Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 22866 |
|---|---|
| ensemblid | ENSG00000149970.16 |
| hgncid | 19701 |
| symbol | CNKSR2 |
| name | connector enhancer of kinase suppressor of Ras 2 |
| refseq_nuc | NM_014927.5 |
| refseq_prot | NP_055742.2 |
| ensembl_nuc | ENST00000379510.5 |
| ensembl_prot | ENSP00000368824.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 21374418 |
| end | 21654689 |
| strand | + |
| ver | v1.2 |
| region | chrX:21374418-21654689 |
| region5000 | chrX:21369418-21659689 |
| regionname0 | CNKSR2_chrX_21374418_21654689 |
| regionname5000 | CNKSR2_chrX_21369418_21659689 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1034 | 161 | 40 | 29 | 67 | 5 | 18 | 52 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0002 | 0/0 | 1034 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0003 | 0/0 | 1034 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3105 | 148 | 36 | 26 | 61 | 5 | 18 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| c0002 | 0/0 | 3105 | 8 | 0 | 2 | 6 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| c0003 | 0/0 | 3105 | 3 | 3 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| c0004 | 0/0 | 3105 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| c0005 | 0/0 | 3105 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| c0006 | 0/0 | 3105 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| c0007 | 0/0 | 3105 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2650 | 48 | 3 | 8 | 25 | 3 | 9 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0002 | 0/0 | 2647 | 22 | 2 | 5 | 14 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0003 | 0/0 | 2650 | 13 | 5 | 1 | 5 | 0 | 2 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0004 | 0/1 | 2653 | 9 | 0 | 5 | 2 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0005 | 1/0 | 2649 | 7 | 0 | 0 | 6 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0006 | 0/0 | 2652 | 6 | 6 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0007 | 0/0 | 2651 | 5 | 1 | 0 | 4 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0008 | 0/0 | 2648 | 4 | 0 | 1 | 3 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0009 | 0/0 | 2646 | 4 | 4 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0010 | 0/0 | 2652 | 3 | 3 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0011 | 0/0 | 2649 | 3 | 3 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0012 | 0/0 | 2646 | 3 | 3 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0013 | 0/0 | 2653 | 2 | 0 | 1 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0014 | 0/0 | 2673 | 2 | 2 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0015 | 0/0 | 2654 | 2 | 0 | 1 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0016 | 0/0 | 2652 | 2 | 0 | 1 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0017 | 0/0 | 2649 | 2 | 0 | 2 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0018 | 0/0 | 2662 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0019 | 0/0 | 2664 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0020 | 0/0 | 2656 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0021 | 0/0 | 2656 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0022 | 0/0 | 2656 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0023 | 0/0 | 2662 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0024 | 0/0 | 2655 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0025 | 0/0 | 2652 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0026 | 0/0 | 2671 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0027 | 0/0 | 2652 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0028 | 0/0 | 2653 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0029 | 0/0 | 2651 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0030 | 0/0 | 2643 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0031 | 0/0 | 2652 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0032 | 0/0 | 2652 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0033 | 0/0 | 2650 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0034 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0035 | 0/0 | 2651 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0036 | 0/0 | 2649 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0037 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0038 | 0/0 | 2646 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0039 | 0/0 | 2646 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0040 | 0/0 | 2647 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0041 | 0/0 | 2646 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0042 | 0/0 | 2634 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| t0043 | 0/0 | 2628 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3105 | 148 | 36 | 26 | 61 | 5 | 18 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0002 | 0/0 | 3105 | 8 | 0 | 2 | 6 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0003 | 0/0 | 3105 | 3 | 3 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0006 | 0/0 | 3105 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0007 | 0/0 | 3105 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0002c0005 | 0/0 | 3105 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0003c0004 | 0/0 | 3105 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5754 | 43 | 3 | 6 | 22 | 3 | 9 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0002 | 0/0 | 5751 | 22 | 2 | 5 | 14 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0003 | 0/0 | 5754 | 12 | 4 | 1 | 5 | 0 | 2 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0004 | 0/1 | 5757 | 9 | 0 | 5 | 2 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0005 | 1/0 | 5753 | 6 | 0 | 0 | 5 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0006 | 0/0 | 5756 | 5 | 5 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0007 | 0/0 | 5755 | 3 | 1 | 0 | 2 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0008 | 0/0 | 5752 | 4 | 0 | 1 | 3 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0009 | 0/0 | 5750 | 4 | 4 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0010 | 0/0 | 5756 | 3 | 3 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0011 | 0/0 | 5753 | 3 | 3 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0012 | 0/0 | 5750 | 3 | 3 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0013 | 0/0 | 5757 | 2 | 0 | 1 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0015 | 0/0 | 5758 | 2 | 0 | 1 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0016 | 0/0 | 5756 | 2 | 0 | 1 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0017 | 0/0 | 5753 | 2 | 0 | 2 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0018 | 0/0 | 5766 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0019 | 0/0 | 5768 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0020 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0021 | 0/0 | 5760 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0022 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0023 | 0/0 | 5766 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0024 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0025 | 0/0 | 5756 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0027 | 0/0 | 5756 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0029 | 0/0 | 5755 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0030 | 0/0 | 5747 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0031 | 0/0 | 5756 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0032 | 0/0 | 5756 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0033 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0034 | 0/0 | 5755 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0035 | 0/0 | 5755 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0037 | 0/0 | 5755 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0038 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0039 | 0/0 | 5750 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0040 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0041 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0042 | 0/0 | 5738 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0001t0043 | 0/0 | 5732 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0002t0001 | 0/0 | 5754 | 5 | 0 | 2 | 3 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0002t0005 | 0/0 | 5753 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0002t0007 | 0/0 | 5755 | 2 | 0 | 0 | 2 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0003t0014 | 0/0 | 5777 | 2 | 2 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0003t0026 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0006t0028 | 0/0 | 5757 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0001c0007t0036 | 0/0 | 5753 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0002c0005t0003 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| a0003c0004t0006 | 0/0 | 5756 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | copy fasta | chrX | 21369418 | 21659689 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0004g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0005g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0007g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0008g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0008g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0009g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0010g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0011g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0012g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0012g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0013g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0013g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0015g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0015g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0016g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0016g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0017g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0017g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0018g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0019g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0020g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0021g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0022g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0023g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0024g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0025g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0027g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0029g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0030g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0031g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0032g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0033g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0034g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0035g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0037g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0038g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0039g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0040g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0041g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0042g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0001t0043g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0002t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0002t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0002t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0003t0014g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0003t0014g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0003t0026g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0006t0028g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0001c0007t0036g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0002c0005t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| a0003c0004t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0114 | EUR | GBR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | CHS | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0064 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0056 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01069 | hp1 | a0001 | c0001 | t0008 | g0005 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01071 | hp2 | a0001 | c0001 | t0017 | g0018 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01081 | hp1 | a0001 | c0007 | t0036 | g0026 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01099 | hp1 | a0001 | c0001 | t0029 | g0023 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01109 | hp1 | a0001 | c0001 | t0017 | g0146 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01167 | hp1 | a0001 | c0001 | t0013 | g0066 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01243 | hp1 | a0001 | c0001 | t0020 | g0141 | AMR | PUR | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0055 | AMR | CLM | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01358 | hp1 | a0001 | c0001 | t0018 | g0123 | AMR | CLM | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01884 | hp1 | a0003 | c0004 | t0006 | g0154 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01884 | hp2 | a0001 | c0001 | t0019 | g0014 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PEL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG01952 | hp1 | a0001 | c0001 | t0015 | g0098 | AMR | PEL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0117 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02027 | hp1 | a0001 | c0002 | t0007 | g0040 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02040 | hp1 | a0001 | c0001 | t0031 | g0065 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02055 | hp1 | a0001 | c0001 | t0022 | g0033 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02132 | hp1 | a0001 | c0001 | t0007 | g0022 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0045 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02300 | hp1 | a0001 | c0001 | t0016 | g0085 | AMR | PEL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02602 | hp1 | a0001 | c0001 | t0016 | g0032 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02615 | hp1 | a0001 | c0003 | t0014 | g0147 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02647 | hp1 | a0001 | c0001 | t0042 | g0008 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02735 | hp1 | a0001 | c0001 | t0034 | g0091 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0159 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02886 | hp2 | a0002 | c0005 | t0003 | g0030 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0140 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0155 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02965 | hp1 | a0001 | c0003 | t0026 | g0148 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0138 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03098 | hp1 | a0001 | c0001 | t0041 | g0009 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03139 | hp1 | a0001 | c0001 | t0012 | g0142 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0162 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0152 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0013 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03486 | hp2 | a0001 | c0001 | t0012 | g0025 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03491 | hp2 | a0001 | c0001 | t0043 | g0007 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03516 | hp2 | a0001 | c0006 | t0028 | g0059 | AFR | ESN | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0017 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03654 | hp1 | a0001 | c0001 | t0023 | g0006 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03688 | hp1 | a0001 | c0001 | t0015 | g0038 | SAS | STU | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | BEB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG04199 | hp1 | a0001 | c0001 | t0030 | g0086 | SAS | STU | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG04204 | hp1 | a0001 | c0001 | t0037 | g0092 | SAS | STU | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0016 | AFR | YRI | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | CHB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0099 | EAS | CHB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0063 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18967 | hp1 | a0001 | c0001 | t0035 | g0054 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18977 | hp1 | a0001 | c0002 | t0007 | g0041 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18986 | hp1 | a0001 | c0001 | t0008 | g0143 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19000 | hp1 | a0001 | c0001 | t0008 | g0135 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19006 | hp1 | a0001 | c0001 | t0033 | g0002 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19012 | hp1 | a0001 | c0001 | t0008 | g0124 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19043 | hp1 | a0001 | c0001 | t0040 | g0027 | AFR | LWK | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19055 | hp1 | a0001 | c0001 | t0039 | g0144 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19060 | hp1 | a0001 | c0001 | t0021 | g0088 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19062 | hp1 | a0001 | c0001 | t0025 | g0130 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19063 | hp1 | a0001 | c0001 | t0032 | g0163 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19072 | hp1 | a0001 | c0001 | t0007 | g0127 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19079 | hp1 | a0001 | c0002 | t0005 | g0106 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19240 | hp1 | a0001 | c0001 | t0038 | g0150 | AFR | YRI | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0153 | AFR | YRI | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0132 | EUR | TSI | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | GIH | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG02486 | hp1 | a0001 | c0001 | t0027 | g0034 | AFR | ACB | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| HG03471 | hp1 | a0001 | c0003 | t0014 | g0149 | AFR | MSL | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA18955 | hp1 | a0001 | c0001 | t0013 | g0100 | EAS | JPT | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | USA | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| NA20300 | hp2 | a0001 | c0001 | t0024 | g0156 | AFR | USA | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0057 | REF | REF | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0139 | REF | REF | CNKSR2_chrX_21369418_21659689 | CNKSR2 | chrX | 21369418 | 21659689 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:21609542
|
C | A | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2617C>A | p.Pro873Thr | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/22 | 3097/5753 | 2617/3105 | 873/1034 | chrX | 21609542 | ||
| chrX:21652399
|
G | A | 1 | a0002 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.2983G>A | p.Asp995Asn | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 3463/5753 | 2983/3105 | 995/1034 | chrX | 21652399 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:21470771
|
T | C | 1 | a0001c0003 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.525T>C | p.Cys175Cys | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/22 | 1005/5753 | 525/3105 | 175/1034 | chrX | 21470771 | ||
| chrX:21490548
|
A | G | 1 | a0001c0002 | 8 | HG01934.hp1 HG01943.hp1 HG02027.hp1 others(5): Show |
synonymous_variant | LOW | c.651A>G | p.Gln217Gln | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/22 | 1131/5753 | 651/3105 | 217/1034 | chrX | 21490548 | ||
