| geneid | 85409 |
|---|---|
| ensemblid | ENSG00000145506.14 |
| hgncid | 17046 |
| symbol | NKD2 |
| name | NKD inhibitor of WNT signaling pathway 2 |
| refseq_nuc | NM_033120.4 |
| refseq_prot | NP_149111.1 |
| ensembl_nuc | ENST00000296849.10 |
| ensembl_prot | ENSP00000296849.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 1008802 |
| end | 1038943 |
| strand | + |
| ver | v1.2 |
| region | chr5:1008802-1038943 |
| region5000 | chr5:1003802-1043943 |
| regionname0 | NKD2_chr5_1008802_1038943 |
| regionname5000 | NKD2_chr5_1003802_1043943 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 451 | 300 | 69 | 66 | 111 | 14 | 39 | 71 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0002 | 0/0 | 448 | 7 | 0 | 0 | 7 | 0 | 0 | 6 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0003 | 0/0 | 451 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0004 | 0/0 | 451 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0005 | 0/0 | 445 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0006 | 0/0 | 451 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0007 | 0/0 | 451 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0008 | 0/0 | 451 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0009 | 0/0 | 451 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1356 | 278 | 59 | 61 | 106 | 14 | 37 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0002 | 0/0 | 1356 | 10 | 6 | 3 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0003 | 0/0 | 1347 | 7 | 0 | 0 | 7 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0004 | 0/0 | 1356 | 4 | 4 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0005 | 0/0 | 1356 | 3 | 3 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0006 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0007 | 0/0 | 1356 | 2 | 1 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0008 | 0/0 | 1356 | 2 | 1 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0009 | 0/0 | 1338 | 2 | 0 | 1 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0010 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0011 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0012 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0013 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0014 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0015 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0016 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| c0017 | 0/0 | 1356 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 827 | 112 | 9 | 32 | 53 | 6 | 11 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0002 | 0/0 | 827 | 100 | 4 | 23 | 47 | 5 | 21 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0003 | 0/0 | 827 | 24 | 21 | 2 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0004 | 0/0 | 827 | 14 | 14 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0005 | 0/0 | 827 | 11 | 2 | 0 | 9 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0006 | 0/0 | 827 | 10 | 2 | 3 | 0 | 2 | 3 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0007 | 0/0 | 827 | 8 | 1 | 0 | 5 | 0 | 2 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0008 | 0/0 | 834 | 6 | 3 | 2 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0009 | 0/0 | 827 | 6 | 3 | 0 | 3 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0010 | 0/0 | 827 | 5 | 4 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0011 | 0/0 | 827 | 3 | 3 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0012 | 0/0 | 827 | 3 | 3 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0013 | 0/0 | 827 | 3 | 2 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0014 | 0/0 | 827 | 2 | 0 | 0 | 0 | 0 | 2 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0015 | 0/0 | 827 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0016 | 0/0 | 827 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0017 | 0/0 | 827 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0018 | 0/0 | 827 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0019 | 0/0 | 834 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0020 | 0/0 | 827 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0021 | 0/0 | 816 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0022 | 0/0 | 827 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0023 | 0/0 | 827 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0024 | 0/0 | 827 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0025 | 0/0 | 827 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| t0026 | 0/0 | 827 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0005 | 0/0 | 4 | 1 | 0 | 1 | 2 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0010 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0011 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1356 | 278 | 59 | 61 | 106 | 14 | 37 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0002 | 0/0 | 1356 | 10 | 6 | 3 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0005 | 0/0 | 1356 | 3 | 3 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0006 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0008 | 0/0 | 1356 | 2 | 1 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0010 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0012 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0016 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0017 | 0/0 | 1356 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0002c0003 | 0/0 | 1347 | 7 | 0 | 0 | 7 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0003c0004 | 0/0 | 1356 | 4 | 4 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0004c0007 | 0/0 | 1356 | 2 | 1 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0005c0009 | 0/0 | 1338 | 2 | 0 | 1 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0006c0015 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0007c0014 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0008c0011 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0009c0013 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2182 | 98 | 5 | 31 | 44 | 6 | 11 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0002 | 0/0 | 2182 | 95 | 4 | 22 | 45 | 5 | 19 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0003 | 0/0 | 2182 | 16 | 16 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0004 | 0/0 | 2182 | 14 | 14 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0005 | 0/0 | 2182 | 11 | 2 | 0 | 9 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0006 | 0/0 | 2182 | 8 | 1 | 2 | 0 | 2 | 3 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0007 | 0/0 | 2182 | 8 | 1 | 0 | 5 | 0 | 2 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0008 | 0/0 | 2189 | 6 | 3 | 2 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0009 | 0/0 | 2182 | 4 | 3 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0010 | 0/0 | 2182 | 4 | 4 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0012 | 0/0 | 2182 | 3 | 3 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0013 | 0/0 | 2182 | 3 | 2 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0014 | 0/0 | 2182 | 2 | 0 | 0 | 0 | 0 | 2 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0015 | 0/0 | 2182 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0019 | 0/0 | 2189 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0020 | 0/0 | 2182 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0021 | 0/0 | 2171 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0022 | 0/0 | 2182 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0001t0026 | 0/0 | 2182 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0002t0001 | 0/0 | 2182 | 2 | 1 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0002t0003 | 0/0 | 2182 | 8 | 5 | 2 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0005t0011 | 0/0 | 2182 | 3 | 3 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0006t0009 | 0/0 | 2182 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0008t0023 | 0/0 | 2182 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0008t0024 | 0/0 | 2182 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0010t0001 | 0/0 | 2182 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0012t0001 | 0/0 | 2182 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0016t0002 | 0/0 | 2182 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0001c0017t0002 | 0/0 | 2182 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0002c0003t0001 | 0/0 | 2173 | 5 | 0 | 0 | 5 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0002c0003t0002 | 0/0 | 2173 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0003c0004t0001 | 0/0 | 2182 | 3 | 3 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0003c0004t0025 | 0/0 | 2182 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0004c0007t0006 | 0/0 | 2182 | 2 | 1 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0005c0009t0002 | 0/0 | 2164 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0005c0009t0010 | 0/0 | 2164 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0006c0015t0001 | 0/0 | 2182 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0007c0014t0018 | 0/0 | 2182 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0008c0011t0016 | 0/0 | 2182 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| a0009c0013t0017 | 0/0 | 2182 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | copy fasta | chr5 | 1003802 | 1043943 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0011 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0005 | 0/0 | 4 | 1 | 0 | 1 | 2 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0003g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0005g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0006g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0006g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0006g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0006g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0007g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0007g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0007g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0007g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0008g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0008g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0009g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0010g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0012g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0012g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0012g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0013g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0013g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0013g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0014g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0014g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0015g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0019g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0020g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0021g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0022g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0001t0026g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0002t0003g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0002t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0002t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0002t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0002t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0005t0011g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0005t0011g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0006t0009g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0006t0009g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0008t0023g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0008t0024g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0010t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0010t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0012t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0016t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0001c0017t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0002c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0002c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0002c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0002c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0002c0003t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0002c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0003c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0003c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0003c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0003c0004t0025g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0004c0007t0006g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0004c0007t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0005c0009t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0005c0009t0010g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0006c0015t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0007c0014t0018g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0008c0011t0016g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| a0009c0013t0017g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | GBR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0269 | EUR | GBR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0238 | EUR | GBR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | GBR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0271 | EUR | FIN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00408 | hp1 | a0001 | c0012 | t0001 | g0012 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00438 | hp1 | a0001 | c0001 | t0009 | g0096 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00597 | hp1 | a0002 | c0003 | t0002 | g0155 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0262 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00639 | hp2 | a0001 | c0016 | t0002 | g0182 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00673 | hp2 | a0001 | c0001 | t0022 | g0199 | EAS | CHS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01099 | hp1 | a0004 | c0007 | t0006 | g0078 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0268 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0082 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01243 | hp2 | a0005 | c0009 | t0010 | g0111 | AMR | PUR | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01361 | hp2 | a0001 | c0008 | t0023 | g0021 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01496 | hp1 | a0001 | c0001 | t0026 | g0024 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0006 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | IBS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01517 | hp2 | a0001 | c0001 | t0021 | g0010 | EUR | IBS | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01891 | hp1 | a0001 | c0001 | t0012 | g0123 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0067 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01928 | hp2 | a0001 | c0001 | t0019 | g0193 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01934 | hp1 | a0001 | c0001 | t0020 | g0202 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02004 | hp1 | a0001 | c0001 | t0008 | g0094 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02027 | hp1 | a0001 | c0010 | t0001 | g0210 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02071 | hp1 | a0009 | c0013 | t0017 | g0098 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02145 | hp1 | a0001 | c0002 | t0003 | g0054 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0270 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | CDX | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CDX | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CDX | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | CDX | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0088 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02273 | hp1 | a0001 | c0001 | t0013 | g0074 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02280 | hp2 | a0001 | c0002 | t0003 | g0055 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0256 | EAS | KHV | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02572 | hp1 | a0003 | c0004 | t0001 | g0100 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02572 | hp2 | a0001 | c0001 | t0010 | g0004 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02602 | hp1 | a0001 | c0001 | t0007 | g0258 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02602 | hp2 | a0001 | c0017 | t0002 | g0016 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02615 | hp2 | a0004 | c0007 | t0006 | g0079 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02622 | hp2 | a0001 | c0001 | t0015 | g0117 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0266 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02809 | hp1 | a0007 | c0014 | t0018 | g0104 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02809 | hp2 | a0001 | c0005 | t0011 | g0002 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0081 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02897 | hp1 | a0001 | c0002 | t0003 | g0056 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0080 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0116 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02970 | hp1 | a0003 | c0004 | t0001 | g0101 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02970 | hp2 | a0001 | c0001 | t0012 | g0120 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0083 | AFR | MSL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03130 | hp1 | a0001 | c0001 | t0013 | g0073 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03130 | hp2 | a0001 | c0008 | t0024 | g0021 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0085 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0004 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03195 | hp2 | a0001 | c0001 | t0013 | g0075 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0066 | AFR | MSL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | MSL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0087 | AFR | MSL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03225 | hp2 | a0001 | c0005 | t0011 | g0114 | AFR | MSL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | MSL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | ESN | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0077 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0086 | AFR | GWD | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | MSL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0110 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03669 | hp1 | a0005 | c0009 | t0002 | g0249 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03834 | hp1 | a0001 | c0001 | t0006 | g0265 | SAS | BEB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | BEB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0267 | SAS | BEB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG04115 | hp1 | a0001 | c0001 | t0007 | g0260 | SAS | STU | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | STU | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | BEB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | BEB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG04199 | hp1 | a0001 | c0001 | t0014 | g0148 | SAS | STU | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | STU | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | STU | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | STU | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG04228 | hp1 | a0001 | c0001 | t0014 | g0149 | SAS | STU | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | STU | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0004 | AFR | YRI | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | YRI | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18612 | hp2 | a0001 | c0001 | t0008 | g0092 | EAS | CHB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | CHB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18747 | hp2 | a0001 | c0010 | t0001 | g0187 | EAS | CHB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18939 | hp1 | a0001 | c0006 | t0009 | g0097 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18944 | hp1 | a0002 | c0003 | t0001 | g0211 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18962 | hp1 | a0001 | c0001 | t0007 | g0257 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18973 | hp1 | a0002 | c0003 | t0002 | g0019 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18980 | hp2 | a0006 | c0015 | t0001 | g0231 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18981 | hp1 | a0001 | c0006 | t0009 | g0072 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18984 | hp2 | a0002 | c0003 | t0001 | g0208 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0034 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | LWK | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | LWK | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19043 | hp1 | a0001 | c0001 | t0012 | g0119 | AFR | LWK | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19064 | hp2 | a0001 | c0001 | t0007 | g0259 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19066 | hp2 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19074 | hp1 | a0002 | c0003 | t0001 | g0041 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19074 | hp2 | a0001 | c0001 | t0007 | g0027 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19091 | hp1 | a0001 | c0001 | t0007 | g0027 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0076 | AFR | YRI | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | YRI | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ASW | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | ASW | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0261 | EUR | TSI | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | TSI | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0192 | EUR | TSI | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0099 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0084 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03471 | hp1 | a0001 | c0005 | t0011 | g0002 | AFR | MSL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| HG03471 | hp2 | a0003 | c0004 | t0025 | g0102 | AFR | MSL | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | USA | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | USA | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA21309 | hp1 | a0008 | c0011 | t0016 | g0263 | AFR | LWK | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0011 | REF | REF | NKD2_chr5_1003802_1043943 | NKD2 | chr5 | 1003802 | 1043943 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:1009517
|
G | T | 1 | a0003 | 4 | HG02109.hp2 HG02572.hp1 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.98G>T | p.Arg33Leu | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/10 | 354/2182 | 98/1356 | 33/451 | chr5 | 1009517 | ||
| chr5:1035440
|
G | A | 1 | a0004 | 2 | HG01099.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.626G>A | p.Arg209Lys | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 8/10 | 882/2182 | 626/1356 | 209/451 | chr5 | 1035440 | ||
| chr5:1038261
|
C | T | 1 | a0006 | 1 | NA18980.hp2 | missense_variant | MODERATE | c.1244C>T | p.Pro415Leu | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 1500/2182 | 1244/1356 | 415/451 | chr5 | 1038261 | ||
| chr5:1038267
|
C | T | 1 | a0007 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.1250C>T | p.Thr417Met | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 1506/2182 | 1250/1356 | 417/451 | chr5 | 1038267 | ||
| chr5:1038288
|
C | T | 1 | a0009 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1271C>T | p.Ala424Val | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 1527/2182 | 1271/1356 | 424/451 | chr5 | 1038288 | ||
| chr5:1038305
|
C | T | 1 | a0008 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1288C>T | p.Arg430Trp | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 1544/2182 | 1288/1356 | 430/451 | chr5 | 1038305 | ||
| chr5:1038307
|
GCACGAGC others(11): Show |
G | 1 | a0005 | 2 | HG01243.hp2 HG03669.hp1 |
conservative_inframe_deletion | MODERATE | c.1312_1329delGAGCAC others(12): Show |
p.Glu438_His443del | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 1568/2182 | 1312/1356 | 438/451 | INFO_REALIGN_3_PRIME | chr5 | 1038307 | |
| chr5:1038331
|
GCACCACC others(2): Show |
G | 1 | a0002 | 7 | HG00597.hp1 NA18944.hp1 NA18973.hp1 others(4): Show |
conservative_inframe_deletion | MODERATE | c.1333_1341delCACCAC others(3): Show |
p.His445_His447del | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 1589/2182 | 1333/1356 | 445/451 | INFO_REALIGN_3_PRIME | chr5 | 1038331 | |
| chr5:1038932
|
AAAGAGAA others(153): Show |
A | 1 | a0001 | 1 | HG01517.hp2 | splice_region_variant | LOW | c.*560_*719del | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | chr5 | 1038932 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:1033475
|
G | A | 1 | a0001c0006 | 2 | NA18939.hp1 NA18981.hp1 |
synonymous_variant | LOW | c.306G>A | p.Pro102Pro | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 5/10 | 562/2182 | 306/1356 | 102/451 | chr5 | 1033475 | ||
| chr5:1034246
|
C | T | 1 | a0001c0017 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.342C>T | p.Cys114Cys | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 6/10 | 598/2182 | 342/1356 | 114/451 | chr5 | 1034246 | ||
| chr5:1034764
|
C | T | 1 | a0001c0010 | 2 | HG02027.hp1 NA18747.hp2 |
synonymous_variant | LOW | c.435C>T | p.Ser145Ser | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/10 | 691/2182 | 435/1356 | 145/451 | chr5 | 1034764 | ||
| chr5:1036320
|
G | A | 3 | a0001c0002a0003c0004a0008c0011 | 15 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(12): Show |
synonymous_variant | LOW | c.723G>A | p.Thr241Thr | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/10 | 979/2182 | 723/1356 | 241/451 | chr5 | 1036320 | ||
| chr5:1037896
|
C | T | 1 | a0001c0005 | 3 | HG02809.hp2 HG03225.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.879C>T | p.Ala293Ala | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 1135/2182 | 879/1356 | 293/451 | chr5 | 1037896 | ||
| chr5:1037974
|
G | A | 1 | a0001c0012 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.957G>A | p.Thr319Thr | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 1213/2182 | 957/1356 | 319/451 | chr5 | 1037974 | ||
| chr5:1038163
|
C | T | 1 | a0001c0016 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.1146C>T | p.His382His | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 1402/2182 | 1146/1356 | 382/451 | chr5 | 1038163 | ||
| chr5:1038220
|
T | C | 1 | a0009c0013 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.1203T>C | p.Ala401Ala | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 1459/2182 | 1203/1356 | 401/451 | chr5 | 1038220 | ||
| chr5:1038262
|
G | A | 1 | a0001c0008 | 2 | HG01361.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.1245G>A | p.Pro415Pro | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 1501/2182 | 1245/1356 | 415/451 | chr5 | 1038262 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:1008805
|
G | A | 7 | a0001c0001t0003a0001c0001t0010a0001c0001t0012others(4): Show | 36 | HG00639.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
5_prime_UTR_variant | MODIFIER | c.-253G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 1/10 | 253 | chr5 | 1008805 | |||||
| chr5:1008832
|
G | A | 1 | a0008c0011t0016 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-226G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 1/10 | 226 | chr5 | 1008832 | |||||
| chr5:1008883
|
T | C | 8 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(5): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-175T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 1/10 | 175 | chr5 | 1008883 | |||||
| chr5:1008951
|
C | A | 4 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(1): Show | 23 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-107C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 1/10 | 107 | chr5 | 1008951 | |||||
| chr5:1038410
|
C | T | 2 | a0001c0001t0007a0008c0011t0016 | 9 | HG02523.hp2 HG02602.hp1 HG03540.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*37C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 37 | chr5 | 1038410 | |||||
| chr5:1038411
|
A | G | 35 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(32): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
3_prime_UTR_variant | MODIFIER | c.*38A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 38 | chr5 | 1038411 | |||||
| chr5:1038416
|
G | A | 1 | a0001c0005t0011 | 3 | HG02809.hp2 HG03225.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*43G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 43 | chr5 | 1038416 | |||||
| chr5:1038447
|
C | T | 1 | a0001c0001t0014 | 2 | HG04199.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*74C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 74 | chr5 | 1038447 | |||||
| chr5:1038460
|
A | G | 1 | a0001c0001t0026 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 87 | chr5 | 1038460 | |||||
| chr5:1038472
|
G | GCCCCCAC | 2 | a0001c0001t0008a0001c0001t0019 | 7 | HG01192.hp1 HG01928.hp2 HG02004.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*108_*114dupCCCCAC others(1): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 115 | INFO_REALIGN_3_PRIME | chr5 | 1038472 | ||||
| chr5:1038486
|
C | T | 1 | a0003c0004t0025 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 113 | chr5 | 1038486 | |||||
| chr5:1038487
|
C | T | 1 | a0001c0008t0024 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 114 | chr5 | 1038487 | |||||
| chr5:1038551
|
G | A | 3 | a0001c0001t0008a0001c0001t0019a0001c0005t0011 | 10 | HG01192.hp1 HG01928.hp2 HG02004.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*178G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 178 | chr5 | 1038551 | |||||
| chr5:1038567
|
C | T | 1 | a0009c0013t0017 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*194C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 194 | chr5 | 1038567 | |||||
| chr5:1038585
|
C | T | 2 | a0001c0008t0023a0001c0008t0024 | 2 | HG01361.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*212C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 212 | chr5 | 1038585 | |||||
| chr5:1038613
|
C | T | 1 | a0001c0001t0022 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*240C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 240 | chr5 | 1038613 | |||||
| chr5:1038712
|
G | A | 1 | a0001c0001t0020 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*339G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 339 | chr5 | 1038712 | |||||
| chr5:1038782
|
C | T | 1 | a0001c0001t0013 | 3 | HG02273.hp1 HG03130.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*409C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 409 | chr5 | 1038782 | |||||
| chr5:1038888
|
C | G | 11 | a0001c0001t0002a0001c0001t0009a0001c0001t0012others(8): Show | 114 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*515C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 10/10 | 515 | chr5 | 1038888 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:1009108
|
A | AGGGC | 4 | a0001c0002t0003g0006a0001c0002t0003g0054a0001c0002t0003g0055others(1): Show | 6 | HG01496.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+40_25+43dupGGCG | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 1009108 | |||||
| chr5:1009108
|
A | AGGGCGGG others(1): Show |
28 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(25): Show | 28 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.25+36_25+43dupGGCG others(4): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 1009108 | |||||
| chr5:1009108
|
AGGGCGGG others(1): Show |
A | 7 | a0001c0001t0006g0265a0001c0001t0006g0266a0001c0001t0006g0267others(4): Show | 7 | HG00099.hp2 HG00323.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+36_25+43delGGCG others(4): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 1009108 | |||||
| chr5:1009135
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.26-44C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 1/9 | chr5 | 1009135 | ||||||
| chr5:1009310
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(260): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.61+96A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 2/9 | chr5 | 1009310 | ||||||
| chr5:1009310
|
A | T | 1 | a0008c0011t0016g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.61+96A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 2/9 | chr5 | 1009310 | ||||||
| chr5:1009391
|
C | T | 1 | a0001c0002t0003g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.62-90C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 2/9 | chr5 | 1009391 | ||||||
| chr5:1009414
|
G | A | 1 | a0001c0006t0009g0072 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.62-67G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 2/9 | chr5 | 1009414 | ||||||
| chr5:1009469
|
C | T | 1 | a0001c0001t0002g0261 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.62-12C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 2/9 | chr5 | 1009469 | ||||||
| chr5:1009576
|
G | A | 36 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(33): Show | 39 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.141+16G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1009576 | ||||||
| chr5:1009616
|
G | A | 4 | a0003c0004t0001g0099a0003c0004t0001g0100a0003c0004t0001g0101others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+56G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1009616 | ||||||
| chr5:1009649
|
G | A | 2 | a0001c0001t0002g0103a0007c0014t0018g0104 | 2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.141+89G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1009649 | ||||||
| chr5:1009689
|
C | CG | 38 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(35): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.141+134dupG | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1009689 | |||||
| chr5:1009741
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.141+181C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1009741 | ||||||
| chr5:1009742
|
G | T | 1 | a0001c0001t0001g0105 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.141+182G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1009742 | ||||||
| chr5:1009771
|
CTGAGTGG others(4): Show |
C | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.141+213_141+223del others(11): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1009771 | |||||
| chr5:1009923
|
C | T | 13 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0246others(10): Show | 15 | HG01106.hp2 HG01123.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.141+363C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1009923 | ||||||
| chr5:1009968
|
A | G | 38 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(35): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.141+408A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1009968 | ||||||
| chr5:1010051
|
G | A | 38 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(35): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.141+491G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010051 | ||||||
| chr5:1010195
|
AG | A | 6 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 7 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+636delG | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010195 | ||||||
| chr5:1010197
|
A | C | 6 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 7 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+637A>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010197 | ||||||
| chr5:1010198
|
A | C | 6 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 7 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+638A>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010198 | ||||||
| chr5:1010201
|
GT | G | 6 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 7 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+642delT | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010201 | ||||||
| chr5:1010203
|
C | G | 6 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 7 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+643C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010203 | ||||||
| chr5:1010204
|
C | A | 6 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 7 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+644C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010204 | ||||||
| chr5:1010223
|
G | A | 2 | a0001c0002t0003g0006a0001c0002t0003g0054 | 4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+663G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010223 | ||||||
| chr5:1010260
|
G | A | 1 | a0001c0001t0006g0076 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.141+700G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010260 | ||||||
| chr5:1010295
|
G | A | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.141+735G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010295 | ||||||
| chr5:1010361
|
C | T | 1 | a0001c0001t0002g0245 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.141+801C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010361 | ||||||
| chr5:1010386
|
GA | G | 8 | a0001c0001t0006g0265a0001c0001t0006g0266a0001c0001t0006g0267others(5): Show | 8 | HG00099.hp2 HG00323.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.141+827delA | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010386 | ||||||
| chr5:1010571
|
C | T | 11 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(8): Show | 14 | HG00438.hp1 HG00438.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+1011C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010571 | ||||||
| chr5:1010583
|
G | C | 3 | a0001c0001t0007g0077a0004c0007t0006g0078a0004c0007t0006g0079 | 3 | HG01099.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.141+1023G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010583 | ||||||
| chr5:1010686
|
C | T | 3 | a0001c0001t0006g0269a0001c0001t0006g0270a0001c0001t0006g0271 | 3 | HG00099.hp2 HG00323.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.141+1126C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010686 | ||||||
| chr5:1010692
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0244others(1): Show | 6 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+1132A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010692 | ||||||
| chr5:1010845
|
C | T | 38 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(35): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.141+1285C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010845 | ||||||
| chr5:1010896
|
T | C | 38 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(35): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.141+1336T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010896 | ||||||
| chr5:1010942
|
G | A | 1 | a0001c0001t0003g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.141+1382G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010942 | ||||||
| chr5:1010959
|
A | G | 1 | a0007c0014t0018g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.141+1399A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1010959 | ||||||
| chr5:1011032
|
T | C | 4 | a0003c0004t0001g0099a0003c0004t0001g0100a0003c0004t0001g0101others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+1472T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1011032 | ||||||
| chr5:1011034
|
G | A | 38 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(35): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.141+1474G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1011034 | ||||||
| chr5:1011359
|
A | G | 3 | a0001c0001t0007g0077a0004c0007t0006g0078a0004c0007t0006g0079 | 3 | HG01099.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.141+1799A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1011359 | ||||||
| chr5:1011375
|
A | G | 1 | a0001c0001t0002g0243 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.141+1815A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1011375 | ||||||
| chr5:1011426
|
C | T | 1 | a0003c0004t0025g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.141+1866C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1011426 | ||||||
| chr5:1011590
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.141+2030A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1011590 | ||||||
| chr5:1011622
|
G | T | 1 | a0001c0001t0001g0241 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.141+2062G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1011622 | ||||||
| chr5:1011891
|
G | A | 3 | a0001c0001t0007g0077a0004c0007t0006g0078a0004c0007t0006g0079 | 3 | HG01099.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.141+2331G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1011891 | ||||||
| chr5:1011894
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.141+2334C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1011894 | ||||||
| chr5:1011924
|
T | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(263): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.141+2364T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1011924 | ||||||
| chr5:1011953
|
C | T | 1 | a0001c0001t0002g0240 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.141+2393C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1011953 | ||||||
| chr5:1012168
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(186): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.141+2608C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012168 | ||||||
| chr5:1012204
|
T | G | 7 | a0001c0001t0006g0076a0001c0001t0007g0027a0001c0001t0007g0256others(4): Show | 8 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.141+2644T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012204 | ||||||
| chr5:1012211
|
T | G | 5 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 5 | HG00544.hp2 NA18944.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+2651T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012211 | ||||||
| chr5:1012304
|
C | T | 1 | a0001c0001t0007g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.141+2744C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012304 | ||||||
| chr5:1012331
|
C | T | 20 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(17): Show | 23 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.141+2771C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012331 | ||||||
| chr5:1012415
|
G | A | 1 | a0001c0001t0002g0131 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.141+2855G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012415 | ||||||
| chr5:1012449
|
G | A | 1 | a0001c0001t0003g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.141+2889G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012449 | ||||||
| chr5:1012471
|
G | A | 28 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0013others(25): Show | 36 | HG00639.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.141+2911G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012471 | ||||||
| chr5:1012517
|
C | G | 7 | a0001c0001t0006g0076a0001c0001t0007g0027a0001c0001t0007g0256others(4): Show | 8 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.141+2957C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012517 | ||||||
| chr5:1012534
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.141+2974G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012534 | ||||||
| chr5:1012543
|
G | A | 1 | a0001c0001t0003g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.141+2983G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012543 | ||||||
| chr5:1012552
|
G | T | 38 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(35): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.141+2992G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012552 | ||||||
| chr5:1012685
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.141+3125C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012685 | ||||||
| chr5:1012686
|
G | C | 1 | a0001c0001t0005g0089 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.141+3126G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012686 | ||||||
| chr5:1012698
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.141+3138G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012698 | ||||||
| chr5:1012700
|
A | G | 38 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(35): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.141+3140A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012700 | ||||||
| chr5:1012765
|
GCTGCCCC others(4): Show |
G | 1 | a0001c0001t0004g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.141+3225_141+3235d others(13): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1012765 | |||||
| chr5:1012852
|
G | A | 28 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0013others(25): Show | 36 | HG00639.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.141+3292G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1012852 | ||||||
| chr5:1013011
|
G | C | 4 | a0003c0004t0001g0099a0003c0004t0001g0100a0003c0004t0001g0101others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+3451G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1013011 | ||||||
| chr5:1013017
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.141+3457G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1013017 | ||||||
| chr5:1013050
|
T | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.141+3490T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1013050 | ||||||
| chr5:1013067
|
C | G | 1 | a0003c0004t0025g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.141+3507C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1013067 | ||||||
| chr5:1013078
|
C | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 4 | HG00408.hp1 NA18965.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+3518C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1013078 | ||||||
| chr5:1013154
|
G | A | 11 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(8): Show | 15 | HG00639.hp1 HG01243.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.141+3594G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1013154 | ||||||
| chr5:1013307
|
A | C | 1 | a0001c0001t0004g0071 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.141+3747A>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1013307 | ||||||
| chr5:1013361
|
C | T | 9 | a0001c0001t0003g0013a0001c0001t0003g0108a0001c0001t0003g0118others(6): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+3801C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1013361 | ||||||
| chr5:1013523
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.141+3963C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1013523 | ||||||
| chr5:1013579
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(184): Show | 215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.141+4019T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1013579 | ||||||
| chr5:1013591
|
C | T | 1 | a0001c0001t0002g0238 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.141+4031C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1013591 | ||||||
| chr5:1013689
|
GGTGCTGA others(10): Show |
G | 1 | a0001c0001t0013g0075 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.141+4146_141+4162d others(19): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1013689 | |||||
| chr5:1013908
|
C | T | 1 | a0003c0004t0001g0101 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.141+4348C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1013908 | ||||||
| chr5:1014125
|
T | G | 8 | a0001c0001t0006g0265a0001c0001t0006g0266a0001c0001t0006g0267others(5): Show | 8 | HG00099.hp2 HG00323.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.141+4565T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014125 | ||||||
| chr5:1014453
|
C | T | 2 | a0001c0001t0008g0087a0001c0001t0008g0088 | 2 | HG02257.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.141+4893C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014453 | ||||||
| chr5:1014495
|
T | G | 7 | a0001c0001t0006g0076a0001c0001t0007g0027a0001c0001t0007g0256others(4): Show | 8 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.141+4935T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014495 | ||||||
| chr5:1014525
|
G | T | 38 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(35): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.141+4965G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014525 | ||||||
| chr5:1014620
|
A | G | 1 | a0008c0011t0016g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.141+5060A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014620 | ||||||
| chr5:1014626
|
A | G | 38 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(35): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.141+5066A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014626 | ||||||
| chr5:1014660
|
C | T | 1 | a0001c0001t0015g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.141+5100C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014660 | ||||||
| chr5:1014738
|
A | G | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.141+5178A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014738 | ||||||
| chr5:1014783
|
A | T | 1 | a0001c0001t0006g0271 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.141+5223A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014783 | ||||||
| chr5:1014812
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.141+5252T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014812 | ||||||
| chr5:1014855
|
C | T | 2 | a0001c0006t0009g0072a0001c0006t0009g0097 | 2 | NA18939.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.141+5295C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014855 | ||||||
| chr5:1014863
|
G | A | 1 | a0001c0001t0013g0075 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.141+5303G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014863 | ||||||
| chr5:1014948
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(94): Show | 110 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.141+5388C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014948 | ||||||
| chr5:1014960
|
C | T | 1 | a0001c0001t0003g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.141+5400C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014960 | ||||||
| chr5:1014994
|
G | A | 2 | a0001c0001t0002g0134a0001c0001t0002g0135 | 2 | HG01099.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.141+5434G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1014994 | ||||||
| chr5:1015006
|
C | A | 10 | a0001c0001t0003g0013a0001c0001t0003g0107a0001c0001t0003g0108others(7): Show | 11 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.141+5446C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1015006 | ||||||
| chr5:1015324
|
C | T | 9 | a0001c0001t0003g0013a0001c0001t0003g0108a0001c0001t0003g0118others(6): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+5764C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1015324 | ||||||
| chr5:1015336
|
A | G | 1 | a0001c0001t0004g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.141+5776A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1015336 | ||||||
| chr5:1015426
|
T | G | 1 | a0001c0001t0001g0186 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.141+5866T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1015426 | ||||||
| chr5:1015432
|
T | G | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.141+5872T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1015432 | ||||||
| chr5:1015480
|
T | C | 33 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(30): Show | 37 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.141+5920T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1015480 | ||||||
| chr5:1015543
|
A | T | 1 | a0001c0001t0001g0186 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.141+5983A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1015543 | ||||||
| chr5:1015699
|
G | A | 20 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(17): Show | 23 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.141+6139G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1015699 | ||||||
| chr5:1015702
|
A | G | 4 | a0003c0004t0001g0099a0003c0004t0001g0100a0003c0004t0001g0101others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+6142A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1015702 | ||||||
