | |||||||
| chr13:52044490 | G | A | 1 | a0001c0001t0035g0127 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2228+5614C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044490 | |||||||
| chr13:52044661 | T | C | 123 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(120): Show |
129 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.2228+5443A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044661 | |||||||
| chr13:52044742 | C | A | 183 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(180): Show |
192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.2228+5362G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52044742 | |||||||
| chr13:52045105 | A | G | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2228+4999T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045105 | |||||||
| chr13:52045130 | C | CT | 158 | a0001c0001t0001g0090 a0001c0001t0001g0164 a0001c0001t0002g0007 others(155): Show |
166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.2228+4973dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045130 | |||||||
| chr13:52045130 | C | CTT | 14 | a0001c0001t0002g0215 a0001c0001t0002g0236 a0001c0001t0002g0241 others(11): Show |
15 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.2228+4972_2228+497 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045130 | |||||||
| chr13:52045200 | G | GCTCACTG others(15): Show |
2 | a0001c0001t0008g0063 a0001c0001t0008g0064 |
2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.2228+4882_2228+490 others(26): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045200 | |||||||
| chr13:52045291 | G | A | 2 | a0001c0001t0023g0014 a0001c0001t0023g0015 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2228+4813C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045291 | |||||||
| chr13:52045332 | G | T | 8 | a0001c0001t0002g0007 a0001c0001t0002g0195 a0001c0001t0002g0255 others(5): Show |
9 | HG01106.hp2 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2228+4772C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045332 | |||||||
| chr13:52045407 | G | A | 1 | a0001c0001t0012g0003 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.2228+4697C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045407 | |||||||
| chr13:52045468 | A | G | 8 | a0001c0001t0002g0007 a0001c0001t0002g0195 a0001c0001t0002g0255 others(5): Show |
9 | HG01106.hp2 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2228+4636T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045468 | |||||||
| chr13:52045500 | G | T | 1 | a0002c0002t0004g0177 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2228+4604C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045500 | |||||||
| chr13:52045581 | A | C | 165 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(162): Show |
173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.2228+4523T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045581 | |||||||
| chr13:52045634 | C | G | 1 | a0001c0001t0001g0102 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2228+4470G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045634 | |||||||
| chr13:52045657 | C | T | 3 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2228+4447G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045657 | |||||||
| chr13:52045714 | A | G | 175 | a0001c0001t0001g0051 a0001c0001t0002g0007 a0001c0001t0002g0009 others(172): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.2228+4390T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045714 | |||||||
| chr13:52045764 | C | CA | 12 | a0001c0001t0001g0100 a0001c0001t0001g0110 a0001c0001t0001g0164 others(9): Show |
12 | HG01943.hp1 HG02258.hp1 HG03130.hp1 others(9): Show |
intron_variant | MODIFIER | c.2228+4339dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045764 | |||||||
| chr13:52045764 | CA | C | 113 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0154 others(110): Show |
119 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.2228+4339delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045764 | |||||||
| chr13:52045873 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+4231G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045873 | |||||||
| chr13:52045933 | C | T | 173 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(170): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.2228+4171G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52045933 | |||||||
| chr13:52046047 | GGCAACAG others(1): Show |
G | 5 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2228+4049_2228+405 others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046047 | |||||||
| chr13:52046070 | C | CA | 9 | a0001c0001t0001g0051 a0001c0001t0002g0229 a0001c0001t0002g0233 others(6): Show |
9 | HG00673.hp1 HG01123.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.2228+4033dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046070 | |||||||
| chr13:52046295 | G | A | 3 | a0001c0010t0048g0290 a0002c0002t0004g0190 a0002c0002t0049g0189 |
3 | HG00621.hp1 HG02132.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2228+3809C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046295 | |||||||
| chr13:52046297 | C | A | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2228+3807G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046297 | |||||||
| chr13:52046340 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0008g0044 |
2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2228+3764C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046340 | |||||||
| chr13:52046349 | T | C | 6 | a0001c0001t0002g0010 a0001c0001t0002g0221 a0001c0001t0002g0253 others(3): Show |
7 | NA18969.hp1 NA18973.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.2228+3755A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046349 | |||||||
| chr13:52046351 | C | T | 1 | a0001c0001t0007g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2228+3753G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046351 | |||||||
| chr13:52046481 | T | TA | 36 | a0001c0001t0001g0158 a0001c0001t0026g0013 a0001c0001t0052g0315 others(33): Show |
37 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.2228+3622dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046481 | |||||||
| chr13:52046481 | T | TAAAAAAA others(298): Show |
1 | a0001c0001t0031g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2228+3622_2228+362 others(309): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046481 | |||||||
| chr13:52046481 | T | TAAAAAAA others(300): Show |
1 | a0010c0015t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2228+3622_2228+362 others(311): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046481 | |||||||
| chr13:52046481 | TA | T | 10 | a0001c0001t0001g0115 a0001c0001t0001g0138 a0001c0001t0001g0139 others(7): Show |
10 | HG01168.hp2 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.2228+3622delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046481 | |||||||
| chr13:52046526 | C | T | 1 | a0001c0001t0058g0284 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2228+3578G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046526 | |||||||
| chr13:52046616 | G | A | 158 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(155): Show |
165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2228+3488C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046616 | |||||||
| chr13:52046622 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+3482A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046622 | |||||||
| chr13:52046712 | T | C | 1 | a0001c0003t0010g0022 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2228+3392A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046712 | |||||||
| chr13:52046731 | A | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0135 a0001c0001t0001g0163 |
3 | NA18948.hp1 NA18956.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2228+3373T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52046731 | |||||||
| chr13:52047111 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2993T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047111 | |||||||
| chr13:52047113 | G | GACAACAC others(14): Show |
1 | a0001c0001t0001g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2990_2228+299 others(25): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047113 | |||||||
| chr13:52047115 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2989C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047115 | |||||||
| chr13:52047117 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2987T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047117 | |||||||
| chr13:52047120 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2984A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047120 | |||||||
| chr13:52047124 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2980G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047124 | |||||||
| chr13:52047127 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2228+2977A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047127 | |||||||
| chr13:52047208 | G | A | 1 | a0002c0002t0004g0187 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2228+2896C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047208 | |||||||
| chr13:52047296 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2228+2808T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047296 | |||||||
| chr13:52047697 | C | A | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+2407G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047697 | |||||||
| chr13:52047744 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2228+2360A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047744 | |||||||
| chr13:52047995 | G | A | 34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.2228+2109C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52047995 | |||||||
| chr13:52048090 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2228+2014C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048090 | |||||||
| chr13:52048290 | A | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1814T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048290 | |||||||
| chr13:52048303 | G | A | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1801C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048303 | |||||||
| chr13:52048304 | G | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1800C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048304 | |||||||
| chr13:52048306 | T | A | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1798A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048306 | |||||||
| chr13:52048317 | A | G | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1787T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048317 | |||||||
| chr13:52048318 | T | A | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1786A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048318 | |||||||
| chr13:52048319 | C | A | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1785G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048319 | |||||||
| chr13:52048320 | C | G | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1784G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048320 | |||||||
| chr13:52048378 | C | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1726G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048378 | |||||||
| chr13:52048379 | C | A | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1725G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048379 | |||||||
| chr13:52048387 | C | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1717G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048387 | |||||||
| chr13:52048414 | A | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1690T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048414 | |||||||
| chr13:52048415 | A | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1689T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048415 | |||||||
| chr13:52048418 | A | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1686T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048418 | |||||||
| chr13:52048419 | A | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1685T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048419 | |||||||
| chr13:52048420 | T | A | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1684A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048420 | |||||||
| chr13:52048424 | A | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1680T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048424 | |||||||
| chr13:52048428 | A | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1676T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048428 | |||||||
| chr13:52048489 | T | C | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2228+1615A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048489 | |||||||
| chr13:52048640 | G | A | 1 | a0001c0001t0012g0039 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2228+1464C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048640 | |||||||
| chr13:52048779 | C | A | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2228+1325G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048779 | |||||||
| chr13:52048945 | A | ATTGTATA others(6): Show |
1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1158_2228+115 others(17): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048945 | |||||||
| chr13:52048967 | A | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1137T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048967 | |||||||
| chr13:52048969 | A | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1135T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048969 | |||||||
| chr13:52048996 | A | C | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1108T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048996 | |||||||
| chr13:52048998 | A | G | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1106T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52048998 | |||||||
| chr13:52049000 | A | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1104T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049000 | |||||||
| chr13:52049008 | C | A | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+1096G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049008 | |||||||
| chr13:52049015 | C | G | 182 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(179): Show |
191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.2228+1089G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049015 | |||||||
| chr13:52049155 | G | C | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+949C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049155 | |||||||
| chr13:52049156 | C | G | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+948G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049156 | |||||||
| chr13:52049200 | A | G | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+904T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049200 | |||||||
| chr13:52049267 | A | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+837T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049267 | |||||||
| chr13:52049348 | C | A | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+756G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049348 | |||||||
| chr13:52049349 | A | G | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+755T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049349 | |||||||
| chr13:52049350 | G | A | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+754C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049350 | |||||||
| chr13:52049352 | A | G | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+752T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049352 | |||||||
| chr13:52049385 | C | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+719G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049385 | |||||||
| chr13:52049414 | G | A | 2 | a0001c0001t0002g0214 a0001c0001t0004g0270 |
2 | HG00639.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2228+690C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049414 | |||||||
| chr13:52049533 | C | T | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2228+571G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049533 | |||||||
| chr13:52049550 | A | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+554T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049550 | |||||||
| chr13:52049562 | A | T | 1 | a0001c0001t0056g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2228+542T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 23/23 | chr13 | 52049562 | |||||||
| chr13:52050364 | T | C | 2 | a0001c0001t0036g0035 a0001c0001t0037g0128 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2111-143A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050364 | |||||||
| chr13:52050611 | C | CT | 159 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0161 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2111-391dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050611 | |||||||
| chr13:52050611 | C | CTT | 6 | a0001c0001t0002g0199 a0001c0001t0012g0038 a0001c0001t0020g0223 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2111-392_2111-391d others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050611 | |||||||
| chr13:52050720 | C | CT | 16 | a0001c0001t0001g0160 a0001c0001t0002g0265 a0001c0001t0011g0240 others(13): Show |
16 | HG00544.hp1 HG01099.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.2111-500dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050720 | |||||||
| chr13:52050720 | CT | C | 10 | a0001c0001t0001g0041 a0001c0001t0001g0083 a0001c0001t0001g0154 others(7): Show |
11 | HG01074.hp2 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2111-500delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050720 | |||||||
| chr13:52050729 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2111-508A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050729 | |||||||
| chr13:52050865 | A | G | 1 | a0001c0001t0003g0211 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2111-644T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050865 | |||||||
| chr13:52050970 | G | A | 1 | a0001c0001t0006g0032 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2111-749C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52050970 | |||||||
| chr13:52051021 | G | C | 2 | a0001c0001t0026g0013 a0001c0001t0052g0315 |
3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2111-800C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051021 | |||||||
| chr13:52051059 | G | A | 159 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2111-838C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051059 | |||||||
| chr13:52051062 | CT | C | 149 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(146): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.2111-842delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051062 | |||||||
| chr13:52051105 | A | G | 2 | a0001c0001t0002g0214 a0001c0001t0004g0270 |
2 | HG00639.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2111-884T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051105 | |||||||
| chr13:52051131 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2111-910C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051131 | |||||||
| chr13:52051227 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2111-1006A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051227 | |||||||
| chr13:52051264 | A | T | 1 | a0001c0001t0011g0205 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2111-1043T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051264 | |||||||
| chr13:52051335 | C | T | 199 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0046 others(196): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2111-1114G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051335 | |||||||
| chr13:52051508 | G | A | 5 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2111-1287C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051508 | |||||||
| chr13:52051684 | C | T | 3 | a0001c0001t0021g0226 a0001c0001t0021g0227 a0001c0001t0021g0285 |
3 | HG00323.hp2 HG02602.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2111-1463G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52051684 | |||||||
| chr13:52052045 | C | A | 159 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2111-1824G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052045 | |||||||
| chr13:52052201 | G | T | 29 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(26): Show |
29 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.2111-1980C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052201 | |||||||
| chr13:52052209 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2111-1988A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052209 | |||||||
| chr13:52052400 | C | A | 1 | a0001c0001t0001g0143 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2111-2179G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052400 | |||||||
| chr13:52052507 | C | T | 184 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.2111-2286G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052507 | |||||||
| chr13:52052811 | C | A | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2111-2590G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052811 | |||||||
| chr13:52052820 | T | G | 2 | a0001c0001t0001g0051 a0001c0001t0030g0045 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2111-2599A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52052820 | |||||||
| chr13:52053039 | A | G | 174 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(171): Show |
182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.2111-2818T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053039 | |||||||
| chr13:52053099 | A | G | 159 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2111-2878T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053099 | |||||||
| chr13:52053173 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2111-2952G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053173 | |||||||
| chr13:52053260 | C | T | 4 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 others(1): Show |
4 | HG01192.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2111-3039G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053260 | |||||||
| chr13:52053582 | C | CT | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2111-3362dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053582 | |||||||
| chr13:52053616 | C | A | 1 | a0001c0001t0002g0268 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2111-3395G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053616 | |||||||
| chr13:52053686 | C | T | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2111-3465G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053686 | |||||||
| chr13:52053938 | T | C | 174 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(171): Show |
182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.2111-3717A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52053938 | |||||||
| chr13:52054292 | G | A | 11 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 others(8): Show |
11 | HG01069.hp2 HG01255.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2111-4071C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054292 | |||||||
| chr13:52054369 | G | A | 1 | a0001c0001t0020g0308 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2111-4148C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054369 | |||||||