| chrX:21652342
|
C | T | 1 | a0001c0007 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.2926C>T | p.Leu976Leu | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 3406/5753 | 2926/3105 | 976/1034 | chrX | 21652342 | ||
| chrX:21652512
|
G | A | 1 | a0001c0006 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.3096G>A | p.Thr1032Thr | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 3576/5753 | 3096/3105 | 1032/1034 | chrX | 21652512 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:21374594
|
G | GGCA | 3 | a0001c0001t0013a0001c0001t0024a0001c0001t0025 | 4 | HG01167.hp1 NA18955.hp1 NA19062.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-268_-266dupAGC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 265 | INFO_REALIGN_3_PRIME | chrX | 21374594 | ||||
| chrX:21374594
|
G | GGCAGCA | 3 | a0001c0001t0020a0001c0001t0021a0001c0001t0022 | 3 | HG01243.hp1 HG02055.hp1 NA19060.hp1 |
5_prime_UTR_variant | MODIFIER | c.-271_-266dupAGCAGC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 265 | INFO_REALIGN_3_PRIME | chrX | 21374594 | ||||
| chrX:21374594
|
G | GGCAGCAG others(5): Show |
1 | a0001c0001t0018 | 1 | HG01358.hp1 | 5_prime_UTR_variant | MODIFIER | c.-277_-266dupAGCAGC others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 265 | INFO_REALIGN_3_PRIME | chrX | 21374594 | ||||
| chrX:21374594
|
GGCA | G | 9 | a0001c0001t0002a0001c0001t0008a0001c0001t0009others(6): Show | 39 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(36): Show |
5_prime_UTR_variant | MODIFIER | c.-268_-266delAGC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 266 | INFO_REALIGN_3_PRIME | chrX | 21374594 | ||||
| chrX:21374594
|
GGCAGCAG others(8): Show |
G | 1 | a0001c0001t0042 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-280_-266delAGCAGC others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 266 | INFO_REALIGN_3_PRIME | chrX | 21374594 | ||||
| chrX:21374594
|
GGCAGCAG others(14): Show |
G | 1 | a0001c0001t0043 | 1 | HG03491.hp2 | 5_prime_UTR_variant | MODIFIER | c.-286_-266delAGCAGC others(15): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 266 | INFO_REALIGN_3_PRIME | chrX | 21374594 | ||||
| chrX:21374630
|
A | AGCAGCAG others(5): Show |
1 | a0001c0001t0019 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-266_-265insAGCAGC others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 265 | INFO_REALIGN_3_PRIME | chrX | 21374630 | ||||
| chrX:21374630
|
A | AGCAGCCG others(5): Show |
1 | a0001c0001t0023 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-266_-265insAGCCGC others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 265 | INFO_REALIGN_3_PRIME | chrX | 21374630 | ||||
| chrX:21374630
|
A | AGCC | 3 | a0001c0001t0004a0001c0001t0015a0001c0001t0016 | 13 | HG00609.hp1 HG00738.hp1 HG00741.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-252_-250dupGCC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 249 | INFO_REALIGN_3_PRIME | chrX | 21374630 | ||||
| chrX:21374630
|
A | AGCCGCAG others(14): Show |
2 | a0001c0003t0014a0001c0003t0026 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-263_-262insAGCAGC others(15): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 262 | INFO_REALIGN_3_PRIME | chrX | 21374630 | ||||
| chrX:21374630
|
A | C | 10 | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(7): Show | 25 | HG01081.hp1 HG01081.hp2 HG02280.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-268A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 268 | chrX | 21374630 | |||||
| chrX:21374633
|
C | A | 1 | a0001c0001t0020 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-265C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 265 | chrX | 21374633 | |||||
| chrX:21374772
|
G | A | 2 | a0001c0003t0014a0001c0003t0026 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-126G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/22 | 126 | chrX | 21374772 | |||||
| chrX:21652832
|
T | G | 1 | a0001c0001t0027 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*311T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 311 | chrX | 21652832 | |||||
| chrX:21652882
|
CA | C | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*365delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 365 | INFO_REALIGN_3_PRIME | chrX | 21652882 | ||||
| chrX:21652888
|
TA | T | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*370delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 370 | INFO_REALIGN_3_PRIME | chrX | 21652888 | ||||
| chrX:21652894
|
ACAT | A | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*374_*376delCAT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 374 | chrX | 21652894 | |||||
| chrX:21652906
|
G | GAATT | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*385_*386insAATT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 386 | chrX | 21652906 | |||||
| chrX:21652937
|
TA | T | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*419delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 419 | INFO_REALIGN_3_PRIME | chrX | 21652937 | ||||
| chrX:21652977
|
C | A | 1 | a0001c0001t0034 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*456C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 456 | chrX | 21652977 | |||||
| chrX:21652987
|
G | GCA | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*469_*470dupCA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 471 | INFO_REALIGN_3_PRIME | chrX | 21652987 | ||||
| chrX:21653041
|
G | GA | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*521dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 522 | INFO_REALIGN_3_PRIME | chrX | 21653041 | ||||
| chrX:21653134
|
T | TG | 1 | a0001c0001t0032 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*615dupG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 616 | INFO_REALIGN_3_PRIME | chrX | 21653134 | ||||
| chrX:21653202
|
T | TA | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*683dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 684 | INFO_REALIGN_3_PRIME | chrX | 21653202 | ||||
| chrX:21653236
|
AT | A | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*719delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 719 | INFO_REALIGN_3_PRIME | chrX | 21653236 | ||||
| chrX:21653273
|
A | ATGAGC | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*756_*757insCTGAG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 757 | INFO_REALIGN_3_PRIME | chrX | 21653273 | ||||
| chrX:21653316
|