| chr5:1015745
|
C | G | 1 | a0001c0001t0009g0096 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.141+6185C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1015745 | ||||||
| chr5:1015818
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.141+6258C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1015818 | ||||||
| chr5:1015893
|
G | A | 34 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(31): Show | 38 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.141+6333G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1015893 | ||||||
| chr5:1015960
|
C | T | 7 | a0001c0001t0006g0265a0001c0001t0006g0266a0001c0001t0006g0267others(4): Show | 7 | HG00099.hp2 HG00323.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+6400C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1015960 | ||||||
| chr5:1016002
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0004g0060a0001c0001t0004g0061 | 3 | HG01261.hp1 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.141+6442G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016002 | ||||||
| chr5:1016078
|
G | A | 1 | a0001c0001t0002g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.141+6518G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016078 | ||||||
| chr5:1016085
|
C | G | 1 | a0001c0001t0003g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.141+6525C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016085 | ||||||
| chr5:1016105
|
C | G | 28 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0013others(25): Show | 36 | HG00639.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.141+6545C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016105 | ||||||
| chr5:1016111
|
G | A | 3 | a0001c0001t0013g0073a0001c0001t0013g0074a0001c0001t0013g0075 | 3 | HG02273.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.141+6551G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016111 | ||||||
| chr5:1016168
|
G | A | 1 | a0001c0001t0002g0246 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.141+6608G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016168 | ||||||
| chr5:1016171
|
G | C | 34 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(31): Show | 38 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.141+6611G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016171 | ||||||
| chr5:1016191
|
A | G | 34 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(31): Show | 38 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.141+6631A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016191 | ||||||
| chr5:1016305
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.141+6745A>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016305 | ||||||
| chr5:1016502
|
CAG | C | 9 | a0001c0001t0003g0013a0001c0001t0003g0108a0001c0001t0003g0118others(6): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+6946_141+6947d others(4): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1016502 | |||||
| chr5:1016509
|
G | A | 1 | a0001c0010t0001g0187 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.141+6949G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016509 | ||||||
| chr5:1016617
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.141+7057C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016617 | ||||||
| chr5:1016653
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.141+7093C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016653 | ||||||
| chr5:1016666
|
C | A | 1 | a0001c0001t0001g0051 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.141+7106C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016666 | ||||||
| chr5:1016727
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(194): Show | 225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.141+7167G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016727 | ||||||
| chr5:1016759
|
C | T | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.141+7199C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1016759 | ||||||
| chr5:1016899
|
T | TCCACAAA others(29): Show |
3 | a0001c0001t0013g0073a0001c0001t0013g0074a0001c0001t0013g0075 | 3 | HG02273.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.141+7359_141+7394d others(38): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1016899 | |||||
| chr5:1017000
|
C | A | 4 | a0003c0004t0001g0099a0003c0004t0001g0100a0003c0004t0001g0101others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+7440C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017000 | ||||||
| chr5:1017066
|
C | T | 2 | a0001c0001t0003g0109a0001c0001t0010g0116 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.141+7506C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017066 | ||||||
| chr5:1017106
|
C | A | 23 | a0001c0001t0003g0004a0001c0001t0003g0013a0001c0001t0003g0108others(20): Show | 28 | HG00639.hp1 HG01243.hp2 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.141+7546C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017106 | ||||||
| chr5:1017131
|
G | C | 6 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 7 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+7571G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017131 | ||||||
| chr5:1017138
|
C | G | 3 | a0001c0001t0002g0019a0001c0001t0002g0031a0002c0003t0002g0019 | 3 | NA18612.hp1 NA18973.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.141+7578C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017138 | ||||||
| chr5:1017196
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(257): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.141+7636T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017196 | ||||||
| chr5:1017214
|
C | T | 1 | a0001c0001t0008g0086 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.141+7654C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017214 | ||||||
| chr5:1017279
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.141+7719C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017279 | ||||||
| chr5:1017280
|
T | G | 1 | a0001c0001t0002g0255 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.141+7720T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017280 | ||||||
| chr5:1017281
|
G | C | 1 | a0001c0001t0002g0255 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.141+7721G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017281 | ||||||
| chr5:1017323
|
G | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(184): Show | 215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.141+7763G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017323 | ||||||
| chr5:1017327
|
G | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.141+7767G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017327 | ||||||
| chr5:1017338
|
G | A | 34 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(31): Show | 38 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.141+7778G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017338 | ||||||
| chr5:1017367
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0186a0001c0001t0001g0236 | 4 | HG00558.hp1 NA18948.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+7807C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017367 | ||||||
| chr5:1017398
|
G | A | 3 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0088 | 3 | HG02257.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.141+7838G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017398 | ||||||
| chr5:1017434
|
G | A | 11 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(8): Show | 15 | HG00639.hp1 HG01243.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.141+7874G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017434 | ||||||
| chr5:1017469
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.141+7909C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017469 | ||||||
| chr5:1017477
|
C | T | 34 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(31): Show | 38 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.141+7917C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017477 | ||||||
| chr5:1017498
|
G | A | 7 | a0001c0001t0006g0265a0001c0001t0006g0266a0001c0001t0006g0267others(4): Show | 7 | HG00099.hp2 HG00323.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+7938G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017498 | ||||||
| chr5:1017572
|
G | C | 3 | a0001c0001t0013g0073a0001c0001t0013g0074a0001c0001t0013g0075 | 3 | HG02273.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.141+8012G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017572 | ||||||
| chr5:1017666
|
GCC | G | 67 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0013others(64): Show | 79 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.141+8111_141+8112d others(4): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1017666 | |||||
| chr5:1017681
|
G | A | 4 | a0003c0004t0001g0099a0003c0004t0001g0100a0003c0004t0001g0101others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+8121G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017681 | ||||||
| chr5:1017731
|
C | T | 28 | a0001c0001t0005g0003a0001c0001t0005g0080a0001c0001t0005g0081others(25): Show | 32 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.141+8171C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017731 | ||||||
| chr5:1017792
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.141+8232C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017792 | ||||||
| chr5:1017800
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 85 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.141+8240G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017800 | ||||||
| chr5:1017929
|
G | C | 2 | a0001c0001t0004g0063a0001c0001t0004g0064 | 2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.141+8369G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017929 | ||||||
| chr5:1017984
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.141+8424G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017984 | ||||||
| chr5:1017985
|
A | G | 1 | a0001c0001t0002g0255 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.141+8425A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1017985 | ||||||
| chr5:1018049
|
A | G | 1 | a0001c0002t0001g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.141+8489A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018049 | ||||||
| chr5:1018070
|
G | A | 6 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(3): Show | 6 | HG00558.hp2 HG02155.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+8510G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018070 | ||||||
| chr5:1018072
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.141+8512G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018072 | ||||||
| chr5:1018083
|
G | A | 9 | a0001c0001t0003g0013a0001c0001t0003g0108a0001c0001t0003g0118others(6): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+8523G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018083 | ||||||
| chr5:1018087
|
G | C | 1 | a0001c0001t0004g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.141+8527G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018087 | ||||||
| chr5:1018110
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.141+8550C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018110 | ||||||
| chr5:1018140
|
G | A | 1 | a0001c0001t0004g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.141+8580G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018140 | ||||||
| chr5:1018175
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.141+8615C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018175 | ||||||
| chr5:1018203
|
C | T | 28 | a0001c0001t0001g0070a0001c0001t0003g0002a0001c0001t0003g0004others(25): Show | 36 | HG00639.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.141+8643C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018203 | ||||||
| chr5:1018205
|
C | G | 4 | a0001c0001t0013g0073a0001c0001t0013g0074a0001c0001t0013g0075others(1): Show | 4 | HG02273.hp1 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+8645C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018205 | ||||||
| chr5:1018333
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.141+8773C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018333 | ||||||
| chr5:1018530
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.141+8970C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018530 | ||||||
| chr5:1018570
|
CAG | C | 25 | a0001c0001t0001g0070a0001c0001t0003g0108a0001c0001t0003g0124others(22): Show | 28 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.141+9011_141+9012d others(4): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018570 | ||||||
| chr5:1018665
|
G | A | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.141+9105G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018665 | ||||||
| chr5:1018817
|
G | A | 1 | a0001c0001t0002g0240 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.141+9257G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018817 | ||||||
| chr5:1018836
|
G | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.141+9276G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018836 | ||||||
| chr5:1018843
|
G | A | 1 | a0001c0002t0003g0110 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.141+9283G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1018843 | ||||||
| chr5:1019116
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(231): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.141+9556G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019116 | ||||||
| chr5:1019168
|
C | A | 7 | a0001c0001t0007g0027a0001c0001t0007g0077a0001c0001t0007g0256others(4): Show | 8 | HG02523.hp2 HG02602.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.141+9608C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019168 | ||||||
| chr5:1019239
|
G | A | 2 | a0001c0002t0001g0185a0001c0002t0003g0055 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.141+9679G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019239 | ||||||
| chr5:1019262
|
C | A | 21 | a0001c0001t0001g0144a0001c0001t0002g0007a0001c0001t0002g0008others(18): Show | 25 | HG00597.hp1 HG00642.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.141+9702C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019262 | ||||||
| chr5:1019318
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.141+9758C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019318 | ||||||
| chr5:1019368
|
G | A | 1 | a0001c0002t0003g0055 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.141+9808G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019368 | ||||||
| chr5:1019458
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG00099.hp1 HG01074.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.141+9898C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019458 | ||||||
| chr5:1019509
|
C | A | 1 | a0001c0001t0001g0032 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.141+9949C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019509 | ||||||
| chr5:1019520
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(233): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.141+9960T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019520 | ||||||
| chr5:1019564
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(196): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.141+10004C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019564 | ||||||
| chr5:1019583
|
G | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.141+10023G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019583 | ||||||
| chr5:1019663
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(233): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.141+10103A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019663 | ||||||
| chr5:1019699
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(233): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.141+10139T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019699 | ||||||
| chr5:1019772
|
G | A | 4 | a0003c0004t0001g0099a0003c0004t0001g0100a0003c0004t0001g0101others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+10212G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019772 | ||||||
| chr5:1019822
|
A | C | 8 | a0001c0001t0003g0107a0001c0002t0001g0185a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG01496.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+10262A>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1019822 | ||||||
| chr5:1020005
|
T | G | 1 | a0001c0001t0002g0245 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.141+10445T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1020005 | ||||||
| chr5:1020031
|
A | T | 1 | a0001c0001t0002g0245 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.141+10471A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1020031 | ||||||
| chr5:1020088
|
C | T | 13 | a0001c0001t0001g0070a0001c0001t0003g0013a0001c0001t0003g0108others(10): Show | 14 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+10528C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1020088 | ||||||
| chr5:1020249
|
C | T | 1 | a0001c0001t0002g0245 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.141+10689C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1020249 | ||||||
| chr5:1020250
|
T | C | 1 | a0001c0001t0002g0245 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.141+10690T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1020250 | ||||||
| chr5:1020435
|
A | G | 266 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(263): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.141+10875A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1020435 | ||||||
| chr5:1020555
|
C | T | 1 | a0006c0015t0001g0231 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.141+10995C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1020555 | ||||||
| chr5:1020603
|
C | T | 1 | a0006c0015t0001g0231 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.141+11043C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1020603 | ||||||
| chr5:1020619
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.141+11059C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1020619 | ||||||
| chr5:1020669
|
C | CT | 35 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0130others(32): Show | 43 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.141+11130dupT | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1020669 | |||||
| chr5:1020669
|
C | CTT | 8 | a0001c0001t0005g0095a0001c0001t0007g0027a0001c0001t0007g0077others(5): Show | 9 | HG02523.hp2 HG02602.hp1 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+11129_141+1113 others(6): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1020669 | |||||
| chr5:1020669
|
CT | C | 20 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0048others(17): Show | 20 | HG00099.hp1 HG00558.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.141+11130delT | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1020669 | |||||
| chr5:1020983
|
A | G | 2 | a0001c0001t0003g0109a0001c0001t0010g0116 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.142-11169A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1020983 | ||||||
| chr5:1021045
|
GACAGAA | G | 19 | a0001c0001t0001g0070a0001c0001t0003g0002a0001c0001t0003g0013others(16): Show | 23 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.142-11103_142-1109 others(10): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1021045 | |||||
| chr5:1021164
|
G | A | 4 | a0003c0004t0001g0099a0003c0004t0001g0100a0003c0004t0001g0101others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-10988G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021164 | ||||||
| chr5:1021263
|
A | G | 1 | a0001c0001t0002g0181 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.142-10889A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021263 | ||||||
| chr5:1021361
|
C | G | 1 | a0001c0001t0001g0229 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.142-10791C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021361 | ||||||
| chr5:1021362
|
G | A | 7 | a0001c0001t0007g0027a0001c0001t0007g0077a0001c0001t0007g0256others(4): Show | 8 | HG02523.hp2 HG02602.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-10790G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021362 | ||||||
| chr5:1021390
|
ACCCG | A | 5 | a0001c0001t0006g0076a0001c0001t0008g0082a0001c0001t0008g0086others(2): Show | 5 | HG01192.hp1 HG02257.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-10761_142-1075 others(8): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021390 | ||||||
| chr5:1021392
|
C | T | 2 | a0004c0007t0006g0078a0004c0007t0006g0079 | 2 | HG01099.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.142-10760C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021392 | ||||||
| chr5:1021394
|
G | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(258): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.142-10758G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021394 | ||||||
| chr5:1021562
|
A | G | 6 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0247others(3): Show | 8 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-10590A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021562 | ||||||
| chr5:1021584
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(225): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.142-10568G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021584 | ||||||
| chr5:1021672
|
G | T | 1 | a0001c0001t0004g0068 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.142-10480G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021672 | ||||||
| chr5:1021674
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(120): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.142-10478G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021674 | ||||||
| chr5:1021708
|
A | T | 3 | a0001c0001t0013g0073a0001c0001t0013g0074a0001c0001t0013g0075 | 3 | HG02273.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.142-10444A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021708 | ||||||
| chr5:1021712
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.142-10440C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021712 | ||||||
| chr5:1021717
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.142-10435G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021717 | ||||||
| chr5:1021773
|
C | T | 2 | a0001c0001t0007g0027a0001c0001t0007g0259 | 3 | NA19064.hp2 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.142-10379C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021773 | ||||||
| chr5:1021789
|
C | A | 1 | a0001c0016t0002g0182 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.142-10363C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021789 | ||||||
| chr5:1021789
|
C | T | 1 | a0001c0001t0002g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.142-10363C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021789 | ||||||
| chr5:1021795
|
A | G | 7 | a0001c0001t0007g0027a0001c0001t0007g0077a0001c0001t0007g0256others(4): Show | 8 | HG02523.hp2 HG02602.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-10357A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021795 | ||||||
| chr5:1021881
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.142-10271C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021881 | ||||||
| chr5:1021911
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | NA18997.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.142-10241C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021911 | ||||||
| chr5:1021912
|
A | T | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-10240A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021912 | ||||||
| chr5:1021947
|
G | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 5 | HG02132.hp1 HG02135.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-10205G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1021947 | ||||||
| chr5:1022046
|
C | A | 1 | a0001c0006t0009g0097 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.142-10106C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022046 | ||||||
| chr5:1022070
|
T | TCCTTGCT others(30): Show |
1 | a0001c0001t0002g0246 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.142-10073_142-1003 others(41): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022070 | |||||
| chr5:1022097
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.142-10055T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022097 | ||||||
| chr5:1022149
|
CTGTCCCT others(34): Show |
C | 1 | a0001c0001t0003g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.142-9983_142-9943d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022149 | |||||
| chr5:1022149
|
CTGTCCCT others(858): Show |
C | 3 | a0001c0001t0002g0019a0001c0001t0002g0031a0002c0003t0002g0019 | 3 | NA18612.hp1 NA18973.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.142-9983_142-9119d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022149 | |||||
| chr5:1022153
|
CCCTGCTC others(6): Show |
C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.142-9992_142-9980d others(15): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022153 | |||||
| chr5:1022160
|
C | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(137): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.142-9992C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022160 | ||||||
| chr5:1022178
|
T | C | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9974T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022178 | ||||||
| chr5:1022182
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9970C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022182 | ||||||
| chr5:1022185
|
A | G | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9967A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022185 | ||||||
| chr5:1022189
|
A | G | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9963A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022189 | ||||||
| chr5:1022201
|
C | G | 1 | a0001c0001t0003g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.142-9951C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022201 | ||||||
| chr5:1022202
|
T | C | 9 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(6): Show | 11 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.142-9950T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022202 | ||||||
| chr5:1022211
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(119): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.142-9941G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022211 | ||||||
| chr5:1022219
|
T | C | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9933T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022219 | ||||||
| chr5:1022223
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9929C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022223 | ||||||
| chr5:1022223
|
CCAGCCCT others(116): Show |
C | 2 | a0003c0004t0001g0099a0003c0004t0001g0101 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.142-9922_142-9800d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022223 | |||||
| chr5:1022230
|
T | G | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9922T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022230 | ||||||
| chr5:1022252
|
G | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9900G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022252 | ||||||
| chr5:1022260
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.142-9892C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022260 | ||||||
| chr5:1022264
|
T | C | 2 | a0001c0001t0001g0162a0009c0013t0017g0098 | 2 | HG02071.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.142-9888T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022264 | ||||||
| chr5:1022271
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.142-9881A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022271 | ||||||
| chr5:1022281
|
C | T | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-9871C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022281 | ||||||
| chr5:1022293
|
G | T | 2 | a0001c0001t0001g0162a0009c0013t0017g0098 | 2 | HG02071.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.142-9859G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022293 | ||||||
| chr5:1022301
|
T | C | 10 | a0001c0001t0002g0133a0001c0001t0003g0004a0001c0001t0003g0112others(7): Show | 12 | HG01243.hp2 HG02055.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-9851T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022301 | ||||||
| chr5:1022305
|
C | T | 10 | a0001c0001t0002g0133a0001c0001t0003g0004a0001c0001t0003g0112others(7): Show | 12 | HG01243.hp2 HG02055.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-9847C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022305 | ||||||
| chr5:1022307
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.142-9845A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022307 | ||||||
| chr5:1022312
|
T | A | 28 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0029others(25): Show | 34 | HG00597.hp1 HG01243.hp2 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.142-9840T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022312 | ||||||
| chr5:1022312
|
T | G | 71 | a0001c0001t0001g0047a0001c0001t0001g0162a0001c0001t0001g0168others(68): Show | 80 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.142-9840T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022312 | ||||||
| chr5:1022312
|
T | TTTGTCCC others(34): Show |
1 | a0001c0001t0007g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-9821_142-9820i others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022312 | |||||
| chr5:1022332
|
C | T | 6 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 7 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-9820C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022332 | ||||||
| chr5:1022334
|
G | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(155): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.142-9818G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022334 | ||||||
| chr5:1022342
|
T | C | 99 | a0001c0001t0001g0047a0001c0001t0001g0162a0001c0001t0001g0168others(96): Show | 113 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.142-9810T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022342 | ||||||
| chr5:1022342
|
T | TGTCCCAG others(35): Show |
1 | a0001c0001t0002g0045 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142-9807_142-9806i others(44): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022342 | |||||
| chr5:1022342
|
TGTCTCAG others(75): Show |
T | 49 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(46): Show | 58 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.142-9758_142-9677d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022342 | |||||
| chr5:1022342
|
TGTCTCAG others(199): Show |
T | 12 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(9): Show | 12 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-9799_142-9594d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022342 | |||||
| chr5:1022343
|
G | A | 1 | a0001c0001t0007g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-9809G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022343 | ||||||
| chr5:1022346
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(111): Show | 129 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.142-9806T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022346 | ||||||
| chr5:1022346
|
TCAGCCCA others(34): Show |
T | 1 | a0001c0001t0002g0261 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.142-9799_142-9759d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022346 | |||||
| chr5:1022346
|
TCAGCCCA others(158): Show |
T | 4 | a0001c0001t0007g0256a0001c0001t0007g0257a0001c0001t0007g0258others(1): Show | 4 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-9799_142-9635d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022346 | |||||
| chr5:1022348
|
A | G | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-9804A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022348 | ||||||
| chr5:1022349
|
G | A | 2 | a0003c0004t0001g0099a0003c0004t0001g0101 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.142-9803G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022349 | ||||||
| chr5:1022353
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(84): Show | 97 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.142-9799A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022353 | ||||||
| chr5:1022353
|
ATTGTCCC others(34): Show |
A | 66 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(63): Show | 75 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.142-9769_142-9729d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022353 | |||||
| chr5:1022370
|
C | T | 17 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0029others(14): Show | 21 | HG00597.hp1 HG01358.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.142-9782C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022370 | ||||||
| chr5:1022374
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.142-9778C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022374 | ||||||
| chr5:1022375
|
G | T | 8 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(5): Show | 10 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-9777G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022375 | ||||||
| chr5:1022377
|
T | TA | 10 | a0001c0001t0001g0162a0001c0001t0002g0029a0001c0002t0001g0185others(7): Show | 12 | HG00639.hp1 HG00741.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-9775_142-9774i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022377 | ||||||
| chr5:1022377
|
TGTGGGTG others(33): Show |
T | 1 | a0001c0001t0002g0163 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.142-9774_142-9735d others(42): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022377 | ||||||
| chr5:1022377
|
TGTGGGTG others(157): Show |
T | 16 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0030others(13): Show | 20 | HG00597.hp1 HG02040.hp2 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.142-9774_142-9611d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022377 | ||||||
| chr5:1022377
|
TGTGGGTG others(406): Show |
T | 2 | a0004c0007t0006g0078a0004c0007t0006g0079 | 2 | HG01099.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.142-9758_142-9346d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022377 | |||||
| chr5:1022383
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(99): Show | 114 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.142-9769T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022383 | ||||||
| chr5:1022384
|
G | A | 2 | a0001c0001t0007g0027a0001c0001t0007g0259 | 3 | NA19064.hp2 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.142-9768G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022384 | ||||||
| chr5:1022385
|
T | C | 8 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(5): Show | 10 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-9767T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022385 | ||||||
| chr5:1022387
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(96): Show | 111 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.142-9765C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022387 | ||||||
| chr5:1022389
|
A | G | 1 | a0001c0001t0007g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-9763A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022389 | ||||||
| chr5:1022394
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(107): Show | 124 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.142-9758G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022394 | ||||||
| chr5:1022394
|
G | T | 2 | a0001c0001t0002g0045a0001c0001t0003g0107 | 2 | HG04199.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-9758G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022394 | ||||||
| chr5:1022415
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.142-9737C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022415 | ||||||
| chr5:1022416
|
G | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9736G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022416 | ||||||
| chr5:1022416
|
GCTGTGGG others(571): Show |
G | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-9724_142-9147d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022416 | |||||
| chr5:1022418
|
T | A | 1 | a0001c0001t0002g0163 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.142-9734T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022418 | ||||||
| chr5:1022418
|
T | TA | 92 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(89): Show | 103 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.142-9734_142-9733i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022418 | ||||||
| chr5:1022424
|
C | T | 7 | a0001c0001t0002g0029a0001c0001t0002g0133a0001c0001t0002g0136others(4): Show | 8 | HG01358.hp1 HG02071.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-9728C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022424 | ||||||
| chr5:1022426
|
T | C | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9726T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022426 | ||||||
| chr5:1022428
|
T | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(55): Show | 68 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.142-9724T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022428 | ||||||
| chr5:1022430
|
A | G | 2 | a0001c0001t0007g0027a0001c0001t0007g0259 | 3 | NA19064.hp2 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.142-9722A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022430 | ||||||
| chr5:1022435
|
A | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 59 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142-9717A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022435 | ||||||
| chr5:1022435
|
A | T | 1 | a0001c0001t0002g0029 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.142-9717A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022435 | ||||||
| chr5:1022435
|
ATTGTCCC others(76): Show |
A | 12 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0044others(9): Show | 12 | HG00408.hp1 HG00741.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-9687_142-9605d others(85): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022435 | |||||
| chr5:1022452
|
C | T | 2 | a0001c0001t0002g0045a0001c0001t0002g0133 | 2 | HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.142-9700C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022452 | ||||||
| chr5:1022457
|
G | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9695G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022457 | ||||||
| chr5:1022459
|
TGTGGGTG others(75): Show |
T | 1 | a0001c0001t0002g0133 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.142-9692_142-9611d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022459 | ||||||
| chr5:1022465
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(122): Show | 147 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.142-9687T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022465 | ||||||
| chr5:1022465
|
TGTCCCAG others(117): Show |
T | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.142-9651_142-9528d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022465 | |||||
| chr5:1022467
|
T | C | 5 | a0001c0001t0001g0162a0001c0001t0003g0002a0001c0001t0003g0115others(2): Show | 8 | HG02132.hp2 HG02809.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-9685T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022467 | ||||||
| chr5:1022469
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(113): Show | 135 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.142-9683C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022469 | ||||||
| chr5:1022476
|
T | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(192): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.142-9676T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022476 | ||||||
| chr5:1022476
|
T | G | 3 | a0001c0001t0002g0045a0001c0001t0007g0027a0001c0001t0007g0259 | 4 | HG04199.hp2 NA19064.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-9676T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022476 | ||||||
| chr5:1022493
|
C | T | 11 | a0001c0001t0002g0029a0001c0001t0002g0136a0001c0001t0015g0117others(8): Show | 13 | HG00639.hp1 HG00741.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.142-9659C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022493 | ||||||
| chr5:1022498
|
G | T | 11 | a0001c0001t0001g0162a0001c0001t0003g0002a0001c0001t0003g0004others(8): Show | 16 | HG01243.hp2 HG02132.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-9654G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022498 | ||||||
| chr5:1022500
|
TA | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(147): Show | 171 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.142-9651delA | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022500 | ||||||
| chr5:1022501
|
AGTGGGTG others(734): Show |
A | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-9645_142-8905d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022501 | |||||
| chr5:1022507
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 76 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.142-9645T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022507 | ||||||
| chr5:1022509
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(60): Show | 69 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.142-9643T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022509 | ||||||
| chr5:1022511
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(54): Show | 67 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.142-9641C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022511 | ||||||
| chr5:1022518
|
T | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(126): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.142-9634T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022518 | ||||||
| chr5:1022518
|
T | G | 9 | a0001c0001t0002g0029a0001c0001t0002g0136a0001c0001t0007g0256others(6): Show | 9 | HG01358.hp1 HG02109.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-9634T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022518 | ||||||
| chr5:1022535
|
C | T | 70 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(67): Show | 79 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.142-9617C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022535 | ||||||
| chr5:1022538
|
C | T | 5 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(2): Show | 7 | HG01243.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-9614C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022538 | ||||||
| chr5:1022540
|
G | A | 1 | a0001c0001t0007g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-9612G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022540 | ||||||
| chr5:1022540
|
G | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(67): Show | 78 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.142-9612G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022540 | ||||||
| chr5:1022542
|
T | A | 17 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0030others(14): Show | 21 | HG00597.hp1 HG02040.hp2 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.142-9610T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022542 | ||||||
| chr5:1022542
|
T | TA | 78 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(75): Show | 88 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.142-9610_142-9609i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022542 | ||||||
| chr5:1022548
|
C | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(62): Show | 71 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.142-9604C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022548 | ||||||
| chr5:1022549
|
G | A | 15 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(12): Show | 17 | HG00438.hp1 HG01243.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.142-9603G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022549 | ||||||
| chr5:1022549
|
GTCTCAGC others(611): Show |
G | 12 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0024others(9): Show | 12 | HG01496.hp1 HG01515.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-9600_142-8983d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022549 | |||||
| chr5:1022552
|
T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(69): Show | 80 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.142-9600T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022552 | ||||||
| chr5:1022559
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(123): Show | 147 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.142-9593G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022559 | ||||||
| chr5:1022559
|
G | T | 3 | a0001c0001t0002g0029a0001c0001t0002g0136a0001c0001t0015g0117 | 3 | HG01358.hp1 HG02622.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-9593G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022559 | ||||||
| chr5:1022580
|
C | T | 5 | a0001c0001t0005g0003a0001c0001t0005g0091a0001c0001t0008g0094others(2): Show | 5 | HG00438.hp1 HG02004.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-9572C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022580 | ||||||
| chr5:1022581
|
G | A | 2 | a0001c0001t0007g0027a0001c0001t0007g0259 | 3 | NA19064.hp2 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.142-9571G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022581 | ||||||
| chr5:1022581
|
G | T | 7 | a0001c0001t0002g0029a0001c0001t0003g0004a0001c0001t0003g0112others(4): Show | 9 | HG01243.hp2 HG01358.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-9571G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022581 | ||||||
| chr5:1022583
|
T | TA | 2 | a0001c0001t0007g0027a0001c0001t0007g0259 | 3 | NA19064.hp2 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.142-9569_142-9568i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022583 | ||||||
| chr5:1022589
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(148): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.142-9563C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022589 | ||||||
| chr5:1022591
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(44): Show | 54 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.142-9561T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022591 | ||||||
| chr5:1022593
|
C | CCAGCCCA others(34): Show |
1 | a0001c0001t0002g0045 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142-9553_142-9552i others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022593 | |||||
| chr5:1022593
|
C | T | 26 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(23): Show | 29 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.142-9559C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022593 | ||||||
| chr5:1022595
|
A | G | 4 | a0001c0001t0007g0256a0001c0001t0007g0257a0001c0001t0007g0258others(1): Show | 4 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-9557A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022595 | ||||||
| chr5:1022600
|
T | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(83): Show | 93 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.142-9552T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022600 | ||||||
| chr5:1022600
|
T | G | 8 | a0001c0001t0002g0029a0001c0001t0003g0004a0001c0001t0003g0112others(5): Show | 11 | HG01243.hp2 HG01358.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.142-9552T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022600 | ||||||
| chr5:1022617
|
C | T | 2 | a0001c0001t0002g0136a0001c0001t0015g0117 | 2 | HG02622.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-9535C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022617 | ||||||
| chr5:1022622
|
G | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(53): Show | 65 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.142-9530G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022622 | ||||||
| chr5:1022624
|
T | TA | 25 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(22): Show | 27 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.142-9528_142-9527i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022624 | ||||||
| chr5:1022624
|
TGTGGGCG others(282): Show |
T | 3 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0088 | 3 | HG02257.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.142-9527_142-9239d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022624 | ||||||
| chr5:1022630
|
C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(49): Show | 62 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.142-9522C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022630 | ||||||
| chr5:1022631
|
G | A | 11 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(8): Show | 13 | HG00438.hp2 HG01192.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-9521G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022631 | ||||||
| chr5:1022632
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.142-9520T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022632 | ||||||
| chr5:1022634
|
C | T | 30 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(27): Show | 33 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.142-9518C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022634 | ||||||
| chr5:1022641
|
T | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(156): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.142-9511T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022641 | ||||||
| chr5:1022641
|
T | G | 10 | a0001c0001t0002g0136a0001c0001t0002g0163a0001c0001t0007g0077others(7): Show | 10 | HG02109.hp2 HG02523.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-9511T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022641 | ||||||
| chr5:1022658
|
C | T | 84 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(81): Show | 97 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.142-9494C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022658 | ||||||
| chr5:1022661
|
C | T | 3 | a0001c0001t0002g0029a0001c0001t0004g0057a0001c0001t0004g0058 | 3 | HG01358.hp1 HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.142-9491C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022661 | ||||||
| chr5:1022662
|
C | T | 11 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(8): Show | 13 | HG00438.hp2 HG01192.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-9490C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022662 | ||||||
| chr5:1022663
|
G | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9489G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022663 | ||||||
| chr5:1022663
|
G | T | 8 | a0001c0001t0002g0029a0001c0001t0004g0057a0001c0001t0004g0058others(5): Show | 8 | HG00438.hp1 HG01358.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-9489G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022663 | ||||||
| chr5:1022663
|
GCTGTGGG others(324): Show |
G | 1 | a0001c0001t0001g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142-9477_142-9147d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022663 | |||||
| chr5:1022663
|
GCTGTGGG others(447): Show |
G | 2 | a0001c0001t0007g0027a0001c0001t0007g0259 | 3 | NA19064.hp2 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.142-9445_142-8992d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022663 | |||||
| chr5:1022665
|
T | TA | 84 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(81): Show | 97 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.142-9487_142-9486i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022665 | ||||||
| chr5:1022665
|
TGTGGGCG others(118): Show |
T | 1 | a0001c0001t0001g0196 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.142-9481_142-9357d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022665 | |||||
| chr5:1022671
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0020others(58): Show | 65 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.142-9481C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022671 | ||||||
| chr5:1022671
|
CGTCTCAG others(35): Show |
C | 1 | a0001c0001t0002g0163 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.142-9477_142-9436d others(44): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022671 | |||||