| chr13:52054455 | G | T | 1 | a0001c0004t0019g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2111-4234C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054455 | |||||||
| chr13:52054516 | A | G | 149 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(146): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.2111-4295T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054516 | |||||||
| chr13:52054587 | C | T | 5 | a0001c0001t0001g0166 a0001c0001t0012g0003 a0001c0001t0012g0038 others(2): Show |
6 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2111-4366G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054587 | |||||||
| chr13:52054608 | A | G | 1 | a0001c0001t0002g0283 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2111-4387T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054608 | |||||||
| chr13:52054613 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2111-4392C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054613 | |||||||
| chr13:52054669 | G | A | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2111-4448C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054669 | |||||||
| chr13:52054679 | G | A | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2111-4458C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054679 | |||||||
| chr13:52054682 | G | C | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2111-4461C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054682 | |||||||
| chr13:52054688 | G | C | 2 | a0001c0001t0003g0012 a0001c0001t0017g0314 |
3 | HG03491.hp2 HG03492.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.2111-4467C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054688 | |||||||
| chr13:52054707 | C | A | 1 | a0001c0001t0003g0012 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2111-4486G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054707 | |||||||
| chr13:52054713 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2111-4492G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054713 | |||||||
| chr13:52054791 | C | T | 3 | a0001c0001t0002g0225 a0001c0001t0002g0229 a0001c0001t0002g0234 |
3 | HG01192.hp2 HG01433.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.2111-4570G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054791 | |||||||
| chr13:52054868 | T | G | 1 | a0001c0001t0002g0214 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2111-4647A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054868 | |||||||
| chr13:52054878 | A | G | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2111-4657T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054878 | |||||||
| chr13:52054890 | A | G | 1 | a0001c0001t0007g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2111-4669T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054890 | |||||||
| chr13:52054911 | C | T | 1 | a0005c0014t0004g0297 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2111-4690G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054911 | |||||||
| chr13:52054946 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0009g0052 |
3 | HG02109.hp1 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2111-4725C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054946 | |||||||
| chr13:52054962 | A | G | 3 | a0001c0001t0015g0197 a0001c0001t0020g0277 a0001c0001t0056g0282 |
3 | HG02074.hp1 NA19065.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.2111-4741T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054962 | |||||||
| chr13:52054987 | G | A | 30 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(27): Show |
30 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.2111-4766C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52054987 | |||||||
| chr13:52055142 | C | T | 1 | a0001c0001t0003g0288 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2111-4921G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055142 | |||||||
| chr13:52055170 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2111-4949C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055170 | |||||||
| chr13:52055188 | G | A | 1 | a0001c0001t0012g0039 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2111-4967C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055188 | |||||||
| chr13:52055287 | T | C | 1 | a0001c0001t0061g0302 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2111-5066A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055287 | |||||||
| chr13:52055292 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0030g0045 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2111-5071C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055292 | |||||||
| chr13:52055319 | C | A | 5 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2111-5098G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055319 | |||||||
| chr13:52055344 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2111-5123C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055344 | |||||||
| chr13:52055419 | C | A | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2111-5198G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055419 | |||||||
| chr13:52055468 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2111-5247C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055468 | |||||||
| chr13:52055508 | A | G | 4 | a0001c0003t0013g0021 a0001c0003t0013g0024 a0001c0003t0013g0025 others(1): Show |
4 | HG00544.hp1 NA18994.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2111-5287T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055508 | |||||||
| chr13:52055593 | T | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0159 a0001c0001t0001g0160 others(3): Show |
6 | HG02258.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2111-5372A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055593 | |||||||
| chr13:52055634 | G | GGCCAATA others(3178): Show |
2 | a0001c0001t0001g0041 a0006c0007t0001g0055 |
2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2111-5414_2111-541 others(3189): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055634 | |||||||
| chr13:52055821 | C | T | 41 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0171 others(38): Show |
43 | HG00597.hp1 HG00621.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2111-5600G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055821 | |||||||
| chr13:52055832 | A | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(16): Show |
21 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.2111-5611T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055832 | |||||||
| chr13:52055865 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2111-5644C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52055865 | |||||||
| chr13:52056068 | A | G | 2 | a0001c0001t0001g0041 a0006c0007t0001g0055 |
2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2110+5751T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056068 | |||||||
| chr13:52056123 | A | G | 2 | a0001c0001t0003g0259 a0001c0001t0029g0258 |
2 | NA18956.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2110+5696T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056123 | |||||||
| chr13:52056291 | A | G | 4 | a0001c0001t0016g0301 a0001c0001t0016g0304 a0001c0001t0016g0305 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2110+5528T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056291 | |||||||
| chr13:52056330 | T | A | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2110+5489A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056330 | |||||||
| chr13:52056378 | G | A | 1 | a0001c0001t0012g0039 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2110+5441C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056378 | |||||||
| chr13:52056388 | C | T | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2110+5431G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056388 | |||||||
| chr13:52056389 | G | A | 3 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2110+5430C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056389 | |||||||
| chr13:52056399 | A | G | 2 | a0002c0002t0050g0317 a0002c0002t0051g0316 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2110+5420T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056399 | |||||||
| chr13:52056560 | C | A | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2110+5259G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056560 | |||||||
| chr13:52056652 | A | G | 2 | a0003c0005t0027g0318 a0003c0005t0027g0319 |
2 | HG01192.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2110+5167T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056652 | |||||||
| chr13:52056655 | G | A | 161 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(158): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2110+5164C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056655 | |||||||
| chr13:52056668 | G | A | 1 | a0001c0001t0007g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2110+5151C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056668 | |||||||
| chr13:52056677 | C | A | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2110+5142G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056677 | |||||||
| chr13:52056698 | G | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0107 others(2): Show |
7 | HG00408.hp1 HG01192.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2110+5121C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056698 | |||||||
| chr13:52056744 | C | A | 174 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(171): Show |
182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.2110+5075G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056744 | |||||||
| chr13:52056783 | G | A | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2110+5036C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056783 | |||||||
| chr13:52056786 | G | A | 4 | a0001c0001t0011g0240 a0003c0005t0027g0318 a0003c0005t0027g0319 others(1): Show |
4 | HG01192.hp1 HG01952.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2110+5033C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056786 | |||||||
| chr13:52056876 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2110+4943A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056876 | |||||||
| chr13:52056928 | C | G | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2110+4891G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056928 | |||||||
| chr13:52056928 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2110+4891G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056928 | |||||||
| chr13:52056929 | G | A | 2 | a0001c0001t0003g0257 a0001c0001t0003g0288 |
2 | HG01981.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2110+4890C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52056929 | |||||||
| chr13:52057125 | A | G | 156 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(153): Show |
163 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2110+4694T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057125 | |||||||
| chr13:52057284 | T | G | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2110+4535A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057284 | |||||||
| chr13:52057352 | C | T | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2110+4467G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057352 | |||||||
| chr13:52057446 | T | G | 2 | a0001c0001t0001g0033 a0001c0001t0008g0034 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2110+4373A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057446 | |||||||
| chr13:52057463 | C | T | 32 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(29): Show |
32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.2110+4356G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057463 | |||||||
| chr13:52057783 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2110+4036C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057783 | |||||||
| chr13:52057980 | A | G | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2110+3839T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52057980 | |||||||
| chr13:52058023 | C | T | 1 | a0001c0001t0043g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2110+3796G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058023 | |||||||
| chr13:52058110 | G | C | 1 | a0001c0001t0002g0264 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2110+3709C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058110 | |||||||
| chr13:52058149 | A | C | 2 | a0001c0001t0026g0013 a0001c0001t0052g0315 |
3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2110+3670T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058149 | |||||||
| chr13:52058202 | A | T | 1 | a0001c0001t0031g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2110+3617T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058202 | |||||||
| chr13:52058257 | A | G | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2110+3562T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058257 | |||||||
| chr13:52058329 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2110+3490A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058329 | |||||||
| chr13:52058331 | T | C | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2110+3488A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058331 | |||||||
| chr13:52058484 | T | C | 1 | a0009c0008t0009g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2110+3335A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058484 | |||||||
| chr13:52058591 | C | G | 1 | a0001c0003t0013g0026 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2110+3228G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058591 | |||||||
| chr13:52058659 | A | G | 3 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2110+3160T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058659 | |||||||
| chr13:52058720 | T | C | 1 | a0001c0001t0002g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2110+3099A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058720 | |||||||
| chr13:52058768 | G | A | 1 | a0001c0003t0010g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2110+3051C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058768 | |||||||
| chr13:52058782 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0162 |
2 | HG02155.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2110+3037A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058782 | |||||||
| chr13:52058825 | C | T | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.2110+2994G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058825 | |||||||
| chr13:52058829 | A | G | 1 | a0002c0002t0005g0065 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2110+2990T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058829 | |||||||
| chr13:52058873 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2110+2946G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058873 | |||||||
| chr13:52058933 | A | G | 159 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2110+2886T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52058933 | |||||||
| chr13:52059161 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2110+2658G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059161 | |||||||
| chr13:52059162 | T | G | 1 | a0001c0001t0038g0119 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2110+2657A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059162 | |||||||
| chr13:52059248 | A | T | 1 | a0001c0001t0002g0219 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2110+2571T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059248 | |||||||
| chr13:52059809 | T | TG | 15 | a0001c0001t0001g0047 a0001c0001t0001g0124 a0001c0001t0001g0138 others(12): Show |
15 | HG00438.hp1 HG00621.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.2110+2009dupC | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059809 | |||||||
| chr13:52059822 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2110+1997C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059822 | |||||||
| chr13:52059823 | A | G | 1 | a0001c0001t0003g0288 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2110+1996T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059823 | |||||||
| chr13:52059848 | A | G | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2110+1971T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059848 | |||||||
| chr13:52059883 | A | T | 2 | a0003c0005t0027g0318 a0003c0005t0027g0319 |
2 | HG01192.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2110+1936T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059883 | |||||||
| chr13:52059942 | C | T | 1 | a0001c0001t0009g0089 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2110+1877G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52059942 | |||||||
| chr13:52060004 | T | C | 3 | a0002c0002t0005g0066 a0002c0002t0005g0069 a0002c0002t0033g0076 |
3 | HG00099.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2110+1815A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060004 | |||||||
| chr13:52060102 | G | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0162 a0001c0001t0017g0129 |
3 | HG02155.hp1 NA18979.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.2110+1717C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060102 | |||||||
| chr13:52060158 | A | T | 1 | a0001c0001t0002g0235 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2110+1661T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060158 | |||||||
| chr13:52060363 | G | T | 2 | a0001c0001t0002g0241 a0001c0001t0060g0280 |
2 | NA18985.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.2110+1456C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060363 | |||||||
| chr13:52060475 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2110+1344G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060475 | |||||||
| chr13:52060597 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2110+1222G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060597 | |||||||
| chr13:52060668 | C | T | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2110+1151G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060668 | |||||||
| chr13:52060832 | A | C | 166 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2110+987T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060832 | |||||||
| chr13:52060870 | T | C | 5 | a0001c0001t0006g0002 a0001c0001t0006g0029 a0001c0001t0006g0030 others(2): Show |
6 | HG01109.hp1 HG01255.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.2110+949A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52060870 | |||||||
| chr13:52061180 | C | T | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2110+639G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52061180 | |||||||
| chr13:52061197 | G | A | 3 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2110+622C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52061197 | |||||||
| chr13:52061198 | T | C | 3 | a0001c0001t0018g0017 a0001c0001t0018g0018 a0001c0001t0044g0019 |
3 | HG03017.hp1 HG03490.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2110+621A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52061198 | |||||||
| chr13:52061429 | G | T | 1 | a0001c0001t0006g0027 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2110+390C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52061429 | |||||||
| chr13:52061547 | G | A | 1 | a0001c0001t0009g0150 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2110+272C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52061547 | |||||||
| chr13:52061712 | C | T | 2 | a0001c0001t0001g0041 a0006c0007t0001g0055 |
2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2110+107G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 22/23 | chr13 | 52061712 | |||||||
| chr13:52062408 | C | T | 1 | a0001c0001t0003g0012 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1976-455G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062408 | |||||||
| chr13:52062468 | A | C | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1976-515T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062468 | |||||||
| chr13:52062506 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1976-553G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062506 | |||||||
| chr13:52062545 | C | G | 1 | a0001c0001t0011g0306 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1976-592G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062545 | |||||||
| chr13:52062652 | C | T | 1 | a0001c0001t0040g0091 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1976-699G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062652 | |||||||
| chr13:52062978 | T | C | 4 | a0001c0001t0012g0003 a0001c0001t0012g0038 a0001c0001t0012g0039 others(1): Show |
5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1976-1025A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062978 | |||||||
| chr13:52062990 | C | T | 1 | a0001c0001t0002g0241 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1976-1037G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52062990 | |||||||
| chr13:52063044 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1976-1091G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063044 | |||||||
| chr13:52063049 | CCCCTCTC others(27): Show |
C | 1 | a0001c0004t0019g0299 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1976-1130_1976-109 others(38): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063049 | |||||||
| chr13:52063108 | T | C | 4 | a0001c0001t0002g0196 a0001c0001t0002g0198 a0001c0001t0002g0199 others(1): Show |
4 | HG00642.hp1 HG02486.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1976-1155A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063108 | |||||||
| chr13:52063209 | A | T | 6 | a0001c0001t0003g0008 a0001c0001t0003g0011 a0001c0001t0003g0216 others(3): Show |
8 | NA18944.hp1 NA18960.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.1976-1256T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063209 | |||||||
| chr13:52063219 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1976-1266G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063219 | |||||||
| chr13:52063280 | G | A | 159 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1976-1327C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063280 | |||||||
| chr13:52063306 | C | A | 10 | a0001c0001t0004g0270 a0001c0003t0010g0020 a0001c0003t0010g0022 others(7): Show |
10 | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1976-1353G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063306 | |||||||
| chr13:52063341 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1976-1388G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063341 | |||||||
| chr13:52063379 | A | G | 3 | a0001c0001t0002g0228 a0001c0001t0002g0265 a0001c0001t0002g0272 |
3 | NA18974.hp1 NA18978.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1976-1426T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063379 | |||||||
| chr13:52063397 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1976-1444A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063397 | |||||||
| chr13:52063411 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0002g0195 a0001c0001t0047g0194 |
3 | HG01074.hp1 HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1976-1458G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063411 | |||||||
| chr13:52063497 | C | T | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1976-1544G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063497 | |||||||