TA | T | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*800delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 800 | INFO_REALIGN_3_PRIME | chrX | 21653316 | ||||
| chrX:21653355
|
C | CTA | 1 | a0001c0001t0031 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*847_*848dupTA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 849 | INFO_REALIGN_3_PRIME | chrX | 21653355 | ||||
| chrX:21653374
|
TCA | T | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*854_*855delCA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 854 | chrX | 21653374 | |||||
| chrX:21653389
|
G | GT | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 874 | INFO_REALIGN_3_PRIME | chrX | 21653389 | ||||
| chrX:21653445
|
TTC | T | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*925_*926delTC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 925 | chrX | 21653445 | |||||
| chrX:21653450
|
CT | C | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*931delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 931 | INFO_REALIGN_3_PRIME | chrX | 21653450 | ||||
| chrX:21653480
|
A | T | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*959A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 959 | chrX | 21653480 | |||||
| chrX:21653563
|
GA | G | 1 | a0001c0001t0039 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1047delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1047 | INFO_REALIGN_3_PRIME | chrX | 21653563 | ||||
| chrX:21653606
|
T | A | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1085T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1085 | chrX | 21653606 | |||||
| chrX:21653656
|
GT | G | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1142delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1142 | INFO_REALIGN_3_PRIME | chrX | 21653656 | ||||
| chrX:21653680
|
G | GT | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1161dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1162 | INFO_REALIGN_3_PRIME | chrX | 21653680 | ||||
| chrX:21653729
|
C | CA | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1209dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1210 | INFO_REALIGN_3_PRIME | chrX | 21653729 | ||||
| chrX:21653808
|
G | A | 1 | a0001c0001t0042 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1287G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1287 | chrX | 21653808 | |||||
| chrX:21653827
|
G | GT | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1313dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1314 | INFO_REALIGN_3_PRIME | chrX | 21653827 | ||||
| chrX:21653874
|
T | TA | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1357dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1358 | INFO_REALIGN_3_PRIME | chrX | 21653874 | ||||
| chrX:21653943
|
A | AG | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1423dupG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1424 | INFO_REALIGN_3_PRIME | chrX | 21653943 | ||||
| chrX:21654084
|
CCT | C | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1564_*1565delCT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1564 | chrX | 21654084 | |||||
| chrX:21654098
|
A | T | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1577A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1577 | chrX | 21654098 | |||||
| chrX:21654113
|
A | C | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1592A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1592 | chrX | 21654113 | |||||
| chrX:21654115
|
AT | A | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1597delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1597 | INFO_REALIGN_3_PRIME | chrX | 21654115 | ||||
| chrX:21654161
|
AT | A | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1644delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1644 | INFO_REALIGN_3_PRIME | chrX | 21654161 | ||||
| chrX:21654180
|
AT | A | 1 | a0001c0001t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1664delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1664 | INFO_REALIGN_3_PRIME | chrX | 21654180 | ||||
| chrX:21654269
|
A | ATG | 2 | a0001c0001t0034a0001c0001t0037 | 2 | HG02735.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1750_*1751dupGT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1752 | INFO_REALIGN_3_PRIME | chrX | 21654269 | ||||
| chrX:21654272
|
T | TA | 16 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | 103 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*1773dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1774 | INFO_REALIGN_3_PRIME | chrX | 21654272 | ||||
| chrX:21654272
|
T | TAA | 7 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(4): Show | 14 | HG01069.hp1 HG01952.hp1 HG02027.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1772_*1773dupAA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1774 | INFO_REALIGN_3_PRIME | chrX | 21654272 | ||||
| chrX:21654272
|
T | TAAA | 8 | a0001c0001t0006a0001c0001t0010a0001c0001t0017others(5): Show | 16 | HG01071.hp2 HG01109.hp1 HG01884.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1771_*1773dupAAA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1774 | INFO_REALIGN_3_PRIME | chrX | 21654272 | ||||
| chrX:21654272
|
T | TAAAA | 1 | a0001c0006t0028 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1770_*1773dupAAAA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1774 | INFO_REALIGN_3_PRIME | chrX | 21654272 | ||||
| chrX:21654272
|
TAAAAAA | T | 1 | a0001c0001t0030 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1768_*1773delAAAA others(2): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1768 | INFO_REALIGN_3_PRIME | chrX | 21654272 | ||||
| chrX:21654287
|
A | C | 3 | a0001c0001t0009a0001c0001t0041a0001c0001t0042 | 6 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1766A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1766 | chrX | 21654287 | |||||
| chrX:21654288
|
A | AAC | 1 | a0001c0001t0029 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1768_*1769insCA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1769 | INFO_REALIGN_3_PRIME | chrX | 21654288 | ||||
| chrX:21654288
|
A | C | 1 | a0001c0007t0036 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1767A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1767 | chrX | 21654288 | |||||
| chrX:21654289
|
A | AC | 1 | a0001c0001t0022 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1768_*1769insC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1769 | chrX | 21654289 | |||||
| chrX:21654295
|
C | A | 1 | a0001c0001t0025 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1774C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1774 | chrX | 21654295 | |||||