| chr5:1022672
|
G | A | 3 | a0001c0001t0002g0227a0001c0001t0004g0057a0001c0001t0004g0058 | 3 | HG02055.hp2 HG02155.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.142-9480G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022672 | ||||||
| chr5:1022673
|
T | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0020others(48): Show | 55 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.142-9479T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022673 | ||||||
| chr5:1022675
|
T | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(109): Show | 127 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.142-9477T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022675 | ||||||
| chr5:1022682
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(77): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.142-9470G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022682 | ||||||
| chr5:1022682
|
G | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0020others(62): Show | 71 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.142-9470G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022682 | ||||||
| chr5:1022682
|
GTTGTCCC others(118): Show |
G | 1 | a0001c0005t0011g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-9445_142-9321d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022682 | |||||
| chr5:1022704
|
G | T | 12 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0003g0004others(9): Show | 14 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-9448G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022704 | ||||||
| chr5:1022704
|
GCTAGTGG others(283): Show |
G | 1 | a0001c0001t0003g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.142-9445_142-9156d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022704 | |||||
| chr5:1022704
|
GCTAGTGG others(406): Show |
G | 45 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0020others(42): Show | 49 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.142-9445_142-9033d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022704 | |||||
| chr5:1022706
|
TA | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(176): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.142-9445delA | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022706 | ||||||
| chr5:1022706
|
TAGTGGGT others(160): Show |
T | 1 | a0001c0001t0002g0007 | 2 | NA18968.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.142-9445_142-9279d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022706 | ||||||
| chr5:1022713
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 105 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.142-9439T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022713 | ||||||
| chr5:1022714
|
G | A | 5 | a0001c0001t0005g0003a0001c0001t0005g0091a0001c0001t0008g0094others(2): Show | 5 | HG00438.hp1 HG02004.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-9438G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022714 | ||||||
| chr5:1022715
|
T | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(9): Show | 12 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-9437T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022715 | ||||||
| chr5:1022717
|
C | T | 52 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0039others(49): Show | 60 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.142-9435C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022717 | ||||||
| chr5:1022723
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9429C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022723 | ||||||
| chr5:1022724
|
T | A | 38 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0039others(35): Show | 40 | HG00408.hp1 HG00438.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.142-9428T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022724 | ||||||
| chr5:1022724
|
T | G | 14 | a0001c0001t0002g0136a0001c0001t0003g0002a0001c0001t0003g0004others(11): Show | 19 | HG01243.hp2 HG02055.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.142-9428T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022724 | ||||||
| chr5:1022724
|
TTTGTCCC others(692): Show |
T | 1 | a0001c0001t0002g0239 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.142-9398_142-8700d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022724 | |||||
| chr5:1022744
|
C | T | 2 | a0001c0001t0002g0163a0001c0001t0002g0181 | 2 | HG01081.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.142-9408C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022744 | ||||||
| chr5:1022746
|
T | A | 5 | a0001c0001t0007g0256a0001c0001t0007g0257a0001c0001t0007g0258others(2): Show | 5 | HG02071.hp1 HG02523.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-9406T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022746 | ||||||
| chr5:1022746
|
T | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(62): Show | 75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.142-9406T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022746 | ||||||
| chr5:1022748
|
TGTGGGTG others(75): Show |
T | 1 | a0001c0001t0007g0256 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.142-9403_142-9322d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022748 | ||||||
| chr5:1022748
|
TGTGGGTG others(199): Show |
T | 3 | a0001c0001t0007g0257a0001c0001t0007g0258a0001c0001t0007g0260 | 3 | HG02602.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.142-9403_142-9198d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022748 | ||||||
| chr5:1022754
|
T | C | 113 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0049others(110): Show | 129 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.142-9398T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022754 | ||||||
| chr5:1022756
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 52 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.142-9396T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022756 | ||||||
| chr5:1022758
|
C | T | 99 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0049others(96): Show | 112 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.142-9394C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022758 | ||||||
| chr5:1022765
|
T | A | 30 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(27): Show | 32 | HG00438.hp2 HG00733.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.142-9387T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022765 | ||||||
| chr5:1022765
|
T | G | 91 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(88): Show | 107 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.142-9387T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022765 | ||||||
| chr5:1022782
|
C | T | 1 | a0001c0001t0015g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-9370C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022782 | ||||||
| chr5:1022785
|
C | T | 1 | a0001c0001t0002g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.142-9367C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022785 | ||||||
| chr5:1022787
|
G | T | 22 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0044others(19): Show | 24 | HG00408.hp1 HG00741.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.142-9365G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022787 | ||||||
| chr5:1022789
|
TA | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(161): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.142-9362delA | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022789 | ||||||
| chr5:1022796
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(165): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.142-9356T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022796 | ||||||
| chr5:1022797
|
G | A | 11 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(8): Show | 13 | HG00438.hp2 HG01192.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-9355G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022797 | ||||||
| chr5:1022798
|
T | C | 2 | a0001c0001t0001g0196a0001c0001t0002g0045 | 2 | HG01346.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.142-9354T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022798 | ||||||
| chr5:1022800
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(56): Show | 71 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.142-9352C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022800 | ||||||
| chr5:1022801
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.142-9351C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022801 | ||||||
| chr5:1022807
|
T | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.142-9345T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022807 | ||||||
| chr5:1022807
|
T | G | 10 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0112others(7): Show | 15 | HG01243.hp2 HG02258.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-9345T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022807 | ||||||
| chr5:1022827
|
C | T | 84 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(81): Show | 95 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-9325C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022827 | ||||||
| chr5:1022828
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9324C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022828 | ||||||
| chr5:1022829
|
G | T | 94 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(91): Show | 107 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.142-9323G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022829 | ||||||
| chr5:1022831
|
T | A | 1 | a0001c0001t0007g0256 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.142-9321T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022831 | ||||||
| chr5:1022837
|
C | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(5): Show | 8 | HG00733.hp2 HG01074.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-9315C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022837 | ||||||
| chr5:1022839
|
T | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(4): Show | 7 | HG00733.hp2 HG01074.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-9313T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022839 | ||||||
| chr5:1022841
|
T | C | 24 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(21): Show | 26 | HG00438.hp2 HG00733.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.142-9311T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022841 | ||||||
| chr5:1022848
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(150): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.142-9304G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022848 | ||||||
| chr5:1022848
|
G | T | 20 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(17): Show | 22 | HG00438.hp2 HG00733.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.142-9304G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022848 | ||||||
| chr5:1022863
|
CCCACCCG others(350): Show |
C | 1 | a0001c0001t0008g0082 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.142-9288_142-8932d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022863 | ||||||
| chr5:1022869
|
CGCTAGTG others(76): Show |
C | 5 | a0001c0001t0002g0181a0001c0001t0004g0057a0001c0001t0004g0058others(2): Show | 5 | HG01081.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-9279_142-9197d others(85): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022869 | |||||
| chr5:1022870
|
G | T | 9 | a0001c0001t0002g0029a0001c0001t0002g0163a0001c0001t0003g0004others(6): Show | 11 | HG01243.hp2 HG01358.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.142-9282G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022870 | ||||||
| chr5:1022870
|
GCTAGTGG others(35): Show |
G | 19 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0030others(16): Show | 21 | HG00597.hp1 HG02040.hp2 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.142-9279_142-9238d others(44): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022870 | |||||
| chr5:1022870
|
GCTAGTGG others(199): Show |
G | 1 | a0001c0001t0010g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.142-9279_142-9074d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022870 | |||||
| chr5:1022872
|
TA | T | 118 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(115): Show | 132 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.142-9279delA | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022872 | ||||||
| chr5:1022873
|
AGTGGGTG others(34): Show |
A | 2 | a0001c0001t0003g0002a0001c0005t0011g0002 | 4 | HG02809.hp2 HG03453.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-9262_142-9222d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022873 | |||||
| chr5:1022873
|
AGTGGGTG others(157): Show |
A | 1 | a0001c0001t0001g0220 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142-9273_142-9110d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022873 | |||||
| chr5:1022873
|
AGTGGGTG others(321): Show |
A | 1 | a0001c0001t0001g0196 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.142-9273_142-8946d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022873 | |||||
| chr5:1022873
|
AGTGGGTG others(444): Show |
A | 2 | a0001c0001t0001g0225a0001c0001t0012g0123 | 2 | HG01891.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.142-9273_142-8823d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022873 | |||||
| chr5:1022879
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(112): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.142-9273T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022879 | ||||||
| chr5:1022880
|
G | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9272G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022880 | ||||||
| chr5:1022881
|
T | C | 13 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(10): Show | 13 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.142-9271T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022881 | ||||||
| chr5:1022883
|
C | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(37): Show | 49 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.142-9269C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022883 | ||||||
| chr5:1022886
|
G | A | 3 | a0001c0001t0013g0073a0001c0001t0013g0074a0001c0001t0013g0075 | 3 | HG02273.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.142-9266G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022886 | ||||||
| chr5:1022890
|
T | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(103): Show | 122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.142-9262T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022890 | ||||||
| chr5:1022890
|
T | G | 12 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0109others(9): Show | 14 | HG01099.hp1 HG01243.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-9262T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022890 | ||||||
| chr5:1022890
|
TTTGTCCC others(75): Show |
T | 5 | a0001c0001t0005g0003a0001c0001t0005g0091a0001c0001t0008g0094others(2): Show | 5 | HG00438.hp1 HG02004.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-9232_142-9151d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022890 | |||||
| chr5:1022890
|
TTTGTCCC others(321): Show |
T | 1 | a0001c0001t0005g0095 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.142-9240_142-8913d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022890 | |||||
| chr5:1022911
|
CTCTGTGG others(34): Show |
C | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9240_142-9200d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022911 | ||||||
| chr5:1022912
|
T | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.142-9240T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022912 | ||||||
| chr5:1022914
|
T | A | 3 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0088 | 3 | HG02257.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.142-9238T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022914 | ||||||
| chr5:1022914
|
T | TA | 6 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(3): Show | 6 | HG00733.hp2 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-9238_142-9237i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022914 | ||||||
| chr5:1022920
|
T | C | 115 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0049others(112): Show | 135 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.142-9232T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022920 | ||||||
| chr5:1022921
|
G | A | 3 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0088 | 3 | HG02257.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.142-9231G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022921 | ||||||
| chr5:1022922
|
T | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(28): Show | 38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.142-9230T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022922 | ||||||
| chr5:1022924
|
C | T | 85 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0049others(82): Show | 97 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.142-9228C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022924 | ||||||
| chr5:1022931
|
G | A | 94 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0049others(91): Show | 105 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.142-9221G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022931 | ||||||
| chr5:1022931
|
G | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.142-9221G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022931 | ||||||
| chr5:1022952
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(168): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.142-9200T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022952 | ||||||
| chr5:1022953
|
G | GCTGTGGG others(34): Show |
1 | a0001c0001t0004g0071 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.142-9187_142-9147d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022953 | |||||
| chr5:1022953
|
G | T | 76 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(73): Show | 87 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.142-9199G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022953 | ||||||
| chr5:1022955
|
T | A | 3 | a0001c0001t0007g0257a0001c0001t0007g0258a0001c0001t0007g0260 | 3 | HG02602.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.142-9197T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022955 | ||||||
| chr5:1022955
|
T | TA | 7 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(4): Show | 7 | HG00733.hp2 HG01074.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-9197_142-9196i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022955 | ||||||
| chr5:1022955
|
TGTGGGCG others(279): Show |
T | 31 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(28): Show | 38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.142-9196_142-8911d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022955 | ||||||
| chr5:1022961
|
C | T | 11 | a0001c0001t0002g0029a0001c0001t0002g0163a0001c0001t0005g0003others(8): Show | 13 | HG00438.hp2 HG01358.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-9191C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022961 | ||||||
| chr5:1022963
|
T | C | 1 | a0001c0001t0002g0163 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.142-9189T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022963 | ||||||
| chr5:1022965
|
T | C | 82 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(79): Show | 97 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.142-9187T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022965 | ||||||
| chr5:1022969
|
C | G | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-9183C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022969 | ||||||
| chr5:1022972
|
G | A | 127 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0028others(124): Show | 145 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.142-9180G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022972 | ||||||
| chr5:1022972
|
G | T | 12 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(9): Show | 14 | HG00438.hp2 HG01928.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-9180G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022972 | ||||||
| chr5:1022972
|
GTTGTCCC others(198): Show |
G | 1 | a0001c0001t0007g0256 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.142-9146_142-8942d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1022972 | |||||
| chr5:1022992
|
C | T | 1 | a0001c0001t0002g0007 | 2 | NA18968.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.142-9160C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022992 | ||||||
| chr5:1022994
|
T | G | 64 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0028others(61): Show | 72 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.142-9158T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022994 | ||||||
| chr5:1022996
|
T | TA | 7 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(4): Show | 7 | HG00733.hp2 HG01074.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-9156_142-9155i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022996 | ||||||
| chr5:1022996
|
TGTGGGCG others(74): Show |
T | 7 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0044others(4): Show | 7 | HG00408.hp1 HG01168.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-9155_142-9075d others(83): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022996 | ||||||
| chr5:1022996
|
TGTGGGCG others(197): Show |
T | 5 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0160others(2): Show | 5 | HG00741.hp2 HG01106.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-9155_142-8952d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1022996 | ||||||
| chr5:1023002
|
C | T | 14 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0028others(11): Show | 14 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-9150C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023002 | ||||||
| chr5:1023004
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0002g0045a0001c0001t0002g0136 | 3 | HG04199.hp2 NA18747.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.142-9148T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023004 | ||||||
| chr5:1023006
|
C | T | 13 | a0001c0001t0002g0007a0001c0001t0002g0163a0001c0001t0003g0002others(10): Show | 14 | HG01099.hp1 HG02071.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-9146C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023006 | ||||||
| chr5:1023013
|
G | A | 45 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(42): Show | 53 | HG00597.hp1 HG00733.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.142-9139G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023013 | ||||||
| chr5:1023013
|
G | T | 30 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0028others(27): Show | 33 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.142-9139G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023013 | ||||||
| chr5:1023035
|
T | G | 37 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(34): Show | 45 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.142-9117T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023035 | ||||||
| chr5:1023035
|
T | TCTGTGGG others(239): Show |
3 | a0001c0001t0013g0073a0001c0001t0013g0074a0001c0001t0013g0075 | 3 | HG02273.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.142-9058_142-9057i others(248): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023035 | |||||
| chr5:1023037
|
T | TA | 6 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(3): Show | 6 | HG00733.hp2 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-9115_142-9114i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023037 | ||||||
| chr5:1023043
|
C | T | 96 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(93): Show | 108 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.142-9109C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023043 | ||||||
| chr5:1023045
|
T | C | 65 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(62): Show | 74 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.142-9107T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023045 | ||||||
| chr5:1023047
|
C | T | 7 | a0001c0001t0001g0022a0001c0001t0002g0136a0001c0001t0003g0002others(4): Show | 10 | HG02055.hp2 HG02809.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-9105C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023047 | ||||||
| chr5:1023054
|
A | G | 42 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(39): Show | 44 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.142-9098A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023054 | ||||||
| chr5:1023054
|
A | T | 2 | a0001c0001t0003g0002a0001c0005t0011g0002 | 5 | HG02809.hp2 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-9098A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023054 | ||||||
| chr5:1023076
|
T | A | 3 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0088 | 3 | HG02257.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.142-9076T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023076 | ||||||
| chr5:1023076
|
T | G | 55 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0028others(52): Show | 65 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.142-9076T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023076 | ||||||
| chr5:1023078
|
T | A | 7 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0044others(4): Show | 7 | HG00408.hp1 HG01168.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-9074T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023078 | ||||||
| chr5:1023078
|
T | TA | 24 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(21): Show | 27 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.142-9074_142-9073i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023078 | ||||||
| chr5:1023084
|
C | T | 22 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0030others(19): Show | 24 | HG00597.hp1 HG02040.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.142-9068C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023084 | ||||||
| chr5:1023085
|
G | A | 16 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(13): Show | 19 | HG00438.hp1 HG00438.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-9067G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023085 | ||||||
| chr5:1023086
|
T | C | 21 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0029others(18): Show | 23 | HG00597.hp1 HG01358.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.142-9066T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023086 | ||||||
| chr5:1023088
|
T | C | 40 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(37): Show | 42 | HG00597.hp1 HG00733.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.142-9064T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023088 | ||||||
| chr5:1023088
|
TCAGCCCG others(157): Show |
T | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.142-9035_142-8872d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023088 | |||||
| chr5:1023095
|
G | A | 53 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0028others(50): Show | 59 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.142-9057G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023095 | ||||||
| chr5:1023095
|
G | T | 24 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(21): Show | 29 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.142-9057G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023095 | ||||||
| chr5:1023117
|
T | G | 121 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0028others(118): Show | 139 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.142-9035T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023117 | ||||||
| chr5:1023119
|
T | TA | 16 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0028others(13): Show | 20 | HG00544.hp1 HG00733.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.142-9033_142-9032i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023119 | ||||||
| chr5:1023119
|
TGTGGGCG others(74): Show |
T | 5 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0048others(2): Show | 5 | HG00099.hp1 HG01358.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-9032_142-8952d others(83): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023119 | ||||||
| chr5:1023125
|
C | T | 60 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(57): Show | 69 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.142-9027C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023125 | ||||||
| chr5:1023127
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.142-9025T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023127 | ||||||
| chr5:1023129
|
T | C | 88 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(85): Show | 102 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.142-9023T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023129 | ||||||
| chr5:1023135
|
C | T | 1 | a0001c0001t0002g0157 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.142-9017C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023135 | ||||||
| chr5:1023136
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(156): Show | 178 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.142-9016G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023136 | ||||||
| chr5:1023136
|
G | T | 24 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(21): Show | 27 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.142-9016G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023136 | ||||||
| chr5:1023142
|
C | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(3): Show | 6 | HG00733.hp2 HG01074.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-9010C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023142 | ||||||
| chr5:1023156
|
C | T | 6 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(3): Show | 8 | HG01243.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-8996C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023156 | ||||||
| chr5:1023158
|
G | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-8994G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023158 | ||||||
| chr5:1023158
|
G | T | 74 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(71): Show | 86 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.142-8994G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023158 | ||||||
| chr5:1023158
|
GCTGTGGG others(34): Show |
G | 2 | a0001c0001t0002g0029a0001c0005t0011g0114 | 2 | HG01358.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.142-8985_142-8945d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023158 | |||||
| chr5:1023160
|
T | TA | 7 | a0001c0001t0001g0162a0001c0001t0001g0220a0001c0001t0003g0002others(4): Show | 10 | HG01123.hp2 HG02132.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-8992_142-8991i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023160 | ||||||
| chr5:1023166
|
C | T | 43 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0039others(40): Show | 48 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.142-8986C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023166 | ||||||
| chr5:1023167
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(192): Show | 222 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.142-8985A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023167 | ||||||
| chr5:1023168
|
T | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0039others(6): Show | 9 | HG00408.hp1 HG01168.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-8984T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023168 | ||||||
| chr5:1023170
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(66): Show | 77 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.142-8982C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023170 | ||||||
| chr5:1023177
|
A | G | 75 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(72): Show | 86 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.142-8975A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023177 | ||||||
| chr5:1023177
|
A | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0039others(8): Show | 11 | HG00408.hp1 HG01168.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.142-8975A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023177 | ||||||
| chr5:1023199
|
T | A | 1 | a0001c0001t0001g0189 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.142-8953T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023199 | ||||||
| chr5:1023199
|
T | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(81): Show | 94 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.142-8953T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023199 | ||||||
| chr5:1023201
|
T | A | 10 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0046others(7): Show | 10 | HG00099.hp1 HG00741.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-8951T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023201 | ||||||
| chr5:1023201
|
T | TA | 51 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0020others(48): Show | 57 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.142-8951_142-8950i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023201 | ||||||
| chr5:1023207
|
C | T | 46 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0028others(43): Show | 50 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.142-8945C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023207 | ||||||
| chr5:1023209
|
T | C | 23 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0028others(20): Show | 24 | HG00544.hp1 HG00733.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.142-8943T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023209 | ||||||
| chr5:1023211
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(147): Show | 169 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.142-8941T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023211 | ||||||
| chr5:1023218
|
A | ATTGTCCC others(117): Show |
1 | a0001c0001t0002g0045 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142-8901_142-8900i others(126): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023218 | |||||
| chr5:1023218
|
A | G | 96 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(93): Show | 108 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.142-8934A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023218 | ||||||
| chr5:1023218
|
A | T | 23 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0028others(20): Show | 25 | HG00544.hp1 HG00733.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.142-8934A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023218 | ||||||
| chr5:1023240
|
G | T | 95 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(92): Show | 108 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.142-8912G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023240 | ||||||
| chr5:1023240
|
GCTGTGGG others(485): Show |
G | 1 | a0001c0001t0019g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.142-8900_142-8409d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023240 | |||||
| chr5:1023242
|
T | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(28): Show | 38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.142-8910T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023242 | ||||||
| chr5:1023242
|
T | TA | 15 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0162others(12): Show | 16 | HG00733.hp2 HG01074.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-8910_142-8909i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023242 | ||||||
| chr5:1023248
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(58): Show | 67 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.142-8904C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023248 | ||||||
| chr5:1023249
|
G | A | 5 | a0001c0001t0002g0019a0001c0001t0002g0031a0002c0003t0002g0019others(2): Show | 5 | HG01099.hp1 HG02615.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-8903G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023249 | ||||||
| chr5:1023250
|
T | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0020others(49): Show | 58 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.142-8902T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023250 | ||||||
| chr5:1023252
|
C | T | 43 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0038others(40): Show | 50 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.142-8900C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023252 | ||||||
| chr5:1023259
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(81): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.142-8893G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023259 | ||||||
| chr5:1023259
|
G | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(66): Show | 76 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.142-8893G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023259 | ||||||
| chr5:1023259
|
GTTGTCCC others(75): Show |
G | 4 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(1): Show | 4 | HG01074.hp2 HG01261.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-8852_142-8771d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023259 | |||||
| chr5:1023276
|
C | T | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-8876C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023276 | ||||||
| chr5:1023281
|
G | T | 106 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(103): Show | 122 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.142-8871G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023281 | ||||||
| chr5:1023283
|
T | TA | 81 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(78): Show | 95 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-8869_142-8868i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023283 | ||||||
| chr5:1023283
|
T | TAGTGGGT others(35): Show |
1 | a0001c0001t0007g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-8869_142-8868i others(44): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023283 | ||||||
| chr5:1023289
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0024others(118): Show | 136 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.142-8863C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023289 | ||||||
| chr5:1023291
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0024others(107): Show | 121 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.142-8861T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023291 | ||||||
| chr5:1023293
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(51): Show | 64 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.142-8859C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023293 | ||||||
| chr5:1023295
|
A | G | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-8857A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023295 | ||||||
| chr5:1023300
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 140 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.142-8852G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023300 | ||||||
| chr5:1023300
|
G | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0024others(39): Show | 42 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.142-8852G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023300 | ||||||
| chr5:1023306
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142-8846C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023306 | ||||||
| chr5:1023322
|
T | A | 1 | a0002c0003t0001g0040 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.142-8830T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023322 | ||||||
| chr5:1023322
|
T | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(217): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.142-8830T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023322 | ||||||
| chr5:1023324
|
T | TA | 92 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(89): Show | 108 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.142-8828_142-8827i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023324 | ||||||
| chr5:1023330
|
C | T | 41 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(38): Show | 43 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-8822C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023330 | ||||||
| chr5:1023330
|
CGTCTCAG others(649): Show |
C | 1 | a0004c0007t0006g0078 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.142-8818_142-8163d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023330 | |||||
| chr5:1023331
|
G | A | 11 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(8): Show | 14 | HG00438.hp1 HG00438.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-8821G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023331 | ||||||
| chr5:1023332
|
T | C | 25 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0044others(22): Show | 27 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.142-8820T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023332 | ||||||
| chr5:1023334
|
T | C | 66 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0028others(63): Show | 71 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.142-8818T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023334 | ||||||
| chr5:1023341
|
A | G | 24 | a0001c0001t0001g0241a0001c0001t0002g0007a0001c0001t0002g0008others(21): Show | 28 | HG00597.hp1 HG00733.hp2 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.142-8811A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023341 | ||||||
| chr5:1023341
|
A | T | 37 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(34): Show | 41 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.142-8811A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023341 | ||||||
| chr5:1023363
|
G | T | 4 | a0001c0001t0001g0220a0001c0001t0002g0007a0001c0001t0002g0045others(1): Show | 5 | HG01123.hp2 HG02622.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-8789G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023363 | ||||||
| chr5:1023363
|
GCTGTGGG others(362): Show |
G | 2 | a0001c0001t0002g0031a0002c0003t0002g0019 | 2 | NA18973.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.142-8777_142-8409d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023363 | |||||
| chr5:1023363
|
GCTGTGGG others(403): Show |
G | 1 | a0001c0001t0002g0019 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.142-8707_142-8298d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023363 | |||||
| chr5:1023365
|
T | TA | 89 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(86): Show | 106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.142-8787_142-8786i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023365 | ||||||
| chr5:1023371
|
C | T | 24 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(21): Show | 27 | HG00544.hp1 HG01123.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.142-8781C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023371 | ||||||
| chr5:1023372
|
G | A | 3 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0088 | 3 | HG02257.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.142-8780G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023372 | ||||||
| chr5:1023373
|
T | C | 13 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(10): Show | 13 | HG00544.hp1 HG01123.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.142-8779T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023373 | ||||||
| chr5:1023375
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(95): Show | 107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.142-8777C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023375 | ||||||
| chr5:1023382
|
A | G | 20 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0030others(17): Show | 24 | HG00597.hp1 HG02040.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.142-8770A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023382 | ||||||
| chr5:1023382
|
A | T | 34 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(31): Show | 39 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.142-8770A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023382 | ||||||
| chr5:1023382
|
ATTGTCCC others(649): Show |
A | 1 | a0004c0007t0006g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.142-8748_142-8093d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023382 | |||||
| chr5:1023404
|
G | T | 6 | a0001c0001t0002g0007a0001c0001t0002g0029a0001c0001t0002g0136others(3): Show | 7 | HG01358.hp1 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-8748G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023404 | ||||||
| chr5:1023406
|
T | TA | 85 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(82): Show | 99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.142-8746_142-8745i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023406 | ||||||
| chr5:1023406
|
T | TGTGGGTG others(35): Show |
2 | a0001c0001t0003g0002a0001c0005t0011g0002 | 4 | HG02809.hp2 HG03453.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-8741_142-8740i others(44): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023406 | |||||
| chr5:1023406
|
TGTGGGCG others(74): Show |
T | 10 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0126others(7): Show | 10 | HG01515.hp1 HG02622.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-8745_142-8665d others(83): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023406 | ||||||
| chr5:1023406
|
TGTGGGCG others(361): Show |
T | 2 | a0001c0001t0001g0235a0006c0015t0001g0231 | 2 | HG03942.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.142-8745_142-8378d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023406 | ||||||
| chr5:1023406
|
TGTGGGCG others(935): Show |
T | 1 | a0001c0001t0001g0222 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.142-8745_142-7804d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023406 | ||||||
| chr5:1023412
|
C | T | 95 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(92): Show | 110 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.142-8740C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023412 | ||||||
| chr5:1023414
|
T | C | 4 | a0001c0001t0002g0007a0001c0001t0002g0029a0001c0001t0002g0045others(1): Show | 5 | HG01358.hp1 HG02622.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-8738T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023414 | ||||||
| chr5:1023416
|
C | G | 1 | a0001c0001t0002g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.142-8736C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023416 | ||||||
| chr5:1023416
|
C | T | 29 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0028others(26): Show | 31 | HG00408.hp1 HG00544.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.142-8736C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023416 | ||||||
| chr5:1023416
|
CCAGCCCA others(116): Show |
C | 3 | a0001c0001t0008g0086a0001c0001t0008g0087a0001c0001t0008g0088 | 3 | HG02257.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.142-8729_142-8607d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023416 | |||||
| chr5:1023423
|
A | G | 12 | a0001c0001t0001g0220a0001c0001t0002g0007a0001c0001t0002g0227others(9): Show | 15 | HG01123.hp2 HG01243.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.142-8729A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023423 | ||||||
| chr5:1023423
|
A | T | 29 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0038others(26): Show | 34 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.142-8729A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023423 | ||||||
| chr5:1023429
|
CCTGCTCT others(75): Show |
C | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0009c0013t0017g0098 | 3 | HG00741.hp2 HG01106.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.142-8654_142-8573d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023429 | |||||
| chr5:1023440
|
C | T | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-8712C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023440 | ||||||
| chr5:1023445
|
T | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(154): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.142-8707T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023445 | ||||||
| chr5:1023447
|
T | TA | 91 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 108 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.142-8705_142-8704i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023447 | ||||||
| chr5:1023447
|
TGTGGGCG others(74): Show |
T | 1 | a0001c0001t0002g0029 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.142-8704_142-8624d others(83): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023447 | ||||||
| chr5:1023447
|
TGTGGGCG others(320): Show |
T | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142-8704_142-8378d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023447 | ||||||
| chr5:1023453
|
C | T | 22 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(19): Show | 25 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.142-8699C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023453 | ||||||
| chr5:1023454
|
G | A | 1 | a0001c0001t0008g0082 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.142-8698G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023454 | ||||||
| chr5:1023455
|
T | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 12 | HG00099.hp1 HG01358.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-8697T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023455 | ||||||
| chr5:1023457
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(114): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.142-8695T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023457 | ||||||
| chr5:1023457
|
TCAGCCCG others(116): Show |
T | 1 | a0001c0001t0002g0132 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.142-8688_142-8566d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023457 | |||||
| chr5:1023464
|
G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(153): Show | 174 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.142-8688G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023464 | ||||||
| chr5:1023464
|
G | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(52): Show | 65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.142-8688G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023464 | ||||||
| chr5:1023464
|
GTTGTCCC others(362): Show |
G | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-8654_142-8286d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023464 | |||||
| chr5:1023470
|
C | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0049a0001c0001t0001g0219others(1): Show | 5 | HG01074.hp2 HG01261.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-8682C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023470 | ||||||
| chr5:1023470
|
CCTGCTCT others(34): Show |
C | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-8666_142-8626d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023470 | |||||
| chr5:1023486
|
G | T | 18 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0030others(15): Show | 20 | HG00597.hp1 HG02040.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.142-8666G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023486 | ||||||
| chr5:1023486
|
GCTGTGGG others(34): Show |
G | 8 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0044others(5): Show | 8 | HG00408.hp1 HG01168.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-8641_142-8601d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023486 | |||||
| chr5:1023486
|
GCTGTGGG others(239): Show |
G | 1 | a0001c0001t0002g0103 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.142-8647_142-8402d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023486 | |||||
| chr5:1023488
|
T | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0126others(7): Show | 10 | HG01515.hp1 HG02622.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-8664T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023488 | ||||||
| chr5:1023488
|
T | TA | 13 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(10): Show | 16 | HG00544.hp1 HG01123.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-8664_142-8663i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023488 | ||||||
| chr5:1023488
|
T | TGTGGGTG others(76): Show |