| chr13:52063498 | G | A | 2 | a0002c0002t0004g0190 a0002c0002t0049g0189 |
2 | HG00621.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1976-1545C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063498 | |||||||
| chr13:52063525 | C | T | 2 | a0001c0001t0002g0241 a0001c0001t0060g0280 |
2 | NA18985.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1976-1572G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063525 | |||||||
| chr13:52063553 | G | A | 1 | a0001c0001t0003g0218 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1976-1600C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063553 | |||||||
| chr13:52063591 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1976-1638G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063591 | |||||||
| chr13:52063602 | A | C | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1976-1649T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063602 | |||||||
| chr13:52063641 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1976-1688G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063641 | |||||||
| chr13:52063646 | A | G | 166 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1976-1693T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063646 | |||||||
| chr13:52063671 | A | ACCTCTGC others(30): Show |
34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1976-1719_1976-171 others(41): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063671 | |||||||
| chr13:52063703 | G | C | 1 | a0008c0012t0001g0101 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1976-1750C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063703 | |||||||
| chr13:52063730 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0134 a0001c0001t0030g0045 |
3 | HG03209.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1975+1754C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063730 | |||||||
| chr13:52063757 | C | T | 2 | a0001c0001t0026g0013 a0001c0001t0052g0315 |
3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1975+1727G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063757 | |||||||
| chr13:52063762 | A | G | 317 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(314): Show |
331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.1975+1722T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063762 | |||||||
| chr13:52063801 | C | T | 3 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1975+1683G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063801 | |||||||
| chr13:52063861 | G | A | 1 | a0001c0001t0002g0253 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1975+1623C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063861 | |||||||
| chr13:52063915 | T | C | 199 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0046 others(196): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1975+1569A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063915 | |||||||
| chr13:52063958 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1975+1526C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063958 | |||||||
| chr13:52063982 | G | A | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1975+1502C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063982 | |||||||
| chr13:52063996 | T | TG | 34 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 others(31): Show |
34 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1975+1487dupC | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063996 | |||||||
| chr13:52063996 | TG | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0160 a0001c0001t0002g0234 others(16): Show |
19 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1975+1487delC | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063996 | |||||||
| chr13:52063996 | TGG | T | 162 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
170 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1975+1486_1975+148 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52063996 | |||||||
| chr13:52064017 | C | G | 7 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0152 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1975+1467G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064017 | |||||||
| chr13:52064035 | A | ATCCGGGA others(120): Show |
4 | a0001c0001t0012g0003 a0001c0001t0012g0038 a0001c0001t0012g0039 others(1): Show |
5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975+1448_1975+144 others(131): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064035 | |||||||
| chr13:52064108 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1975+1376C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064108 | |||||||
| chr13:52064112 | G | A | 1 | a0001c0001t0044g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1975+1372C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064112 | |||||||
| chr13:52064161 | TGTCCGGG others(42): Show |
T | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1975+1274_1975+132 others(53): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064161 | |||||||
| chr13:52064192 | C | G | 34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1975+1292G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064192 | |||||||
| chr13:52064194 | G | A | 1 | a0001c0001t0007g0242 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1975+1290C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064194 | |||||||
| chr13:52064206 | G | A | 5 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975+1278C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064206 | |||||||
| chr13:52064211 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0148 a0001c0001t0012g0038 |
3 | HG00438.hp2 HG02970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1975+1273C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064211 | |||||||
| chr13:52064242 | C | T | 4 | a0001c0001t0012g0003 a0001c0001t0012g0038 a0001c0001t0012g0039 others(1): Show |
5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975+1242G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064242 | |||||||
| chr13:52064324 | T | C | 159 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1975+1160A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064324 | |||||||
| chr13:52064365 | C | A | 5 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975+1119G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064365 | |||||||
| chr13:52064388 | G | A | 4 | a0001c0001t0012g0003 a0001c0001t0012g0038 a0001c0001t0012g0039 others(1): Show |
5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975+1096C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064388 | |||||||
| chr13:52064391 | C | T | 1 | a0001c0001t0002g0263 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1975+1093G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064391 | |||||||
| chr13:52064416 | G | C | 1 | a0001c0001t0041g0085 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1975+1068C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064416 | |||||||
| chr13:52064451 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0221 a0001c0001t0002g0253 others(3): Show |
7 | NA18969.hp1 NA18973.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.1975+1033C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064451 | |||||||
| chr13:52064486 | T | C | 159 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1975+998A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064486 | |||||||
| chr13:52064514 | C | T | 11 | a0001c0001t0036g0035 a0001c0001t0037g0128 a0001c0003t0010g0020 others(8): Show |
11 | HG00544.hp1 HG01099.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1975+970G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064514 | |||||||
| chr13:52064527 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0057 others(1): Show |
4 | HG02622.hp1 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+957C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064527 | |||||||
| chr13:52064535 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0008g0096 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1975+949G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064535 | |||||||
| chr13:52064559 | C | T | 3 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1975+925G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064559 | |||||||
| chr13:52064606 | C | T | 30 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(27): Show |
30 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.1975+878G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064606 | |||||||
| chr13:52064618 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1975+866C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064618 | |||||||
| chr13:52064648 | G | A | 1 | a0002c0002t0004g0178 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1975+836C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064648 | |||||||
| chr13:52064649 | G | T | 1 | a0002c0002t0004g0178 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1975+835C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064649 | |||||||
| chr13:52064683 | C | T | 1 | a0010c0015t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1975+801G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064683 | |||||||
| chr13:52064995 | A | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1975+489T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52064995 | |||||||
| chr13:52065042 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1975+442G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52065042 | |||||||
| chr13:52065094 | C | T | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1975+390G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52065094 | |||||||
| chr13:52065095 | G | A | 28 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0171 others(25): Show |
30 | HG00597.hp1 HG00621.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.1975+389C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52065095 | |||||||
| chr13:52065162 | C | A | 159 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1975+322G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52065162 | |||||||
| chr13:52065326 | T | C | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1975+158A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 21/23 | chr13 | 52065326 | |||||||
| chr13:52065688 | A | G | 3 | a0001c0001t0022g0310 a0001c0001t0022g0311 a0001c0001t0022g0312 |
3 | HG02451.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1850-79T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52065688 | |||||||
| chr13:52065878 | A | G | 1 | a0001c0001t0006g0027 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1850-269T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52065878 | |||||||
| chr13:52065891 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA18951.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1850-282T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52065891 | |||||||
| chr13:52065983 | A | G | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1850-374T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52065983 | |||||||
| chr13:52066013 | GA | G | 175 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0121 others(172): Show |
182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1850-405delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066013 | |||||||
| chr13:52066325 | T | C | 1 | a0002c0002t0004g0191 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1850-716A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066325 | |||||||
| chr13:52066465 | G | T | 184 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1850-856C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066465 | |||||||
| chr13:52066493 | T | G | 2 | a0001c0001t0022g0311 a0001c0001t0022g0312 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1850-884A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066493 | |||||||
| chr13:52066632 | C | T | 159 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1850-1023G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066632 | |||||||
| chr13:52066736 | G | A | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1850-1127C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066736 | |||||||
| chr13:52066758 | C | A | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1850-1149G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066758 | |||||||
| chr13:52066760 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0144 a0001c0001t0008g0034 |
3 | HG02886.hp2 HG02970.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1850-1151G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066760 | |||||||
| chr13:52066795 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1850-1186G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066795 | |||||||
| chr13:52066796 | G | A | 4 | a0001c0003t0013g0021 a0001c0003t0013g0024 a0001c0003t0013g0025 others(1): Show |
4 | HG00544.hp1 NA18994.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1850-1187C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066796 | |||||||
| chr13:52066803 | C | CA | 9 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0084 others(6): Show |
9 | HG00621.hp1 HG01123.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1850-1195dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066803 | |||||||
| chr13:52066917 | G | A | 8 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0048 others(5): Show |
8 | HG01069.hp2 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1850-1308C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52066917 | |||||||
| chr13:52067002 | T | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0135 a0001c0001t0001g0163 |
3 | NA18948.hp1 NA18956.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1850-1393A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067002 | |||||||
| chr13:52067078 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1850-1469T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067078 | |||||||
| chr13:52067317 | T | G | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1850-1708A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067317 | |||||||
| chr13:52067444 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1850-1835G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067444 | |||||||
| chr13:52067457 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1850-1848T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067457 | |||||||
| chr13:52067651 | C | T | 34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1850-2042G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067651 | |||||||
| chr13:52067670 | C | G | 10 | a0001c0001t0001g0033 a0001c0001t0001g0146 a0001c0001t0001g0159 others(7): Show |
10 | HG02258.hp2 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1850-2061G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067670 | |||||||
| chr13:52067676 | A | AT | 27 | a0001c0001t0001g0110 a0001c0001t0001g0132 a0001c0001t0001g0160 others(24): Show |
28 | HG00099.hp2 HG00408.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1850-2068dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067676 | |||||||
| chr13:52067676 | A | ATT | 124 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(121): Show |
131 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1850-2069_1850-206 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067676 | |||||||
| chr13:52067676 | A | ATTT | 16 | a0001c0001t0002g0231 a0001c0001t0002g0307 a0001c0001t0007g0202 others(13): Show |
16 | HG00323.hp1 HG00733.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1850-2070_1850-206 others(7): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067676 | |||||||
| chr13:52067760 | T | C | 184 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1850-2151A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067760 | |||||||
| chr13:52067770 | C | A | 1 | a0001c0001t0062g0275 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1850-2161G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067770 | |||||||
| chr13:52067977 | C | T | 1 | a0001c0001t0015g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1850-2368G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52067977 | |||||||
| chr13:52068089 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1850-2480G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068089 | |||||||
| chr13:52068220 | G | A | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1850-2611C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068220 | |||||||
| chr13:52068230 | C | A | 1 | a0001c0001t0038g0119 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1850-2621G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068230 | |||||||
| chr13:52068231 | A | C | 1 | a0001c0001t0038g0119 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1850-2622T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068231 | |||||||
| chr13:52068232 | C | A | 1 | a0001c0001t0038g0119 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1850-2623G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068232 | |||||||
| chr13:52068293 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1850-2684G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068293 | |||||||
| chr13:52068338 | A | G | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1850-2729T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068338 | |||||||
| chr13:52068466 | T | TAC | 14 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0057 others(11): Show |
15 | HG01192.hp1 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1850-2859_1850-285 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068466 | |||||||
| chr13:52068466 | T | TACAC | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
105 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1850-2861_1850-285 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068466 | |||||||
| chr13:52068466 | T | TACACAC | 10 | a0001c0001t0001g0109 a0001c0001t0001g0116 a0001c0001t0001g0117 others(7): Show |
10 | HG00609.hp1 HG01109.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1850-2863_1850-285 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068466 | |||||||
| chr13:52068466 | TAC | T | 161 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(158): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1850-2859_1850-285 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068466 | |||||||
| chr13:52068466 | TACAC | T | 4 | a0001c0001t0016g0301 a0001c0001t0016g0305 a0002c0002t0004g0190 others(1): Show |
4 | HG00621.hp1 HG02132.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1850-2861_1850-285 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068466 | |||||||
| chr13:52068466 | TACACACA others(5): Show |
T | 1 | a0001c0001t0002g0255 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1850-2869_1850-285 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068466 | |||||||
| chr13:52068706 | C | T | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1850-3097G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068706 | |||||||
| chr13:52068790 | T | C | 1 | a0001c0001t0016g0304 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1849+3154A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068790 | |||||||
| chr13:52068803 | C | G | 1 | a0002c0002t0004g0176 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1849+3141G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068803 | |||||||
| chr13:52068844 | G | A | 3 | a0001c0001t0021g0226 a0001c0001t0021g0227 a0001c0001t0021g0285 |
3 | HG00323.hp2 HG02602.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1849+3100C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068844 | |||||||
| chr13:52068864 | G | A | 3 | a0001c0001t0018g0017 a0001c0001t0018g0018 a0001c0001t0044g0019 |
3 | HG03017.hp1 HG03490.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1849+3080C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068864 | |||||||
| chr13:52068879 | G | A | 1 | a0001c0001t0007g0242 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1849+3065C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068879 | |||||||
| chr13:52068938 | TC | T | 159 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1849+3005delG | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068938 | |||||||
| chr13:52068970 | CA | C | 173 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(170): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1849+2973delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52068970 | |||||||
| chr13:52069000 | A | G | 2 | a0002c0002t0050g0317 a0002c0002t0051g0316 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1849+2944T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069000 | |||||||
| chr13:52069034 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1849+2910G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069034 | |||||||
| chr13:52069119 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1849+2825A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069119 | |||||||
| chr13:52069176 | G | T | 2 | a0001c0001t0002g0214 a0001c0001t0004g0270 |
2 | HG00639.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1849+2768C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069176 | |||||||
| chr13:52069321 | C | A | 2 | a0001c0001t0002g0291 a0001c0001t0002g0292 |
2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1849+2623G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069321 | |||||||
| chr13:52069466 | G | A | 2 | a0001c0001t0001g0041 a0006c0007t0001g0055 |
2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1849+2478C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069466 | |||||||
| chr13:52069621 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1849+2323G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069621 | |||||||
| chr13:52069639 | T | C | 1 | a0001c0001t0012g0039 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1849+2305A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069639 | |||||||
| chr13:52069937 | T | C | 2 | a0001c0001t0002g0291 a0001c0001t0002g0292 |
2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1849+2007A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52069937 | |||||||
| chr13:52070115 | A | G | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1849+1829T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52070115 | |||||||
| chr13:52070328 | C | CA | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1849+1615dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52070328 | |||||||
| chr13:52070769 | A | T | 1 | a0001c0001t0038g0119 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1849+1175T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52070769 | |||||||
| chr13:52070927 | C | T | 5 | a0002c0002t0005g0066 a0002c0002t0005g0069 a0002c0002t0005g0072 others(2): Show |
5 | HG00099.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1849+1017G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52070927 | |||||||
| chr13:52071145 | A | G | 29 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(26): Show |
29 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.1849+799T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071145 | |||||||
| chr13:52071275 | C | T | 4 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 others(1): Show |
4 | HG01192.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1849+669G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071275 | |||||||
| chr13:52071366 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1849+578G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071366 | |||||||