| chrX:21654296
|
A | C | 1 | a0001c0001t0025 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1775A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1775 | chrX | 21654296 | |||||
| chrX:21654502
|
TAA | T | 1 | a0001c0001t0038 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1983_*1984delAA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 22/22 | 1983 | INFO_REALIGN_3_PRIME | chrX | 21654502 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:21375025
|
A | AG | 1 | a0001c0001t0032g0163 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.64+69dupG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21375025 | |||||
| chrX:21375244
|
C | G | 12 | a0001c0001t0001g0158a0001c0001t0003g0151a0001c0001t0006g0155others(9): Show | 12 | HG01081.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+283C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21375244 | ||||||
| chrX:21375625
|
G | A | 1 | a0001c0001t0001g0001 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.64+664G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21375625 | ||||||
| chrX:21375918
|
C | T | 1 | a0001c0001t0038g0150 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.64+957C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21375918 | ||||||
| chrX:21376153
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+1192A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21376153 | ||||||
| chrX:21376234
|
A | AT | 1 | a0001c0001t0010g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+1281dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21376234 | |||||
| chrX:21376601
|
C | T | 1 | a0001c0001t0017g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.64+1640C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21376601 | ||||||
| chrX:21376778
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.64+1817A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21376778 | ||||||
| chrX:21377049
|
G | A | 1 | a0001c0001t0033g0002 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.64+2088G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21377049 | ||||||
| chrX:21377618
|
G | T | 2 | a0001c0001t0008g0143a0001c0001t0039g0144 | 2 | NA18986.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.64+2657G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21377618 | ||||||
| chrX:21377901
|
A | T | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+2940A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21377901 | ||||||
| chrX:21377911
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.64+2950G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21377911 | ||||||
| chrX:21378232
|
A | G | 2 | a0001c0001t0007g0140a0001c0001t0020g0141 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.64+3271A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21378232 | ||||||
| chrX:21378261
|
C | A | 2 | a0001c0001t0007g0140a0001c0001t0020g0141 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.64+3300C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21378261 | ||||||
| chrX:21378644
|
T | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0036others(159): Show | 162 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.64+3683T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21378644 | ||||||
| chrX:21379575
|
T | G | 2 | a0001c0001t0002g0004a0001c0001t0008g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.64+4614T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21379575 | ||||||
| chrX:21380310
|
C | T | 1 | a0001c0001t0011g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64+5349C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21380310 | ||||||
| chrX:21380443
|
C | CT | 5 | a0001c0001t0001g0137a0001c0001t0003g0136a0001c0001t0008g0135others(2): Show | 5 | HG03490.hp1 NA18965.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+5503dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21380443 | |||||
| chrX:21380443
|
CT | C | 31 | a0001c0001t0001g0158a0001c0001t0002g0004a0001c0001t0002g0019others(28): Show | 31 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.64+5503delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21380443 | |||||
| chrX:21380443
|
CTT | C | 15 | a0001c0001t0003g0015a0001c0001t0003g0151a0001c0001t0007g0140others(12): Show | 15 | HG01071.hp2 HG01081.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.64+5502_64+5503del others(2): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21380443 | |||||
| chrX:21380443
|
CTTT | C | 2 | a0001c0001t0023g0006a0001c0001t0043g0007 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.64+5501_64+5503del others(3): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21380443 | |||||
| chrX:21380634
|
C | G | 33 | a0001c0001t0001g0158a0001c0001t0003g0015a0001c0001t0003g0151others(30): Show | 33 | HG01071.hp2 HG01081.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.64+5673C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21380634 | ||||||
| chrX:21380722
|
A | C | 2 | a0001c0001t0001g0134a0001c0001t0003g0133 | 2 | HG02071.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.64+5761A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21380722 | ||||||
| chrX:21380739
|
C | T | 2 | a0001c0001t0004g0132a0001c0001t0016g0032 | 2 | HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.64+5778C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21380739 | ||||||
| chrX:21381138
|
G | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+6177G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21381138 | ||||||
| chrX:21381225
|
C | T | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64+6264C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21381225 | ||||||
| chrX:21381649
|
A | G | 2 | a0001c0001t0007g0140a0001c0001t0020g0141 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.64+6688A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21381649 | ||||||
| chrX:21381690
|
G | A | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.64+6729G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21381690 | ||||||
| chrX:21381910
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.64+6949C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21381910 | ||||||
| chrX:21382102
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.64+7141C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21382102 | ||||||
| chrX:21382859
|
C | G | 1 | a0001c0001t0025g0130 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.64+7898C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21382859 | ||||||