1 | a0001c0001t0002g0045 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142-8659_142-8658i others(85): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023488 | |||||
| chr5:1023488
|
TGTGGGCG others(33): Show |
T | 1 | a0001c0001t0012g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-8663_142-8624d others(42): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023488 | ||||||
| chr5:1023488
|
TGTGGGCG others(74): Show |
T | 27 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(24): Show | 32 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.142-8663_142-8583d others(83): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023488 | ||||||
| chr5:1023488
|
TGTGGGCG others(156): Show |
T | 2 | a0001c0001t0001g0024a0001c0001t0026g0024 | 2 | HG01496.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.142-8663_142-8501d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023488 | ||||||
| chr5:1023488
|
TGTGGGCG others(279): Show |
T | 42 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0020others(39): Show | 46 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.142-8663_142-8378d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023488 | ||||||
| chr5:1023488
|
TGTGGGCG others(443): Show |
T | 1 | a0001c0001t0014g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.142-8663_142-8214d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023488 | ||||||
| chr5:1023488
|
TGTGGGCG others(689): Show |
T | 3 | a0001c0001t0001g0011a0001c0001t0001g0203a0001c0001t0001g0244 | 5 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-8663_142-7968d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023488 | ||||||
| chr5:1023489
|
G | T | 1 | a0001c0001t0004g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142-8663G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023489 | ||||||
| chr5:1023490
|
T | G | 1 | a0001c0001t0004g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142-8662T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023490 | ||||||
| chr5:1023491
|
G | T | 1 | a0001c0001t0004g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142-8661G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023491 | ||||||
| chr5:1023494
|
C | T | 17 | a0001c0001t0001g0241a0001c0001t0002g0136a0001c0001t0003g0108others(14): Show | 20 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.142-8658C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023494 | ||||||
| chr5:1023494
|
CGTCTCAG others(485): Show |
C | 1 | a0001c0001t0008g0082 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.142-8654_142-8163d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023494 | |||||
| chr5:1023495
|
G | A | 2 | a0001c0001t0002g0045a0001c0001t0005g0095 | 2 | HG04199.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.142-8657G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023495 | ||||||
| chr5:1023496
|
T | C | 3 | a0001c0001t0002g0136a0001c0001t0003g0109a0001c0001t0003g0115 | 3 | HG03516.hp1 NA18747.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.142-8656T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023496 | ||||||
| chr5:1023498
|
T | C | 29 | a0001c0001t0001g0220a0001c0001t0001g0241a0001c0001t0002g0136others(26): Show | 34 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.142-8654T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023498 | ||||||
| chr5:1023505
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(134): Show | 154 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.142-8647G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023505 | ||||||
| chr5:1023505
|
G | T | 17 | a0001c0001t0001g0162a0001c0001t0001g0220a0001c0001t0001g0221others(14): Show | 20 | HG00438.hp1 HG00438.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.142-8647G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023505 | ||||||
| chr5:1023505
|
GTTGTCTC others(239): Show |
G | 1 | a0001c0001t0003g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.142-8641_142-8396d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023505 | |||||
| chr5:1023505
|
GTTGTCTC others(731): Show |
G | 1 | a0001c0001t0001g0241 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.142-8641_142-7904d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023505 | |||||
| chr5:1023510
|
CTCTGCTC others(33): Show |
C | 1 | a0001c0001t0001g0225 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.142-8641_142-8602d others(42): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023510 | ||||||
| chr5:1023511
|
T | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0221 | 2 | HG02015.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.142-8641T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023511 | ||||||
| chr5:1023511
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(152): Show | 178 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.142-8641T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023511 | ||||||
| chr5:1023525
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.142-8627C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023525 | ||||||
| chr5:1023527
|
T | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(64): Show | 78 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.142-8625T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023527 | ||||||
| chr5:1023529
|
T | A | 2 | a0001c0001t0002g0029a0001c0001t0012g0123 | 2 | HG01358.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.142-8623T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023529 | ||||||
| chr5:1023529
|
T | TA | 4 | a0001c0001t0001g0220a0001c0001t0002g0136a0001c0001t0003g0002others(1): Show | 7 | HG01123.hp2 HG02809.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-8623_142-8622i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023529 | ||||||
| chr5:1023535
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(97): Show | 110 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.142-8617C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023535 | ||||||
| chr5:1023536
|
G | A | 2 | a0001c0001t0002g0029a0001c0001t0002g0136 | 2 | HG01358.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.142-8616G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023536 | ||||||
| chr5:1023537
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(95): Show | 108 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.142-8615T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023537 | ||||||
| chr5:1023539
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(104): Show | 121 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.142-8613T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023539 | ||||||
| chr5:1023541
|
A | G | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-8611A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023541 | ||||||
| chr5:1023546
|
G | A | 114 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0046others(111): Show | 129 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.142-8606G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023546 | ||||||
| chr5:1023546
|
G | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(34): Show | 41 | HG00408.hp1 HG00544.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.142-8606G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023546 | ||||||
| chr5:1023552
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142-8600C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023552 | ||||||
| chr5:1023568
|
G | T | 20 | a0001c0001t0001g0162a0001c0001t0001g0221a0001c0001t0002g0007others(17): Show | 22 | HG00597.hp1 HG02015.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.142-8584G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023568 | ||||||
| chr5:1023570
|
T | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(24): Show | 32 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.142-8582T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023570 | ||||||
| chr5:1023570
|
T | TA | 109 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(106): Show | 122 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.142-8582_142-8581i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023570 | ||||||
| chr5:1023570
|
TGTGGGCG others(33): Show |
T | 3 | a0001c0001t0002g0150a0001c0001t0002g0157a0001c0001t0002g0163 | 3 | HG04184.hp1 NA19011.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.142-8581_142-8542d others(42): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023570 | ||||||
| chr5:1023570
|
TGTGGGCG others(320): Show |
T | 1 | a0007c0014t0018g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.142-8581_142-8255d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023570 | ||||||
| chr5:1023576
|
C | T | 41 | a0001c0001t0001g0162a0001c0001t0001g0221a0001c0001t0002g0007others(38): Show | 48 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.142-8576C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023576 | ||||||
| chr5:1023577
|
G | A | 65 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(62): Show | 74 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.142-8575G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023577 | ||||||
| chr5:1023578
|
T | C | 17 | a0001c0001t0001g0162a0001c0001t0001g0221a0001c0001t0002g0007others(14): Show | 19 | HG00597.hp1 HG02015.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-8574T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023578 | ||||||
| chr5:1023580
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(110): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.142-8572C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023580 | ||||||
| chr5:1023580
|
CCAGCCCA others(854): Show |
C | 8 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(5): Show | 10 | HG00438.hp2 NA18612.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-8543_142-7683d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023580 | |||||
| chr5:1023587
|
A | G | 73 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0168others(70): Show | 83 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.142-8565A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023587 | ||||||
| chr5:1023587
|
A | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(34): Show | 44 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.142-8565A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023587 | ||||||
| chr5:1023592
|
C | T | 4 | a0001c0001t0005g0003a0001c0001t0005g0091a0001c0001t0008g0094others(1): Show | 4 | HG00438.hp1 HG02004.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-8560C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023592 | ||||||
| chr5:1023593
|
C | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(24): Show | 32 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.142-8559C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023593 | ||||||
| chr5:1023607
|
C | T | 6 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(3): Show | 8 | HG01243.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-8545C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023607 | ||||||
| chr5:1023609
|
T | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(159): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.142-8543T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023609 | ||||||
| chr5:1023611
|
T | A | 3 | a0001c0001t0002g0150a0001c0001t0002g0157a0001c0001t0002g0163 | 3 | HG04184.hp1 NA19011.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.142-8541T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023611 | ||||||
| chr5:1023611
|
T | TA | 51 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(48): Show | 56 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.142-8541_142-8540i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023611 | ||||||
| chr5:1023617
|
C | T | 29 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0046others(26): Show | 31 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.142-8535C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023617 | ||||||
| chr5:1023618
|
G | A | 18 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0030others(15): Show | 20 | HG00597.hp1 HG02040.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.142-8534G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023618 | ||||||
| chr5:1023619
|
T | C | 11 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0046others(8): Show | 11 | HG00099.hp1 HG01123.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.142-8533T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023619 | ||||||
| chr5:1023621
|
T | C | 97 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0046others(94): Show | 108 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.142-8531T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023621 | ||||||
| chr5:1023628
|
A | G | 39 | a0001c0001t0001g0162a0001c0001t0002g0007a0001c0001t0002g0008others(36): Show | 46 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.142-8524A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023628 | ||||||
| chr5:1023628
|
A | T | 77 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0046others(74): Show | 86 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.142-8524A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023628 | ||||||
| chr5:1023630
|
T | A | 4 | a0001c0001t0005g0003a0001c0001t0005g0091a0001c0001t0008g0094others(1): Show | 4 | HG00438.hp1 HG02004.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-8522T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023630 | ||||||
| chr5:1023648
|
C | CCGCTAGT others(35): Show |
1 | a0001c0001t0007g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-8503_142-8502i others(44): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023648 | |||||
| chr5:1023650
|
T | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(83): Show | 97 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.142-8502T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023650 | ||||||
| chr5:1023652
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0026g0024 | 2 | HG01496.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.142-8500T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023652 | ||||||
| chr5:1023652
|
T | TA | 43 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(40): Show | 47 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.142-8500_142-8499i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023652 | ||||||
| chr5:1023652
|
TGTGGGCG others(115): Show |
T | 3 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0259 | 4 | HG02523.hp2 NA19064.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-8499_142-8378d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023652 | ||||||
| chr5:1023658
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(101): Show | 118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.142-8494C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023658 | ||||||
| chr5:1023660
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(97): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.142-8492T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023660 | ||||||
| chr5:1023662
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(140): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.142-8490T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023662 | ||||||
| chr5:1023662
|
TCAGCCCA others(157): Show |
T | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-8461_142-8298d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023662 | |||||
| chr5:1023669
|
A | ATTGTCCC others(158): Show |
4 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(1): Show | 6 | HG02258.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-8462_142-8461i others(167): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023669 | |||||
| chr5:1023669
|
A | G | 8 | a0001c0001t0001g0221a0001c0001t0004g0057a0001c0001t0004g0058others(5): Show | 8 | HG00438.hp1 HG02004.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-8483A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023669 | ||||||
| chr5:1023669
|
A | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(49): Show | 59 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.142-8483A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023669 | ||||||
| chr5:1023673
|
TCCCTGCT others(34): Show |
T | 1 | a0001c0001t0002g0029 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.142-8438_142-8398d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023673 | |||||
| chr5:1023689
|
CCTCTGTG others(75): Show |
C | 1 | a0001c0001t0008g0086 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.142-8449_142-8368d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023689 | |||||
| chr5:1023691
|
T | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(149): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.142-8461T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023691 | ||||||
| chr5:1023693
|
T | TA | 60 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(57): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.142-8459_142-8458i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023693 | ||||||
| chr5:1023693
|
TGTGGGCG others(74): Show |
T | 19 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(16): Show | 19 | HG00408.hp1 HG01074.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-8458_142-8378d others(83): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023693 | ||||||
| chr5:1023699
|
C | T | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0002g0007others(28): Show | 38 | HG00597.hp1 HG00741.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.142-8453C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023699 | ||||||
| chr5:1023700
|
G | A | 2 | a0001c0001t0002g0132a0001c0001t0015g0117 | 2 | HG02622.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.142-8452G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023700 | ||||||
| chr5:1023701
|
T | C | 20 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0002g0007others(17): Show | 24 | HG00597.hp1 HG00741.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.142-8451T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023701 | ||||||
| chr5:1023703
|
T | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(66): Show | 81 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.142-8449T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023703 | ||||||
| chr5:1023703
|
TCAGCCCA others(239): Show |
T | 4 | a0001c0001t0005g0003a0001c0001t0005g0091a0001c0001t0008g0094others(1): Show | 4 | HG00438.hp1 HG02004.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-8438_142-8193d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023703 | |||||
| chr5:1023710
|
A | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(36): Show | 46 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.142-8442A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023710 | ||||||
| chr5:1023710
|
A | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0160a0001c0001t0001g0161others(5): Show | 8 | HG00741.hp2 HG01106.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-8442A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023710 | ||||||
| chr5:1023714
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(173): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.142-8438C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023714 | ||||||
| chr5:1023716
|
C | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0225a0001c0001t0012g0123 | 3 | HG01891.hp1 NA18997.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.142-8436C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023716 | ||||||
| chr5:1023724
|
TC | T | 3 | a0001c0001t0007g0257a0001c0001t0007g0258a0001c0001t0007g0260 | 3 | HG02602.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.142-8425delC | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023724 | |||||
| chr5:1023731
|
C | CGCTGTGG others(158): Show |
1 | a0008c0011t0016g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142-8421_142-8420i others(167): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023731 | ||||||
| chr5:1023731
|
C | T | 4 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(1): Show | 6 | HG02258.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-8421C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023731 | ||||||
| chr5:1023732
|
T | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(92): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.142-8420T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023732 | ||||||
| chr5:1023734
|
T | TA | 30 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0028others(27): Show | 34 | HG00099.hp1 HG00544.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.142-8418_142-8417i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023734 | ||||||
| chr5:1023734
|
TGTGGGCG others(33): Show |
T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0006g0265 | 3 | HG00741.hp2 HG01106.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.142-8417_142-8378d others(42): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023734 | ||||||
| chr5:1023734
|
TGTGGGCG others(197): Show |
T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-8417_142-8214d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023734 | ||||||
| chr5:1023740
|
C | T | 4 | a0001c0001t0002g0029a0001c0001t0002g0136a0001c0001t0002g0239others(1): Show | 4 | HG01243.hp2 HG01358.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-8412C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023740 | ||||||
| chr5:1023741
|
G | A | 4 | a0001c0001t0002g0007a0001c0001t0005g0095a0001c0001t0008g0087others(1): Show | 5 | HG02257.hp1 HG03225.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-8411G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023741 | ||||||
| chr5:1023742
|
T | C | 3 | a0001c0001t0002g0029a0001c0001t0002g0136a0001c0001t0002g0239 | 3 | HG01358.hp1 HG03927.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-8410T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023742 | ||||||
| chr5:1023744
|
T | C | 85 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0032others(82): Show | 97 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.142-8408T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023744 | ||||||
| chr5:1023751
|
A | G | 7 | a0001c0001t0001g0221a0001c0001t0002g0007a0001c0001t0002g0045others(4): Show | 8 | HG01243.hp2 HG02015.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-8401A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023751 | ||||||
| chr5:1023751
|
A | T | 8 | a0001c0001t0002g0132a0001c0001t0003g0002a0001c0001t0005g0095others(5): Show | 11 | HG02257.hp1 HG02622.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.142-8401A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023751 | ||||||
| chr5:1023771
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(161): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.142-8381T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023771 | ||||||
| chr5:1023773
|
T | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(62): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.142-8379T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023773 | ||||||
| chr5:1023775
|
T | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(66): Show | 75 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.142-8377T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023775 | ||||||
| chr5:1023775
|
T | G | 2 | a0001c0001t0002g0150a0001c0001t0002g0157 | 2 | NA19011.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.142-8377T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023775 | ||||||
| chr5:1023775
|
T | TA | 49 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(46): Show | 57 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.142-8377_142-8376i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023775 | ||||||
| chr5:1023781
|
C | T | 95 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0168others(92): Show | 106 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.142-8371C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023781 | ||||||
| chr5:1023783
|
T | C | 91 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0168others(88): Show | 102 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.142-8369T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023783 | ||||||
| chr5:1023785
|
C | T | 12 | a0001c0001t0001g0221a0001c0001t0002g0019a0001c0001t0002g0239others(9): Show | 15 | HG01243.hp2 HG02015.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-8367C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023785 | ||||||
| chr5:1023792
|
A | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(33): Show | 43 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-8360A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023792 | ||||||
| chr5:1023792
|
A | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(56): Show | 64 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.142-8360A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023792 | ||||||
| chr5:1023797
|
C | G | 1 | a0001c0001t0003g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.142-8355C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023797 | ||||||
| chr5:1023814
|
G | T | 8 | a0001c0001t0002g0007a0001c0001t0002g0019a0001c0001t0002g0029others(5): Show | 10 | HG01358.hp1 HG02523.hp2 HG03540.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-8338G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023814 | ||||||
| chr5:1023816
|
T | TA | 94 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(91): Show | 103 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.142-8336_142-8335i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023816 | ||||||
| chr5:1023822
|
C | T | 35 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(32): Show | 40 | HG00597.hp1 HG01243.hp2 HG02040.hp2 others(37): Show |
intron_variant | MODIFIER | c.142-8330C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023822 | ||||||
| chr5:1023823
|
G | A | 3 | a0001c0001t0002g0103a0001c0001t0008g0086a0001c0001t0019g0193 | 3 | HG01928.hp2 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.142-8329G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023823 | ||||||
| chr5:1023824
|
T | C | 22 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(19): Show | 26 | HG00597.hp1 HG02040.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.142-8328T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023824 | ||||||
| chr5:1023826
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(144): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.142-8326C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023826 | ||||||
| chr5:1023826
|
CCAGCCCA others(444): Show |
C | 3 | a0001c0001t0005g0095a0001c0001t0008g0087a0001c0001t0008g0088 | 3 | HG02257.hp1 HG03225.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.142-8319_142-7869d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023826 | |||||
| chr5:1023828
|
A | G | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-8324A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023828 | ||||||
| chr5:1023833
|
A | ATTGTCCC others(35): Show |
1 | a0001c0001t0002g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.142-8303_142-8302i others(44): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023833 | |||||
| chr5:1023833
|
A | G | 11 | a0001c0001t0001g0162a0001c0001t0001g0225a0001c0001t0002g0103others(8): Show | 12 | HG01891.hp1 HG02055.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-8319A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023833 | ||||||
| chr5:1023833
|
A | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(59): Show | 68 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.142-8319A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023833 | ||||||
| chr5:1023839
|
C | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(45): Show | 52 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.142-8313C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023839 | ||||||
| chr5:1023851
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.142-8301A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023851 | ||||||
| chr5:1023855
|
G | T | 89 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(86): Show | 100 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.142-8297G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023855 | ||||||
| chr5:1023855
|
GCTGTGGG others(34): Show |
G | 1 | a0001c0001t0002g0029 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.142-8217_142-8177d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023855 | |||||
| chr5:1023855
|
GCTGTGGG others(75): Show |
G | 1 | a0001c0001t0002g0103 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.142-8258_142-8177d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023855 | |||||
| chr5:1023857
|
T | G | 1 | a0001c0001t0002g0132 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.142-8295T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023857 | ||||||
| chr5:1023857
|
T | TA | 39 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(36): Show | 40 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.142-8295_142-8294i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023857 | ||||||
| chr5:1023863
|
C | T | 81 | a0001c0001t0001g0047a0001c0001t0001g0162a0001c0001t0001g0168others(78): Show | 92 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.142-8289C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023863 | ||||||
| chr5:1023865
|
T | C | 68 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(65): Show | 77 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.142-8287T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023865 | ||||||
| chr5:1023867
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(59): Show | 67 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.142-8285C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023867 | ||||||
| chr5:1023867
|
CCAGCCCA others(403): Show |
C | 1 | a0001c0001t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.142-8278_142-7869d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023867 | |||||
| chr5:1023867
|
CCAGCCCA others(485): Show |
C | 3 | a0001c0001t0001g0191a0001c0001t0001g0217a0001c0001t0005g0081 | 3 | HG00140.hp2 HG01515.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.142-8258_142-7767d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023867 | |||||
| chr5:1023874
|
A | G | 11 | a0001c0001t0001g0162a0001c0001t0001g0198a0001c0001t0001g0218others(8): Show | 13 | HG01243.hp2 HG02132.hp2 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.142-8278A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023874 | ||||||
| chr5:1023874
|
A | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(37): Show | 43 | HG00099.hp1 HG00408.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.142-8278A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023874 | ||||||
| chr5:1023874
|
ATTGTCCC others(116): Show |
A | 3 | a0001c0001t0007g0257a0001c0001t0007g0258a0001c0001t0007g0260 | 3 | HG02602.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.142-8258_142-8136d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023874 | |||||
| chr5:1023874
|
ATTGTCCC others(403): Show |
A | 4 | a0001c0001t0001g0023a0001c0001t0001g0129a0001c0001t0001g0207others(1): Show | 5 | HG00558.hp1 HG02738.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-8258_142-7849d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023874 | |||||
| chr5:1023880
|
C | A | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142-8272C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023880 | ||||||
| chr5:1023892
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.142-8260A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023892 | ||||||
| chr5:1023894
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(220): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.142-8258T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023894 | ||||||
| chr5:1023895
|
C | T | 1 | a0005c0009t0010g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.142-8257C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023895 | ||||||
| chr5:1023896
|
T | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(166): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.142-8256T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023896 | ||||||
| chr5:1023896
|
T | TCTGTGGG others(34): Show |
1 | a0001c0001t0002g0045 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142-8248_142-8247i others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023896 | |||||
| chr5:1023898
|
T | A | 1 | a0007c0014t0018g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.142-8254T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023898 | ||||||
| chr5:1023898
|
T | TA | 46 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(43): Show | 51 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.142-8254_142-8253i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023898 | ||||||
| chr5:1023899
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.142-8253G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023899 | ||||||
| chr5:1023900
|
T | G | 1 | a0001c0001t0001g0225 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.142-8252T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023900 | ||||||
| chr5:1023901
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.142-8251G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023901 | ||||||
| chr5:1023904
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(142): Show | 163 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.142-8248C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023904 | ||||||
| chr5:1023905
|
G | A | 1 | a0007c0014t0018g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.142-8247G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023905 | ||||||
| chr5:1023906
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(113): Show | 130 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.142-8246T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023906 | ||||||
| chr5:1023908
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(76): Show | 87 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.142-8244C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023908 | ||||||
| chr5:1023915
|
A | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(23): Show | 30 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.142-8237A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023915 | ||||||
| chr5:1023915
|
A | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(82): Show | 90 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.142-8237A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023915 | ||||||
| chr5:1023921
|
C | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(30): Show | 33 | HG00099.hp1 HG00408.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.142-8231C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023921 | ||||||
| chr5:1023929
|
TC | T | 3 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0259 | 4 | HG02523.hp2 NA19064.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-8220delC | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023929 | |||||
| chr5:1023932
|
C | T | 1 | a0001c0001t0002g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.142-8220C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023932 | ||||||
| chr5:1023935
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(223): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.142-8217T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023935 | ||||||
| chr5:1023937
|
T | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(132): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.142-8215T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023937 | ||||||
| chr5:1023939
|
T | A | 2 | a0001c0001t0014g0149a0009c0013t0017g0098 | 2 | HG02071.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.142-8213T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023939 | ||||||
| chr5:1023939
|
T | TA | 60 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(57): Show | 65 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.142-8213_142-8212i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023939 | ||||||
| chr5:1023945
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(48): Show | 61 | HG00597.hp1 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.142-8207C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023945 | ||||||
| chr5:1023946
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0002g0045 | 2 | HG02622.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.142-8206G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023946 | ||||||
| chr5:1023947
|
T | C | 22 | a0001c0001t0001g0237a0001c0001t0002g0007a0001c0001t0002g0008others(19): Show | 26 | HG00597.hp1 HG01358.hp1 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.142-8205T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023947 | ||||||
| chr5:1023949
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(46): Show | 50 | HG00099.hp1 HG00408.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.142-8203C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023949 | ||||||
| chr5:1023956
|
A | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(75): Show | 89 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.142-8196A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023956 | ||||||
| chr5:1023956
|
A | T | 30 | a0001c0001t0001g0237a0001c0001t0002g0007a0001c0001t0002g0008others(27): Show | 35 | HG00597.hp1 HG01358.hp1 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.142-8196A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023956 | ||||||
| chr5:1023962
|
C | A | 1 | a0001c0005t0011g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-8190C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023962 | ||||||
| chr5:1023974
|
A | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(16): Show | 23 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.142-8178A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023974 | ||||||
| chr5:1023978
|
G | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(41): Show | 47 | HG00099.hp1 HG00408.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.142-8174G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023978 | ||||||
| chr5:1023978
|
GCTGTGGG others(280): Show |
G | 1 | a0001c0001t0001g0218 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.142-8166_142-7880d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023978 | |||||
| chr5:1023980
|
T | TA | 14 | a0001c0001t0001g0022a0001c0001t0001g0160a0001c0001t0001g0161others(11): Show | 17 | HG00597.hp1 HG00741.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.142-8172_142-8171i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023980 | ||||||
| chr5:1023980
|
TGTGGGTG others(74): Show |
T | 16 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0030others(13): Show | 17 | HG02040.hp2 HG02109.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.142-8171_142-8091d others(83): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023980 | ||||||
| chr5:1023986
|
T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(93): Show | 113 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.142-8166T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023986 | ||||||
| chr5:1023987
|
G | A | 9 | a0001c0001t0002g0008a0001c0001t0002g0029a0001c0001t0002g0152others(6): Show | 9 | HG00597.hp1 HG01358.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-8165G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023987 | ||||||
| chr5:1023988
|
T | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(36): Show | 39 | HG00099.hp1 HG00408.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.142-8164T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023988 | ||||||
| chr5:1023990
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(127): Show | 145 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.142-8162C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023990 | ||||||
| chr5:1023990
|
CCAGCCCT others(280): Show |
C | 1 | a0001c0001t0001g0198 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.142-8155_142-7869d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023990 | |||||
| chr5:1023992
|
A | G | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-8160A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023992 | ||||||
| chr5:1023997
|
T | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(136): Show | 157 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.142-8155T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023997 | ||||||
| chr5:1023997
|
T | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(27): Show | 34 | HG00099.hp2 HG00597.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.142-8155T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1023997 | ||||||
| chr5:1023997
|
T | TTTGTCCC others(34): Show |
1 | a0001c0001t0002g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.142-8134_142-8133i others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1023997 | |||||
| chr5:1024002
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.142-8150C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024002 | ||||||
| chr5:1024003
|
C | A | 1 | a0001c0001t0003g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.142-8149C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024003 | ||||||
| chr5:1024015
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0144 | 3 | HG00642.hp1 HG00673.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.142-8137A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024015 | ||||||
| chr5:1024019
|
G | T | 79 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(76): Show | 90 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.142-8133G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024019 | ||||||
| chr5:1024019
|
GCTGTGGG others(34): Show |
G | 1 | a0001c0001t0008g0086 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.142-8121_142-8081d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024019 | |||||
| chr5:1024019
|
GCTGTGGG others(198): Show |
G | 1 | a0001c0001t0019g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.142-8121_142-7917d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024019 | |||||
| chr5:1024021
|
T | TA | 86 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(83): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.142-8131_142-8130i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024021 | ||||||
| chr5:1024021
|
TGTGGGCG others(156): Show |
T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.142-8130_142-7968d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024021 | ||||||
| chr5:1024027
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(94): Show | 113 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.142-8125C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024027 | ||||||
| chr5:1024028
|
G | A | 1 | a0001c0001t0002g0019 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.142-8124G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024028 | ||||||
| chr5:1024029
|
T | C | 67 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(64): Show | 76 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.142-8123T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024029 | ||||||
| chr5:1024031
|
C | T | 9 | a0001c0001t0001g0237a0001c0001t0002g0007a0001c0001t0002g0019others(6): Show | 10 | HG01099.hp1 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-8121C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024031 | ||||||
| chr5:1024031
|
CCAGCCCG others(239): Show |
C | 4 | a0001c0001t0001g0144a0001c0001t0001g0225a0001c0001t0003g0118others(1): Show | 4 | HG00642.hp1 HG01891.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-8092_142-7847d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024031 | |||||
| chr5:1024038
|
G | A | 19 | a0001c0001t0002g0007a0001c0001t0002g0045a0001c0001t0002g0103others(16): Show | 22 | HG01099.hp1 HG01192.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.142-8114G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024038 | ||||||
| chr5:1024038
|
G | T | 88 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0168others(85): Show | 101 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.142-8114G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024038 | ||||||
| chr5:1024058
|
C | T | 1 | a0001c0001t0002g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.142-8094C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024058 | ||||||
| chr5:1024060
|
T | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(178): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.142-8092T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024060 | ||||||
| chr5:1024060
|
TCTGTGGG others(34): Show |
T | 1 | a0001c0001t0002g0029 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.142-8080_142-8040d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024060 | |||||
| chr5:1024062
|
T | A | 16 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0030others(13): Show | 17 | HG02040.hp2 HG02109.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.142-8090T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024062 | ||||||
| chr5:1024062
|
T | TA | 72 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0168others(69): Show | 81 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.142-8090_142-8089i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024062 | ||||||
| chr5:1024068
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(26): Show | 37 | HG00099.hp2 HG00673.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.142-8084C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024068 | ||||||
| chr5:1024069
|
G | A | 83 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(80): Show | 93 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.142-8083G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024069 | ||||||
| chr5:1024070
|
T | C | 6 | a0001c0001t0002g0007a0001c0001t0002g0103a0001c0001t0003g0107others(3): Show | 7 | HG01099.hp1 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-8082T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024070 | ||||||
| chr5:1024072
|
T | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(37): Show | 49 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.142-8080T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024072 | ||||||
| chr5:1024079
|
A | ATTGTCCC others(116): Show |
1 | a0001c0001t0002g0045 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142-8054_142-8053i others(125): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024079 | |||||
| chr5:1024079
|
A | G | 102 | a0001c0001t0001g0047a0001c0001t0001g0162a0001c0001t0001g0168others(99): Show | 114 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.142-8073A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024079 | ||||||
| chr5:1024079
|
A | T | 6 | a0001c0001t0001g0022a0001c0001t0002g0007a0001c0001t0002g0019others(3): Show | 10 | HG02809.hp2 HG03453.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-8073A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024079 | ||||||
| chr5:1024084
|
C | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(13): Show | 20 | HG00099.hp2 HG00673.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.142-8068C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024084 | ||||||
| chr5:1024085
|
C | A | 1 | a0001c0001t0001g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142-8067C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024085 | ||||||
| chr5:1024099
|
CCGCTGTG others(75): Show |
C | 1 | a0001c0001t0007g0259 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.142-8051_142-7970d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024099 | |||||
| chr5:1024100
|
C | T | 9 | a0001c0001t0003g0108a0001c0002t0001g0185a0001c0002t0001g0194others(6): Show | 11 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.142-8052C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024100 | ||||||
| chr5:1024101
|
G | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-8051G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024101 | ||||||
| chr5:1024101
|
G | T | 7 | a0001c0001t0002g0019a0001c0001t0003g0107a0001c0001t0007g0027others(4): Show | 8 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-8051G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024101 | ||||||
| chr5:1024101
|
GCTGTGGG others(157): Show |
G | 4 | a0001c0001t0005g0003a0001c0001t0005g0091a0001c0001t0008g0094others(1): Show | 4 | HG00438.hp1 HG02004.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-8039_142-7876d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024101 | |||||
| chr5:1024103
|
T | TA | 36 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(33): Show | 37 | HG00099.hp1 HG00408.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.142-8049_142-8048i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024103 | ||||||
| chr5:1024103
|
TGTGGGCG others(74): Show |
T | 1 | a0001c0001t0001g0197 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.142-8048_142-7968d others(83): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024103 | ||||||
| chr5:1024103
|
TGTGGGCG others(156): Show |
T | 1 | a0001c0001t0001g0223 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.142-8048_142-7886d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024103 | ||||||
| chr5:1024103
|
TGTGGGCG others(279): Show |
T | 7 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(4): Show | 9 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-8048_142-7763d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024103 | ||||||
| chr5:1024109
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(26): Show | 36 | HG00099.hp2 HG00673.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.142-8043C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024109 | ||||||
| chr5:1024110
|
G | A | 1 | a0001c0001t0002g0007 | 2 | NA18968.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.142-8042G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024110 | ||||||
| chr5:1024111
|
T | C | 5 | a0001c0001t0002g0103a0001c0001t0003g0108a0004c0007t0006g0078others(2): Show | 5 | HG01099.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-8041T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024111 | ||||||
| chr5:1024113
|
C | T | 18 | a0001c0001t0001g0022a0001c0001t0001g0237a0001c0001t0002g0007others(15): Show | 19 | HG00597.hp1 HG01192.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-8039C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024113 | ||||||
| chr5:1024113
|
CCAGCCCA others(34): Show |
C | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.142-8012_142-7972d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024113 | |||||
| chr5:1024113
|
CCAGCCCA others(116): Show |
C | 1 | a0001c0001t0006g0265 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.142-7991_142-7869d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024113 | |||||
| chr5:1024113
|
CCAGCCCA others(157): Show |
C | 1 | a0001c0001t0001g0001 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.142-8032_142-7869d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024113 | |||||
| chr5:1024113
|
CCAGCCCA others(239): Show |
C | 12 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(9): Show | 14 | HG00099.hp2 HG00673.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-8010_142-7765d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024113 | |||||
| chr5:1024120
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(37): Show | 41 | HG00099.hp1 HG00408.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.142-8032A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024120 | ||||||
| chr5:1024120
|
A | T | 86 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(83): Show | 97 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.142-8032A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024120 | ||||||
| chr5:1024125
|
C | T | 4 | a0001c0001t0003g0002a0001c0001t0003g0109a0001c0001t0008g0086others(1): Show | 7 | HG02809.hp2 HG03453.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-8027C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024125 | ||||||
| chr5:1024140
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142-8012C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024140 | ||||||
| chr5:1024142