| chr13:52071410 | C | G | 2 | a0001c0001t0031g0054 a0010c0015t0001g0056 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1849+534G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071410 | |||||||
| chr13:52071466 | C | T | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1849+478G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071466 | |||||||
| chr13:52071542 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1849+402G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071542 | |||||||
| chr13:52071650 | T | G | 1 | a0001c0001t0001g0118 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1849+294A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071650 | |||||||
| chr13:52071789 | G | T | 1 | a0001c0001t0038g0119 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1849+155C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071789 | |||||||
| chr13:52071859 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1849+85G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071859 | |||||||
| chr13:52071889 | A | G | 2 | a0002c0002t0004g0180 a0002c0002t0004g0181 |
2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1849+55T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 20/23 | chr13 | 52071889 | |||||||
| chr13:52072372 | A | G | 4 | a0001c0001t0012g0003 a0001c0001t0012g0038 a0001c0001t0012g0039 others(1): Show |
5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1723-302T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52072372 | |||||||
| chr13:52072441 | T | C | 2 | a0001c0001t0031g0054 a0010c0015t0001g0056 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1723-371A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52072441 | |||||||
| chr13:52072466 | C | A | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1723-396G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52072466 | |||||||
| chr13:52072558 | G | A | 10 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(7): Show |
10 | HG00544.hp1 HG01099.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1723-488C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52072558 | |||||||
| chr13:52072926 | A | C | 1 | a0001c0003t0013g0021 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1723-856T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52072926 | |||||||
| chr13:52073068 | A | T | 1 | a0001c0001t0001g0043 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1723-998T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073068 | |||||||
| chr13:52073216 | A | G | 3 | a0001c0001t0022g0310 a0001c0001t0022g0311 a0001c0001t0022g0312 |
3 | HG02451.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1723-1146T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073216 | |||||||
| chr13:52073217 | T | A | 149 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(146): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1723-1147A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073217 | |||||||
| chr13:52073378 | T | C | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1723-1308A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073378 | |||||||
| chr13:52073542 | C | T | 1 | a0001c0004t0019g0298 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1723-1472G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073542 | |||||||
| chr13:52073859 | C | T | 159 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1723-1789G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073859 | |||||||
| chr13:52073866 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1723-1796G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073866 | |||||||
| chr13:52073976 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1722+1782T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52073976 | |||||||
| chr13:52074209 | G | A | 1 | a0010c0015t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1722+1549C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52074209 | |||||||
| chr13:52074605 | T | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0137 others(8): Show |
12 | HG02015.hp1 NA18959.hp1 NA18960.hp2 others(9): Show |
intron_variant | MODIFIER | c.1722+1153A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52074605 | |||||||
| chr13:52074791 | C | T | 4 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0154 others(1): Show |
4 | HG02083.hp2 NA18942.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1722+967G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52074791 | |||||||
| chr13:52074937 | C | T | 1 | a0001c0001t0058g0284 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1722+821G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52074937 | |||||||
| chr13:52074983 | G | A | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1722+775C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52074983 | |||||||
| chr13:52075093 | C | A | 1 | a0001c0001t0001g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1722+665G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52075093 | |||||||
| chr13:52075106 | C | A | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1722+652G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52075106 | |||||||
| chr13:52075444 | C | A | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1722+314G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52075444 | |||||||
| chr13:52075645 | A | T | 1 | a0001c0001t0060g0280 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1722+113T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 19/23 | chr13 | 52075645 | |||||||
| chr13:52075976 | G | A | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1653+87C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 18/23 | chr13 | 52075976 | |||||||
| chr13:52075985 | A | G | 3 | a0001c0001t0002g0228 a0001c0001t0002g0265 a0001c0001t0002g0272 |
3 | NA18974.hp1 NA18978.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1653+78T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 18/23 | chr13 | 52075985 | |||||||
| chr13:52076484 | T | C | 1 | a0001c0001t0014g0296 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1573-341A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52076484 | |||||||
| chr13:52076487 | C | T | 1 | a0001c0001t0006g0028 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1573-344G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52076487 | |||||||
| chr13:52076539 | A | G | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1573-396T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52076539 | |||||||
| chr13:52076653 | C | T | 1 | a0001c0001t0037g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1573-510G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52076653 | |||||||
| chr13:52076886 | A | C | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1573-743T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52076886 | |||||||
| chr13:52076902 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1573-759G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52076902 | |||||||
| chr13:52077329 | A | G | 1 | a0001c0003t0010g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1573-1186T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077329 | |||||||
| chr13:52077341 | T | C | 1 | a0002c0002t0004g0190 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1573-1198A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077341 | |||||||
| chr13:52077355 | T | C | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1573-1212A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077355 | |||||||
| chr13:52077663 | C | A | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1573-1520G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077663 | |||||||
| chr13:52077671 | C | T | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1573-1528G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077671 | |||||||
| chr13:52077767 | T | C | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1573-1624A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077767 | |||||||
| chr13:52077856 | C | T | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1573-1713G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077856 | |||||||
| chr13:52077943 | G | A | 32 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(29): Show |
32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1573-1800C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52077943 | |||||||
| chr13:52078045 | G | A | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1573-1902C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078045 | |||||||
| chr13:52078181 | A | C | 1 | a0001c0001t0060g0280 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1573-2038T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078181 | |||||||
| chr13:52078384 | G | A | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1573-2241C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078384 | |||||||
| chr13:52078520 | C | A | 184 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1573-2377G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078520 | |||||||
| chr13:52078592 | G | GT | 54 | a0001c0001t0001g0047 a0001c0001t0001g0313 a0001c0001t0002g0276 others(51): Show |
56 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.1573-2450dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078592 | |||||||
| chr13:52078592 | G | GTT | 114 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(111): Show |
120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1573-2451_1573-245 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078592 | |||||||
| chr13:52078714 | C | T | 3 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1573-2571G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078714 | |||||||
| chr13:52078839 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0049 |
2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1573-2696C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078839 | |||||||
| chr13:52078879 | T | C | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1573-2736A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52078879 | |||||||
| chr13:52079058 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1573-2915C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079058 | |||||||
| chr13:52079203 | T | G | 1 | a0001c0001t0002g0287 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1573-3060A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079203 | |||||||
| chr13:52079251 | C | A | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1573-3108G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079251 | |||||||
| chr13:52079286 | A | ATCCCTC | 147 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0102 others(144): Show |
154 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.1573-3149_1573-314 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079286 | |||||||
| chr13:52079286 | A | ATCCCTCT others(5): Show |
117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
123 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.1573-3155_1573-314 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079286 | |||||||
| chr13:52079286 | ATCCCTC | A | 32 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(29): Show |
32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1573-3149_1573-314 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079286 | |||||||
| chr13:52079286 | ATCCCTCT others(5): Show |
A | 2 | a0001c0001t0001g0041 a0006c0007t0001g0055 |
2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1573-3155_1573-314 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079286 | |||||||
| chr13:52079308 | C | CTCTCCCC others(11): Show |
2 | a0001c0001t0026g0013 a0001c0001t0052g0315 |
3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1573-3166_1573-316 others(22): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079308 | |||||||
| chr13:52079347 | C | T | 2 | a0001c0001t0003g0259 a0001c0001t0029g0258 |
2 | NA18956.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1573-3204G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079347 | |||||||
| chr13:52079348 | G | A | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1573-3205C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079348 | |||||||
| chr13:52079348 | G | T | 1 | a0001c0001t0003g0247 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1573-3205C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079348 | |||||||
| chr13:52079437 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1573-3294A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079437 | |||||||
| chr13:52079457 | G | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0169 a0001c0001t0017g0104 |
3 | HG02735.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1573-3314C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079457 | |||||||
| chr13:52079471 | C | T | 20 | a0001c0001t0002g0250 a0001c0001t0003g0008 a0001c0001t0003g0011 others(17): Show |
22 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1573-3328G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079471 | |||||||
| chr13:52079493 | G | A | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1573-3350C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079493 | |||||||
| chr13:52079725 | G | T | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+3535C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079725 | |||||||
| chr13:52079752 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1572+3508G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079752 | |||||||
| chr13:52079817 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1572+3443C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079817 | |||||||
| chr13:52079829 | C | T | 1 | a0001c0001t0014g0293 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1572+3431G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079829 | |||||||
| chr13:52079872 | C | T | 5 | a0002c0002t0004g0179 a0002c0002t0004g0180 a0002c0002t0004g0181 others(2): Show |
5 | HG00323.hp1 HG00733.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+3388G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079872 | |||||||
| chr13:52079880 | G | A | 3 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0043g0037 |
3 | HG01891.hp1 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1572+3380C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079880 | |||||||
| chr13:52079916 | C | T | 32 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(29): Show |
32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1572+3344G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079916 | |||||||
| chr13:52079984 | C | T | 1 | a0001c0001t0041g0085 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1572+3276G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52079984 | |||||||
| chr13:52080005 | G | A | 1 | a0002c0002t0004g0178 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1572+3255C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080005 | |||||||
| chr13:52080038 | A | AAGAAGTG others(33): Show |
114 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(111): Show |
120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1572+3221_1572+322 others(44): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080038 | |||||||
| chr13:52080060 | C | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG01074.hp1 HG01993.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572+3200G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080060 | |||||||
| chr13:52080061 | C | T | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3199G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080061 | |||||||
| chr13:52080073 | G | C | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3187C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080073 | |||||||
| chr13:52080093 | T | C | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3167A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080093 | |||||||
| chr13:52080094 | A | C | 2 | a0001c0001t0002g0192 a0001c0001t0020g0223 |
2 | HG01106.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1572+3166T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080094 | |||||||
| chr13:52080109 | A | G | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3151T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080109 | |||||||
| chr13:52080113 | C | G | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3147G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080113 | |||||||
| chr13:52080119 | G | A | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3141C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080119 | |||||||
| chr13:52080122 | G | A | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3138C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080122 | |||||||
| chr13:52080132 | G | C | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3128C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080132 | |||||||
| chr13:52080134 | C | A | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3126G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080134 | |||||||
| chr13:52080137 | C | T | 2 | a0001c0001t0016g0301 a0001c0001t0016g0305 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1572+3123G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080137 | |||||||
| chr13:52080161 | A | T | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3099T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080161 | |||||||
| chr13:52080170 | G | A | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3090C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080170 | |||||||
| chr13:52080173 | G | A | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3087C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080173 | |||||||
| chr13:52080174 | T | G | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3086A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080174 | |||||||
| chr13:52080178 | C | T | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3082G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080178 | |||||||
| chr13:52080180 | C | T | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3080G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080180 | |||||||
| chr13:52080186 | A | C | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3074T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080186 | |||||||
| chr13:52080195 | G | A | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3065C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080195 | |||||||
| chr13:52080204 | G | A | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3056C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080204 | |||||||
| chr13:52080214 | TG | T | 32 | a0001c0001t0002g0255 a0002c0002t0004g0175 a0002c0002t0004g0176 others(29): Show |
32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1572+3045delC | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080214 | |||||||
| chr13:52080215 | GGGGGGGG others(43): Show |
G | 8 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(5): Show |
8 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.1572+2995_1572+304 others(54): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080215 | |||||||
| chr13:52080216 | GGGGGGGG others(42): Show |
G | 1 | a0001c0003t0013g0021 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1572+2995_1572+304 others(53): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080216 | |||||||
| chr13:52080237 | C | A | 1 | a0001c0001t0020g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1572+3023G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080237 | |||||||
| chr13:52080251 | A | G | 6 | a0001c0001t0020g0223 a0002c0002t0004g0190 a0002c0002t0049g0189 others(3): Show |
6 | HG00621.hp1 HG01192.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1572+3009T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080251 | |||||||
| chr13:52080259 | G | C | 5 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+3001C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080259 | |||||||
| chr13:52080285 | G | A | 32 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(29): Show |
32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1572+2975C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080285 | |||||||
| chr13:52080288 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1572+2972G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080288 | |||||||
| chr13:52080296 | C | G | 1 | a0010c0015t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1572+2964G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080296 | |||||||
| chr13:52080323 | T | C | 8 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(5): Show |
8 | HG01192.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1572+2937A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080323 | |||||||
| chr13:52080329 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1572+2931G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080329 | |||||||
| chr13:52080353 | A | G | 178 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1572+2907T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080353 | |||||||
| chr13:52080356 | C | A | 1 | a0003c0005t0054g0320 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1572+2904G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080356 | |||||||
| chr13:52080376 | C | T | 3 | a0001c0001t0021g0226 a0001c0001t0021g0227 a0001c0001t0021g0285 |
3 | HG00323.hp2 HG02602.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1572+2884G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080376 | |||||||
| chr13:52080412 | C | G | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1572+2848G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080412 | |||||||
| chr13:52080572 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1572+2688G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080572 | |||||||
| chr13:52080695 | A | G | 1 | a0001c0001t0003g0012 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1572+2565T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080695 | |||||||
| chr13:52080700 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0039g0145 |
2 | HG01516.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1572+2560G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080700 | |||||||
| chr13:52080718 | C | A | 2 | a0002c0002t0005g0066 a0002c0002t0033g0076 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1572+2542G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080718 | |||||||
| chr13:52080723 | T | C | 19 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0121 others(16): Show |
19 | HG00609.hp1 HG00673.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1572+2537A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080723 | |||||||
| chr13:52080770 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1572+2490G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080770 | |||||||
| chr13:52080771 | C | T | 1 | a0001c0001t0016g0304 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1572+2489G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080771 | |||||||
| chr13:52080781 | G | A | 1 | a0001c0004t0019g0298 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1572+2479C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080781 | |||||||
| chr13:52080785 | A | G | 1 | a0001c0001t0003g0271 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1572+2475T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080785 | |||||||