| chrX:21383652
|
C | T | 1 | a0001c0001t0004g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.64+8691C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21383652 | ||||||
| chrX:21384319
|
A | T | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.64+9358A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21384319 | ||||||
| chrX:21384626
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.64+9665A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21384626 | ||||||
| chrX:21385318
|
A | G | 1 | a0001c0001t0017g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.64+10357A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21385318 | ||||||
| chrX:21386018
|
C | CA | 32 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(29): Show | 32 | HG00621.hp1 HG00642.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.64+11081dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21386018 | |||||
| chrX:21386018
|
C | CAA | 2 | a0001c0001t0010g0152a0001c0001t0010g0153 | 2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.64+11080_64+11081d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21386018 | |||||
| chrX:21386018
|
CA | C | 9 | a0001c0001t0003g0015a0001c0001t0007g0127a0001c0001t0011g0016others(6): Show | 9 | HG02615.hp1 HG02717.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+11081delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21386018 | |||||
| chrX:21386428
|
T | C | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+11467T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21386428 | ||||||
| chrX:21386611
|
A | T | 2 | a0001c0001t0002g0125a0001c0001t0002g0126 | 2 | NA18943.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.64+11650A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21386611 | ||||||
| chrX:21386713
|
A | G | 1 | a0001c0001t0008g0124 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.64+11752A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21386713 | ||||||
| chrX:21386845
|
A | G | 2 | a0001c0001t0023g0006a0001c0001t0043g0007 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.64+11884A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21386845 | ||||||
| chrX:21387080
|
T | C | 2 | a0001c0001t0007g0140a0001c0001t0020g0141 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.64+12119T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21387080 | ||||||
| chrX:21387855
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0002g0126 | 2 | NA18943.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.64+12894C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21387855 | ||||||
| chrX:21387990
|
C | A | 1 | a0001c0001t0017g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.64+13029C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21387990 | ||||||
| chrX:21388086
|
A | G | 1 | a0001c0001t0018g0123 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.64+13125A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21388086 | ||||||
| chrX:21388338
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+13377A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21388338 | ||||||
| chrX:21388979
|
T | C | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.64+14018T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21388979 | ||||||
| chrX:21389119
|
C | T | 13 | a0001c0001t0001g0158a0001c0001t0006g0155a0001c0001t0006g0157others(10): Show | 13 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.64+14158C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21389119 | ||||||
| chrX:21389120
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.64+14159G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21389120 | ||||||
| chrX:21389258
|
C | T | 8 | a0001c0001t0002g0046a0001c0001t0002g0118a0001c0001t0002g0119others(5): Show | 8 | HG02083.hp1 NA18612.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+14297C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21389258 | ||||||
| chrX:21389721
|
A | G | 2 | a0001c0001t0003g0116a0001c0001t0004g0117 | 2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.64+14760A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21389721 | ||||||
| chrX:21390356
|
A | G | 1 | a0001c0001t0043g0007 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.64+15395A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21390356 | ||||||
| chrX:21390535
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+15574A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21390535 | ||||||
| chrX:21390688
|
C | T | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64+15727C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21390688 | ||||||
| chrX:21391166
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.64+16205A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391166 | ||||||
| chrX:21391470
|
C | G | 1 | a0001c0001t0006g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64+16509C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391470 | ||||||
| chrX:21391479
|
T | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+16518T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391479 | ||||||
| chrX:21391533
|
G | T | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+16572G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391533 | ||||||
| chrX:21391632
|
C | G | 3 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0162 | 3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.64+16671C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391632 | ||||||
| chrX:21391713
|
C | T | 1 | a0001c0001t0041g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.64+16752C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391713 | ||||||
| chrX:21391884
|
C | T | 1 | a0001c0001t0002g0115 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.64+16923C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21391884 | ||||||
| chrX:21392162
|
G | GT | 15 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(12): Show | 15 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+17202dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21392162 | |||||
| chrX:21392426
|
G | A | 3 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0138 | 3 | HG02717.hp1 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.64+17465G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21392426 | ||||||
| chrX:21392481
|
T | A | 15 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(12): Show | 15 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+17520T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21392481 | ||||||