|
T | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(101): Show | 113 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.142-8010T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024142 | ||||||
| chr5:1024142
|
TCTGTGGG others(239): Show |
T | 1 | a0001c0002t0003g0054 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.142-7998_142-7753d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024142 | |||||
| chr5:1024150
|
C | T | 8 | a0001c0001t0001g0022a0001c0001t0002g0008a0001c0001t0002g0152others(5): Show | 8 | HG00597.hp1 HG01192.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-8002C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024150 | ||||||
| chr5:1024152
|
T | C | 6 | a0001c0001t0001g0022a0001c0001t0002g0008a0001c0001t0002g0152others(3): Show | 6 | HG00597.hp1 HG02135.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-8000T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024152 | ||||||
| chr5:1024154
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(151): Show | 174 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.142-7998T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024154 | ||||||
| chr5:1024154
|
TCAGCCCA others(34): Show |
T | 16 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0036others(13): Show | 16 | HG00408.hp1 HG01168.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-7971_142-7931d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024154 | |||||
| chr5:1024160
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-7992C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024160 | ||||||
| chr5:1024161
|
A | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(58): Show | 69 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.142-7991A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024161 | ||||||
| chr5:1024161
|
A | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0162a0001c0001t0002g0007others(4): Show | 8 | HG02055.hp2 HG02132.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-7991A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024161 | ||||||
| chr5:1024161
|
ATTGTCCC others(116): Show |
A | 11 | a0001c0001t0001g0022a0001c0001t0001g0035a0001c0001t0001g0049others(8): Show | 11 | HG00597.hp1 HG01074.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.142-7971_142-7849d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024161 | |||||
| chr5:1024163
|
T | A | 1 | a0001c0001t0008g0086 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.142-7989T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024163 | ||||||
| chr5:1024166
|
C | T | 1 | a0001c0001t0003g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.142-7986C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024166 | ||||||
| chr5:1024181
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(178): Show | 203 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.142-7971T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024181 | ||||||
| chr5:1024183
|
T | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-7969T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024183 | ||||||
| chr5:1024183
|
T | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(163): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.142-7969T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024183 | ||||||
| chr5:1024185
|
T | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0160a0001c0001t0001g0161others(3): Show | 8 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-7967T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024185 | ||||||
| chr5:1024185
|
T | TA | 6 | a0001c0001t0001g0022a0001c0001t0003g0115a0001c0001t0008g0082others(3): Show | 6 | HG01192.hp1 HG03225.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-7967_142-7966i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024185 | ||||||
| chr5:1024191
|
C | CGTCCCAG others(157): Show |
1 | a0001c0001t0002g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.142-7917_142-7916i others(166): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024191 | |||||
| chr5:1024191
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(56): Show | 66 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.142-7961C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024191 | ||||||
| chr5:1024192
|
G | A | 1 | a0001c0001t0008g0082 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.142-7960G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024192 | ||||||
| chr5:1024193
|
T | C | 3 | a0001c0001t0002g0019a0001c0001t0002g0029a0001c0001t0007g0077 | 3 | HG01358.hp1 HG03540.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.142-7959T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024193 | ||||||
| chr5:1024195
|
C | T | 102 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0001g0160others(99): Show | 115 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.142-7957C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024195 | ||||||
| chr5:1024202
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(59): Show | 68 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.142-7950A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024202 | ||||||
| chr5:1024202
|
A | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0160a0001c0001t0001g0161others(11): Show | 19 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-7950A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024202 | ||||||
| chr5:1024202
|
ATTGTCCC others(772): Show |
A | 1 | a0001c0001t0001g0216 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.142-7928_142-7150d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024202 | |||||
| chr5:1024208
|
C | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 7 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-7944C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024208 | ||||||
| chr5:1024220
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(44): Show | 51 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.142-7932A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024220 | ||||||
| chr5:1024222
|
C | T | 5 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(2): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-7930C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024222 | ||||||
| chr5:1024224
|
T | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(105): Show | 120 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.142-7928T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024224 | ||||||
| chr5:1024226
|
T | TA | 8 | a0001c0001t0001g0162a0001c0001t0003g0108a0001c0001t0007g0077others(5): Show | 8 | HG02132.hp2 HG02602.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-7926_142-7925i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024226 | ||||||
| chr5:1024232
|
C | T | 91 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(88): Show | 104 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.142-7920C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024232 | ||||||
| chr5:1024233
|
G | A | 1 | a0001c0001t0007g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-7919G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024233 | ||||||
| chr5:1024234
|
T | C | 88 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(85): Show | 98 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.142-7918T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024234 | ||||||
| chr5:1024236
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(173): Show | 194 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.142-7916T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024236 | ||||||
| chr5:1024236
|
T | TCAGCCCG others(240): Show |
1 | a0005c0009t0010g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.142-7910_142-7909i others(249): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024236 | |||||
| chr5:1024236
|
TCAGCCCA others(75): Show |
T | 1 | a0001c0001t0002g0019 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.142-7909_142-7828d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024236 | |||||
| chr5:1024236
|
TCAGCCCA others(362): Show |
T | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.142-7887_142-7519d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024236 | |||||
| chr5:1024243
|
A | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(62): Show | 69 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.142-7909A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024243 | ||||||
| chr5:1024243
|
A | T | 12 | a0001c0001t0001g0186a0001c0001t0002g0045a0001c0001t0003g0013others(9): Show | 12 | HG01099.hp1 HG01192.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-7909A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024243 | ||||||
| chr5:1024243
|
ATTGTCCC others(157): Show |
A | 1 | a0001c0001t0008g0086 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.142-7868_142-7705d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024243 | |||||
| chr5:1024248
|
C | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0109a0001c0005t0011g0002 | 6 | HG02809.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-7904C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024248 | ||||||
| chr5:1024261
|
A | G | 4 | a0001c0001t0001g0046a0001c0001t0001g0237a0001c0001t0001g0241others(1): Show | 4 | HG00733.hp2 HG02922.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-7891A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024261 | ||||||
| chr5:1024263
|
C | T | 4 | a0001c0001t0002g0045a0001c0001t0007g0257a0001c0001t0007g0258others(1): Show | 4 | HG02602.hp1 HG04115.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7889C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024263 | ||||||
| chr5:1024264
|
C | A | 1 | a0001c0001t0003g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.142-7888C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024264 | ||||||
| chr5:1024264
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-7888C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024264 | ||||||
| chr5:1024265
|
T | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(89): Show | 100 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.142-7887T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024265 | ||||||
| chr5:1024267
|
T | A | 1 | a0001c0001t0001g0223 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.142-7885T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024267 | ||||||
| chr5:1024267
|
T | TA | 8 | a0001c0001t0001g0022a0001c0001t0002g0239a0001c0001t0003g0115others(5): Show | 8 | HG01099.hp1 HG02071.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-7885_142-7884i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024267 | ||||||
| chr5:1024267
|
TGTGGGCG others(74): Show |
T | 1 | a0004c0007t0006g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.142-7884_142-7804d others(83): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024267 | ||||||
| chr5:1024273
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(63): Show | 73 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.142-7879C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024273 | ||||||
| chr5:1024274
|
G | A | 2 | a0001c0001t0002g0239a0004c0007t0006g0078 | 2 | HG01099.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.142-7878G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024274 | ||||||
| chr5:1024275
|
T | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0160a0001c0001t0001g0161others(3): Show | 9 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-7877T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024275 | ||||||
| chr5:1024277
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(94): Show | 105 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.142-7875T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024277 | ||||||
| chr5:1024284
|
G | A | 10 | a0001c0001t0001g0197a0001c0001t0002g0007a0001c0001t0003g0004others(7): Show | 13 | HG02071.hp1 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-7868G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024284 | ||||||
| chr5:1024284
|
G | T | 15 | a0001c0001t0001g0011a0001c0001t0001g0160a0001c0001t0001g0161others(12): Show | 18 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.142-7868G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024284 | ||||||
| chr5:1024289
|
C | T | 1 | a0001c0001t0019g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.142-7863C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024289 | ||||||
| chr5:1024290
|
C | A | 2 | a0001c0001t0014g0149a0002c0003t0001g0040 | 2 | HG04228.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.142-7862C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024290 | ||||||
| chr5:1024302
|
A | G | 9 | a0001c0001t0001g0024a0001c0001t0001g0046a0001c0001t0001g0048others(6): Show | 9 | HG00099.hp1 HG01123.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-7850A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024302 | ||||||
| chr5:1024306
|
G | T | 8 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0045others(5): Show | 9 | HG00597.hp1 HG02135.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-7846G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024306 | ||||||
| chr5:1024306
|
GCTGTGGG others(34): Show |
G | 81 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(78): Show | 91 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.142-7834_142-7794d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024306 | |||||
| chr5:1024306
|
GCTGTGGG others(116): Show |
G | 1 | a0001c0001t0002g0142 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.142-7834_142-7712d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024306 | |||||
| chr5:1024308
|
T | TA | 12 | a0001c0001t0001g0011a0001c0001t0001g0160a0001c0001t0001g0161others(9): Show | 15 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-7844_142-7843i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024308 | ||||||
| chr5:1024308
|
TGTGGGCG others(74): Show |
T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-7843_142-7763d others(83): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024308 | ||||||
| chr5:1024308
|
TGTGGGCG others(525): Show |
T | 4 | a0001c0001t0001g0186a0001c0001t0003g0013a0001c0001t0003g0121others(1): Show | 4 | HG02145.hp2 HG02895.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7843_142-7312d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024308 | ||||||
| chr5:1024314
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(75): Show | 86 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.142-7838C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024314 | ||||||
| chr5:1024316
|
T | C | 1 | a0001c0001t0002g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.142-7836T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024316 | ||||||
| chr5:1024318
|
C | T | 28 | a0001c0001t0001g0022a0001c0001t0001g0223a0001c0001t0002g0007others(25): Show | 30 | HG00597.hp1 HG01192.hp1 HG01928.hp2 others(27): Show |
intron_variant | MODIFIER | c.142-7834C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024318 | ||||||
| chr5:1024325
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(67): Show | 80 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.142-7827G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024325 | ||||||
| chr5:1024325
|
G | T | 10 | a0001c0001t0002g0239a0001c0001t0003g0109a0001c0001t0003g0115others(7): Show | 10 | HG00438.hp1 HG01099.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-7827G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024325 | ||||||
| chr5:1024325
|
GTTGTCCC others(34): Show |
G | 1 | a0001c0001t0001g0225 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.142-7805_142-7765d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024325 | |||||
| chr5:1024327
|
T | A | 1 | a0001c0001t0019g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.142-7825T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024327 | ||||||
| chr5:1024330
|
C | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(47): Show | 54 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.142-7822C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024330 | ||||||
| chr5:1024332
|
C | T | 1 | a0004c0007t0006g0078 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.142-7820C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024332 | ||||||
| chr5:1024343
|
A | G | 21 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0036others(18): Show | 21 | HG00099.hp1 HG00408.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.142-7809A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024343 | ||||||
| chr5:1024345
|
C | T | 2 | a0001c0001t0007g0027a0001c0001t0007g0256 | 3 | HG02523.hp2 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.142-7807C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024345 | ||||||
| chr5:1024347
|
T | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 144 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.142-7805T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024347 | ||||||
| chr5:1024349
|
T | A | 2 | a0001c0001t0001g0222a0004c0007t0006g0079 | 2 | HG02004.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.142-7803T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024349 | ||||||
| chr5:1024355
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(79): Show | 91 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.142-7797C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024355 | ||||||
| chr5:1024356
|
G | A | 1 | a0004c0007t0006g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.142-7796G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024356 | ||||||
| chr5:1024356
|
GTCTCAGC others(239): Show |
G | 1 | a0001c0001t0002g0029 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.142-7793_142-7548d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024356 | |||||
| chr5:1024357
|
T | C | 6 | a0001c0001t0002g0136a0001c0001t0002g0239a0001c0001t0003g0107others(3): Show | 6 | HG02965.hp1 HG03927.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-7795T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024357 | ||||||
| chr5:1024359
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(113): Show | 127 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.142-7793T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024359 | ||||||
| chr5:1024363
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.142-7789C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024363 | ||||||
| chr5:1024366
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(194): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.142-7786A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024366 | ||||||
| chr5:1024366
|
A | T | 17 | a0001c0001t0003g0115a0001c0001t0005g0003a0001c0001t0005g0091others(14): Show | 17 | HG00438.hp1 HG01192.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.142-7786A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024366 | ||||||
| chr5:1024371
|
C | G | 3 | a0001c0001t0001g0237a0001c0001t0001g0241a0001c0001t0005g0080 | 3 | HG00733.hp2 HG02922.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.142-7781C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024371 | ||||||
| chr5:1024371
|
C | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0109a0001c0005t0011g0002 | 6 | HG02809.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-7781C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024371 | ||||||
| chr5:1024372
|
C | A | 1 | a0001c0001t0014g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.142-7780C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024372 | ||||||
| chr5:1024372
|
C | G | 2 | a0001c0001t0002g0103a0007c0014t0018g0104 | 2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.142-7780C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024372 | ||||||
| chr5:1024384
|
A | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0129a0001c0001t0001g0197others(3): Show | 7 | HG00558.hp1 HG02622.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-7768A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024384 | ||||||
| chr5:1024386
|
C | T | 3 | a0001c0001t0007g0257a0001c0001t0007g0258a0001c0001t0007g0260 | 3 | HG02602.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.142-7766C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024386 | ||||||
| chr5:1024388
|
G | T | 3 | a0001c0001t0007g0257a0001c0001t0007g0258a0001c0001t0007g0260 | 3 | HG02602.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.142-7764G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024388 | ||||||
| chr5:1024390
|
T | A | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-7762T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024390 | ||||||
| chr5:1024390
|
T | TA | 12 | a0001c0001t0001g0011a0001c0001t0001g0160a0001c0001t0001g0161others(9): Show | 15 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-7762_142-7761i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024390 | ||||||
| chr5:1024390
|
TGTGGGCG others(1058): Show |
T | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-7761_142-6697d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024390 | ||||||
| chr5:1024396
|
C | CGTCTCAG others(240): Show |
3 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0010g0004 | 5 | HG02486.hp2 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-7753_142-7752i others(249): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024396 | |||||
| chr5:1024396
|
C | CGTCTCAG others(240): Show |
2 | a0001c0001t0003g0113a0008c0011t0016g0263 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.142-7753_142-7752i others(249): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024396 | |||||
| chr5:1024396
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(50): Show | 55 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.142-7756C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024396 | ||||||
| chr5:1024397
|
G | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-7755G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024397 | ||||||
| chr5:1024398
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.142-7754T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024398 | ||||||
| chr5:1024400
|
C | T | 19 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0002g0239others(16): Show | 20 | HG01099.hp1 HG01192.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.142-7752C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024400 | ||||||
| chr5:1024407
|
G | A | 111 | a0001c0001t0001g0024a0001c0001t0001g0046a0001c0001t0001g0047others(108): Show | 126 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.142-7745G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024407 | ||||||
| chr5:1024407
|
G | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0222a0001c0001t0003g0004others(6): Show | 11 | HG01243.hp2 HG02004.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.142-7745G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024407 | ||||||
| chr5:1024412
|
C | G | 9 | a0001c0001t0001g0024a0001c0001t0001g0046a0001c0001t0001g0048others(6): Show | 9 | HG00099.hp1 HG01123.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-7740C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024412 | ||||||
| chr5:1024412
|
C | T | 6 | a0001c0001t0003g0115a0001c0001t0005g0003a0001c0001t0005g0091others(3): Show | 6 | HG00438.hp1 HG02004.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-7740C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024412 | ||||||
| chr5:1024414
|
C | T | 1 | a0004c0007t0006g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.142-7738C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024414 | ||||||
| chr5:1024425
|
A | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0035a0001c0001t0001g0049others(4): Show | 7 | HG01074.hp2 HG01261.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-7727A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024425 | ||||||
| chr5:1024427
|
C | T | 3 | a0001c0001t0004g0057a0001c0001t0004g0058a0001c0001t0007g0259 | 3 | HG02055.hp2 HG02965.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.142-7725C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024427 | ||||||
| chr5:1024429
|
T | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(135): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.142-7723T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024429 | ||||||
| chr5:1024437
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(109): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.142-7715C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024437 | ||||||
| chr5:1024439
|
T | C | 1 | a0004c0007t0006g0078 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.142-7713T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024439 | ||||||
| chr5:1024441
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(218): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.142-7711T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024441 | ||||||
| chr5:1024443
|
A | G | 1 | a0001c0002t0003g0054 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.142-7709A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024443 | ||||||
| chr5:1024445
|
C | G | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-7707C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024445 | ||||||
| chr5:1024448
|
A | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0023others(65): Show | 76 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.142-7704A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024448 | ||||||
| chr5:1024448
|
A | T | 6 | a0001c0001t0003g0002a0001c0001t0007g0027a0001c0001t0007g0256others(3): Show | 10 | HG01928.hp2 HG02523.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-7704A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024448 | ||||||
| chr5:1024450
|
T | A | 4 | a0001c0001t0005g0003a0001c0001t0005g0091a0001c0001t0008g0094others(1): Show | 4 | HG00438.hp1 HG02004.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7702T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024450 | ||||||
| chr5:1024453
|
C | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0036others(16): Show | 19 | HG00408.hp1 HG01168.hp2 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.142-7699C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024453 | ||||||
| chr5:1024453
|
C | T | 13 | a0001c0001t0003g0109a0001c0001t0005g0003a0001c0001t0005g0089others(10): Show | 15 | HG00438.hp2 HG01192.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.142-7699C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024453 | ||||||
| chr5:1024466
|
A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0191a0001c0001t0001g0217others(2): Show | 5 | HG00140.hp2 HG01515.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-7686A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024466 | ||||||
| chr5:1024468
|
C | T | 2 | a0001c0001t0007g0027a0001c0001t0007g0256 | 3 | HG02523.hp2 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.142-7684C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024468 | ||||||
| chr5:1024470
|
G | T | 12 | a0001c0001t0002g0239a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 15 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-7682G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024470 | ||||||
| chr5:1024472
|
T | TA | 3 | a0001c0001t0001g0001a0001c0001t0001g0222a0002c0003t0001g0040 | 3 | HG02004.hp2 HG03669.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.142-7680_142-7679i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024472 | ||||||
| chr5:1024472
|
TGTGGGCG others(156): Show |
T | 1 | a0001c0001t0007g0259 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.142-7679_142-7517d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024472 | ||||||
| chr5:1024473
|
G | A | 1 | a0001c0001t0010g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.142-7679G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024473 | ||||||
| chr5:1024474
|
T | G | 1 | a0001c0001t0010g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.142-7678T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024474 | ||||||
| chr5:1024475
|
G | T | 1 | a0001c0001t0010g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.142-7677G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024475 | ||||||
| chr5:1024478
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0023others(39): Show | 46 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.142-7674C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024478 | ||||||
| chr5:1024479
|
GTCCCAGC others(116): Show |
G | 18 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0036others(15): Show | 18 | HG00408.hp1 HG01168.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-7641_142-7519d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024479 | |||||
| chr5:1024480
|
T | C | 2 | a0001c0001t0002g0239a0004c0007t0006g0078 | 2 | HG01099.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.142-7672T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024480 | ||||||
| chr5:1024482
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0168others(116): Show | 137 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.142-7670C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024482 | ||||||
| chr5:1024484
|
A | G | 7 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(4): Show | 9 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-7668A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024484 | ||||||
| chr5:1024489
|
A | G | 32 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0035others(29): Show | 34 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.142-7663A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024489 | ||||||
| chr5:1024489
|
A | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(68): Show | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.142-7663A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024489 | ||||||
| chr5:1024491
|
T | A | 12 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(9): Show | 14 | HG00438.hp2 HG01192.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-7661T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024491 | ||||||
| chr5:1024494
|
C | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0129a0001c0001t0001g0207others(2): Show | 6 | HG00558.hp1 HG02738.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-7658C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024494 | ||||||
| chr5:1024494
|
C | T | 4 | a0001c0001t0005g0003a0001c0001t0005g0091a0001c0001t0008g0094others(1): Show | 4 | HG00438.hp1 HG02004.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7658C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024494 | ||||||
| chr5:1024507
|
A | G | 4 | a0001c0001t0001g0191a0001c0001t0001g0217a0001c0001t0005g0081others(1): Show | 4 | HG00140.hp2 HG01515.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7645A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024507 | ||||||
| chr5:1024509
|
C | T | 89 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(86): Show | 102 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.142-7643C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024509 | ||||||
| chr5:1024511
|
T | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(63): Show | 77 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.142-7641T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024511 | ||||||
| chr5:1024519
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(103): Show | 120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.142-7633C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024519 | ||||||
| chr5:1024520
|
G | A | 89 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(86): Show | 102 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.142-7632G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024520 | ||||||
| chr5:1024521
|
T | C | 2 | a0001c0001t0002g0045a0004c0007t0006g0079 | 2 | HG02615.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.142-7631T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024521 | ||||||
| chr5:1024523
|
C | T | 13 | a0001c0001t0001g0222a0001c0001t0002g0136a0001c0001t0002g0239others(10): Show | 14 | HG01928.hp2 HG02004.hp2 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.142-7629C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024523 | ||||||
| chr5:1024530
|
A | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(93): Show | 110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.142-7622A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024530 | ||||||
| chr5:1024530
|
A | T | 10 | a0001c0001t0001g0237a0001c0001t0001g0241a0001c0001t0003g0002others(7): Show | 13 | HG00438.hp1 HG00733.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-7622A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024530 | ||||||
| chr5:1024530
|
ATTGTCCC others(321): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.142-7588_142-7261d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024530 | |||||
| chr5:1024530
|
ATTGTCCC others(444): Show |
A | 2 | a0001c0001t0001g0024a0001c0001t0026g0024 | 2 | HG01496.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.142-7581_142-7131d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024530 | |||||
| chr5:1024535
|
C | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0035a0001c0001t0001g0049others(4): Show | 7 | HG01074.hp2 HG01261.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-7617C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024535 | ||||||
| chr5:1024535
|
C | T | 2 | a0001c0001t0003g0115a0001c0005t0011g0114 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.142-7617C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024535 | ||||||
| chr5:1024550
|
CCGCTGTG others(34): Show |
C | 1 | a0001c0002t0003g0054 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.142-7600_142-7560d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024550 | |||||
| chr5:1024552
|
G | T | 18 | a0001c0001t0001g0237a0001c0001t0001g0241a0001c0001t0002g0142others(15): Show | 23 | HG00733.hp2 HG02055.hp2 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.142-7600G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024552 | ||||||
| chr5:1024554
|
T | TA | 63 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(60): Show | 71 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.142-7598_142-7597i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024554 | ||||||
| chr5:1024554
|
TGTGGGCG others(279): Show |
T | 1 | a0001c0001t0003g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.142-7597_142-7312d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024554 | ||||||
| chr5:1024554
|
TGTGGGCG others(443): Show |
T | 1 | a0001c0001t0001g0161 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.142-7597_142-7148d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024554 | ||||||
| chr5:1024560
|
C | T | 30 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0035others(27): Show | 36 | HG00323.hp1 HG00639.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.142-7592C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024560 | ||||||
| chr5:1024561
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142-7591G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024561 | ||||||
| chr5:1024561
|
GTCTCAGC others(34): Show |
G | 7 | a0001c0001t0001g0022a0001c0001t0001g0035a0001c0001t0001g0049others(4): Show | 7 | HG01074.hp2 HG01261.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-7588_142-7548d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024561 | |||||
| chr5:1024562
|
T | C | 4 | a0001c0001t0002g0239a0001c0001t0010g0116a0004c0007t0006g0078others(1): Show | 4 | HG01099.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-7590T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024562 | ||||||
| chr5:1024563
|
C | A | 1 | a0001c0001t0002g0045 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142-7589C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024563 | ||||||
| chr5:1024564
|
T | C | 42 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(39): Show | 48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.142-7588T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024564 | ||||||
| chr5:1024564
|
TCAGCCCA others(34): Show |
T | 75 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(72): Show | 86 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.142-7561_142-7521d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024564 | |||||
| chr5:1024571
|
A | G | 24 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0129others(21): Show | 29 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.142-7581A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024571 | ||||||
| chr5:1024571
|
A | T | 8 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0050others(5): Show | 8 | HG00099.hp1 HG01123.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-7581A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024571 | ||||||
| chr5:1024576
|
C | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0223 | 2 | NA18965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.142-7576C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024576 | ||||||
| chr5:1024589
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0203a0001c0001t0001g0244 | 5 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-7563A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024589 | ||||||
| chr5:1024591
|
T | C | 64 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(61): Show | 75 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.142-7561T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024591 | ||||||
| chr5:1024593
|
T | G | 40 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(37): Show | 45 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.142-7559T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024593 | ||||||
| chr5:1024595
|
T | TA | 5 | a0001c0001t0001g0222a0001c0001t0001g0237a0001c0001t0001g0241others(2): Show | 5 | HG00733.hp2 HG02004.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-7557_142-7556i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024595 | ||||||
| chr5:1024595
|
T | TGTGGGTG others(35): Show |
1 | a0001c0001t0002g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.142-7552_142-7551i others(44): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024595 | |||||
| chr5:1024601
|
C | T | 38 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0046others(35): Show | 46 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.142-7551C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024601 | ||||||
| chr5:1024602
|
A | G | 64 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(61): Show | 75 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.142-7550A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024602 | ||||||
| chr5:1024603
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.142-7549T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024603 | ||||||
| chr5:1024605
|
C | T | 11 | a0001c0001t0001g0237a0001c0001t0001g0241a0001c0001t0002g0136others(8): Show | 12 | HG00733.hp2 HG01243.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-7547C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024605 | ||||||
| chr5:1024612
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 58 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.142-7540A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024612 | ||||||
| chr5:1024612
|
A | T | 1 | a0001c0001t0001g0038 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.142-7540A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024612 | ||||||
| chr5:1024612
|
ATTGTCCC others(239): Show |
A | 1 | a0001c0002t0003g0054 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.142-7479_142-7234d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024612 | |||||
| chr5:1024617
|
C | G | 4 | a0001c0001t0001g0191a0001c0001t0001g0217a0001c0001t0005g0081others(1): Show | 4 | HG00140.hp2 HG01515.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7535C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024617 | ||||||
| chr5:1024633
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0003g0108 | 2 | HG02148.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.142-7519C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024633 | ||||||
| chr5:1024634
|
G | T | 3 | a0001c0001t0001g0038a0001c0001t0002g0045a0001c0001t0002g0239 | 3 | HG02135.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.142-7518G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024634 | ||||||
| chr5:1024636
|
T | A | 1 | a0001c0001t0007g0259 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.142-7516T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024636 | ||||||
| chr5:1024636
|
T | TA | 8 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0050others(5): Show | 8 | HG00099.hp1 HG01123.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-7516_142-7515i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024636 | ||||||
| chr5:1024636
|
TGTGGGCG others(279): Show |
T | 1 | a0001c0001t0001g0160 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.142-7515_142-7230d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024636 | ||||||
| chr5:1024642
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(93): Show | 109 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.142-7510C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024642 | ||||||
| chr5:1024643
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.142-7509G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024643 | ||||||
| chr5:1024644
|
T | C | 4 | a0001c0001t0001g0198a0001c0001t0001g0218a0001c0001t0003g0108others(1): Show | 4 | HG02148.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-7508T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024644 | ||||||
| chr5:1024646
|
C | T | 23 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0050others(20): Show | 26 | HG00099.hp1 HG01099.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.142-7506C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024646 | ||||||
| chr5:1024653
|
T | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(91): Show | 105 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.142-7499T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024653 | ||||||
| chr5:1024653
|
T | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(33): Show | 39 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.142-7499T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024653 | ||||||
| chr5:1024653
|
TTTGTCCC others(34): Show |
T | 2 | a0001c0001t0003g0002a0001c0005t0011g0002 | 3 | HG02809.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.142-7477_142-7437d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024653 | |||||
| chr5:1024658
|
C | T | 2 | a0001c0001t0003g0115a0001c0005t0011g0114 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.142-7494C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024658 | ||||||
| chr5:1024661
|
T | A | 2 | a0001c0001t0002g0103a0007c0014t0018g0104 | 2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.142-7491T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024661 | ||||||
| chr5:1024671
|
A | G | 1 | a0002c0003t0001g0040 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.142-7481A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024671 | ||||||
| chr5:1024673
|
C | T | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-7479C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024673 | ||||||
| chr5:1024674
|
C | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(60): Show | 71 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.142-7478C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024674 | ||||||
| chr5:1024675
|
G | T | 23 | a0001c0001t0001g0023a0001c0001t0001g0129a0001c0001t0001g0207others(20): Show | 26 | HG00558.hp1 HG00639.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.142-7477G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024675 | ||||||
| chr5:1024675
|
GCTGTGGG others(239): Show |
G | 2 | a0001c0001t0001g0218a0001c0001t0003g0108 | 2 | HG02886.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.142-7465_142-7220d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024675 | |||||
| chr5:1024675
|
GCTGTGGG others(977): Show |
G | 1 | a0004c0007t0006g0078 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.142-7469_142-6486d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024675 | |||||
| chr5:1024677
|
T | TA | 9 | a0001c0001t0001g0038a0001c0001t0001g0222a0001c0001t0002g0045others(6): Show | 11 | HG02004.hp2 HG02135.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.142-7475_142-7474i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024677 | ||||||
| chr5:1024683
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(108): Show | 127 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.142-7469C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024683 | ||||||
| chr5:1024685
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(60): Show | 71 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.142-7467T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024685 | ||||||
| chr5:1024687
|
C | T | 17 | a0001c0001t0001g0038a0001c0001t0001g0198a0001c0001t0001g0222others(14): Show | 19 | HG00639.hp1 HG00741.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-7465C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024687 | ||||||
| chr5:1024694
|
A | G | 20 | a0001c0001t0001g0023a0001c0001t0001g0129a0001c0001t0001g0191others(17): Show | 22 | HG00140.hp2 HG00558.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.142-7458A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024694 | ||||||
| chr5:1024694
|
A | T | 23 | a0001c0001t0001g0222a0001c0001t0003g0004a0001c0001t0003g0112others(20): Show | 28 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.142-7458A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024694 | ||||||
| chr5:1024694
|
ATTGTCCC others(75): Show |
A | 2 | a0001c0001t0008g0086a0001c0001t0019g0193 | 2 | HG01928.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.142-7436_142-7355d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024694 | |||||
| chr5:1024694
|
ATTGTCCC others(157): Show |
A | 3 | a0001c0001t0001g0050a0001c0001t0014g0148a0006c0015t0001g0231 | 3 | HG01358.hp2 HG04199.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.142-7436_142-7273d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024694 | |||||
| chr5:1024694
|
ATTGTCCC others(280): Show |
A | 1 | a0001c0001t0001g0235 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.142-7436_142-7150d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024694 | |||||
| chr5:1024699
|
C | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0203a0001c0001t0001g0244 | 5 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-7453C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024699 | ||||||
| chr5:1024700
|
C | A | 1 | a0001c0001t0001g0222 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.142-7452C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024700 | ||||||
| chr5:1024714
|
C | T | 3 | a0001c0001t0004g0057a0001c0001t0004g0058a0001c0001t0007g0259 | 3 | HG02055.hp2 HG02965.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.142-7438C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024714 | ||||||
| chr5:1024715
|
C | T | 10 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0220others(7): Show | 12 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-7437C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024715 | ||||||
| chr5:1024716
|
T | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.142-7436T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024716 | ||||||
| chr5:1024718
|
T | TA | 6 | a0001c0001t0001g0023a0001c0001t0001g0129a0001c0001t0001g0207others(3): Show | 7 | HG00558.hp1 HG02738.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-7434_142-7433i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024718 | ||||||
| chr5:1024718
|
TGTGGGCG others(115): Show |
T | 1 | a0001c0001t0001g0225 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.142-7433_142-7312d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024718 | ||||||
| chr5:1024719
|
GTGGGCGT others(318): Show |
G | 1 | a0001c0001t0001g0046 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.142-7432_142-7108d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024719 | ||||||
| chr5:1024724
|
C | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0048others(19): Show | 24 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.142-7428C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024724 | ||||||
| chr5:1024725
|
G | A | 1 | a0001c0001t0007g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-7427G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024725 | ||||||
| chr5:1024726
|
T | C | 6 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0220others(3): Show | 6 | HG00099.hp1 HG01123.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-7426T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024726 | ||||||
| chr5:1024728
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.142-7424T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024728 | ||||||
| chr5:1024735
|
A | G | 29 | a0001c0001t0001g0011a0001c0001t0001g0198a0001c0001t0001g0203others(26): Show | 36 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.142-7417A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024735 | ||||||
| chr5:1024735
|
A | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(24): Show | 28 | HG00408.hp1 HG01074.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.142-7417A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024735 | ||||||
| chr5:1024735
|
ATTGTCCC others(485): Show |
A | 1 | a0001c0001t0001g0052 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.142-7395_142-6904d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024735 | |||||
| chr5:1024735
|
ATTGTCCC others(895): Show |
A | 1 | a0004c0007t0006g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.142-7387_142-6486d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024735 | |||||
| chr5:1024750
|
C | T | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.142-7402C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024750 | ||||||
| chr5:1024755
|
C | T | 90 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(87): Show | 103 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.142-7397C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024755 | ||||||
| chr5:1024755
|
CCTCTGTG others(75): Show |
C | 1 | a0001c0001t0008g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142-7294_142-7213d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024755 | |||||
| chr5:1024756
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0129 | 2 | HG02135.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.142-7396C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024756 | ||||||
| chr5:1024757
|
T | G | 54 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0038others(51): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.142-7395T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024757 | ||||||
| chr5:1024759
|
TGTGGGCG others(74): Show |
T | 1 | a0001c0001t0006g0265 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.142-7392_142-7312d others(83): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024759 | ||||||
| chr5:1024759
|
TGTGGGCG others(156): Show |
T | 1 | a0001c0001t0001g0198 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.142-7392_142-7230d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024759 | ||||||
| chr5:1024765
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(99): Show | 118 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.142-7387C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024765 | ||||||
| chr5:1024766
|
G | A | 3 | a0001c0001t0002g0142a0001c0001t0002g0239a0001c0001t0015g0117 | 3 | HG02622.hp2 HG03927.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.142-7386G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024766 | ||||||
| chr5:1024767
|
T | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0129a0001c0001t0001g0222others(1): Show | 4 | HG02004.hp2 HG02135.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-7385T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024767 | ||||||
| chr5:1024769