| chr13:52080810 | G | A | 2 | a0001c0001t0014g0295 a0001c0001t0053g0294 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1572+2450C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080810 | |||||||
| chr13:52080832 | G | A | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1572+2428C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080832 | |||||||
| chr13:52080889 | TA | T | 13 | a0001c0001t0001g0053 a0001c0001t0001g0081 a0001c0001t0001g0152 others(10): Show |
14 | HG01069.hp2 HG01243.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1572+2370delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080889 | |||||||
| chr13:52080889 | TAA | T | 156 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(153): Show |
162 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1572+2369_1572+237 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080889 | |||||||
| chr13:52080892 | A | T | 1 | a0001c0001t0002g0225 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1572+2368T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080892 | |||||||
| chr13:52080988 | T | A | 1 | a0001c0001t0011g0205 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1572+2272A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080988 | |||||||
| chr13:52080988 | T | TA | 114 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(111): Show |
120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1572+2271dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080988 | |||||||
| chr13:52080989 | A | T | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1572+2271T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52080989 | |||||||
| chr13:52081187 | T | A | 1 | a0001c0001t0014g0286 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1572+2073A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52081187 | |||||||
| chr13:52081752 | T | A | 1 | a0001c0001t0002g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1572+1508A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52081752 | |||||||
| chr13:52081870 | C | T | 1 | a0005c0014t0004g0297 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1572+1390G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52081870 | |||||||
| chr13:52082141 | C | A | 1 | a0001c0001t0002g0243 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1572+1119G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082141 | |||||||
| chr13:52082149 | C | T | 32 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(29): Show |
32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1572+1111G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082149 | |||||||
| chr13:52082246 | C | T | 5 | a0002c0002t0004g0184 a0002c0002t0004g0185 a0002c0002t0004g0186 others(2): Show |
5 | HG00408.hp2 HG00621.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1572+1014G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082246 | |||||||
| chr13:52082255 | C | T | 5 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+1005G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082255 | |||||||
| chr13:52082256 | G | A | 3 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0288 |
3 | HG01981.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1572+1004C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082256 | |||||||
| chr13:52082542 | T | C | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1572+718A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082542 | |||||||
| chr13:52082771 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1572+489T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52082771 | |||||||
| chr13:52083090 | G | A | 1 | a0001c0001t0012g0003 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1572+170C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52083090 | |||||||
| chr13:52083104 | C | T | 32 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(29): Show |
32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1572+156G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52083104 | |||||||
| chr13:52083151 | A | G | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1572+109T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52083151 | |||||||
| chr13:52083171 | G | A | 8 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1572+89C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52083171 | |||||||
| chr13:52083237 | C | T | 1 | a0002c0002t0032g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1572+23G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 17/23 | chr13 | 52083237 | |||||||
| chr13:52083373 | A | G | 2 | a0002c0002t0050g0317 a0002c0002t0051g0316 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1480-21T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52083373 | |||||||
| chr13:52083553 | T | G | 114 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(111): Show |
120 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1480-201A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52083553 | |||||||
| chr13:52083572 | T | G | 5 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480-220A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52083572 | |||||||
| chr13:52083727 | A | G | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1480-375T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52083727 | |||||||
| chr13:52083784 | C | T | 1 | a0001c0001t0058g0284 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1480-432G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52083784 | |||||||
| chr13:52083932 | G | C | 2 | a0001c0001t0008g0063 a0001c0001t0008g0064 |
2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1480-580C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52083932 | |||||||
| chr13:52084293 | A | G | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1480-941T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084293 | |||||||
| chr13:52084324 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1480-972G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084324 | |||||||
| chr13:52084361 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1480-1009C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084361 | |||||||
| chr13:52084384 | A | C | 1 | a0001c0001t0004g0270 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1480-1032T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084384 | |||||||
| chr13:52084696 | T | C | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1480-1344A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084696 | |||||||
| chr13:52084699 | G | A | 11 | a0001c0001t0001g0048 a0001c0001t0008g0044 a0001c0003t0010g0020 others(8): Show |
11 | HG00544.hp1 HG01099.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1480-1347C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084699 | |||||||
| chr13:52084724 | A | C | 1 | a0001c0001t0002g0221 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1480-1372T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084724 | |||||||
| chr13:52084730 | A | T | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG01074.hp1 HG01993.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-1378T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084730 | |||||||
| chr13:52084732 | A | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0152 |
3 | HG02622.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1480-1380T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084732 | |||||||
| chr13:52084732 | AGT | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0167 a0001c0001t0008g0063 |
3 | HG01109.hp2 HG01993.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1480-1382_1480-138 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084732 | |||||||
| chr13:52084732 | AGTGAGAG others(41): Show |
A | 1 | a0001c0001t0020g0277 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1480-1428_1480-138 others(52): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084732 | |||||||
| chr13:52084734 | T | A | 121 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0097 others(118): Show |
127 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.1480-1382A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084734 | |||||||
| chr13:52084734 | T | TGA | 12 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0100 others(9): Show |
15 | HG00408.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1480-1384_1480-138 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084734 | |||||||
| chr13:52084734 | TGA | T | 8 | a0001c0001t0001g0059 a0001c0001t0001g0113 a0001c0001t0001g0122 others(5): Show |
8 | HG00597.hp2 HG01516.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1480-1384_1480-138 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084734 | |||||||
| chr13:52084734 | TGAGA | T | 7 | a0001c0001t0035g0127 a0002c0002t0004g0180 a0002c0002t0004g0181 others(4): Show |
7 | HG00323.hp1 HG01081.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1480-1386_1480-138 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084734 | |||||||
| chr13:52084734 | TGAGAGA | T | 4 | a0002c0002t0005g0065 a0002c0002t0005g0069 a0002c0002t0005g0071 others(1): Show |
4 | HG00099.hp2 HG00738.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480-1388_1480-138 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084734 | |||||||
| chr13:52084736 | A | T | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1480-1384T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084736 | |||||||
| chr13:52084736 | AGAGAGAG others(37): Show |
A | 2 | a0001c0001t0002g0244 a0001c0001t0002g0263 |
2 | HG02015.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1480-1428_1480-138 others(48): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084736 | |||||||
| chr13:52084738 | A | T | 1 | a0001c0001t0008g0064 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1480-1386T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084738 | |||||||
| chr13:52084738 | AGAGAGAG others(33): Show |
A | 4 | a0001c0001t0002g0229 a0001c0001t0003g0216 a0001c0001t0003g0256 others(1): Show |
4 | HG01433.hp2 HG02004.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480-1426_1480-138 others(44): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084738 | |||||||
| chr13:52084738 | AGAGAGAG others(35): Show |
A | 9 | a0001c0001t0002g0220 a0001c0001t0002g0222 a0001c0001t0003g0008 others(6): Show |
11 | HG00099.hp1 HG02602.hp2 NA18944.hp1 others(8): Show |
intron_variant | MODIFIER | c.1480-1428_1480-138 others(46): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084738 | |||||||
| chr13:52084738 | AGAGAGAG others(37): Show |
A | 90 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(87): Show |
94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.1480-1430_1480-138 others(48): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084738 | |||||||
| chr13:52084740 | A | T | 1 | a0001c0001t0008g0063 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1480-1388T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084740 | |||||||
| chr13:52084740 | AGAGAGAG others(33): Show |
A | 3 | a0001c0001t0003g0257 a0001c0001t0003g0271 a0001c0001t0029g0252 |
3 | HG01981.hp2 NA18948.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1480-1428_1480-138 others(44): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084740 | |||||||
| chr13:52084740 | AGAGAGAG others(35): Show |
A | 4 | a0001c0001t0002g0225 a0001c0001t0002g0268 a0001c0001t0002g0274 others(1): Show |
4 | HG01934.hp1 HG02129.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480-1430_1480-138 others(46): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084740 | |||||||
| chr13:52084740 | AGAGAGAG others(37): Show |
A | 2 | a0001c0001t0002g0241 a0001c0001t0007g0232 |
2 | HG03704.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1480-1432_1480-138 others(48): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084740 | |||||||
| chr13:52084742 | A | T | 2 | a0002c0002t0004g0179 a0002c0002t0004g0183 |
2 | HG00733.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1480-1390T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084742 | |||||||
| chr13:52084756 | A | AGT | 6 | a0001c0001t0026g0013 a0002c0002t0004g0184 a0002c0002t0004g0185 others(3): Show |
6 | HG00408.hp2 HG00621.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1480-1405_1480-140 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084756 | |||||||
| chr13:52084756 | A | T | 3 | a0002c0002t0004g0191 a0002c0002t0050g0317 a0005c0014t0004g0297 |
3 | HG01074.hp2 HG02280.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1480-1404T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084756 | |||||||
| chr13:52084756 | AGAGAGAG others(1): Show |
A | 5 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0182 others(2): Show |
5 | HG00642.hp2 HG01243.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480-1412_1480-140 others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084756 | |||||||
| chr13:52084756 | AGAGAGAG others(3): Show |
A | 7 | a0001c0001t0006g0027 a0001c0001t0006g0028 a0001c0001t0006g0029 others(4): Show |
7 | HG01255.hp1 HG01256.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1480-1414_1480-140 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084756 | |||||||
| chr13:52084756 | AGAGAGAG others(5): Show |
A | 4 | a0001c0001t0006g0002 a0001c0001t0006g0031 a0001c0004t0019g0300 others(1): Show |
5 | HG01099.hp1 HG01109.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480-1416_1480-140 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084756 | |||||||
| chr13:52084756 | AGAGAGAG others(23): Show |
A | 2 | a0001c0001t0001g0048 a0001c0001t0008g0044 |
2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1480-1434_1480-140 others(34): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084756 | |||||||
| chr13:52084758 | A | T | 10 | a0001c0001t0026g0013 a0002c0002t0004g0178 a0002c0002t0004g0184 others(7): Show |
10 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1480-1406T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084758 | |||||||
| chr13:52084758 | AGAGAGTG others(3): Show |
A | 3 | a0001c0003t0010g0023 a0001c0003t0010g0174 a0001c0004t0019g0298 |
3 | HG02258.hp1 HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1480-1416_1480-140 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084758 | |||||||
| chr13:52084758 | AGAGAGTG others(5): Show |
A | 4 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0013g0021 others(1): Show |
4 | HG01099.hp2 HG03688.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-1418_1480-140 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084758 | |||||||
| chr13:52084758 | AGAGAGTG others(7): Show |
A | 3 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0043g0037 |
3 | HG01891.hp1 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1480-1420_1480-140 others(18): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084758 | |||||||
| chr13:52084758 | AGAGAGTG others(17): Show |
A | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1480-1430_1480-140 others(28): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084758 | |||||||
| chr13:52084760 | A | AGT | 4 | a0001c0001t0001g0077 a0001c0001t0001g0155 a0001c0001t0001g0157 others(1): Show |
4 | HG02074.hp2 HG03831.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-1409_1480-140 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084760 | |||||||
| chr13:52084760 | A | AGTGTGTG others(3): Show |
1 | a0002c0002t0004g0176 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1480-1409_1480-140 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084760 | |||||||
| chr13:52084760 | A | T | 15 | a0001c0001t0026g0013 a0002c0002t0004g0175 a0002c0002t0004g0177 others(12): Show |
15 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1480-1408T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084760 | |||||||
| chr13:52084760 | AGAGTGTG others(3): Show |
A | 1 | a0001c0003t0013g0024 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1480-1418_1480-140 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084760 | |||||||
| chr13:52084760 | AGAGTGTG others(5): Show |
A | 1 | a0001c0003t0013g0025 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1480-1420_1480-140 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084760 | |||||||
| chr13:52084760 | AGAGTGTG others(7): Show |
A | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1480-1422_1480-140 others(18): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084760 | |||||||
| chr13:52084762 | A | AGAGAGAG others(7): Show |
1 | a0001c0001t0009g0089 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1480-1411_1480-141 others(18): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | A | AGAGAGTG others(1): Show |
3 | a0001c0001t0001g0090 a0001c0001t0008g0106 a0001c0001t0014g0293 |
3 | HG00733.hp1 NA18994.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1480-1411_1480-141 others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | A | AGAGAGTG others(7): Show |
1 | a0001c0001t0001g0088 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1480-1411_1480-141 others(18): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | A | AGAGT | 8 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0001g0080 others(5): Show |
8 | HG00558.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1480-1411_1480-141 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | A | AGAGTGT | 4 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0124 others(1): Show |
4 | HG02258.hp2 HG02647.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480-1411_1480-141 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | A | AGAGTGTG others(3): Show |
3 | a0001c0001t0001g0086 a0001c0001t0001g0146 a0006c0007t0001g0055 |
3 | HG02572.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1480-1411_1480-141 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | A | AGAGTGTG others(5): Show |
1 | a0001c0001t0008g0034 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1480-1411_1480-141 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | A | AGT | 4 | a0001c0001t0001g0051 a0001c0001t0001g0093 a0001c0001t0001g0108 others(1): Show |
4 | HG01346.hp1 HG03471.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480-1412_1480-141 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | A | AGTGT | 5 | a0001c0001t0001g0092 a0001c0001t0012g0003 a0001c0001t0022g0311 others(2): Show |
5 | HG01943.hp1 HG02004.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480-1414_1480-141 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | A | AGTGTGT | 5 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0134 others(2): Show |
5 | HG00438.hp2 HG02622.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480-1416_1480-141 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | A | AGTGTGTG others(1): Show |
4 | a0001c0001t0001g0033 a0001c0001t0001g0152 a0001c0001t0001g0154 others(1): Show |
4 | HG02886.hp2 HG06807.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-1418_1480-141 others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | A | AGTGTGTG others(5): Show |
1 | a0001c0001t0001g0111 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1480-1422_1480-141 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | A | T | 33 | a0001c0001t0001g0077 a0001c0001t0001g0113 a0001c0001t0001g0123 others(30): Show |
33 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1480-1410T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | AGT | A | 19 | a0001c0001t0001g0084 a0001c0001t0001g0102 a0001c0001t0001g0103 others(16): Show |
19 | HG01192.hp1 HG01243.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1480-1412_1480-141 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | AGTGT | A | 9 | a0001c0001t0001g0053 a0001c0001t0001g0116 a0001c0001t0001g0139 others(6): Show |
9 | HG01069.hp2 HG02486.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1480-1414_1480-141 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | AGTGTGT | A | 6 | a0001c0001t0001g0098 a0001c0001t0016g0301 a0001c0001t0016g0304 others(3): Show |
6 | HG01074.hp1 HG01516.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1480-1416_1480-141 others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0022g0310 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1480-1420_1480-141 others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084762 | AGTGTGTG others(9): Show |
A | 1 | a0008c0012t0001g0101 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1480-1426_1480-141 others(20): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084762 | |||||||
| chr13:52084764 | T | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0058 others(20): Show |
25 | HG00408.hp1 HG00544.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1480-1412A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084764 | |||||||
| chr13:52084766 | T | A | 19 | a0001c0001t0001g0084 a0001c0001t0001g0103 a0001c0001t0001g0105 others(16): Show |
19 | HG00544.hp2 HG01081.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1480-1414A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084766 | |||||||
| chr13:52084768 | T | A | 19 | a0001c0001t0001g0084 a0001c0001t0001g0105 a0001c0001t0001g0116 others(16): Show |
19 | HG01109.hp2 HG01192.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1480-1416A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084768 | |||||||
| chr13:52084770 | T | A | 10 | a0001c0001t0001g0137 a0001c0001t0001g0142 a0001c0001t0016g0301 others(7): Show |
10 | HG01192.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1480-1418A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084770 | |||||||
| chr13:52084772 | T | A | 1 | a0001c0001t0031g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1480-1420A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084772 | |||||||
| chr13:52084774 | T | A | 1 | a0001c0001t0031g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1480-1422A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084774 | |||||||
| chr13:52084780 | T | A | 1 | a0008c0012t0001g0101 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1480-1428A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084780 | |||||||
| chr13:52084781 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1480-1429C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084781 | |||||||
| chr13:52084782 | T | A | 1 | a0001c0001t0020g0277 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1480-1430A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084782 | |||||||
| chr13:52084815 | GT | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0162 a0002c0002t0004g0177 |
3 | HG02135.hp1 NA18979.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1479+1461delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084815 | |||||||
| chr13:52084817 | T | G | 1 | a0006c0007t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1479+1460A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084817 | |||||||
| chr13:52084818 | T | G | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1479+1459A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52084818 | |||||||
| chr13:52085137 | A | C | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1479+1140T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085137 | |||||||
| chr13:52085140 | G | A | 2 | a0001c0001t0024g0036 a0001c0001t0024g0078 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1479+1137C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085140 | |||||||
| chr13:52085523 | A | G | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1479+754T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085523 | |||||||