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(114): Show | 137 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.142-7383T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024769 | ||||||
| chr5:1024769
|
TCAGCCCG others(34): Show |
T | 1 | a0001c0001t0015g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-7376_142-7336d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024769 | |||||
| chr5:1024776
|
G | A | 112 | a0001c0001t0001g0023a0001c0001t0001g0038a0001c0001t0001g0047others(109): Show | 127 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.142-7376G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024776 | ||||||
| chr5:1024776
|
G | T | 16 | a0001c0001t0001g0191a0001c0001t0001g0217a0001c0001t0001g0222others(13): Show | 18 | HG00140.hp2 HG00438.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.142-7376G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024776 | ||||||
| chr5:1024781
|
C | CCCTGCTC others(34): Show |
1 | a0001c0001t0003g0002 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.142-7347_142-7346i others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024781 | |||||
| chr5:1024781
|
C | G | 1 | a0002c0003t0001g0040 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.142-7371C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024781 | ||||||
| chr5:1024796
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.142-7356C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024796 | ||||||
| chr5:1024796
|
CCGCTGTG others(34): Show |
C | 20 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0029others(17): Show | 21 | HG01106.hp2 HG01358.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.142-7354_142-7314d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024796 | |||||
| chr5:1024797
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0207a0001c0001t0001g0236 | 4 | HG00558.hp1 HG02738.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7355C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024797 | ||||||
| chr5:1024798
|
G | T | 83 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0168others(80): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.142-7354G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024798 | ||||||
| chr5:1024798
|
GCTGTGGG others(116): Show |
G | 1 | a0001c0001t0001g0038 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.142-7342_142-7220d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024798 | |||||
| chr5:1024800
|
T | TA | 4 | a0001c0001t0001g0022a0001c0001t0001g0222a0001c0001t0010g0116others(1): Show | 4 | HG02004.hp2 HG02071.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-7352_142-7351i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024800 | ||||||
| chr5:1024800
|
TGTGGGCG others(33): Show |
T | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(21): Show | 24 | HG00408.hp1 HG01074.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.142-7351_142-7312d others(42): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024800 | ||||||
| chr5:1024800
|
TGTGGGCG others(197): Show |
T | 61 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(58): Show | 69 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.142-7351_142-7148d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024800 | ||||||
| chr5:1024806
|
C | T | 35 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0048others(32): Show | 42 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.142-7346C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024806 | ||||||
| chr5:1024806
|
CGTCCCAG others(239): Show |
C | 7 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(4): Show | 9 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-7335_142-7090d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024806 | |||||
| chr5:1024808
|
T | C | 8 | a0001c0001t0001g0023a0001c0001t0001g0207a0001c0001t0001g0236others(5): Show | 9 | HG00558.hp1 HG02602.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-7344T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024808 | ||||||
| chr5:1024810
|
C | T | 79 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0129others(76): Show | 90 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.142-7342C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024810 | ||||||
| chr5:1024810
|
CCAGCCCT others(34): Show |
C | 3 | a0001c0001t0001g0023a0001c0001t0001g0207a0001c0001t0001g0236 | 4 | HG00558.hp1 HG02738.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7335_142-7295d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024810 | |||||
| chr5:1024810
|
CCAGCCCT others(157): Show |
C | 3 | a0001c0001t0001g0011a0001c0001t0001g0203a0001c0001t0001g0244 | 5 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-7335_142-7172d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024810 | |||||
| chr5:1024817
|
T | A | 22 | a0001c0001t0001g0022a0001c0001t0001g0129a0001c0001t0002g0045others(19): Show | 25 | HG02055.hp2 HG02258.hp1 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.142-7335T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024817 | ||||||
| chr5:1024817
|
T | G | 11 | a0001c0001t0001g0048a0001c0001t0001g0191a0001c0001t0001g0217others(8): Show | 11 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.142-7335T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024817 | ||||||
| chr5:1024817
|
TTTGTCCC others(280): Show |
T | 9 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(6): Show | 11 | HG00438.hp2 HG01192.hp1 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.142-7315_142-7029d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024817 | |||||
| chr5:1024822
|
C | T | 3 | a0001c0001t0008g0086a0001c0001t0019g0193a0001c0005t0011g0002 | 3 | HG01928.hp2 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.142-7330C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024822 | ||||||
| chr5:1024837
|
T | C | 115 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0048others(112): Show | 131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.142-7315T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024837 | ||||||
| chr5:1024839
|
T | G | 94 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0048others(91): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.142-7313T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024839 | ||||||
| chr5:1024839
|
T | TCTGTGGG others(1715): Show |
1 | a0001c0001t0013g0075 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.142-7273_142-7272i others(1724): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024839 | |||||
| chr5:1024839
|
T | TCTGTGGG others(1674): Show |
2 | a0001c0001t0013g0073a0001c0001t0013g0074 | 2 | HG02273.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142-7273_142-7272i others(1683): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024839 | |||||
| chr5:1024841
|
T | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(28): Show | 31 | HG00408.hp1 HG01074.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.142-7311T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024841 | ||||||
| chr5:1024841
|
T | TA | 10 | a0001c0001t0001g0048a0001c0001t0001g0191a0001c0001t0001g0217others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-7311_142-7310i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024841 | ||||||
| chr5:1024847
|
C | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0129a0001c0001t0003g0002others(2): Show | 6 | HG02809.hp2 HG03453.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-7305C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024847 | ||||||
| chr5:1024848
|
G | A | 4 | a0001c0001t0002g0142a0001c0001t0007g0257a0001c0001t0007g0258others(1): Show | 4 | HG02602.hp1 HG04115.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-7304G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024848 | ||||||
| chr5:1024851
|
T | C | 82 | a0001c0001t0001g0022a0001c0001t0001g0047a0001c0001t0001g0129others(79): Show | 94 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.142-7301T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024851 | ||||||
| chr5:1024858
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(57): Show | 65 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.142-7294G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024858 | ||||||
| chr5:1024858
|
G | T | 94 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(91): Show | 107 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.142-7294G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024858 | ||||||
| chr5:1024860
|
T | A | 2 | a0001c0001t0008g0086a0001c0001t0019g0193 | 2 | HG01928.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.142-7292T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024860 | ||||||
| chr5:1024863
|
C | T | 2 | a0001c0001t0003g0002a0001c0005t0011g0002 | 3 | HG02809.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.142-7289C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024863 | ||||||
| chr5:1024879
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0050others(2): Show | 5 | HG01358.hp2 HG03669.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-7273C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024879 | ||||||
| chr5:1024880
|
G | T | 9 | a0001c0001t0001g0048a0001c0001t0001g0220a0001c0001t0003g0002others(6): Show | 10 | HG00099.hp1 HG01123.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-7272G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024880 | ||||||
| chr5:1024880
|
GCTGTGGG others(34): Show |
G | 6 | a0001c0001t0001g0023a0001c0001t0001g0207a0001c0001t0001g0236others(3): Show | 7 | HG00558.hp1 HG02055.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-7260_142-7220d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024880 | |||||
| chr5:1024882
|
T | TA | 3 | a0001c0001t0001g0222a0001c0001t0003g0109a0001c0001t0010g0116 | 3 | HG02004.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.142-7270_142-7269i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024882 | ||||||
| chr5:1024882
|
TGTGGGCG others(115): Show |
T | 1 | a0001c0001t0001g0129 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.142-7269_142-7148d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024882 | ||||||
| chr5:1024888
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(52): Show | 58 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.142-7264C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024888 | ||||||
| chr5:1024890
|
T | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0050others(4): Show | 8 | HG01358.hp2 HG02523.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-7262T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024890 | ||||||
| chr5:1024892
|
C | T | 9 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0003g0109others(6): Show | 9 | HG02273.hp1 HG02965.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-7260C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024892 | ||||||
| chr5:1024892
|
CCAGCCCT others(34): Show |
C | 6 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0051others(3): Show | 6 | HG01074.hp2 HG02015.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-7253_142-7213d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024892 | |||||
| chr5:1024899
|
T | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(111): Show | 127 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.142-7253T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024899 | ||||||
| chr5:1024899
|
T | G | 15 | a0001c0001t0001g0048a0001c0001t0001g0220a0001c0001t0001g0222others(12): Show | 15 | HG00099.hp1 HG01123.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-7253T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024899 | ||||||
| chr5:1024899
|
TTTGTCCC others(75): Show |
T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-7233_142-7152d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024899 | |||||
| chr5:1024899
|
TTTGTCCC others(198): Show |
T | 1 | a0001c0001t0008g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142-7233_142-7029d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024899 | |||||
| chr5:1024899
|
TTTGTCCC others(280): Show |
T | 4 | a0001c0001t0005g0003a0001c0001t0005g0091a0001c0001t0008g0094others(1): Show | 4 | HG00438.hp1 HG02004.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7233_142-6947d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024899 | |||||
| chr5:1024899
|
TTTGTCCC others(444): Show |
T | 19 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0030others(16): Show | 20 | HG01106.hp2 HG02040.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.142-7233_142-6783d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024899 | |||||
| chr5:1024904
|
C | T | 4 | a0001c0001t0008g0086a0001c0001t0019g0193a0001c0006t0009g0072others(1): Show | 4 | HG01928.hp2 HG03540.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-7248C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024904 | ||||||
| chr5:1024918
|
CTCT | C | 29 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(26): Show | 29 | HG00140.hp2 HG00408.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.142-7233_142-7231d others(5): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024918 | ||||||
| chr5:1024919
|
T | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0048others(31): Show | 38 | HG00099.hp1 HG01123.hp2 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.142-7233T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024919 | ||||||
| chr5:1024921
|
T | G | 31 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0048others(28): Show | 32 | HG00099.hp1 HG01123.hp2 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.142-7231T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024921 | ||||||
| chr5:1024921
|
TCTGTGGG others(75): Show |
T | 54 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0001t0002g0005others(51): Show | 59 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.142-7212_142-7131d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024921 | |||||
| chr5:1024921
|
TCTGTGGG others(444): Show |
T | 1 | a0007c0014t0018g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.142-7212_142-6762d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024921 | |||||
| chr5:1024921
|
TCTGTGGG others(485): Show |
T | 18 | a0001c0001t0001g0047a0001c0001t0002g0005a0001c0001t0002g0007others(15): Show | 20 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.142-7212_142-6721d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024921 | |||||
| chr5:1024921
|
TCTGTGGG others(526): Show |
T | 1 | a0001c0001t0002g0151 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.142-7212_142-6680d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024921 | |||||
| chr5:1024923
|
T | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0198 | 2 | HG00741.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.142-7229T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024923 | ||||||
| chr5:1024923
|
T | TA | 6 | a0001c0001t0001g0048a0001c0001t0001g0220a0001c0001t0003g0002others(3): Show | 7 | HG00099.hp1 HG01123.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-7229_142-7228i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024923 | ||||||
| chr5:1024924
|
GTGGGCGT others(113): Show |
G | 29 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(26): Show | 29 | HG00140.hp2 HG00408.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.142-7227_142-7108d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024924 | ||||||
| chr5:1024929
|
C | T | 4 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0003g0109others(1): Show | 4 | HG03471.hp1 HG04199.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-7223C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024929 | ||||||
| chr5:1024930
|
G | A | 2 | a0001c0001t0007g0027a0001c0001t0007g0256 | 3 | HG02523.hp2 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.142-7222G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024930 | ||||||
| chr5:1024931
|
T | C | 2 | a0001c0001t0002g0045a0001c0001t0002g0136 | 2 | HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-7221T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024931 | ||||||
| chr5:1024933
|
T | C | 16 | a0001c0001t0002g0029a0001c0001t0002g0045a0001c0001t0002g0136others(13): Show | 16 | HG01358.hp1 HG01928.hp2 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-7219T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024933 | ||||||
| chr5:1024940
|
A | G | 13 | a0001c0001t0001g0048a0001c0001t0001g0160a0001c0001t0001g0220others(10): Show | 15 | HG00099.hp1 HG00741.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-7212A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024940 | ||||||
| chr5:1024940
|
A | T | 10 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0003g0115others(7): Show | 10 | HG01928.hp2 HG02602.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-7212A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024940 | ||||||
| chr5:1024940
|
ATTGTCCC others(116): Show |
A | 2 | a0001c0006t0009g0072a0001c0006t0009g0097 | 2 | NA18939.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.142-7190_142-7068d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024940 | |||||
| chr5:1024945
|
C | T | 1 | a0001c0001t0003g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.142-7207C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024945 | ||||||
| chr5:1024960
|
C | T | 3 | a0001c0001t0002g0029a0001c0001t0002g0103a0001c0001t0015g0117 | 3 | HG01358.hp1 HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.142-7192C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024960 | ||||||
| chr5:1024961
|
C | T | 8 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0051others(5): Show | 8 | HG01074.hp2 HG02015.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-7191C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024961 | ||||||
| chr5:1024962
|
T | G | 32 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0001g0049others(29): Show | 35 | HG00099.hp1 HG00741.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.142-7190T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024962 | ||||||
| chr5:1024962
|
T | TCTGTGGG others(444): Show |
1 | a0001c0001t0004g0066 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.142-6988_142-6987i others(453): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024962 | |||||
| chr5:1024962
|
T | TCTGTGGG others(403): Show |
1 | a0001c0001t0004g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.142-7108_142-6699d others(412): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024962 | |||||
| chr5:1024962
|
T | TCTGTGGG others(444): Show |
5 | a0001c0001t0004g0063a0001c0001t0004g0064a0001c0001t0004g0068others(2): Show | 5 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-7108_142-6658d others(453): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024962 | |||||
| chr5:1024962
|
T | TCTGTGGG others(444): Show |
1 | a0001c0001t0004g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142-6886_142-6885i others(453): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024962 | |||||
| chr5:1024962
|
T | TCTGTGGG others(977): Show |
1 | a0001c0001t0004g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.142-6937_142-6936i others(986): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024962 | |||||
| chr5:1024964
|
T | TA | 4 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0010g0116others(1): Show | 4 | HG02965.hp1 HG03471.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7188_142-7187i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024964 | ||||||
| chr5:1024970
|
C | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0023others(18): Show | 24 | HG00558.hp1 HG01074.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.142-7182C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024970 | ||||||
| chr5:1024971
|
G | A | 2 | a0001c0001t0002g0045a0001c0001t0002g0136 | 2 | HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-7181G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024971 | ||||||
| chr5:1024972
|
T | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0051others(4): Show | 7 | HG01074.hp2 HG02015.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-7180T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024972 | ||||||
| chr5:1024974
|
T | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0023others(24): Show | 31 | HG00558.hp1 HG01074.hp2 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.142-7178T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024974 | ||||||
| chr5:1024974
|
TCAGCCCG others(75): Show |
T | 1 | a0001c0001t0002g0029 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.142-7108_142-7027d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1024974 | |||||
| chr5:1024981
|
G | A | 30 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0049others(27): Show | 34 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.142-7171G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024981 | ||||||
| chr5:1024981
|
G | T | 1 | a0001c0001t0007g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-7171G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1024981 | ||||||
| chr5:1025001
|
C | T | 1 | a0001c0001t0002g0142 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.142-7151C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025001 | ||||||
| chr5:1025002
|
C | T | 1 | a0001c0001t0003g0002 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.142-7150C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025002 | ||||||
| chr5:1025003
|
G | GCTGTGGG others(34): Show |
1 | a0005c0009t0010g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.142-7138_142-7137i others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025003 | |||||
| chr5:1025003
|
G | T | 8 | a0001c0001t0002g0142a0001c0001t0003g0004a0001c0001t0003g0112others(5): Show | 10 | HG02055.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-7149G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025003 | ||||||
| chr5:1025005
|
T | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(60): Show | 71 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.142-7147T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025005 | ||||||
| chr5:1025005
|
T | TA | 16 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 18 | HG00558.hp1 HG01358.hp2 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-7147_142-7146i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025005 | ||||||
| chr5:1025005
|
TGTGGGCG others(74): Show |
T | 1 | a0001c0001t0001g0198 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.142-7146_142-7066d others(83): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025005 | ||||||
| chr5:1025011
|
C | T | 7 | a0001c0001t0003g0002a0001c0001t0003g0115a0001c0001t0008g0086others(4): Show | 7 | HG01928.hp2 HG02071.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-7141C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025011 | ||||||
| chr5:1025013
|
T | C | 1 | a0001c0001t0003g0002 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.142-7139T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025013 | ||||||
| chr5:1025015
|
T | C | 19 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0203others(16): Show | 22 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.142-7137T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025015 | ||||||
| chr5:1025022
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(86): Show | 98 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.142-7130G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025022 | ||||||
| chr5:1025022
|
G | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0203others(11): Show | 17 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.142-7130G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025022 | ||||||
| chr5:1025042
|
C | T | 1 | a0001c0001t0007g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-7110C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025042 | ||||||
| chr5:1025043
|
C | T | 1 | a0001c0005t0011g0002 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.142-7109C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025043 | ||||||
| chr5:1025044
|
T | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-7108T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025044 | ||||||
| chr5:1025044
|
T | G | 19 | a0001c0001t0001g0222a0001c0001t0003g0002a0001c0001t0003g0004others(16): Show | 24 | HG01243.hp2 HG01928.hp2 HG02004.hp2 others(21): Show |
intron_variant | MODIFIER | c.142-7108T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025044 | ||||||
| chr5:1025044
|
TCTGTGGG others(403): Show |
T | 1 | a0001c0001t0015g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-7100_142-6691d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025044 | |||||
| chr5:1025052
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(99): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.142-7100T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025052 | ||||||
| chr5:1025054
|
T | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.142-7098T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025054 | ||||||
| chr5:1025056
|
C | T | 17 | a0001c0001t0002g0142a0001c0001t0003g0002a0001c0001t0003g0004others(14): Show | 20 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.142-7096C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025056 | ||||||
| chr5:1025056
|
CCAGCCCG others(403): Show |
C | 54 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0001t0002g0005others(51): Show | 59 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.142-7028_142-6619d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025056 | |||||
| chr5:1025063
|
G | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(37): Show | 44 | HG00140.hp2 HG00408.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.142-7089G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025063 | ||||||
| chr5:1025063
|
G | T | 7 | a0001c0001t0002g0142a0001c0001t0003g0115a0001c0001t0008g0086others(4): Show | 7 | HG01928.hp2 HG02071.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-7089G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025063 | ||||||
| chr5:1025065
|
T | A | 2 | a0001c0006t0009g0072a0001c0006t0009g0097 | 2 | NA18939.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.142-7087T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025065 | ||||||
| chr5:1025069
|
C | A | 1 | a0001c0001t0010g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.142-7083C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025069 | ||||||
| chr5:1025081
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.142-7071A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025081 | ||||||
| chr5:1025084
|
C | T | 3 | a0001c0001t0003g0002a0001c0005t0011g0002a0002c0003t0001g0040 | 4 | HG02809.hp2 HG03453.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7068C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025084 | ||||||
| chr5:1025085
|
G | T | 6 | a0001c0001t0002g0029a0001c0001t0003g0004a0001c0001t0003g0112others(3): Show | 8 | HG01358.hp1 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-7067G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025085 | ||||||
| chr5:1025085
|
GCTGTGGG others(116): Show |
G | 1 | a0002c0003t0001g0040 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.142-7014_142-6892d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025085 | |||||
| chr5:1025087
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.142-7065T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025087 | ||||||
| chr5:1025087
|
T | TA | 86 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(83): Show | 98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.142-7065_142-7064i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025087 | ||||||
| chr5:1025087
|
TGTGGGCG others(33): Show |
T | 4 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0051others(1): Show | 4 | HG01074.hp2 HG02015.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7064_142-7025d others(42): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025087 | ||||||
| chr5:1025087
|
TGTGGGCG others(197): Show |
T | 1 | a0001c0001t0003g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.142-7064_142-6861d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025087 | ||||||
| chr5:1025093
|
C | T | 7 | a0001c0001t0002g0029a0001c0001t0003g0002a0001c0001t0003g0115others(4): Show | 9 | HG01358.hp1 HG02809.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-7059C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025093 | ||||||
| chr5:1025095
|
T | C | 2 | a0001c0001t0003g0002a0001c0005t0011g0002 | 3 | HG02809.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.142-7057T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025095 | ||||||
| chr5:1025096
|
CTCAGCCC others(406): Show |
C | 1 | a0001c0001t0002g0103 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.142-7055_142-6643d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025096 | ||||||
| chr5:1025097
|
T | C | 15 | a0001c0001t0001g0222a0001c0001t0002g0029a0001c0001t0002g0142others(12): Show | 17 | HG01358.hp1 HG02004.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.142-7055T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025097 | ||||||
| chr5:1025097
|
T | TCAGCCCA others(34): Show |
1 | a0001c0005t0011g0002 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.142-7049_142-7048i others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025097 | |||||
| chr5:1025103
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-7049C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025103 | ||||||
| chr5:1025104
|
G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(49): Show | 59 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.142-7048G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025104 | ||||||
| chr5:1025104
|
G | T | 1 | a0001c0001t0002g0142 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.142-7048G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025104 | ||||||
| chr5:1025109
|
C | T | 4 | a0001c0001t0003g0115a0001c0005t0011g0114a0001c0006t0009g0072others(1): Show | 4 | HG03225.hp2 HG03516.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-7043C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025109 | ||||||
| chr5:1025124
|
C | CCGCTGTG others(444): Show |
3 | a0001c0001t0001g0062a0001c0001t0004g0060a0001c0001t0004g0061 | 3 | HG01261.hp1 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.142-6658_142-6657i others(453): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025124 | |||||
| chr5:1025126
|
G | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-7026G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025126 | ||||||
| chr5:1025126
|
G | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(43): Show | 48 | HG00140.hp2 HG00408.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.142-7026G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025126 | ||||||
| chr5:1025126
|
GCTGTGGG others(34): Show |
G | 4 | a0001c0001t0001g0023a0001c0001t0001g0207a0001c0001t0001g0236others(1): Show | 4 | HG00558.hp1 HG02738.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7014_142-6974d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025126 | |||||
| chr5:1025126
|
GCTGTGGG others(75): Show |
G | 3 | a0001c0001t0001g0023a0001c0001t0007g0027a0001c0001t0007g0256 | 4 | HG02523.hp2 NA19007.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7014_142-6933d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025126 | |||||
| chr5:1025128
|
T | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0051others(1): Show | 4 | HG01074.hp2 HG02015.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-7024T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025128 | ||||||
| chr5:1025134
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 45 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.142-7018C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025134 | ||||||
| chr5:1025136
|
T | C | 2 | a0001c0001t0002g0045a0001c0001t0002g0136 | 2 | HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-7016T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025136 | ||||||
| chr5:1025138
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(75): Show | 88 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.142-7014C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025138 | ||||||
| chr5:1025145
|
T | A | 20 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0035others(17): Show | 23 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.142-7007T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025145 | ||||||
| chr5:1025145
|
T | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(115): Show | 135 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.142-7007T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025145 | ||||||
| chr5:1025145
|
TTTGTCCC others(34): Show |
T | 2 | a0001c0006t0009g0072a0001c0006t0009g0097 | 2 | NA18939.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.142-6987_142-6947d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025145 | |||||
| chr5:1025165
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.142-6987T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025165 | ||||||
| chr5:1025165
|
T | TCTCTGTG others(485): Show |
1 | a0001c0001t0004g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142-6658_142-6657i others(494): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025165 | |||||
| chr5:1025166
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0203others(2): Show | 7 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-6986C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025166 | ||||||
| chr5:1025167
|
T | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(121): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.142-6985T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025167 | ||||||
| chr5:1025169
|
T | TA | 35 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(32): Show | 35 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.142-6983_142-6982i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025169 | ||||||
| chr5:1025175
|
C | T | 29 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0203others(26): Show | 36 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.142-6977C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025175 | ||||||
| chr5:1025177
|
T | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0203others(3): Show | 8 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-6975T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025177 | ||||||
| chr5:1025179
|
T | C | 36 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0035others(33): Show | 43 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-6973T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025179 | ||||||
| chr5:1025186
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 60 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.142-6966G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025186 | ||||||
| chr5:1025186
|
G | T | 2 | a0001c0001t0008g0086a0001c0001t0019g0193 | 2 | HG01928.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.142-6966G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025186 | ||||||
| chr5:1025191
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.142-6961C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025191 | ||||||
| chr5:1025191
|
C | T | 13 | a0001c0001t0001g0048a0001c0001t0001g0160a0001c0001t0001g0220others(10): Show | 15 | HG00099.hp1 HG00438.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.142-6961C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025191 | ||||||
| chr5:1025201
|
C | T | 1 | a0005c0009t0010g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.142-6951C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025201 | ||||||
| chr5:1025207
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-6945C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025207 | ||||||
| chr5:1025208
|
T | G | 52 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(49): Show | 60 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.142-6944T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025208 | ||||||
| chr5:1025208
|
TCTGTGGG others(239): Show |
T | 1 | a0001c0001t0002g0142 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.142-6864_142-6619d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025208 | |||||
| chr5:1025210
|
T | TA | 11 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0001g0049others(8): Show | 11 | HG00099.hp1 HG00741.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.142-6942_142-6941i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025210 | ||||||
| chr5:1025216
|
C | T | 6 | a0001c0001t0001g0222a0001c0001t0003g0002a0001c0001t0003g0115others(3): Show | 6 | HG02004.hp2 HG03471.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-6936C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025216 | ||||||
| chr5:1025218
|
T | C | 2 | a0001c0001t0007g0259a0002c0003t0001g0040 | 2 | NA19064.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.142-6934T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025218 | ||||||
| chr5:1025220
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(118): Show | 139 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.142-6932T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025220 | ||||||
| chr5:1025226
|
C | G | 2 | a0001c0006t0009g0072a0001c0006t0009g0097 | 2 | NA18939.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.142-6926C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025226 | ||||||
| chr5:1025227
|
G | A | 32 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0203others(29): Show | 38 | HG00323.hp1 HG00438.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.142-6925G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025227 | ||||||
| chr5:1025227
|
G | T | 14 | a0001c0001t0003g0002a0001c0001t0005g0003a0001c0001t0005g0091others(11): Show | 17 | HG00438.hp1 HG00639.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.142-6925G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025227 | ||||||
| chr5:1025229
|
T | A | 10 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(7): Show | 12 | HG00438.hp2 HG01192.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-6923T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025229 | ||||||
| chr5:1025247
|
C | T | 1 | a0001c0001t0004g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.142-6905C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025247 | ||||||
| chr5:1025249
|
G | GCTGTGGG others(34): Show |
6 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(3): Show | 8 | HG01243.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-6892_142-6891i others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025249 | |||||
| chr5:1025249
|
G | GCTGTGGG others(34): Show |
1 | a0001c0001t0007g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-6896_142-6895i others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025249 | |||||
| chr5:1025249
|
G | T | 15 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 18 | HG00323.hp1 HG00558.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.142-6903G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025249 | ||||||
| chr5:1025251
|
T | TA | 105 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(102): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.142-6901_142-6900i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025251 | ||||||
| chr5:1025257
|
C | T | 32 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0203others(29): Show | 39 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.142-6895C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025257 | ||||||
| chr5:1025258
|
G | A | 2 | a0001c0001t0007g0259a0009c0013t0017g0098 | 2 | HG02071.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.142-6894G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025258 | ||||||
| chr5:1025261
|
T | C | 41 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(38): Show | 49 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.142-6891T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025261 | ||||||
| chr5:1025268
|
G | A | 23 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0160others(20): Show | 26 | HG00099.hp1 HG00741.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.142-6884G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025268 | ||||||
| chr5:1025268
|
G | T | 12 | a0001c0001t0008g0086a0001c0001t0019g0193a0001c0002t0001g0185others(9): Show | 14 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.142-6884G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025268 | ||||||
| chr5:1025273
|
C | T | 16 | a0001c0001t0001g0048a0001c0001t0001g0160a0001c0001t0001g0220others(13): Show | 19 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-6879C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025273 | ||||||
| chr5:1025289
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.142-6863C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025289 | ||||||
| chr5:1025290
|
G | T | 16 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0186others(13): Show | 18 | HG02055.hp2 HG02523.hp2 HG02602.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-6862G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025290 | ||||||
| chr5:1025292
|
T | A | 1 | a0001c0001t0003g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.142-6860T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025292 | ||||||
| chr5:1025292
|
T | TA | 11 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 13 | HG00323.hp1 HG00558.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-6860_142-6859i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025292 | ||||||
| chr5:1025298
|
C | T | 10 | a0001c0001t0001g0052a0001c0001t0001g0222a0001c0001t0003g0002others(7): Show | 13 | HG02004.hp2 HG02602.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-6854C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025298 | ||||||
| chr5:1025300
|
T | C | 4 | a0001c0001t0007g0257a0001c0001t0007g0258a0001c0001t0007g0260others(1): Show | 4 | HG02602.hp1 HG02965.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-6852T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025300 | ||||||
| chr5:1025302
|
T | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(109): Show | 129 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.142-6850T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025302 | ||||||
| chr5:1025306
|
C | G | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-6846C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025306 | ||||||
| chr5:1025309
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(101): Show | 117 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.142-6843G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025309 | ||||||
| chr5:1025309
|
G | T | 22 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(19): Show | 26 | HG00438.hp2 HG00639.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.142-6843G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025309 | ||||||
| chr5:1025314
|
C | T | 4 | a0001c0001t0005g0003a0001c0001t0005g0091a0001c0001t0008g0094others(1): Show | 4 | HG00438.hp1 HG02004.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-6838C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025314 | ||||||
| chr5:1025330
|
C | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0115a0001c0005t0011g0002 | 3 | HG03471.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.142-6822C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025330 | ||||||
| chr5:1025331
|
G | T | 15 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0035others(12): Show | 18 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.142-6821G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025331 | ||||||
| chr5:1025333
|
T | TA | 81 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(78): Show | 91 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.142-6819_142-6818i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025333 | ||||||
| chr5:1025339
|
C | T | 8 | a0001c0001t0001g0048a0001c0001t0001g0160a0001c0001t0001g0220others(5): Show | 8 | HG00099.hp1 HG00741.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-6813C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025339 | ||||||
| chr5:1025340
|
G | A | 3 | a0001c0001t0007g0257a0001c0001t0007g0258a0001c0001t0007g0260 | 3 | HG02602.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.142-6812G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025340 | ||||||
| chr5:1025341
|
T | C | 3 | a0001c0001t0003g0002a0001c0001t0003g0115a0001c0005t0011g0002 | 3 | HG03471.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.142-6811T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025341 | ||||||
| chr5:1025343
|
T | C | 37 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(34): Show | 41 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.142-6809T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025343 | ||||||
| chr5:1025343
|
T | TCAGCCCA others(34): Show |
2 | a0001c0001t0002g0045a0001c0001t0002g0136 | 2 | HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-6803_142-6802i others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025343 | |||||
| chr5:1025350
|
G | A | 39 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0052others(36): Show | 44 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.142-6802G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025350 | ||||||
| chr5:1025350
|
G | T | 10 | a0001c0001t0001g0222a0001c0001t0007g0259a0001c0002t0001g0185others(7): Show | 12 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-6802G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025350 | ||||||
| chr5:1025355
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(74): Show | 86 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.142-6797C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025355 | ||||||
| chr5:1025361
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.142-6791T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025361 | ||||||
| chr5:1025372
|
G | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(39): Show | 43 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-6780G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025372 | ||||||
| chr5:1025374
|
T | TA | 84 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(81): Show | 95 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.142-6778_142-6777i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025374 | ||||||
| chr5:1025380
|
C | T | 16 | a0001c0001t0001g0222a0001c0001t0003g0002a0001c0001t0005g0003others(13): Show | 19 | HG00438.hp2 HG01192.hp1 HG02004.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-6772C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025380 | ||||||
| chr5:1025384
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0022others(87): Show | 98 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.142-6768T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025384 | ||||||
| chr5:1025384
|
T | TCAGCCCA others(240): Show |
1 | a0001c0001t0007g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-6762_142-6761i others(249): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025384 | |||||
| chr5:1025391
|
G | A | 39 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0186others(36): Show | 44 | HG01106.hp2 HG01243.hp2 HG01358.hp1 others(41): Show |
intron_variant | MODIFIER | c.142-6761G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025391 | ||||||
| chr5:1025391
|
G | GTTGTCCC others(649): Show |
5 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(2): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-6742_142-6741i others(658): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025391 | |||||
| chr5:1025391
|
G | T | 15 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(12): Show | 18 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-6761G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025391 | ||||||
| chr5:1025396
|
C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0207a0001c0001t0001g0236others(2): Show | 5 | HG00558.hp1 HG01928.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-6756C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025396 | ||||||
| chr5:1025411
|
C | T | 21 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0030others(18): Show | 22 | HG01106.hp2 HG02040.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.142-6741C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025411 | ||||||
| chr5:1025412
|
C | T | 2 | a0001c0001t0003g0002a0001c0005t0011g0002 | 3 | HG02809.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.142-6740C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025412 | ||||||
| chr5:1025413
|
G | T | 36 | a0001c0001t0001g0200a0001c0001t0001g0235a0001c0001t0002g0007others(33): Show | 39 | HG01106.hp2 HG01243.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.142-6739G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025413 | ||||||
| chr5:1025415
|
T | TA | 105 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(102): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.142-6737_142-6736i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025415 | ||||||
| chr5:1025421
|
C | T | 11 | a0001c0001t0003g0002a0001c0001t0003g0115a0001c0002t0001g0185others(8): Show | 16 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.142-6731C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025421 | ||||||
| chr5:1025422
|
G | A | 2 | a0001c0001t0002g0045a0001c0001t0002g0136 | 2 | HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-6730G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025422 | ||||||
| chr5:1025423
|
T | C | 2 | a0001c0001t0003g0002a0001c0005t0011g0002 | 3 | HG02809.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.142-6729T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025423 | ||||||
| chr5:1025423
|
TCTCAGCC others(362): Show |
T | 1 | a0001c0005t0011g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-6727_142-6359d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025423 | |||||
| chr5:1025425
|
T | C | 40 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0200others(37): Show | 48 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.142-6727T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025425 | ||||||
| chr5:1025425
|
T | G | 1 | a0001c0001t0007g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.142-6727T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025425 | ||||||
| chr5:1025432
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(94): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.142-6720G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025432 | ||||||
| chr5:1025432
|
G | T | 25 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(22): Show | 30 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.142-6720G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025432 | ||||||
| chr5:1025437
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(74): Show | 86 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.142-6715C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025437 | ||||||
| chr5:1025453
|
C | T | 3 | a0001c0001t0007g0257a0001c0001t0007g0258a0001c0001t0007g0260 | 3 | HG02602.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.142-6699C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025453 | ||||||
| chr5:1025454
|
G | GCTGTGGG others(75): Show |
1 | a0005c0009t0010g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.142-6687_142-6686i others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025454 | |||||
| chr5:1025454
|
G | T | 44 | a0001c0001t0001g0047a0001c0001t0002g0005a0001c0001t0002g0007others(41): Show | 49 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.142-6698G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025454 | ||||||
| chr5:1025454
|
GCTGTGGG others(75): Show |
G | 2 | a0001c0001t0008g0086a0001c0001t0019g0193 | 2 | HG01928.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.142-6686_142-6605d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025454 | |||||
| chr5:1025454
|
GCTGTGGG others(239): Show |
G | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-6686_142-6441d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025454 | |||||
| chr5:1025456
|