| chr13:52085528 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1479+749G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085528 | |||||||
| chr13:52085711 | A | C | 1 | a0001c0001t0031g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1479+566T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085711 | |||||||
| chr13:52085888 | T | C | 1 | a0001c0001t0002g0213 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1479+389A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085888 | |||||||
| chr13:52085920 | G | A | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1479+357C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085920 | |||||||
| chr13:52085967 | G | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1479+310C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085967 | |||||||
| chr13:52085993 | T | C | 1 | a0002c0002t0004g0187 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1479+284A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52085993 | |||||||
| chr13:52086098 | A | G | 32 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(29): Show |
32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1479+179T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52086098 | |||||||
| chr13:52086169 | T | C | 1 | a0001c0003t0010g0174 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1479+108A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52086169 | |||||||
| chr13:52086170 | G | T | 34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1479+107C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52086170 | |||||||
| chr13:52086171 | A | C | 34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1479+106T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52086171 | |||||||
| chr13:52086248 | C | T | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1479+29G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | 52086248 | |||||||
| chr13:52086446 | A | C | 1 | a0001c0001t0015g0197 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1393-83T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52086446 | |||||||
| chr13:52086459 | T | C | 30 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(27): Show |
30 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.1393-96A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52086459 | |||||||
| chr13:52086802 | CAAG | C | 35 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0001c0010t0048g0290 others(32): Show |
36 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1393-442_1393-440d others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52086802 | |||||||
| chr13:52087168 | C | T | 5 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1392+170G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52087168 | |||||||
| chr13:52087245 | A | T | 1 | a0001c0001t0002g0220 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1392+93T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52087245 | |||||||
| chr13:52087275 | C | T | 8 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1392+63G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52087275 | |||||||
| chr13:52087279 | A | G | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1392+59T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52087279 | |||||||
| chr13:52087280 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1392+58G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 15/23 | chr13 | 52087280 | |||||||
| chr13:52087502 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276-48T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087502 | |||||||
| chr13:52087519 | A | C | 8 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-65T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087519 | |||||||
| chr13:52087652 | G | A | 8 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-198C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087652 | |||||||
| chr13:52087679 | A | ACAGCGGC others(3): Show |
1 | a0001c0001t0007g0245 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1276-235_1276-226d others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087679 | |||||||
| chr13:52087771 | A | G | 2 | a0001c0001t0002g0201 a0001c0001t0002g0269 |
2 | HG01069.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1276-317T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087771 | |||||||
| chr13:52087786 | C | T | 1 | a0001c0001t0002g0220 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1276-332G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087786 | |||||||
| chr13:52087877 | G | A | 8 | a0001c0001t0009g0150 a0001c0003t0010g0020 a0001c0003t0010g0023 others(5): Show |
8 | HG00544.hp1 HG01099.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1276-423C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087877 | |||||||
| chr13:52087928 | C | CT | 10 | a0001c0001t0001g0124 a0001c0003t0010g0020 a0001c0003t0010g0022 others(7): Show |
10 | HG00544.hp1 HG01099.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1276-475dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087928 | |||||||
| chr13:52087928 | CT | C | 9 | a0001c0001t0001g0167 a0001c0001t0002g0219 a0001c0001t0002g0246 others(6): Show |
9 | HG01256.hp1 HG01993.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-475delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52087928 | |||||||
| chr13:52088019 | C | A | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1276-565G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088019 | |||||||
| chr13:52088099 | T | C | 2 | a0001c0001t0023g0014 a0001c0001t0023g0015 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1276-645A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088099 | |||||||
| chr13:52088171 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1276-717G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088171 | |||||||
| chr13:52088249 | G | T | 183 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(180): Show |
192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1276-795C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088249 | |||||||
| chr13:52088255 | G | GT | 18 | a0001c0001t0001g0102 a0001c0001t0001g0168 a0001c0001t0002g0219 others(15): Show |
18 | HG00323.hp1 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1276-802dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088255 | |||||||
| chr13:52088294 | G | A | 9 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(6): Show |
9 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-840C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088294 | |||||||
| chr13:52088362 | C | G | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1275+885G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088362 | |||||||
| chr13:52088443 | C | T | 1 | a0001c0001t0012g0003 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1275+804G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088443 | |||||||
| chr13:52088542 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1275+705G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088542 | |||||||
| chr13:52088581 | A | C | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1275+666T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088581 | |||||||
| chr13:52088734 | A | G | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1275+513T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088734 | |||||||
| chr13:52088839 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1275+408G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088839 | |||||||
| chr13:52088957 | G | A | 119 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(116): Show |
125 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1275+290C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52088957 | |||||||
| chr13:52089054 | G | A | 2 | a0001c0001t0024g0036 a0001c0001t0024g0078 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1275+193C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52089054 | |||||||
| chr13:52089077 | G | A | 1 | a0010c0015t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+170C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52089077 | |||||||
| chr13:52089093 | A | AAACAACA others(2): Show |
185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
193 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1275+145_1275+153d others(11): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52089093 | |||||||
| chr13:52089093 | A | AAACAACA others(5): Show |
132 | a0001c0001t0001g0051 a0001c0001t0001g0121 a0001c0001t0001g0122 others(129): Show |
138 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1275+142_1275+153d others(14): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 14/23 | chr13 | 52089093 | |||||||
| chr13:52089355 | A | G | 171 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(168): Show |
179 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.1209-42T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089355 | |||||||
| chr13:52089526 | G | T | 23 | a0001c0001t0002g0250 a0001c0001t0003g0008 a0001c0001t0003g0011 others(20): Show |
25 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1209-213C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089526 | |||||||
| chr13:52089557 | C | T | 3 | a0002c0002t0004g0184 a0002c0002t0004g0185 a0002c0002t0004g0186 |
3 | HG00408.hp2 NA18941.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1209-244G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089557 | |||||||
| chr13:52089559 | T | C | 34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1209-246A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089559 | |||||||
| chr13:52089704 | G | A | 1 | a0003c0005t0027g0319 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1209-391C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089704 | |||||||
| chr13:52089754 | G | A | 1 | a0001c0009t0001g0042 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1209-441C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089754 | |||||||
| chr13:52089842 | G | A | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1209-529C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089842 | |||||||
| chr13:52089852 | G | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0165 |
2 | HG02071.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1209-539C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089852 | |||||||
| chr13:52089961 | C | CA | 35 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0001c0003t0010g0020 others(32): Show |
36 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1209-649dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52089961 | |||||||
| chr13:52090069 | T | C | 119 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(116): Show |
125 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1209-756A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090069 | |||||||
| chr13:52090081 | C | T | 2 | a0001c0001t0006g0027 a0001c0001t0006g0028 |
2 | HG01256.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1209-768G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090081 | |||||||
| chr13:52090129 | C | T | 1 | a0001c0001t0002g0307 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1209-816G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090129 | |||||||
| chr13:52090156 | C | A | 3 | a0001c0001t0003g0011 a0001c0001t0003g0247 a0001c0001t0003g0248 |
4 | NA18944.hp1 NA18960.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1209-843G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090156 | |||||||
| chr13:52090287 | A | G | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-974T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090287 | |||||||
| chr13:52090638 | A | G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0009g0089 |
3 | NA18950.hp2 NA19077.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1209-1325T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090638 | |||||||
| chr13:52090792 | A | G | 172 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(169): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1209-1479T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52090792 | |||||||
| chr13:52091106 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0008g0044 |
2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1209-1793A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52091106 | |||||||
| chr13:52091131 | C | A | 3 | a0001c0001t0002g0250 a0001c0001t0003g0251 a0001c0001t0055g0249 |
3 | HG02300.hp2 NA19005.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1209-1818G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52091131 | |||||||
| chr13:52091250 | CAA | C | 41 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(38): Show |
43 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.1208+1802_1208+180 others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52091250 | |||||||
| chr13:52091280 | T | C | 4 | a0001c0001t0012g0003 a0001c0001t0012g0038 a0001c0001t0012g0039 others(1): Show |
5 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208+1774A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52091280 | |||||||
| chr13:52091773 | T | G | 1 | a0001c0001t0029g0252 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1208+1281A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52091773 | |||||||
| chr13:52092185 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1208+869G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092185 | |||||||
| chr13:52092221 | CTTTA | C | 34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1208+829_1208+832d others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092221 | |||||||
| chr13:52092335 | C | A | 1 | a0001c0001t0002g0264 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1208+719G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092335 | |||||||
| chr13:52092336 | G | A | 1 | a0001c0001t0002g0264 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1208+718C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092336 | |||||||
| chr13:52092424 | C | CA | 131 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(128): Show |
137 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1208+629dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092424 | |||||||
| chr13:52092469 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1208+585T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092469 | |||||||
| chr13:52092556 | C | A | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1208+498G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092556 | |||||||
| chr13:52092618 | G | A | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208+436C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52092618 | |||||||
| chr13:52093013 | T | C | 2 | a0001c0001t0031g0054 a0010c0015t0001g0056 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1208+41A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 13/23 | chr13 | 52093013 | |||||||
| chr13:52093330 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1027-95G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52093330 | |||||||
| chr13:52093403 | T | C | 2 | a0001c0001t0001g0051 a0001c0001t0030g0045 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1027-168A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52093403 | |||||||
| chr13:52093428 | C | T | 4 | a0001c0003t0013g0021 a0001c0003t0013g0024 a0001c0003t0013g0025 others(1): Show |
4 | HG00544.hp1 NA18994.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-193G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52093428 | |||||||
| chr13:52093560 | C | CA | 33 | a0001c0001t0060g0280 a0002c0002t0004g0175 a0002c0002t0004g0176 others(30): Show |
33 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.1027-326dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52093560 | |||||||
| chr13:52093904 | T | G | 1 | a0002c0002t0004g0177 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1027-669A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52093904 | |||||||
| chr13:52093922 | A | G | 3 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1027-687T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52093922 | |||||||
| chr13:52094602 | T | C | 1 | a0001c0001t0002g0253 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1027-1367A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52094602 | |||||||
| chr13:52094872 | T | C | 34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1027-1637A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52094872 | |||||||
| chr13:52094994 | C | T | 156 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(153): Show |
164 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1027-1759G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52094994 | |||||||
| chr13:52095066 | G | A | 5 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027-1831C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095066 | |||||||
| chr13:52095093 | A | T | 6 | a0001c0001t0001g0077 a0001c0001t0001g0155 a0001c0001t0001g0156 others(3): Show |
6 | HG00673.hp2 HG02074.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027-1858T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095093 | |||||||
| chr13:52095169 | G | A | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1027-1934C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095169 | |||||||
| chr13:52095204 | G | A | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1027-1969C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095204 | |||||||
| chr13:52095255 | CAAG | C | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1027-2023_1027-202 others(7): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095255 | |||||||
| chr13:52095503 | A | G | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1027-2268T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095503 | |||||||
| chr13:52095626 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1027-2391C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095626 | |||||||
| chr13:52095659 | G | A | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1027-2424C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095659 | |||||||
| chr13:52095848 | C | A | 2 | a0001c0001t0031g0054 a0010c0015t0001g0056 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1027-2613G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095848 | |||||||
| chr13:52095927 | C | G | 1 | a0001c0001t0008g0034 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1027-2692G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095927 | |||||||
| chr13:52095947 | G | A | 2 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
2 | HG01261.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1027-2712C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095947 | |||||||
| chr13:52095957 | A | T | 2 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
2 | HG01261.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1027-2722T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095957 | |||||||
| chr13:52095976 | T | A | 1 | a0010c0015t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1027-2741A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52095976 | |||||||
| chr13:52096071 | C | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0107 others(2): Show |
7 | HG00408.hp1 HG02071.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1027-2836G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52096071 | |||||||
| chr13:52096293 | G | A | 34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1027-3058C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52096293 | |||||||
| chr13:52096331 | A | G | 2 | a0001c0001t0002g0214 a0001c0001t0004g0270 |
2 | HG00639.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1027-3096T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52096331 | |||||||
| chr13:52096438 | G | A | 8 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1027-3203C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52096438 | |||||||
| chr13:52096881 | C | T | 1 | a0002c0002t0051g0316 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1026+2862G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52096881 | |||||||
| chr13:52096986 | G | A | 1 | a0001c0001t0044g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1026+2757C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52096986 | |||||||
| chr13:52097113 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1026+2630G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52097113 | |||||||
| chr13:52097161 | C | T | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1026+2582G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52097161 | |||||||
| chr13:52097408 | C | T | 3 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1026+2335G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52097408 | |||||||
| chr13:52098073 | G | A | 1 | a0001c0001t0003g0254 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1026+1670C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098073 | |||||||
| chr13:52098220 | C | T | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1026+1523G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098220 | |||||||
| chr13:52098261 | C | CAAAT | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
97 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1026+1478_1026+148 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098261 | |||||||
| chr13:52098261 | C | CAAATAAA others(1): Show |
27 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0098 others(24): Show |
28 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1026+1474_1026+148 others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098261 | |||||||
| chr13:52098261 | C | CAAATAAA others(5): Show |
7 | a0001c0001t0009g0052 a0002c0002t0004g0176 a0002c0002t0005g0065 others(4): Show |
7 | HG00099.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026+1470_1026+148 others(16): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098261 | |||||||
| chr13:52098261 | C | CAAATAAA others(9): Show |
1 | a0002c0002t0005g0067 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1026+1466_1026+148 others(20): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098261 | |||||||
| chr13:52098261 | CAAAT | C | 6 | a0001c0001t0001g0059 a0001c0001t0012g0003 a0001c0001t0012g0038 others(3): Show |
7 | HG01358.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026+1478_1026+148 others(8): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098261 | |||||||
| chr13:52098261 | CAAATAAA others(9): Show |
C | 126 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(123): Show |
132 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1026+1466_1026+148 others(20): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098261 | |||||||
| chr13:52098432 | T | TC | 160 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(157): Show |
167 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1026+1310_1026+131 others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098432 | |||||||
| chr13:52098581 | G | T | 5 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0209 others(2): Show |
5 | HG00621.hp2 NA18612.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026+1162C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098581 | |||||||
| chr13:52098698 | T | C | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1026+1045A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098698 | |||||||
| chr13:52098814 | C | G | 3 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1026+929G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098814 | |||||||
| chr13:52098868 | T | G | 184 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1026+875A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52098868 | |||||||
| chr13:52099053 | G | C | 2 | a0001c0001t0031g0054 a0010c0015t0001g0056 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1026+690C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099053 | |||||||
| chr13:52099210 | AT | A | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026+532delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099210 | |||||||
| chr13:52099292 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1026+451C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099292 | |||||||
| chr13:52099394 | G | A | 1 | a0008c0012t0001g0101 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1026+349C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099394 | |||||||
| chr13:52099542 | C | G | 2 | a0002c0002t0050g0317 a0002c0002t0051g0316 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1026+201G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099542 | |||||||
| chr13:52099543 | G | A | 2 | a0001c0001t0001g0132 a0002c0002t0004g0175 |
2 | HG01981.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1026+200C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099543 | |||||||
| chr13:52099637 | T | C | 1 | a0001c0001t0002g0269 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1026+106A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099637 | |||||||
| chr13:52099651 | A | T | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026+92T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 12/23 | chr13 | 52099651 | |||||||
| chr13:52099918 | T | C | 1 | a0001c0001t0002g0269 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.893-42A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52099918 | |||||||
| chr13:52100103 | T | C | 167 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(164): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.893-227A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100103 | |||||||
| chr13:52100108 | C | A | 1 | a0010c0015t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.893-232G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100108 | |||||||
| chr13:52100162 | T | C | 3 | a0001c0001t0003g0256 a0001c0001t0003g0257 a0001c0001t0003g0288 |
3 | HG01981.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.893-286A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100162 | |||||||
| chr13:52100305 | G | A | 2 | a0001c0001t0026g0013 a0001c0001t0052g0315 |
3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.893-429C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100305 | |||||||
| chr13:52100312 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.893-436C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100312 | |||||||
| chr13:52100322 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.893-446G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100322 | |||||||
| chr13:52100496 | C | T | 1 | a0001c0001t0012g0003 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.893-620G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100496 | |||||||
| chr13:52100720 | A | G | 1 | a0001c0001t0006g0029 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.893-844T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100720 | |||||||
| chr13:52100772 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.893-896A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100772 | |||||||
| chr13:52100911 | G | A | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.892+1022C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52100911 | |||||||
| chr13:52101097 | G | C | 3 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.892+836C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52101097 | |||||||
| chr13:52101139 | C | G | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.892+794G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52101139 | |||||||
| chr13:52101180 | C | T | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.892+753G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52101180 | |||||||
| chr13:52101195 | G | A | 2 | a0002c0002t0050g0317 a0002c0002t0051g0316 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.892+738C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52101195 | |||||||
| chr13:52101399 | C | T | 8 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.892+534G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52101399 | |||||||
| chr13:52101792 | A | G | 1 | a0002c0002t0004g0184 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.892+141T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 11/23 | chr13 | 52101792 | |||||||
| chr13:52102023 | G | A | 1 | a0010c0015t0001g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.811-9C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 10/23 | chr13 | 52102023 | |||||||
| chr13:52102392 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.610-100T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102392 | |||||||
| chr13:52102564 | G | A | 1 | a0001c0001t0044g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.610-272C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102564 | |||||||
| chr13:52102606 | T | C | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.610-314A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102606 | |||||||
| chr13:52102646 | T | A | 1 | a0001c0001t0012g0039 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.610-354A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102646 | |||||||
| chr13:52102650 | G | A | 1 | a0009c0008t0009g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.610-358C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102650 | |||||||
| chr13:52102812 | ATTTTG | A | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.610-525_610-521del others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102812 | |||||||
| chr13:52102880 | G | T | 1 | a0001c0001t0001g0313 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.610-588C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52102880 | |||||||
| chr13:52103033 | G | A | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.610-741C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52103033 | |||||||
| chr13:52103351 | T | A | 184 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.610-1059A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52103351 | |||||||
| chr13:52103711 | A | T | 1 | a0001c0001t0001g0095 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.609+787T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52103711 | |||||||
| chr13:52103745 | G | C | 1 | a0001c0001t0001g0083 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.609+753C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52103745 | |||||||
| chr13:52103843 | T | C | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.609+655A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52103843 | |||||||
| chr13:52104175 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.609+323A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52104175 | |||||||
| chr13:52104221 | C | T | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.609+277G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52104221 | |||||||
| chr13:52104264 | A | G | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.609+234T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 9/23 | chr13 | 52104264 | |||||||
| chr13:52104605 | A | G | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-53T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52104605 | |||||||
| chr13:52104831 | G | A | 34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.555-279C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52104831 | |||||||
| chr13:52104831 | G | T | 1 | a0001c0001t0002g0210 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.555-279C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52104831 | |||||||
| chr13:52104987 | T | G | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.555-435A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52104987 | |||||||
| chr13:52105237 | G | A | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.555-685C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105237 | |||||||
| chr13:52105238 | A | AGT | 14 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(11): Show |
14 | HG00544.hp2 HG01074.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.555-688_555-687dup others(2): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | |||||||
| chr13:52105238 | A | AGTGT | 4 | a0001c0001t0001g0079 a0001c0001t0008g0096 a0001c0001t0018g0017 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-690_555-687dup others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | |||||||
| chr13:52105238 | A | AGTGTGT | 5 | a0001c0001t0016g0301 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-692_555-687dup others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | |||||||
| chr13:52105238 | AGT | A | 45 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0049 others(42): Show |
47 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.555-688_555-687del others(2): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | |||||||
| chr13:52105238 | AGTGT | A | 112 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0137 others(109): Show |
120 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.555-690_555-687del others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | |||||||
| chr13:52105238 | AGTGTGT | A | 7 | a0001c0001t0002g0264 a0001c0001t0002g0291 a0001c0001t0002g0292 others(4): Show |
7 | HG00738.hp2 HG01168.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.555-692_555-687del others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | |||||||
| chr13:52105238 | AGTGTGTG others(3): Show |
A | 4 | a0001c0001t0003g0259 a0001c0001t0003g0260 a0001c0001t0029g0258 others(1): Show |
4 | NA18956.hp2 NA18959.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-696_555-687del others(10): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | |||||||
| chr13:52105238 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0002g0276 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.555-698_555-687del others(12): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105238 | |||||||
| chr13:52105244 | T | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0143 |
3 | NA19060.hp2 NA19063.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.555-692A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105244 | |||||||
| chr13:52105266 | T | C | 2 | a0001c0001t0002g0262 a0001c0001t0002g0263 |
2 | HG00597.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.555-714A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105266 | |||||||
| chr13:52105279 | GAGA | G | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.555-730_555-728del others(3): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105279 | |||||||
| chr13:52105284 | G | C | 2 | a0001c0001t0014g0295 a0001c0001t0053g0294 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.555-732C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105284 | |||||||
| chr13:52105332 | G | C | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.555-780C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105332 | |||||||
| chr13:52105452 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.555-900G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105452 | |||||||
| chr13:52105505 | C | T | 1 | a0001c0001t0041g0085 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.555-953G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105505 | |||||||
| chr13:52105626 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0045g0094 |
3 | NA18954.hp2 NA18971.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.555-1074G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105626 | |||||||
| chr13:52105669 | T | C | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.555-1117A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105669 | |||||||
| chr13:52105729 | C | T | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-1177G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105729 | |||||||
| chr13:52105786 | C | T | 4 | a0001c0001t0014g0293 a0001c0001t0014g0295 a0001c0001t0014g0296 others(1): Show |
4 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.555-1234G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52105786 | |||||||
| chr13:52106053 | T | A | 2 | a0001c0001t0002g0264 a0001c0001t0057g0279 |
2 | NA18972.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.555-1501A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106053 | |||||||
| chr13:52106179 | C | CA | 10 | a0001c0001t0001g0135 a0001c0001t0006g0027 a0001c0001t0012g0039 others(7): Show |
11 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.555-1628dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106179 | |||||||
| chr13:52106179 | CA | C | 115 | a0001c0001t0001g0046 a0001c0001t0002g0007 a0001c0001t0002g0009 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.555-1628delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106179 | |||||||
| chr13:52106441 | C | T | 1 | a0001c0004t0019g0298 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.554+1877G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106441 | |||||||
| chr13:52106660 | G | T | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.554+1658C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106660 | |||||||
| chr13:52106753 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.554+1565G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106753 | |||||||
| chr13:52106797 | G | A | 6 | a0001c0001t0012g0003 a0001c0001t0012g0038 a0001c0001t0012g0039 others(3): Show |
7 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.554+1521C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52106797 | |||||||
| chr13:52107264 | T | TACTA | 177 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.554+1053_554+1054i others(6): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107264 | |||||||
| chr13:52107295 | A | T | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.554+1023T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107295 | |||||||
| chr13:52107426 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.554+892T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107426 | |||||||
| chr13:52107463 | C | G | 167 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(164): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.554+855G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107463 | |||||||
| chr13:52107508 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.554+810G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107508 | |||||||
| chr13:52107599 | TA | T | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.554+718delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107599 | |||||||
| chr13:52107621 | C | G | 3 | a0002c0002t0004g0184 a0002c0002t0004g0185 a0002c0002t0004g0186 |
3 | HG00408.hp2 NA18941.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.554+697G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107621 | |||||||
| chr13:52107626 | A | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.554+692T>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107626 | |||||||
| chr13:52107882 | TTAAG | T | 3 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0043g0037 |
3 | HG01891.hp1 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.554+432_554+435del others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52107882 | |||||||
| chr13:52108243 | T | C | 3 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0009g0089 |
3 | NA18950.hp2 NA19077.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.554+75A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 8/23 | chr13 | 52108243 | |||||||
| chr13:52108941 | T | G | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.468-537A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52108941 | |||||||
| chr13:52108953 | A | C | 1 | a0001c0001t0012g0003 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.468-549T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52108953 | |||||||
| chr13:52109020 | C | T | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.468-616G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52109020 | |||||||
| chr13:52109127 | A | C | 184 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.468-723T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52109127 | |||||||
| chr13:52109787 | T | C | 167 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(164): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.467+553A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52109787 | |||||||
| chr13:52109921 | C | T | 2 | a0001c0001t0002g0198 a0001c0001t0002g0199 |
2 | HG00642.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.467+419G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52109921 | |||||||
| chr13:52109938 | T | C | 1 | a0009c0008t0009g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.467+402A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52109938 | |||||||
| chr13:52110115 | G | C | 184 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.467+225C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 7/23 | chr13 | 52110115 | |||||||
| chr13:52110665 | TAC | T | 123 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(120): Show |
129 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.313-90_313-89delGT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110665 | |||||||
| chr13:52110667 | C | T | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.313-90G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110667 | |||||||
| chr13:52110675 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0040g0091 |
3 | HG01346.hp1 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.313-98G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110675 | |||||||
| chr13:52110681 | C | T | 18 | a0001c0001t0002g0192 a0001c0001t0002g0196 a0001c0001t0002g0198 others(15): Show |
18 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-104G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110681 | |||||||
| chr13:52110685 | T | C | 2 | a0002c0002t0050g0317 a0002c0002t0051g0316 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.313-108A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110685 | |||||||
| chr13:52110878 | T | A | 164 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.313-301A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110878 | |||||||
| chr13:52110961 | A | G | 314 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(311): Show |
328 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.313-384T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52110961 | |||||||
| chr13:52111569 | G | A | 1 | a0001c0001t0003g0012 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.312+699C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52111569 | |||||||
| chr13:52111710 | T | C | 1 | a0001c0001t0016g0304 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.312+558A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52111710 | |||||||
| chr13:52111897 | C | A | 2 | a0001c0001t0008g0063 a0001c0001t0008g0064 |
2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.312+371G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52111897 | |||||||
| chr13:52111936 | T | C | 1 | a0001c0001t0009g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.312+332A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52111936 | |||||||
| chr13:52111985 | A | G | 1 | a0001c0001t0009g0150 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.312+283T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52111985 | |||||||
| chr13:52112104 | T | C | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.312+164A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 5/23 | chr13 | 52112104 | |||||||
| chr13:52112523 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.215-158G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52112523 | |||||||
| chr13:52112837 | C | G | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.215-472G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52112837 | |||||||
| chr13:52112933 | C | T | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.215-568G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52112933 | |||||||
| chr13:52113107 | T | A | 34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.215-742A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113107 | |||||||
| chr13:52113198 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0137 others(7): Show |
11 | NA18959.hp1 NA18960.hp2 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.215-833C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113198 | |||||||
| chr13:52113343 | G | A | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.215-978C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113343 | |||||||
| chr13:52113574 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.215-1209C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113574 | |||||||
| chr13:52113654 | T | C | 2 | a0001c0001t0001g0151 a0001c0001t0039g0145 |
2 | HG01516.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.215-1289A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113654 | |||||||
| chr13:52113716 | C | T | 123 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(120): Show |
129 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.215-1351G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113716 | |||||||
| chr13:52113747 | T | G | 10 | a0001c0001t0001g0033 a0001c0001t0001g0146 a0001c0001t0001g0159 others(7): Show |
10 | HG02258.hp2 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-1382A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113747 | |||||||
| chr13:52113955 | T | G | 1 | a0001c0001t0015g0197 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.215-1590A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52113955 | |||||||
| chr13:52114143 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.215-1778A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52114143 | |||||||
| chr13:52114731 | A | G | 1 | a0007c0011t0042g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.215-2366T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52114731 | |||||||
| chr13:52114833 | G | T | 184 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.215-2468C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52114833 | |||||||
| chr13:52115159 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.215-2794C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115159 | |||||||
| chr13:52115172 | C | A | 1 | a0001c0001t0002g0265 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.215-2807G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115172 | |||||||
| chr13:52115344 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0009g0089 |
3 | NA18950.hp2 NA19077.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.215-2979G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115344 | |||||||
| chr13:52115352 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.215-2987G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115352 | |||||||
| chr13:52115557 | T | A | 2 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
2 | HG01261.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.215-3192A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115557 | |||||||