T | A | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-6696T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025456 | ||||||
| chr5:1025456
|
T | TA | 16 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0049others(13): Show | 17 | HG00558.hp1 HG01074.hp2 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.142-6696_142-6695i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025456 | ||||||
| chr5:1025456
|
TGTGGGCG others(485): Show |
T | 1 | a0001c0001t0001g0186 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.142-6695_142-6204d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025456 | ||||||
| chr5:1025462
|
C | T | 42 | a0001c0001t0001g0047a0001c0001t0002g0005a0001c0001t0002g0007others(39): Show | 47 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.142-6690C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025462 | ||||||
| chr5:1025463
|
G | A | 5 | a0001c0001t0003g0107a0001c0001t0003g0113a0001c0001t0004g0057others(2): Show | 5 | HG02055.hp2 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-6689G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025463 | ||||||
| chr5:1025463
|
GTCTCAGC others(363): Show |
G | 2 | a0001c0001t0001g0050a0001c0001t0014g0148 | 2 | HG01358.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.142-6645_142-6276d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025463 | |||||
| chr5:1025464
|
T | C | 3 | a0001c0001t0002g0029a0001c0001t0007g0027a0001c0001t0007g0256 | 4 | HG01358.hp1 HG02523.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-6688T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025464 | ||||||
| chr5:1025464
|
TCTCAGCC others(321): Show |
T | 24 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0036others(21): Show | 24 | HG00140.hp2 HG00408.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.142-6686_142-6359d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025464 | |||||
| chr5:1025466
|
T | C | 51 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0053others(48): Show | 56 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.142-6686T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025466 | ||||||
| chr5:1025473
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(94): Show | 111 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.142-6679G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025473 | ||||||
| chr5:1025473
|
G | T | 3 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0003g0115 | 3 | HG03516.hp1 HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-6679G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025473 | ||||||
| chr5:1025478
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0049others(7): Show | 10 | HG00099.hp1 HG00558.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-6674C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025478 | ||||||
| chr5:1025493
|
CCGCTGTG others(34): Show |
C | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-6657_142-6617d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025493 | |||||
| chr5:1025495
|
G | T | 10 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0112others(7): Show | 13 | HG02055.hp2 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-6657G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025495 | ||||||
| chr5:1025495
|
GCTGTGGG others(157): Show |
G | 67 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(64): Show | 76 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.142-6649_142-6486d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025495 | |||||
| chr5:1025497
|
T | TA | 22 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0023others(19): Show | 25 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.142-6655_142-6654i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025497 | ||||||
| chr5:1025497
|
TGTGGGCG others(156): Show |
T | 4 | a0001c0001t0007g0257a0001c0001t0007g0258a0001c0001t0007g0260others(1): Show | 4 | HG02602.hp1 HG04115.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-6654_142-6492d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025497 | ||||||
| chr5:1025503
|
C | T | 19 | a0001c0001t0001g0022a0001c0001t0001g0043a0001c0001t0001g0161others(16): Show | 22 | HG00408.hp2 HG00438.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.142-6649C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025503 | ||||||
| chr5:1025504
|
G | A | 2 | a0001c0001t0007g0027a0001c0001t0007g0256 | 3 | HG02523.hp2 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.142-6648G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025504 | ||||||
| chr5:1025505
|
TCTCAGCC others(280): Show |
T | 2 | a0001c0001t0001g0200a0001c0001t0001g0235 | 2 | HG03942.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.142-6645_142-6359d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025505 | |||||
| chr5:1025507
|
T | C | 119 | a0001c0001t0001g0022a0001c0001t0001g0043a0001c0001t0001g0047others(116): Show | 135 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.142-6645T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025507 | ||||||
| chr5:1025507
|
TCAGCCCG others(280): Show |
T | 2 | a0001c0001t0001g0023a0001c0001t0001g0035 | 2 | HG03239.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.142-6638_142-6352d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025507 | |||||
| chr5:1025510
|
G | C | 1 | a0001c0001t0002g0103 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.142-6642G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025510 | ||||||
| chr5:1025514
|
G | A | 31 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(28): Show | 36 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.142-6638G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025514 | ||||||
| chr5:1025514
|
G | T | 105 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(102): Show | 120 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.142-6638G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025514 | ||||||
| chr5:1025514
|
GTTGTCCC others(404): Show |
G | 1 | a0001c0001t0002g0042 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.142-6618_142-6208d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025514 | |||||
| chr5:1025519
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0048a0001c0001t0001g0053others(4): Show | 7 | HG00099.hp1 HG00741.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-6633C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025519 | ||||||
| chr5:1025534
|
T | C | 62 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0022others(59): Show | 72 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.142-6618T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025534 | ||||||
| chr5:1025536
|
T | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-6616T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025536 | ||||||
| chr5:1025536
|
T | G | 35 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0048others(32): Show | 39 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.142-6616T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025536 | ||||||
| chr5:1025538
|
T | TA | 9 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0051others(6): Show | 10 | HG01074.hp2 HG01168.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-6614_142-6613i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025538 | ||||||
| chr5:1025544
|
C | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0207a0001c0001t0001g0222others(4): Show | 7 | HG00558.hp1 HG02004.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-6608C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025544 | ||||||
| chr5:1025548
|
C | T | 23 | a0001c0001t0001g0010a0001c0001t0001g0048a0001c0001t0001g0049others(20): Show | 26 | HG00099.hp1 HG00741.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.142-6604C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025548 | ||||||
| chr5:1025554
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.142-6598C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025554 | ||||||
| chr5:1025555
|
G | A | 18 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0207others(15): Show | 20 | HG00558.hp1 HG01074.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.142-6597G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025555 | ||||||
| chr5:1025555
|
G | T | 15 | a0001c0001t0001g0051a0001c0001t0005g0003a0001c0001t0005g0089others(12): Show | 17 | HG00438.hp2 HG01192.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.142-6597G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025555 | ||||||
| chr5:1025560
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0221 | 2 | HG01074.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.142-6592C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025560 | ||||||
| chr5:1025561
|
C | A | 1 | a0001c0001t0001g0051 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.142-6591C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025561 | ||||||
| chr5:1025575
|
C | T | 9 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0003g0004others(6): Show | 11 | HG02055.hp2 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.142-6577C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025575 | ||||||
| chr5:1025576
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.142-6576C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025576 | ||||||
| chr5:1025577
|
T | G | 35 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0022others(32): Show | 40 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.142-6575T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025577 | ||||||
| chr5:1025577
|
TCTGTGGG others(281): Show |
T | 3 | a0001c0001t0001g0023a0001c0001t0001g0207a0001c0001t0001g0236 | 3 | HG00558.hp1 HG02738.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.142-6563_142-6276d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025577 | |||||
| chr5:1025579
|
T | TA | 16 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(13): Show | 18 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.142-6573_142-6572i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025579 | ||||||
| chr5:1025585
|
C | T | 6 | a0001c0001t0001g0048a0001c0001t0001g0160a0001c0001t0001g0220others(3): Show | 6 | HG00099.hp1 HG00741.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-6567C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025585 | ||||||
| chr5:1025586
|
GTCTCAGC others(240): Show |
G | 2 | a0001c0001t0001g0049a0001c0001t0001g0221 | 2 | HG01074.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.142-6534_142-6288d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025586 | |||||
| chr5:1025587
|
T | C | 1 | a0001c0001t0010g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.142-6565T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025587 | ||||||
| chr5:1025589
|
T | C | 113 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0160others(110): Show | 129 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.142-6563T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025589 | ||||||
| chr5:1025589
|
TCAGCCCG others(116): Show |
T | 2 | a0001c0001t0001g0043a0001c0001t0001g0198 | 2 | HG01175.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.142-6556_142-6434d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025589 | |||||
| chr5:1025589
|
TCAGCCCG others(322): Show |
T | 3 | a0001c0001t0001g0022a0001c0001t0001g0161a0001c0001t0001g0215 | 3 | HG00408.hp2 HG01106.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.142-6556_142-6228d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025589 | |||||
| chr5:1025596
|
G | A | 23 | a0001c0001t0001g0010a0001c0001t0001g0051a0001c0001t0001g0053others(20): Show | 27 | HG01168.hp2 HG01243.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.142-6556G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025596 | ||||||
| chr5:1025596
|
G | T | 3 | a0001c0001t0008g0086a0001c0001t0019g0193a0009c0013t0017g0098 | 3 | HG01928.hp2 HG02071.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.142-6556G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025596 | ||||||
| chr5:1025601
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0053a0001c0001t0001g0225others(3): Show | 6 | HG01168.hp2 HG01515.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-6551C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025601 | ||||||
| chr5:1025617
|
C | T | 3 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0259 | 4 | HG02523.hp2 NA19064.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-6535C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025617 | ||||||
| chr5:1025618
|
T | G | 45 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(42): Show | 52 | HG00323.hp1 HG00438.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.142-6534T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025618 | ||||||
| chr5:1025618
|
T | TCTGTGGG others(280): Show |
1 | a0005c0009t0010g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.142-6523_142-6522i others(289): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025618 | |||||
| chr5:1025620
|
T | TA | 3 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0259 | 4 | HG02523.hp2 NA19064.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-6532_142-6531i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025620 | ||||||
| chr5:1025626
|
C | T | 13 | a0001c0001t0001g0051a0001c0001t0003g0107a0001c0001t0003g0115others(10): Show | 15 | HG00438.hp2 HG01192.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.142-6526C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025626 | ||||||
| chr5:1025626
|
CGTCCCAG others(939): Show |
C | 1 | a0001c0001t0001g0222 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.142-6515_142-5570d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025626 | |||||
| chr5:1025627
|
GTCCCAGC others(199): Show |
G | 3 | a0001c0001t0001g0010a0001c0001t0001g0053a0001c0010t0001g0187 | 3 | HG01168.hp2 HG01515.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.142-6522_142-6317d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025627 | |||||
| chr5:1025628
|
T | C | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-6524T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025628 | ||||||
| chr5:1025628
|
TCCCAGCC others(157): Show |
T | 5 | a0001c0001t0001g0052a0001c0001t0003g0109a0001c0006t0009g0072others(2): Show | 5 | NA18939.hp1 NA18981.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-6515_142-6352d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025628 | |||||
| chr5:1025630
|
C | T | 110 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0047others(107): Show | 126 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.142-6522C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025630 | ||||||
| chr5:1025637
|
G | A | 16 | a0001c0001t0001g0051a0001c0001t0001g0225a0001c0001t0003g0004others(13): Show | 19 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.142-6515G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025637 | ||||||
| chr5:1025637
|
G | T | 13 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0005g0003others(10): Show | 15 | HG00438.hp2 HG01192.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.142-6515G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025637 | ||||||
| chr5:1025642
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.142-6510C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025642 | ||||||
| chr5:1025646
|
G | C | 3 | a0001c0001t0001g0062a0001c0001t0004g0060a0001c0001t0004g0061 | 3 | HG01261.hp1 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.142-6506G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025646 | ||||||
| chr5:1025652
|
CCCACCCT others(198): Show |
C | 1 | a0001c0001t0001g0225 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.142-6497_142-6293d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025652 | |||||
| chr5:1025657
|
C | T | 8 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(5): Show | 10 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-6495C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025657 | ||||||
| chr5:1025658
|
C | T | 1 | a0001c0001t0003g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.142-6494C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025658 | ||||||
| chr5:1025659
|
T | A | 1 | a0001c0001t0003g0013 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.142-6493T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025659 | ||||||
| chr5:1025659
|
T | G | 123 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0047others(120): Show | 144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.142-6493T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025659 | ||||||
| chr5:1025659
|
TCTGTGGG others(199): Show |
T | 1 | a0001c0001t0001g0051 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.142-6485_142-6280d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025659 | |||||
| chr5:1025661
|
T | A | 4 | a0001c0001t0007g0257a0001c0001t0007g0258a0001c0001t0007g0260others(1): Show | 4 | HG02602.hp1 HG04115.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-6491T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025661 | ||||||
| chr5:1025661
|
T | TA | 98 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(95): Show | 113 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.142-6491_142-6490i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025661 | ||||||
| chr5:1025667
|
T | C | 133 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0047others(130): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.142-6485T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025667 | ||||||
| chr5:1025669
|
T | C | 4 | a0001c0001t0003g0107a0001c0001t0003g0115a0004c0007t0006g0078others(1): Show | 4 | HG01099.hp1 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-6483T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025669 | ||||||
| chr5:1025671
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(82): Show | 97 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.142-6481T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025671 | ||||||
| chr5:1025671
|
T | TCAGCCCG others(34): Show |
3 | a0001c0001t0001g0062a0001c0001t0004g0060a0001c0001t0004g0061 | 3 | HG01261.hp1 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.142-6475_142-6474i others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025671 | |||||
| chr5:1025671
|
TCAGCCCA others(898): Show |
T | 3 | a0001c0001t0001g0048a0001c0001t0001g0160a0001c0001t0001g0220 | 3 | HG00099.hp1 HG00741.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.142-6452_142-5548d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025671 | |||||
| chr5:1025673
|
A | G | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-6479A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025673 | ||||||
| chr5:1025678
|
A | G | 104 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0047others(101): Show | 120 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.142-6474A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025678 | ||||||
| chr5:1025678
|
A | T | 17 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0005g0003others(14): Show | 20 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.142-6474A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025678 | ||||||
| chr5:1025679
|
T | G | 1 | a0001c0001t0002g0103 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.142-6473T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025679 | ||||||
| chr5:1025683
|
C | T | 2 | a0001c0001t0003g0013a0001c0001t0012g0119 | 2 | HG02897.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.142-6469C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025683 | ||||||
| chr5:1025700
|
T | G | 28 | a0001c0001t0001g0062a0001c0001t0002g0045a0001c0001t0002g0136others(25): Show | 32 | HG00438.hp1 HG00438.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.142-6452T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025700 | ||||||
| chr5:1025708
|
C | T | 25 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(22): Show | 30 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.142-6444C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025708 | ||||||
| chr5:1025709
|
GTCCCAGC others(117): Show |
G | 1 | a0001c0001t0003g0013 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.142-6440_142-6317d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025709 | |||||
| chr5:1025712
|
C | T | 98 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(95): Show | 112 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.142-6440C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025712 | ||||||
| chr5:1025719
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(79): Show | 98 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.142-6433A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025719 | ||||||
| chr5:1025724
|
C | T | 25 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(22): Show | 30 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.142-6428C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025724 | ||||||
| chr5:1025739
|
C | T | 2 | a0001c0001t0002g0045a0001c0001t0002g0136 | 2 | HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-6413C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025739 | ||||||
| chr5:1025741
|
G | T | 4 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0003g0115others(1): Show | 4 | HG02622.hp2 HG03516.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-6411G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025741 | ||||||
| chr5:1025743
|
T | TA | 8 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0203others(5): Show | 10 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-6409_142-6408i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025743 | ||||||
| chr5:1025749
|
C | T | 9 | a0001c0001t0003g0107a0001c0001t0003g0115a0001c0001t0007g0027others(6): Show | 10 | HG02071.hp1 HG02523.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-6403C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025749 | ||||||
| chr5:1025753
|
T | C | 2 | a0001c0001t0003g0115a0009c0013t0017g0098 | 2 | HG02071.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.142-6399T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025753 | ||||||
| chr5:1025760
|
A | G | 11 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0203others(8): Show | 13 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-6392A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025760 | ||||||
| chr5:1025765
|
C | T | 13 | a0001c0001t0001g0043a0001c0001t0001g0198a0001c0001t0005g0003others(10): Show | 15 | HG00438.hp2 HG01175.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.142-6387C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025765 | ||||||
| chr5:1025782
|
T | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(82): Show | 98 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.142-6370T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025782 | ||||||
| chr5:1025784
|
T | TA | 4 | a0001c0001t0001g0043a0001c0001t0001g0198a0001c0001t0003g0115others(1): Show | 4 | HG01175.hp1 HG02148.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-6368_142-6367i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025784 | ||||||
| chr5:1025784
|
TGTGGGTG others(35): Show |
T | 10 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(7): Show | 12 | HG00438.hp2 HG01192.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-6362_142-6321d others(44): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025784 | |||||
| chr5:1025790
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(73): Show | 90 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.142-6362T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025790 | ||||||
| chr5:1025792
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(92): Show | 111 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.142-6360C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025792 | ||||||
| chr5:1025794
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(66): Show | 78 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.142-6358C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025794 | ||||||
| chr5:1025801
|
A | G | 25 | a0001c0001t0001g0043a0001c0001t0001g0198a0001c0001t0002g0045others(22): Show | 28 | HG00438.hp1 HG00639.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.142-6351A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025801 | ||||||
| chr5:1025801
|
A | T | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-6351A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025801 | ||||||
| chr5:1025806
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(67): Show | 79 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.142-6346C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025806 | ||||||
| chr5:1025822
|
C | T | 16 | a0001c0001t0005g0003a0001c0001t0005g0091a0001c0001t0008g0086others(13): Show | 18 | HG00438.hp1 HG00639.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-6330C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025822 | ||||||
| chr5:1025823
|
G | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-6329G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025823 | ||||||
| chr5:1025825
|
TA | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0043others(7): Show | 10 | HG01175.hp1 HG02148.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-6326delA | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025825 | ||||||
| chr5:1025825
|
TAGTGGGC others(159): Show |
T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-6326_142-6161d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025825 | ||||||
| chr5:1025830
|
G | A | 6 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 7 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-6322G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025830 | ||||||
| chr5:1025832
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.142-6320C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025832 | ||||||
| chr5:1025833
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(133): Show | 156 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.142-6319A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025833 | ||||||
| chr5:1025835
|
C | A | 89 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(86): Show | 102 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.142-6317C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025835 | ||||||
| chr5:1025836
|
T | C | 14 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0005g0003others(11): Show | 16 | HG00438.hp2 HG01192.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-6316T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025836 | ||||||
| chr5:1025843
|
G | A | 115 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0035others(112): Show | 130 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.142-6309G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025843 | ||||||
| chr5:1025843
|
G | T | 2 | a0001c0001t0002g0045a0001c0001t0002g0136 | 2 | HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-6309G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025843 | ||||||
| chr5:1025848
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(109): Show | 126 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.142-6304C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025848 | ||||||
| chr5:1025860
|
C | T | 6 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 7 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-6292C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025860 | ||||||
| chr5:1025863
|
C | T | 2 | a0001c0001t0002g0045a0001c0001t0002g0136 | 2 | HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-6289C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025863 | ||||||
| chr5:1025864
|
C | T | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-6288C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025864 | ||||||
| chr5:1025865
|
G | T | 3 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0003g0115 | 3 | HG03516.hp1 HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-6287G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025865 | ||||||
| chr5:1025867
|
T | TA | 38 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(35): Show | 40 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.142-6285_142-6284i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025867 | ||||||
| chr5:1025873
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0035others(11): Show | 14 | HG01074.hp2 HG01168.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-6279C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025873 | ||||||
| chr5:1025877
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(114): Show | 131 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.142-6275C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025877 | ||||||
| chr5:1025884
|
G | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0035others(25): Show | 31 | HG00438.hp1 HG00639.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.142-6268G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025884 | ||||||
| chr5:1025884
|
G | T | 19 | a0001c0001t0003g0107a0001c0001t0005g0003a0001c0001t0005g0089others(16): Show | 22 | HG00438.hp2 HG01192.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.142-6268G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025884 | ||||||
| chr5:1025889
|
C | T | 1 | a0001c0005t0011g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-6263C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025889 | ||||||
| chr5:1025891
|
C | T | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-6261C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025891 | ||||||
| chr5:1025895
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.142-6257T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025895 | ||||||
| chr5:1025906
|
T | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(130): Show | 153 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.142-6246T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025906 | ||||||
| chr5:1025908
|
T | TA | 39 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(36): Show | 44 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.142-6244_142-6243i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025908 | ||||||
| chr5:1025914
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(76): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.142-6238C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025914 | ||||||
| chr5:1025918
|
C | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(47): Show | 56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.142-6234C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025918 | ||||||
| chr5:1025924
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142-6228C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025924 | ||||||
| chr5:1025925
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(76): Show | 89 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.142-6227A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025925 | ||||||
| chr5:1025925
|
A | T | 13 | a0001c0001t0001g0223a0001c0001t0005g0003a0001c0001t0005g0089others(10): Show | 15 | HG00438.hp2 HG01192.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.142-6227A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025925 | ||||||
| chr5:1025930
|
C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(35): Show | 43 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-6222C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025930 | ||||||
| chr5:1025931
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.142-6221C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025931 | ||||||
| chr5:1025946
|
C | T | 123 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(120): Show | 141 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.142-6206C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025946 | ||||||
| chr5:1025947
|
G | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(63): Show | 75 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.142-6205G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025947 | ||||||
| chr5:1025949
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.142-6203T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025949 | ||||||
| chr5:1025949
|
T | TA | 110 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(107): Show | 127 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.142-6203_142-6202i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025949 | ||||||
| chr5:1025959
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(61): Show | 73 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.142-6193T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025959 | ||||||
| chr5:1025966
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(80): Show | 95 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.142-6186A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025966 | ||||||
| chr5:1025966
|
A | T | 16 | a0001c0001t0005g0003a0001c0001t0005g0091a0001c0001t0008g0086others(13): Show | 18 | HG00438.hp1 HG00639.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-6186A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025966 | ||||||
| chr5:1025971
|
C | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(5): Show | 8 | HG00408.hp2 HG00558.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-6181C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025971 | ||||||
| chr5:1025988
|
G | T | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-6164G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025988 | ||||||
| chr5:1025988
|
GCTAGTGG others(199): Show |
G | 1 | a0001c0001t0012g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-6161_142-5956d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025988 | |||||
| chr5:1025988
|
GCTAGTGG others(610): Show |
G | 4 | a0001c0001t0001g0043a0001c0001t0001g0198a0001c0001t0003g0013others(1): Show | 4 | HG01175.hp1 HG02148.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-6161_142-5545d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1025988 | |||||
| chr5:1025990
|
TA | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(134): Show | 155 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.142-6161delA | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025990 | ||||||
| chr5:1025990
|
TAGTGGGC others(241): Show |
T | 6 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 7 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-6161_142-5914d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025990 | ||||||
| chr5:1025997
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(48): Show | 55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.142-6155C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025997 | ||||||
| chr5:1025999
|
T | C | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-6153T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1025999 | ||||||
| chr5:1026001
|
T | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(48): Show | 55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.142-6151T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026001 | ||||||
| chr5:1026001
|
TCAGCCCA others(34): Show |
T | 92 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(89): Show | 105 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.142-6122_142-6082d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026001 | |||||
| chr5:1026001
|
TCAGCCCA others(568): Show |
T | 79 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(76): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.142-6122_142-5548d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026001 | |||||
| chr5:1026008
|
A | G | 10 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(7): Show | 10 | HG00408.hp2 HG00558.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-6144A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026008 | ||||||
| chr5:1026008
|
A | T | 12 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(9): Show | 14 | HG00438.hp2 HG01192.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-6144A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026008 | ||||||
| chr5:1026013
|
C | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(17): Show | 22 | HG00408.hp2 HG00558.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.142-6139C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026013 | ||||||
| chr5:1026030
|
T | G | 34 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(31): Show | 38 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.142-6122T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026030 | ||||||
| chr5:1026032
|
T | TA | 10 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0035others(7): Show | 10 | HG01074.hp2 HG01168.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-6120_142-6119i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026032 | ||||||
| chr5:1026038
|
C | T | 14 | a0001c0001t0003g0107a0001c0001t0005g0003a0001c0001t0005g0089others(11): Show | 16 | HG00438.hp2 HG01192.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-6114C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026038 | ||||||
| chr5:1026039
|
G | T | 2 | a0001c0001t0004g0063a0001c0001t0004g0064 | 2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.142-6113G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026039 | ||||||
| chr5:1026040
|
T | C | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-6112T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026040 | ||||||
| chr5:1026042
|
C | T | 22 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(19): Show | 24 | HG00408.hp2 HG00558.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.142-6110C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026042 | ||||||
| chr5:1026049
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.142-6103A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026049 | ||||||
| chr5:1026054
|
C | T | 22 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0035others(19): Show | 24 | HG00438.hp2 HG01074.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.142-6098C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026054 | ||||||
| chr5:1026071
|
G | T | 2 | a0001c0001t0003g0107a0009c0013t0017g0098 | 2 | HG02071.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.142-6081G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026071 | ||||||
| chr5:1026079
|
C | T | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(10): Show | 14 | HG00408.hp2 HG00558.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-6073C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026079 | ||||||
| chr5:1026083
|
T | C | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(10): Show | 14 | HG00408.hp2 HG00558.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-6069T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026083 | ||||||
| chr5:1026090
|
A | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 18 | HG00408.hp2 HG00558.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.142-6062A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026090 | ||||||
| chr5:1026090
|
ATTGTCCC others(75): Show |
A | 47 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(44): Show | 49 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.142-6032_142-5951d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026090 | |||||
| chr5:1026095
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.142-6057C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026095 | ||||||
| chr5:1026112
|
T | G | 13 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0035others(10): Show | 13 | HG01074.hp2 HG01168.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-6040T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026112 | ||||||
| chr5:1026120
|
T | C | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(10): Show | 14 | HG00408.hp2 HG00558.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-6032T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026120 | ||||||
| chr5:1026120
|
TGCCCCAG others(75): Show |
T | 2 | a0001c0001t0005g0003a0001c0001t0008g0088 | 2 | HG02257.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.142-6030_142-5949d others(84): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026120 | |||||
| chr5:1026122
|
C | T | 25 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(22): Show | 27 | HG00408.hp2 HG00558.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.142-6030C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026122 | ||||||
| chr5:1026124
|
C | CCAGCCCA others(35): Show |
2 | a0001c0001t0002g0045a0001c0001t0002g0136 | 2 | HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-5997_142-5996i others(44): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026124 | |||||
| chr5:1026124
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.142-6028C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026124 | ||||||
| chr5:1026131
|
A | G | 23 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(20): Show | 25 | HG00408.hp2 HG00558.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.142-6021A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026131 | ||||||
| chr5:1026148
|
C | CACCCGCT others(35): Show |
1 | a0001c0001t0007g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-5997_142-5996i others(44): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026148 | |||||
| chr5:1026152
|
C | T | 2 | a0001c0001t0005g0003a0001c0001t0005g0093 | 2 | NA18951.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.142-6000C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026152 | ||||||
| chr5:1026153
|
G | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0035others(10): Show | 13 | HG01074.hp2 HG01168.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-5999G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026153 | ||||||
| chr5:1026155
|
T | TA | 4 | a0001c0001t0003g0115a0001c0001t0005g0003a0001c0001t0005g0093others(1): Show | 4 | HG02965.hp1 HG03516.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-5997_142-5996i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026155 | ||||||
| chr5:1026161
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-5991C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026161 | ||||||
| chr5:1026161
|
CGTCCCAG others(404): Show |
C | 7 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(4): Show | 7 | HG00408.hp2 HG00558.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-5980_142-5570d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026161 | |||||
| chr5:1026165
|
C | T | 8 | a0001c0001t0001g0186a0001c0001t0002g0042a0001c0001t0003g0002others(5): Show | 9 | HG02809.hp2 HG02965.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-5987C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026165 | ||||||
| chr5:1026165
|
CCAGCCCT others(76): Show |
C | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-5980_142-5898d others(85): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026165 | |||||
| chr5:1026172
|
T | A | 7 | a0001c0001t0001g0186a0001c0001t0002g0042a0001c0001t0003g0002others(4): Show | 8 | HG02809.hp2 HG02965.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-5980T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026172 | ||||||
| chr5:1026172
|
T | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0035others(11): Show | 14 | HG01074.hp2 HG01168.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.142-5980T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026172 | ||||||
| chr5:1026172
|
TTTGTCCC others(76): Show |
T | 91 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(88): Show | 104 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.142-5958_142-5876d others(85): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026172 | |||||
| chr5:1026177
|
C | T | 2 | a0001c0001t0003g0115a0001c0001t0010g0116 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.142-5975C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026177 | ||||||
| chr5:1026194
|
T | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(52): Show | 60 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.142-5958T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026194 | ||||||
| chr5:1026202
|
C | T | 11 | a0001c0001t0003g0107a0001c0001t0005g0003a0001c0001t0005g0089others(8): Show | 11 | HG00438.hp2 HG01192.hp1 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.142-5950C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026202 | ||||||
| chr5:1026206
|
T | C | 14 | a0001c0001t0002g0045a0001c0001t0002g0136a0001c0001t0005g0003others(11): Show | 15 | HG00438.hp2 HG01192.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.142-5946T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026206 | ||||||
| chr5:1026206
|
TCAGCCCA others(363): Show |
T | 10 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0035others(7): Show | 10 | HG01074.hp2 HG01168.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-5918_142-5549d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026206 | |||||
| chr5:1026213
|
A | G | 16 | a0001c0001t0003g0013a0001c0001t0003g0115a0001c0001t0003g0118others(13): Show | 17 | HG00438.hp2 HG01192.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.142-5939A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026213 | ||||||
| chr5:1026213
|
ATTGTCCC others(76): Show |
A | 1 | a0001c0001t0015g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-5918_142-5836d others(85): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026213 | |||||
| chr5:1026218
|
C | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(37): Show | 45 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.142-5934C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026218 | ||||||
| chr5:1026234
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(42): Show | 50 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.142-5918T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026234 | ||||||
| chr5:1026235
|
G | A | 4 | a0001c0001t0003g0013a0001c0001t0003g0118a0001c0001t0003g0121others(1): Show | 4 | HG02145.hp2 HG02895.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-5917G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026235 | ||||||
| chr5:1026237
|
TA | T | 4 | a0001c0001t0003g0107a0001c0001t0005g0003a0001c0001t0005g0093others(1): Show | 4 | HG02965.hp1 NA18951.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-5914delA | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026237 | ||||||
| chr5:1026244
|
C | T | 4 | a0001c0001t0003g0107a0001c0001t0005g0003a0001c0001t0005g0093others(1): Show | 4 | HG02965.hp1 NA18951.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-5908C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026244 | ||||||
| chr5:1026246
|
T | C | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-5906T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026246 | ||||||
| chr5:1026248
|
T | C | 10 | a0001c0001t0003g0107a0001c0001t0005g0003a0001c0001t0005g0093others(7): Show | 11 | HG02523.hp2 HG02602.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.142-5904T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026248 | ||||||
| chr5:1026248
|
TCAGCCCA others(34): Show |
T | 1 | a0001c0001t0001g0186 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.142-5897_142-5857d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026248 | |||||
| chr5:1026252
|
C | T | 1 | a0001c0001t0008g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142-5900C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026252 | ||||||
| chr5:1026255
|
A | ATTGTCCC others(158): Show |
2 | a0001c0001t0002g0045a0001c0001t0002g0136 | 2 | HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.142-5873_142-5872i others(167): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026255 | |||||
| chr5:1026255
|
A | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(43): Show | 49 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.142-5897A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026255 | ||||||
| chr5:1026255
|
A | T | 6 | a0001c0001t0007g0027a0001c0001t0007g0256a0001c0001t0007g0257others(3): Show | 7 | HG02523.hp2 HG02602.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-5897A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026255 | ||||||
| chr5:1026260
|
C | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(37): Show | 45 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.142-5892C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026260 | ||||||
| chr5:1026276
|
C | T | 2 | a0001c0001t0005g0003a0001c0001t0005g0093 | 2 | NA18951.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.142-5876C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026276 | ||||||
| chr5:1026277
|
G | T | 3 | a0001c0001t0010g0116a0001c0001t0013g0074a0009c0013t0017g0098 | 3 | HG02071.hp1 HG02273.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.142-5875G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026277 | ||||||
| chr5:1026277
|
GCTGTGGG others(157): Show |
G | 4 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0008g0092others(1): Show | 5 | HG00438.hp2 NA18612.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-5863_142-5700d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026277 | |||||
| chr5:1026281
|
T | C | 1 | a0001c0001t0003g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.142-5871T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026281 | ||||||
| chr5:1026285
|
C | T | 2 | a0001c0001t0003g0107a0009c0013t0017g0098 | 2 | HG02071.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.142-5867C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026285 | ||||||
| chr5:1026289
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(46): Show | 54 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.142-5863C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026289 | ||||||
| chr5:1026296
|
T | A | 10 | a0001c0001t0003g0107a0001c0001t0003g0115a0001c0001t0005g0090others(7): Show | 10 | HG01192.hp1 HG02071.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-5856T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026296 | ||||||
| chr5:1026296
|
T | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(38): Show | 46 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.142-5856T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026296 | ||||||
| chr5:1026301
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0003g0107 | 2 | NA18948.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-5851C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026301 | ||||||
| chr5:1026317
|
CGCTGTGG others(157): Show |
C | 40 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(37): Show | 45 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.142-5820_142-5657d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026317 | |||||
| chr5:1026318
|
G | GCTGTGGG others(34): Show |
9 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(6): Show | 11 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.142-5823_142-5822i others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026318 | |||||
| chr5:1026318
|
G | T | 101 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(98): Show | 115 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.142-5834G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026318 | ||||||
| chr5:1026318
|
GCTGTGGG others(116): Show |
G | 1 | a0001c0001t0001g0186 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.142-5820_142-5698d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026318 | |||||
| chr5:1026326
|
C | T | 8 | a0001c0001t0003g0115a0001c0001t0005g0090a0001c0001t0005g0095others(5): Show | 8 | HG01192.hp1 HG02071.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-5826C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026326 | ||||||
| chr5:1026330
|
T | C | 8 | a0001c0001t0003g0115a0001c0001t0005g0090a0001c0001t0005g0095others(5): Show | 8 | HG01192.hp1 HG02071.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-5822T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026330 | ||||||
| chr5:1026330
|
TCGGTCCA others(239): Show |
T | 2 | a0001c0001t0005g0003a0001c0001t0005g0093 | 2 | NA18951.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.142-5820_142-5575d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026330 | |||||
| chr5:1026332
|
G | A | 10 | a0001c0001t0003g0107a0001c0001t0003g0115a0001c0001t0005g0090others(7): Show | 10 | HG01192.hp1 HG02071.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-5820G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026332 | ||||||
| chr5:1026334
|
T | C | 10 | a0001c0001t0003g0107a0001c0001t0003g0115a0001c0001t0005g0090others(7): Show | 10 | HG01192.hp1 HG02071.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-5818T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026334 | ||||||
| chr5:1026334
|
T | TCCATTGT others(34): Show |
3 | a0001c0001t0001g0062a0001c0001t0004g0060a0001c0001t0004g0061 | 3 | HG01261.hp1 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.142-5793_142-5753d others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026334 | |||||
| chr5:1026358
|
C | T | 6 | a0001c0001t0005g0090a0001c0001t0005g0095a0001c0001t0006g0076others(3): Show | 6 | HG01192.hp1 HG03225.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-5794C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026358 | ||||||
| chr5:1026359
|
T | G | 7 | a0001c0001t0005g0090a0001c0001t0005g0095a0001c0001t0006g0076others(4): Show | 7 | HG01192.hp1 HG02965.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-5793T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026359 | ||||||
| chr5:1026359
|
TCTGTGGG others(116): Show |
T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-5779_142-5657d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026359 | |||||
| chr5:1026366
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.142-5786G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026366 | ||||||
| chr5:1026367
|
C | T | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-5785C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026367 | ||||||
| chr5:1026371
|
T | C | 2 | a0001c0001t0003g0107a0001c0001t0003g0115 | 2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.142-5781T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026371 | ||||||
| chr5:1026373
|
G | A | 9 | a0001c0001t0003g0107a0001c0001t0003g0115a0001c0001t0005g0090others(6): Show | 9 | HG01192.hp1 HG02965.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-5779G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026373 | ||||||
| chr5:1026378
|
A | G | 2 | a0001c0001t0003g0107a0001c0001t0003g0115 | 2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.142-5774A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026378 | ||||||
| chr5:1026378
|
A | T | 6 | a0001c0001t0005g0090a0001c0001t0005g0095a0001c0001t0006g0076others(3): Show | 6 | HG01192.hp1 HG03225.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-5774A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026378 | ||||||
| chr5:1026383
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.142-5769C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026383 | ||||||
| chr5:1026399
|
C | T | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-5753C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026399 | ||||||
| chr5:1026408
|
CGTCCCAG others(157): Show |
C | 5 | a0001c0001t0005g0095a0001c0001t0006g0076a0001c0001t0008g0082others(2): Show | 5 | HG01192.hp1 HG03225.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-5733_142-5570d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026408 | |||||
| chr5:1026412
|
C | T | 4 | a0001c0001t0003g0107a0001c0001t0003g0115a0001c0001t0005g0090others(1): Show | 4 | HG02965.hp1 HG03516.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-5740C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026412 | ||||||
| chr5:1026419
|
T | A | 2 | a0001c0001t0003g0115a0001c0001t0010g0116 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.142-5733T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026419 | ||||||
| chr5:1026419
|
T | G | 2 | a0001c0001t0003g0107a0001c0001t0005g0090 | 2 | NA18939.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-5733T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026419 | ||||||
| chr5:1026422
|
T | G | 4 | a0001c0001t0003g0107a0001c0001t0003g0115a0001c0001t0005g0090others(1): Show | 4 | HG02965.hp1 HG03516.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-5730T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026422 | ||||||
| chr5:1026424
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.142-5728C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026424 | ||||||
| chr5:1026424
|
CCCTGCTC others(156): Show |
C | 1 | a0001c0001t0005g0090 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.142-5725_142-5563d others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026424 | |||||
| chr5:1026441
|
T | G | 3 | a0001c0001t0003g0107a0001c0001t0003g0115a0001c0001t0010g0116 | 3 | HG02965.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.142-5711T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026441 | ||||||
| chr5:1026443
|
T | TGTGGGCG others(35): Show |
1 | a0001c0001t0003g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.142-5688_142-5687i others(44): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026443 | |||||
| chr5:1026445
|
T | C | 1 | a0001c0001t0010g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.142-5707T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026445 | ||||||
| chr5:1026460
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0010g0116 | 2 | HG02965.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.142-5692A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026460 | ||||||
| chr5:1026465
|
C | T | 1 | a0001c0001t0003g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.142-5687C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026465 | ||||||
| chr5:1026479
|
T | C | 16 | a0001c0001t0001g0186a0001c0001t0003g0004a0001c0001t0003g0107others(13): Show | 19 | HG00438.hp2 HG01243.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-5673T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026479 | ||||||
| chr5:1026481
|
T | C | 120 | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(117): Show | 137 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.142-5671T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026481 | ||||||
| chr5:1026482
|
G | T | 8 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(5): Show | 10 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-5670G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026482 | ||||||
| chr5:1026490
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(45): Show | 54 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.142-5662C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026490 | ||||||
| chr5:1026494
|
T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(45): Show | 54 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.142-5658T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026494 | ||||||
| chr5:1026501
|
A | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(34): Show | 39 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.142-5651A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026501 | ||||||
| chr5:1026522
|
C | T | 6 | a0001c0001t0003g0107a0001c0001t0005g0003a0001c0001t0005g0089others(3): Show | 7 | HG00438.hp2 HG02257.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-5630C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026522 | ||||||
| chr5:1026523
|
G | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(39): Show | 47 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.142-5629G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026523 | ||||||
| chr5:1026531
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(44): Show | 53 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.142-5621T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026531 | ||||||
| chr5:1026535
|
C | T | 6 | a0001c0001t0003g0107a0001c0001t0005g0003a0001c0001t0005g0089others(3): Show | 7 | HG00438.hp2 HG02257.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-5617C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026535 | ||||||
| chr5:1026542
|
A | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(38): Show | 46 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.142-5610A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026542 | ||||||
| chr5:1026542
|
A | T | 6 | a0001c0001t0003g0107a0001c0001t0005g0003a0001c0001t0005g0089others(3): Show | 7 | HG00438.hp2 HG02257.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-5610A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026542 | ||||||
| chr5:1026564
|
T | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(45): Show | 54 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.142-5588T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026564 | ||||||
| chr5:1026572
|
T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(45): Show | 54 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.142-5580T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026572 | ||||||
| chr5:1026576
|
C | CCAGCCCG others(34): Show |
1 | a0001c0001t0003g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.142-5570_142-5569i others(43): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1026576 | |||||
| chr5:1026576
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(56): Show | 66 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.142-5576C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026576 | ||||||
| chr5:1026583
|
A | G | 27 | a0001c0001t0003g0107a0001c0001t0005g0003a0001c0001t0005g0089others(24): Show | 32 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.142-5569A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026583 | ||||||
| chr5:1026605
|
A | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.142-5547A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026605 | ||||||
| chr5:1026714
|
C | T | 2 | a0001c0001t0006g0266a0001c0001t0006g0268 | 2 | HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.142-5438C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026714 | ||||||
| chr5:1026888
|
T | C | 28 | a0001c0001t0003g0107a0001c0001t0005g0003a0001c0001t0005g0089others(25): Show | 33 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.142-5264T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026888 | ||||||
| chr5:1026906
|
T | C | 29 | a0001c0001t0003g0107a0001c0001t0005g0003a0001c0001t0005g0089others(26): Show | 34 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.142-5246T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026906 | ||||||
| chr5:1026940
|
C | T | 3 | a0001c0001t0003g0107a0004c0007t0006g0078a0004c0007t0006g0079 | 3 | HG01099.hp1 HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-5212C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026940 | ||||||
| chr5:1026941
|
G | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-5211G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026941 | ||||||
| chr5:1026993
|
T | G | 29 | a0001c0001t0003g0107a0001c0001t0005g0003a0001c0001t0005g0089others(26): Show | 34 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.142-5159T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1026993 | ||||||
| chr5:1027017
|
G | A | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | NA18972.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.142-5135G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027017 | ||||||
| chr5:1027036
|
A | G | 26 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(23): Show | 31 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.142-5116A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027036 | ||||||
| chr5:1027039
|
A | G | 26 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(23): Show | 31 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.142-5113A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027039 | ||||||
| chr5:1027067
|
A | G | 25 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(22): Show | 30 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.142-5085A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027067 | ||||||
| chr5:1027194
|
C | T | 3 | a0001c0001t0003g0107a0004c0007t0006g0078a0004c0007t0006g0079 | 3 | HG01099.hp1 HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-4958C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027194 | ||||||
| chr5:1027252
|
A | G | 2 | a0001c0001t0015g0117a0009c0013t0017g0098 | 2 | HG02071.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.142-4900A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027252 | ||||||
| chr5:1027282
|
T | C | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-4870T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027282 | ||||||
| chr5:1027291
|
C | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 4 | HG00673.hp1 HG02015.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-4861C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027291 | ||||||
| chr5:1027341
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(119): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.142-4811A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027341 | ||||||
| chr5:1027358
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.142-4794T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027358 | ||||||
| chr5:1027487
|
C | T | 1 | a0001c0001t0002g0042 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.142-4665C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027487 | ||||||
| chr5:1027598
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.142-4554G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027598 | ||||||
| chr5:1027895
|
C | T | 1 | a0001c0002t0001g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.142-4257C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027895 | ||||||
| chr5:1027946
|
C | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0188a0001c0001t0001g0214 | 3 | HG00735.hp1 HG02683.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.142-4206C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1027946 | ||||||
| chr5:1028012
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.142-4140G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028012 | ||||||
| chr5:1028054
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.142-4098G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028054 | ||||||
| chr5:1028078
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.142-4074C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028078 | ||||||
| chr5:1028122
|
TGGGCTGG others(18): Show |
T | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-4028_142-4004d others(27): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1028122 | |||||
| chr5:1028138
|
C | T | 8 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(5): Show | 10 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-4014C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028138 | ||||||
| chr5:1028160
|
C | T | 1 | a0001c0001t0015g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-3992C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028160 | ||||||
| chr5:1028188
|
G | T | 1 | a0001c0001t0008g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.142-3964G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028188 | ||||||
| chr5:1028335
|
C | T | 4 | a0001c0001t0003g0002a0001c0001t0003g0115a0001c0005t0011g0002others(1): Show | 7 | HG02809.hp2 HG03225.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-3817C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028335 | ||||||
| chr5:1028377
|
C | T | 1 | a0001c0001t0012g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.142-3775C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028377 | ||||||
| chr5:1028387
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-3765C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028387 | ||||||
| chr5:1028467
|
C | G | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-3685C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028467 | ||||||
| chr5:1028475
|
T | G | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0230 | 3 | NA18968.hp1 NA18992.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.142-3677T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028475 | ||||||
| chr5:1028568
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(134): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.142-3584C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028568 | ||||||
| chr5:1028731
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.142-3421C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028731 | ||||||
| chr5:1028761
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(162): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.142-3391A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028761 | ||||||
| chr5:1028803
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(113): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.142-3349G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028803 | ||||||
| chr5:1028851
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.142-3301G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028851 | ||||||
| chr5:1028873
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-3279C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028873 | ||||||
| chr5:1028928
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-3224C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028928 | ||||||
| chr5:1028987
|
T | C | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-3165T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1028987 | ||||||
| chr5:1029012
|
G | A | 3 | a0001c0001t0003g0107a0004c0007t0006g0078a0004c0007t0006g0079 | 3 | HG01099.hp1 HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.142-3140G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029012 | ||||||
| chr5:1029058
|
C | T | 1 | a0001c0001t0004g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.142-3094C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029058 | ||||||
| chr5:1029066
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.142-3086C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029066 | ||||||
| chr5:1029100
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.142-3052G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029100 | ||||||
| chr5:1029128
|
AT | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.142-3022delT | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1029128 | |||||
| chr5:1029256
|
A | G | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-2896A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029256 | ||||||
| chr5:1029316
|
G | C | 6 | a0001c0001t0006g0265a0001c0001t0006g0266a0001c0001t0006g0268others(3): Show | 6 | HG00099.hp2 HG00323.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-2836G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029316 | ||||||
| chr5:1029438
|
G | A | 4 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0153others(1): Show | 4 | HG03239.hp1 HG04184.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-2714G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029438 | ||||||
| chr5:1029496
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.142-2656C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029496 | ||||||
| chr5:1029548
|
A | T | 1 | a0001c0001t0001g0177 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.142-2604A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029548 | ||||||
| chr5:1029584
|
C | T | 17 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(14): Show | 20 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.142-2568C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029584 | ||||||
| chr5:1029597
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.142-2555G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029597 | ||||||
| chr5:1029622
|
T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(276): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.142-2530T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029622 | ||||||
| chr5:1029736
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.142-2416T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029736 | ||||||
| chr5:1029737
|
G | A | 2 | a0001c0002t0003g0006a0001c0002t0003g0054 | 4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-2415G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029737 | ||||||
| chr5:1029753
|
G | A | 17 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(14): Show | 20 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.142-2399G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029753 | ||||||
| chr5:1029760
|
C | T | 1 | a0001c0001t0005g0093 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.142-2392C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029760 | ||||||
| chr5:1029834
|
A | G | 17 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(14): Show | 20 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.142-2318A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1029834 | ||||||
| chr5:1030015
|
C | CG | 29 | a0001c0001t0001g0177a0001c0001t0002g0016a0001c0001t0002g0017others(26): Show | 33 | HG00597.hp2 HG00642.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.142-2126dupG | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1030015 | |||||
| chr5:1030020
|
G | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-2132G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030020 | ||||||
| chr5:1030022
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(117): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.142-2130G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030022 | ||||||
| chr5:1030023
|
G | GC | 25 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(22): Show | 29 | HG01358.hp1 HG02040.hp2 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.142-2129_142-2128i others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030023 | ||||||
| chr5:1030027
|
T | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.142-2125T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030027 | ||||||
| chr5:1030100
|
C | A | 11 | a0001c0001t0003g0107a0001c0002t0001g0185a0001c0002t0001g0194others(8): Show | 13 | HG00639.hp1 HG00741.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.142-2052C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030100 | ||||||
| chr5:1030132
|
G | A | 15 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(12): Show | 18 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-2020G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030132 | ||||||
| chr5:1030337
|
T | C | 1 | a0001c0001t0022g0199 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.142-1815T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030337 | ||||||
| chr5:1030425
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(154): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.142-1727A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030425 | ||||||
| chr5:1030473
|
T | C | 1 | a0001c0001t0005g0091 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.142-1679T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030473 | ||||||
| chr5:1030474
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.142-1678C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030474 | ||||||
| chr5:1030527
|
A | AC | 8 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-1622dupC | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1030527 | |||||
| chr5:1030530
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.142-1622C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030530 | ||||||
| chr5:1030545
|
GAAAT | G | 3 | a0001c0001t0003g0002a0001c0001t0003g0115a0001c0005t0011g0002 | 6 | HG02809.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-1592_142-1589d others(6): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1030545 | |||||
| chr5:1030556
|
A | G | 1 | a0001c0001t0003g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-1596A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030556 | ||||||
| chr5:1030567
|
C | T | 1 | a0007c0014t0018g0104 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.142-1585C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030567 | ||||||
| chr5:1030635
|
C | T | 17 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(14): Show | 20 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.142-1517C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030635 | ||||||
| chr5:1030671
|
G | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0186a0001c0001t0001g0236 | 4 | HG00558.hp1 NA18948.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-1481G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030671 | ||||||
| chr5:1030700
|
C | G | 1 | a0001c0001t0001g0244 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.142-1452C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030700 | ||||||
| chr5:1030706
|
C | T | 26 | a0001c0001t0001g0168a0001c0001t0002g0017a0001c0001t0002g0018others(23): Show | 28 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.142-1446C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030706 | ||||||
| chr5:1030853
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.142-1299G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030853 | ||||||
| chr5:1030857
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(148): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.142-1295A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030857 | ||||||
| chr5:1030989
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.142-1163C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1030989 | ||||||
| chr5:1031165
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.142-987C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1031165 | ||||||
| chr5:1031255
|
G | T | 1 | a0001c0001t0015g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-897G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1031255 | ||||||
| chr5:1031519
|
G | A | 4 | a0001c0001t0003g0013a0001c0001t0003g0118a0001c0001t0003g0121others(1): Show | 5 | HG02145.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-633G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1031519 | ||||||
| chr5:1031544
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0050 | 2 | HG00099.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.142-608C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1031544 | ||||||
| chr5:1031559
|
C | G | 1 | a0005c0009t0002g0249 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.142-593C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1031559 | ||||||
| chr5:1031567
|
AG | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(154): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.142-583delG | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 1031567 | |||||
| chr5:1031917
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(148): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.142-235T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1031917 | ||||||
| chr5:1032053
|
C | T | 1 | a0001c0001t0004g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142-99C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1032053 | ||||||
| chr5:1032054
|
G | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.142-98G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | 1032054 | ||||||
| chr5:1032276
|
C | T | 1 | a0001c0001t0015g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.202+64C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1032276 | ||||||
| chr5:1032426
|
G | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.202+214G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1032426 | ||||||
| chr5:1032624
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.202+412C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1032624 | ||||||
| chr5:1032673
|
G | A | 1 | a0001c0001t0002g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.202+461G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1032673 | ||||||
| chr5:1032707
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.202+495G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1032707 | ||||||
| chr5:1032771
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.202+559C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1032771 | ||||||
| chr5:1032901
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(154): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.203-471A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1032901 | ||||||
| chr5:1033018
|
G | A | 4 | a0001c0001t0003g0002a0001c0001t0003g0115a0001c0005t0011g0002others(1): Show | 7 | HG02809.hp2 HG03225.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-354G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1033018 | ||||||
| chr5:1033031
|
C | CGCGG | 66 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0001t0002g0005others(63): Show | 75 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.203-341_203-340ins others(4): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1033031 | ||||||
| chr5:1033109
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02738.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.203-263G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1033109 | ||||||
| chr5:1033202
|
G | A | 2 | a0001c0001t0003g0109a0001c0001t0010g0116 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.203-170G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1033202 | ||||||
| chr5:1033241
|
C | T | 1 | a0001c0005t0011g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.203-131C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1033241 | ||||||
| chr5:1033299
|
G | A | 7 | a0001c0001t0007g0027a0001c0001t0007g0077a0001c0001t0007g0256others(4): Show | 8 | HG02523.hp2 HG02602.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.203-73G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1033299 | ||||||
| chr5:1033310
|
A | G | 16 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(13): Show | 19 | HG00438.hp2 HG01192.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.203-62A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 4/9 | chr5 | 1033310 | ||||||
| chr5:1033513
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.330+14C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 5/9 | chr5 | 1033513 | ||||||
| chr5:1033545
|
C | T | 7 | a0001c0001t0007g0027a0001c0001t0007g0077a0001c0001t0007g0256others(4): Show | 8 | HG02523.hp2 HG02602.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+46C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 5/9 | chr5 | 1033545 | ||||||
| chr5:1033718
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.330+219A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 5/9 | chr5 | 1033718 | ||||||
| chr5:1033765
|
T | G | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.330+266T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 5/9 | chr5 | 1033765 | ||||||
| chr5:1033865
|
G | A | 7 | a0001c0001t0001g0168a0001c0001t0002g0018a0001c0001t0002g0134others(4): Show | 8 | HG01070.hp2 HG01099.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+366G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 5/9 | chr5 | 1033865 | ||||||
| chr5:1033933
|
C | T | 16 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(13): Show | 19 | HG00438.hp2 HG01192.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.331-302C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 5/9 | chr5 | 1033933 | ||||||
| chr5:1033999
|
G | C | 1 | a0001c0001t0002g0165 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.331-236G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 5/9 | chr5 | 1033999 | ||||||
| chr5:1034047
|
T | C | 1 | a0001c0001t0003g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.331-188T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 5/9 | chr5 | 1034047 | ||||||
| chr5:1034131
|
A | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(120): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.331-104A>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 5/9 | chr5 | 1034131 | ||||||
| chr5:1034139
|
C | A | 1 | a0001c0001t0015g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.331-96C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 5/9 | chr5 | 1034139 | ||||||
| chr5:1034204
|
G | T | 2 | a0003c0004t0001g0099a0003c0004t0001g0101 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.331-31G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 5/9 | chr5 | 1034204 | ||||||
| chr5:1034376
|
G | A | 2 | a0004c0007t0006g0078a0004c0007t0006g0079 | 2 | HG01099.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.426+46G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 6/9 | chr5 | 1034376 | ||||||
| chr5:1034464
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0021g0010 | 3 | HG00738.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.426+134C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 6/9 | chr5 | 1034464 | ||||||
| chr5:1034487
|
G | A | 2 | a0001c0001t0002g0103a0007c0014t0018g0104 | 2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.426+157G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 6/9 | chr5 | 1034487 | ||||||
| chr5:1034570
|
C | T | 8 | a0001c0001t0001g0050a0001c0001t0003g0004a0001c0001t0003g0112others(5): Show | 10 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.427-186C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 6/9 | chr5 | 1034570 | ||||||
| chr5:1034576
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.427-180C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 6/9 | chr5 | 1034576 | ||||||
| chr5:1034622
|
T | C | 1 | a0001c0001t0001g0020 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.427-134T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 6/9 | chr5 | 1034622 | ||||||
| chr5:1034668
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.427-88G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 6/9 | chr5 | 1034668 | ||||||
| chr5:1035057
|
T | A | 7 | a0001c0001t0007g0027a0001c0001t0007g0077a0001c0001t0007g0256others(4): Show | 8 | HG02523.hp2 HG02602.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.574+154T>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | chr5 | 1035057 | ||||||
| chr5:1035072
|
G | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.574+169G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | chr5 | 1035072 | ||||||
| chr5:1035089
|
T | G | 9 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(6): Show | 11 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.574+186T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | chr5 | 1035089 | ||||||
| chr5:1035148
|
A | G | 2 | a0001c0001t0002g0136a0002c0003t0002g0155 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.575-241A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | chr5 | 1035148 | ||||||
| chr5:1035160
|
ATGAG | A | 13 | a0001c0001t0002g0138a0001c0001t0002g0142a0001c0001t0003g0109others(10): Show | 15 | HG00558.hp2 HG00639.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.575-222_575-219del others(4): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 1035160 | |||||
| chr5:1035168
|
GTGTT | G | 7 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(4): Show | 9 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.575-220_575-217del others(4): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | chr5 | 1035168 | ||||||
| chr5:1035170
|
G | A | 2 | a0001c0001t0002g0136a0002c0003t0002g0155 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.575-219G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | chr5 | 1035170 | ||||||
| chr5:1035172
|
T | G | 2 | a0001c0001t0002g0136a0002c0003t0002g0155 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.575-217T>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | chr5 | 1035172 | ||||||
| chr5:1035174
|
A | G | 2 | a0001c0001t0002g0136a0002c0003t0002g0155 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.575-215A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | chr5 | 1035174 | ||||||
| chr5:1035179
|
T | C | 2 | a0001c0001t0002g0136a0002c0003t0002g0155 | 2 | HG00597.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.575-210T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | chr5 | 1035179 | ||||||
| chr5:1035248
|
AAGTG | A | 2 | a0001c0001t0002g0009a0001c0001t0002g0181 | 4 | HG01081.hp1 HG01081.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-133_575-130del others(4): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 1035248 | |||||
| chr5:1035260
|
TAATG | T | 3 | a0004c0007t0006g0078a0004c0007t0006g0079a0009c0013t0017g0098 | 3 | HG01099.hp1 HG02071.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.575-123_575-120del others(4): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 1035260 | |||||
| chr5:1035284
|
T | TAATG | 218 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.575-91_575-88dupAT others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 1035284 | |||||
| chr5:1035294
|
ATGAATGA others(1): Show |
A | 7 | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(4): Show | 9 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.575-91_575-84delAT others(6): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 1035294 | |||||
| chr5:1035298
|
A | ATGAG | 18 | a0001c0001t0006g0076a0001c0001t0007g0027a0001c0001t0007g0077others(15): Show | 21 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.575-81_575-78dupGA others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 1035298 | |||||
| chr5:1035312
|
TAATGAAT others(5): Show |
T | 1 | a0001c0001t0004g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.575-60_575-49delAA others(10): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 1035312 | |||||
| chr5:1035315
|
T | C | 7 | a0001c0001t0007g0027a0001c0001t0007g0077a0001c0001t0007g0256others(4): Show | 8 | HG02523.hp2 HG02602.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.575-74T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | chr5 | 1035315 | ||||||
| chr5:1035367
|
A | G | 266 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(263): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.575-22A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 7/9 | chr5 | 1035367 | ||||||
| chr5:1035487
|
T | C | 35 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(32): Show | 41 | HG00438.hp2 HG00639.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.659+14T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 8/9 | chr5 | 1035487 | ||||||
| chr5:1035543
|
GCAGGCCA | G | 3 | a0001c0001t0001g0215a0001c0001t0002g0154a0002c0003t0001g0208 | 3 | HG00408.hp2 HG02135.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.659+87_659+93delGG others(5): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 1035543 | |||||
| chr5:1035596
|
G | T | 2 | a0004c0007t0006g0078a0004c0007t0006g0079 | 2 | HG01099.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.659+123G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 8/9 | chr5 | 1035596 | ||||||
| chr5:1035633
|
C | T | 1 | a0002c0003t0001g0211 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.659+160C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 8/9 | chr5 | 1035633 | ||||||
| chr5:1035677
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.659+204G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 8/9 | chr5 | 1035677 | ||||||
| chr5:1035746
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(158): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.659+273A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 8/9 | chr5 | 1035746 | ||||||
| chr5:1035775
|
G | C | 1 | a0001c0001t0007g0257 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.659+302G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 8/9 | chr5 | 1035775 | ||||||
| chr5:1035817
|
GAGGGTGG others(37): Show |
G | 2 | a0001c0001t0002g0176a0001c0001t0002g0245 | 2 | NA18945.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.659+358_660-383del others(44): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 1035817 | |||||
| chr5:1035831
|
C | A | 87 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0001t0002g0005others(84): Show | 100 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.659+358C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 8/9 | chr5 | 1035831 | ||||||
| chr5:1035948
|
C | A | 1 | a0001c0001t0002g0233 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.660-309C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 8/9 | chr5 | 1035948 | ||||||
| chr5:1036134
|
C | T | 1 | a0001c0001t0003g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.660-123C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 8/9 | chr5 | 1036134 | ||||||
| chr5:1036209
|
G | A | 13 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(10): Show | 15 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.660-48G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 8/9 | chr5 | 1036209 | ||||||
| chr5:1036402
|
C | G | 19 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(16): Show | 22 | HG00438.hp2 HG01192.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.787+18C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036402 | ||||||
| chr5:1036403
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.787+19C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036403 | ||||||
| chr5:1036406
|
G | A | 85 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0001t0002g0005others(82): Show | 96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.787+22G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036406 | ||||||
| chr5:1036485
|
C | T | 1 | a0001c0001t0003g0124 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.787+101C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036485 | ||||||
| chr5:1036496
|
CCCCCCAA others(14): Show |
C | 3 | a0003c0004t0001g0099a0003c0004t0001g0100a0003c0004t0001g0101 | 3 | HG02109.hp2 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.787+117_787+137del others(21): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 1036496 | |||||
| chr5:1036497
|
CCCCCAAC others(13): Show |
C | 10 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(7): Show | 12 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.787+119_787+138del others(20): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 1036497 | |||||
| chr5:1036498
|
C | CCCA | 14 | a0001c0001t0002g0132a0001c0001t0005g0003a0001c0001t0005g0089others(11): Show | 17 | HG00438.hp2 HG01928.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.787+116_787+117ins others(3): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 1036498 | |||||
| chr5:1036498
|
CCCCAACC others(12): Show |
C | 2 | a0004c0007t0006g0078a0004c0007t0006g0079 | 2 | HG01099.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.787+118_787+136del others(19): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 1036498 | |||||
| chr5:1036500
|
CCA | C | 23 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(20): Show | 30 | HG01358.hp1 HG01891.hp1 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.787+117_787+118del others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036500 | ||||||
| chr5:1036501
|
CA | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.787+119delA | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 1036501 | |||||
| chr5:1036502
|
A | C | 36 | a0001c0001t0001g0024a0001c0001t0001g0050a0001c0001t0001g0127others(33): Show | 39 | HG00438.hp2 HG00544.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.787+118A>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036502 | ||||||
| chr5:1036503
|
A | C | 57 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0049others(54): Show | 62 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.787+119A>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036503 | ||||||
| chr5:1036507
|
C | A | 15 | a0001c0001t0002g0132a0001c0001t0005g0003a0001c0001t0005g0089others(12): Show | 18 | HG00438.hp2 HG01192.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.787+123C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036507 | ||||||
| chr5:1036507
|
C | CCCCA | 9 | a0001c0001t0003g0004a0001c0001t0003g0113a0001c0001t0004g0057others(6): Show | 11 | HG01243.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.787+126_787+127ins others(4): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 1036507 | |||||
| chr5:1036610
|
G | A | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.787+226G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036610 | ||||||
| chr5:1036639
|
C | T | 2 | a0001c0001t0002g0132a0001c0001t0002g0150 | 2 | NA18967.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.787+255C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036639 | ||||||
| chr5:1036640
|
G | A | 3 | a0001c0001t0013g0073a0001c0001t0013g0074a0001c0001t0013g0075 | 3 | HG02273.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.787+256G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036640 | ||||||
| chr5:1036645
|
C | G | 7 | a0001c0001t0007g0027a0001c0001t0007g0077a0001c0001t0007g0256others(4): Show | 8 | HG02523.hp2 HG02602.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.787+261C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036645 | ||||||
| chr5:1036687
|
G | C | 16 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(13): Show | 19 | HG00438.hp2 HG01192.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.787+303G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036687 | ||||||
| chr5:1036785
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(119): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.787+401C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036785 | ||||||
| chr5:1036813
|
C | T | 2 | a0001c0001t0003g0109a0001c0001t0010g0116 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.787+429C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036813 | ||||||
| chr5:1036847
|
C | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(158): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.787+463C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036847 | ||||||
| chr5:1036851
|
A | AGCAGGCA others(13): Show |
8 | a0001c0001t0007g0027a0001c0001t0007g0077a0001c0001t0007g0256others(5): Show | 9 | HG02071.hp1 HG02523.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.787+486_787+505dup others(20): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 1036851 | |||||
| chr5:1036851
|
AGCAGGCA others(137): Show |
A | 1 | a0001c0001t0008g0086 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.787+486_787+629del | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 1036851 | |||||
| chr5:1036869
|
C | A | 1 | a0001c0001t0003g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.787+485C>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036869 | ||||||
| chr5:1036869
|
C | T | 3 | a0001c0001t0006g0269a0001c0001t0006g0270a0001c0001t0006g0271 | 3 | HG00099.hp2 HG00323.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.787+485C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036869 | ||||||
| chr5:1036908
|
CCAGGCAG others(117): Show |
C | 15 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(12): Show | 18 | HG00438.hp2 HG01192.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.787+560_787+683del | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 1036908 | |||||
| chr5:1036910
|
A | AGGCAGTG others(29): Show |
1 | a0003c0004t0025g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.787+554_787+589dup others(36): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 1036910 | |||||
| chr5:1036929
|
C | T | 2 | a0001c0001t0002g0246a0001c0001t0002g0255 | 2 | HG01106.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.787+545C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036929 | ||||||
| chr5:1036946
|
GGGCAGTG others(117): Show |
G | 21 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0019others(18): Show | 25 | HG00597.hp1 HG01358.hp1 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.787+575_787+698del | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 1036946 | |||||
| chr5:1036950
|
AGT | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(119): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.787+570_787+571del others(2): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 1036950 | |||||
| chr5:1036977
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.787+593C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1036977 | ||||||
| chr5:1037003
|
GTGTGGAT others(9): Show |
G | 2 | a0001c0008t0023g0021a0001c0008t0024g0021 | 2 | HG01361.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.787+630_787+645del others(16): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 1037003 | |||||
| chr5:1037010
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(114): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.787+626T>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037010 | ||||||
| chr5:1037011
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(112): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.787+627G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037011 | ||||||
| chr5:1037015
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(114): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.787+631G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037015 | ||||||
| chr5:1037019
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(134): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.787+635A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037019 | ||||||
| chr5:1037032
|
G | C | 1 | a0001c0001t0008g0086 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.787+648G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037032 | ||||||
| chr5:1037046
|
C | T | 2 | a0004c0007t0006g0078a0004c0007t0006g0079 | 2 | HG01099.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.787+662C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037046 | ||||||
| chr5:1037049
|
C | T | 16 | a0001c0001t0005g0003a0001c0001t0005g0089a0001c0001t0005g0090others(13): Show | 19 | HG00438.hp2 HG01192.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.787+665C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037049 | ||||||
| chr5:1037083
|
A | G | 4 | a0001c0001t0003g0002a0001c0001t0003g0115a0001c0005t0011g0002others(1): Show | 7 | HG02809.hp2 HG03225.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.787+699A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037083 | ||||||
| chr5:1037146
|
G | C | 1 | a0004c0007t0006g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.788-659G>C | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037146 | ||||||
| chr5:1037234
|
G | T | 5 | a0001c0001t0008g0092a0001c0001t0008g0094a0001c0001t0019g0193others(2): Show | 5 | HG01928.hp2 HG02004.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.788-571G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037234 | ||||||
| chr5:1037324
|
C | T | 7 | a0001c0001t0007g0027a0001c0001t0007g0077a0001c0001t0007g0256others(4): Show | 8 | HG02523.hp2 HG02602.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.788-481C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037324 | ||||||
| chr5:1037338
|
C | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0201a0001c0001t0020g0202 | 4 | HG01257.hp1 HG01258.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.788-467C>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037338 | ||||||
| chr5:1037428
|
A | G | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.788-377A>G | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037428 | ||||||
| chr5:1037474
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.788-331G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037474 | ||||||
| chr5:1037508
|
C | T | 2 | a0001c0002t0003g0006a0001c0002t0003g0054 | 4 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-297C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037508 | ||||||
| chr5:1037583
|
G | T | 1 | a0001c0001t0002g0153 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.788-222G>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037583 | ||||||
| chr5:1037599
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.788-206G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037599 | ||||||
| chr5:1037739
|
G | A | 1 | a0001c0001t0004g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.788-66G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037739 | ||||||
| chr5:1037753
|
G | A | 1 | a0002c0003t0001g0034 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.788-52G>A | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037753 | ||||||
| chr5:1037773
|
C | T | 1 | a0009c0013t0017g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.788-32C>T | NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 9/9 | chr5 | 1037773 |