| chr13:52115598 | C | T | 2 | a0001c0001t0008g0063 a0001c0001t0008g0064 |
2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.215-3233G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115598 | |||||||
| chr13:52115601 | C | CA | 47 | a0001c0001t0001g0053 a0001c0001t0001g0149 a0001c0001t0001g0151 others(44): Show |
50 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.215-3237dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115601 | |||||||
| chr13:52115601 | C | CAA | 9 | a0002c0002t0004g0178 a0002c0002t0004g0183 a0002c0002t0004g0190 others(6): Show |
9 | HG00621.hp1 HG00733.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-3238_215-3237d others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115601 | |||||||
| chr13:52115601 | CA | C | 111 | a0001c0001t0001g0043 a0001c0001t0001g0086 a0001c0001t0001g0154 others(108): Show |
117 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.215-3237delT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115601 | |||||||
| chr13:52115656 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.215-3291G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115656 | |||||||
| chr13:52115677 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.215-3312A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52115677 | |||||||
| chr13:52116117 | G | T | 1 | a0001c0001t0036g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.214+3202C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116117 | |||||||
| chr13:52116178 | C | CA | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
155 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.214+3140dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116178 | |||||||
| chr13:52116178 | C | CAA | 117 | a0001c0001t0001g0151 a0001c0001t0001g0163 a0001c0001t0002g0007 others(114): Show |
123 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.214+3139_214+3140d others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116178 | |||||||
| chr13:52116178 | C | CAAA | 12 | a0001c0001t0003g0281 a0001c0001t0006g0002 a0001c0001t0006g0028 others(9): Show |
13 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.214+3138_214+3140d others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116178 | |||||||
| chr13:52116503 | A | C | 11 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(8): Show |
11 | HG01192.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.214+2816T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116503 | |||||||
| chr13:52116507 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.214+2812C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116507 | |||||||
| chr13:52116848 | T | A | 184 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.214+2471A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116848 | |||||||
| chr13:52116980 | G | A | 1 | a0001c0001t0058g0284 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.214+2339C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52116980 | |||||||
| chr13:52117182 | G | A | 3 | a0001c0001t0018g0017 a0001c0001t0018g0018 a0001c0001t0044g0019 |
3 | HG03017.hp1 HG03490.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.214+2137C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52117182 | |||||||
| chr13:52117215 | G | C | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.214+2104C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52117215 | |||||||
| chr13:52117279 | C | T | 4 | a0001c0001t0014g0293 a0001c0001t0014g0295 a0001c0001t0014g0296 others(1): Show |
4 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+2040G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52117279 | |||||||
| chr13:52117311 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.214+2008A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52117311 | |||||||
| chr13:52117859 | T | G | 1 | a0009c0008t0009g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.214+1460A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52117859 | |||||||
| chr13:52117962 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.214+1357C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52117962 | |||||||
| chr13:52118384 | A | G | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.214+935T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118384 | |||||||
| chr13:52118477 | CAT | C | 2 | a0001c0001t0026g0013 a0001c0001t0052g0315 |
3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.214+840_214+841del others(2): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118477 | |||||||
| chr13:52118481 | G | A | 6 | a0001c0001t0001g0077 a0001c0001t0001g0155 a0001c0001t0001g0156 others(3): Show |
6 | HG00673.hp2 HG02074.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+838C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118481 | |||||||
| chr13:52118561 | C | T | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+758G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118561 | |||||||
| chr13:52118580 | G | A | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+739C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118580 | |||||||
| chr13:52118580 | G | T | 1 | a0006c0007t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.214+739C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118580 | |||||||
| chr13:52118587 | C | T | 1 | a0001c0001t0015g0197 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.214+732G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118587 | |||||||
| chr13:52118677 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.214+642G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118677 | |||||||
| chr13:52118713 | C | G | 1 | a0001c0001t0024g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.214+606G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118713 | |||||||
| chr13:52118767 | C | G | 2 | a0001c0001t0026g0013 a0001c0001t0052g0315 |
3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.214+552G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118767 | |||||||
| chr13:52118967 | C | T | 34 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.214+352G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52118967 | |||||||
| chr13:52119138 | G | A | 1 | a0006c0007t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.214+181C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52119138 | |||||||
| chr13:52119299 | C | T | 3 | a0001c0004t0019g0298 a0001c0004t0019g0299 a0001c0004t0019g0300 |
3 | HG02258.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.214+20G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 4/23 | chr13 | 52119299 | |||||||
| chr13:52119470 | A | G | 1 | a0001c0009t0001g0042 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.118-55T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52119470 | |||||||
| chr13:52119678 | C | T | 1 | a0001c0004t0019g0299 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.118-263G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52119678 | |||||||
| chr13:52119732 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.118-317G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52119732 | |||||||
| chr13:52119951 | T | C | 2 | a0001c0004t0019g0299 a0001c0004t0019g0300 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.118-536A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52119951 | |||||||
| chr13:52120229 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.118-814A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120229 | |||||||
| chr13:52120374 | A | G | 5 | a0002c0002t0004g0179 a0002c0002t0004g0180 a0002c0002t0004g0181 others(2): Show |
5 | HG00323.hp1 HG00733.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-959T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120374 | |||||||
| chr13:52120471 | T | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.118-1056A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120471 | |||||||
| chr13:52120566 | G | A | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-1151C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120566 | |||||||
| chr13:52120677 | A | G | 161 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(158): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.118-1262T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120677 | |||||||
| chr13:52120681 | C | T | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.118-1266G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120681 | |||||||
| chr13:52120728 | T | C | 1 | a0001c0001t0014g0296 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.118-1313A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120728 | |||||||
| chr13:52120911 | C | CA | 6 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
6 | HG04115.hp1 NA18978.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-1497dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52120911 | |||||||
| chr13:52121003 | T | C | 176 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.118-1588A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121003 | |||||||
| chr13:52121159 | C | CT | 123 | a0001c0001t0001g0057 a0001c0001t0001g0077 a0001c0001t0002g0009 others(120): Show |
128 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.118-1745dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121159 | |||||||
| chr13:52121159 | C | CTT | 5 | a0001c0001t0002g0007 a0001c0001t0002g0192 a0001c0001t0002g0195 others(2): Show |
6 | HG01106.hp1 HG01106.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-1746_118-1745d others(4): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121159 | |||||||
| chr13:52121299 | C | T | 1 | a0002c0002t0004g0175 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.118-1884G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121299 | |||||||
| chr13:52121667 | T | C | 8 | a0001c0001t0002g0287 a0001c0001t0006g0002 a0001c0001t0006g0027 others(5): Show |
9 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.118-2252A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121667 | |||||||
| chr13:52121845 | C | T | 177 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(174): Show |
185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.118-2430G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121845 | |||||||
| chr13:52121923 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.118-2508C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121923 | |||||||
| chr13:52121935 | C | CT | 12 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(9): Show |
13 | HG01192.hp1 HG01243.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-2521dupA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121935 | |||||||
| chr13:52121935 | CT | C | 8 | a0001c0001t0001g0057 a0001c0001t0001g0166 a0001c0001t0003g0288 others(5): Show |
8 | HG01081.hp2 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-2521delA | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52121935 | |||||||
| chr13:52122077 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.118-2662T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52122077 | |||||||
| chr13:52122308 | A | G | 1 | a0001c0001t0012g0003 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.118-2893T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52122308 | |||||||
| chr13:52122348 | G | A | 2 | a0001c0001t0008g0063 a0001c0001t0008g0064 |
2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.118-2933C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52122348 | |||||||
| chr13:52122476 | G | C | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.118-3061C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52122476 | |||||||
| chr13:52122766 | C | CA | 8 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(5): Show |
8 | HG01192.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-3352dupT | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52122766 | |||||||
| chr13:52123045 | A | G | 32 | a0002c0002t0004g0175 a0002c0002t0004g0176 a0002c0002t0004g0177 others(29): Show |
32 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.118-3630T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123045 | |||||||
| chr13:52123102 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.118-3687C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123102 | |||||||
| chr13:52123137 | G | C | 1 | a0001c0001t0003g0289 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.118-3722C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123137 | |||||||
| chr13:52123341 | A | G | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-3926T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123341 | |||||||
| chr13:52123358 | G | T | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.118-3943C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123358 | |||||||
| chr13:52123376 | A | G | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-3961T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123376 | |||||||
| chr13:52123450 | A | C | 2 | a0001c0001t0008g0063 a0001c0001t0008g0064 |
2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.117+3916T>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123450 | |||||||
| chr13:52123839 | G | GAACAAGT others(2760): Show |
1 | a0001c0003t0013g0026 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2769): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | |||||||
| chr13:52123839 | G | GAACAAGT others(2763): Show |
1 | a0001c0003t0010g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2772): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | |||||||
| chr13:52123839 | G | GAACAAGT others(2762): Show |
1 | a0001c0003t0010g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2771): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | |||||||
| chr13:52123839 | G | GAACAAGT others(2761): Show |
2 | a0001c0003t0010g0174 a0001c0003t0013g0025 |
2 | NA18994.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.117+3526_117+3527i others(2770): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | |||||||
| chr13:52123839 | G | GAACAAGT others(2762): Show |
1 | a0001c0003t0013g0024 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2771): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | |||||||
| chr13:52123839 | G | GAACAAGT others(2764): Show |
1 | a0001c0003t0010g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2773): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | |||||||
| chr13:52123839 | G | GAACAAGT others(2767): Show |
1 | a0001c0003t0010g0022 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2776): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | |||||||
| chr13:52123839 | G | GAACAAGT others(2764): Show |
1 | a0001c0003t0013g0021 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.117+3526_117+3527i others(2773): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123839 | |||||||
| chr13:52123957 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.117+3409A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52123957 | |||||||
| chr13:52124052 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.117+3314C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124052 | |||||||
| chr13:52124263 | G | A | 1 | a0001c0001t0012g0039 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.117+3103C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124263 | |||||||
| chr13:52124296 | C | T | 22 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(19): Show |
23 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+3070G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124296 | |||||||
| chr13:52124415 | ATAT | A | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+2948_117+2950d others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124415 | |||||||
| chr13:52124640 | C | G | 161 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(158): Show |
169 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.117+2726G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124640 | |||||||
| chr13:52124866 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.117+2500A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124866 | |||||||
| chr13:52124866 | T | G | 22 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(19): Show |
23 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+2500A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124866 | |||||||
| chr13:52124909 | G | C | 1 | a0005c0014t0004g0297 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.117+2457C>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52124909 | |||||||
| chr13:52125005 | G | A | 1 | a0001c0001t0012g0039 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.117+2361C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125005 | |||||||
| chr13:52125269 | T | C | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+2097A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125269 | |||||||
| chr13:52125283 | G | A | 22 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(19): Show |
23 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+2083C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125283 | |||||||
| chr13:52125512 | G | A | 22 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(19): Show |
23 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+1854C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125512 | |||||||
| chr13:52125530 | T | A | 22 | a0001c0001t0026g0013 a0001c0001t0052g0315 a0002c0002t0004g0175 others(19): Show |
23 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+1836A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125530 | |||||||
| chr13:52125698 | G | A | 115 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
121 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.117+1668C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125698 | |||||||
| chr13:52125800 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.117+1566A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125800 | |||||||
| chr13:52125847 | C | A | 1 | a0001c0010t0048g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.117+1519G>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125847 | |||||||
| chr13:52125893 | C | T | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+1473G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52125893 | |||||||
| chr13:52126077 | G | A | 2 | a0001c0001t0002g0291 a0001c0001t0002g0292 |
2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.117+1289C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126077 | |||||||
| chr13:52126334 | A | G | 166 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(163): Show |
174 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.117+1032T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126334 | |||||||
| chr13:52126372 | T | C | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+994A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126372 | |||||||
| chr13:52126639 | C | T | 9 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(6): Show |
9 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+727G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126639 | |||||||
| chr13:52126704 | C | T | 2 | a0001c0001t0002g0171 a0001c0001t0002g0172 |
2 | NA18971.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.117+662G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126704 | |||||||
| chr13:52126705 | G | A | 1 | a0005c0014t0004g0297 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.117+661C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126705 | |||||||
| chr13:52126780 | AAAAAG | A | 8 | a0001c0001t0016g0301 a0001c0001t0016g0303 a0001c0001t0016g0304 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+581_117+585del others(5): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126780 | |||||||
| chr13:52126884 | G | A | 1 | a0001c0001t0011g0306 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.117+482C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126884 | |||||||
| chr13:52126903 | G | T | 3 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0043g0037 |
3 | HG01891.hp1 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.117+463C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126903 | |||||||
| chr13:52126993 | T | G | 3 | a0001c0001t0002g0307 a0001c0001t0002g0309 a0001c0001t0020g0308 |
3 | HG01257.hp2 HG01346.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.117+373A>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52126993 | |||||||
| chr13:52127056 | T | A | 1 | a0001c0001t0001g0058 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.117+310A>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52127056 | |||||||
| chr13:52127189 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.117+177A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52127189 | |||||||
| chr13:52127354 | A | ACTT | 190 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0046 others(187): Show |
199 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.117+9_117+11dupAAG | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 3/23 | chr13 | 52127354 | |||||||
| chr13:52127674 | C | T | 2 | a0001c0001t0024g0036 a0001c0001t0036g0035 |
2 | HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-90-12G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52127674 | |||||||
| chr13:52128187 | G | A | 2 | a0001c0001t0001g0313 a0001c0001t0017g0314 |
2 | HG00544.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-90-525C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128187 | |||||||
| chr13:52128194 | TC | T | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90-533delG | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128194 | |||||||
| chr13:52128209 | G | A | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90-547C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128209 | |||||||
| chr13:52128248 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0008g0034 a0001c0001t0023g0014 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90-586G>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128248 | |||||||
| chr13:52128555 | T | C | 2 | a0001c0001t0026g0013 a0001c0001t0052g0315 |
3 | HG01243.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-91+474A>G | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128555 | |||||||
| chr13:52128564 | G | A | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.-91+465C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128564 | |||||||
| chr13:52128594 | G | A | 2 | a0002c0002t0050g0317 a0002c0002t0051g0316 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.-91+435C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128594 | |||||||
| chr13:52128624 | G | A | 3 | a0003c0005t0027g0318 a0003c0005t0027g0319 a0003c0005t0054g0320 |
3 | HG01192.hp1 HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-91+405C>T | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128624 | |||||||
| chr13:52128641 | A | G | 7 | a0001c0001t0006g0002 a0001c0001t0006g0027 a0001c0001t0006g0028 others(4): Show |
8 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.-91+388T>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128641 | |||||||
| chr13:52128824 | C | G | 7 | a0001c0003t0010g0020 a0001c0003t0010g0022 a0001c0003t0010g0023 others(4): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-91+205G>C | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52128824 | |||||||
| chr13:52129023 | G | T | 3 | a0001c0001t0018g0017 a0001c0001t0018g0018 a0001c0001t0044g0019 |
3 | HG03017.hp1 HG03490.hp1 HG03654.hp2 |
splice_region_variant&intron_variant | LOW | c.-91+6C>A | NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 1/23 | chr13 | 52129023 |