| chrX:21392949
|
TC | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+17990delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21392949 | |||||
| chrX:21392968
|
T | C | 12 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(9): Show | 12 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+18007T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21392968 | ||||||
| chrX:21393074
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.64+18113T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21393074 | ||||||
| chrX:21393293
|
C | T | 1 | a0002c0005t0003g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.64+18332C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21393293 | ||||||
| chrX:21393507
|
C | A | 1 | a0001c0001t0004g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.64+18546C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21393507 | ||||||
| chrX:21393876
|
T | C | 5 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+18915T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21393876 | ||||||
| chrX:21394370
|
G | A | 4 | a0001c0001t0002g0047a0001c0001t0002g0049a0001c0001t0002g0050others(1): Show | 4 | NA18944.hp1 NA19000.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+19409G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21394370 | ||||||
| chrX:21394427
|
C | G | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64+19466C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21394427 | ||||||
| chrX:21394594
|
G | C | 15 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(12): Show | 15 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+19633G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21394594 | ||||||
| chrX:21394900
|
G | T | 69 | a0001c0001t0001g0158a0001c0001t0002g0003a0001c0001t0002g0004others(66): Show | 69 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.64+19939G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21394900 | ||||||
| chrX:21395319
|
A | G | 1 | a0001c0001t0003g0044 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.64+20358A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21395319 | ||||||
| chrX:21395413
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.64+20452G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21395413 | ||||||
| chrX:21396442
|
A | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+21481A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21396442 | ||||||
| chrX:21396457
|
A | C | 1 | a0001c0001t0002g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+21496A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21396457 | ||||||
| chrX:21396577
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.64+21616C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21396577 | ||||||
| chrX:21398302
|
C | T | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.64+23341C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21398302 | ||||||
| chrX:21398340
|
A | G | 8 | a0001c0002t0001g0042a0001c0002t0001g0104a0001c0002t0001g0105others(5): Show | 8 | HG01934.hp1 HG01943.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+23379A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21398340 | ||||||
| chrX:21398390
|
T | C | 2 | a0001c0001t0006g0155a0003c0004t0006g0154 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.64+23429T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21398390 | ||||||
| chrX:21398498
|
T | C | 2 | a0001c0001t0007g0140a0001c0001t0020g0141 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.64+23537T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21398498 | ||||||
| chrX:21399197
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+24236A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399197 | ||||||
| chrX:21399551
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+24590G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399551 | ||||||
| chrX:21399632
|
T | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+24671T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399632 | ||||||
| chrX:21399648
|
A | G | 15 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(12): Show | 15 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+24687A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399648 | ||||||
| chrX:21399685
|
T | C | 12 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(9): Show | 12 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+24724T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399685 | ||||||
| chrX:21399752
|
C | T | 2 | a0001c0001t0023g0006a0001c0001t0043g0007 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.64+24791C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399752 | ||||||
| chrX:21399983
|
T | C | 1 | a0001c0001t0002g0125 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.64+25022T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21399983 | ||||||
| chrX:21400142
|
A | G | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64+25181A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21400142 | ||||||
| chrX:21400469
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.64+25508A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21400469 | ||||||
| chrX:21400553
|
T | C | 41 | a0001c0001t0001g0158a0001c0001t0002g0028a0001c0001t0003g0015others(38): Show | 41 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.64+25592T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21400553 | ||||||
| chrX:21400631
|
G | A | 1 | a0002c0005t0003g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.64+25670G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21400631 | ||||||
| chrX:21401316
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.65-25181C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21401316 | ||||||
| chrX:21401536
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-24961C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21401536 | ||||||
| chrX:21401675
|
G | A | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.65-24822G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21401675 | ||||||
| chrX:21401840
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0052 | 2 | HG02056.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.65-24657G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21401840 | ||||||
| chrX:21401850
|
TTAAG | T | 1 | a0001c0001t0041g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.65-24645_65-24642d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21401850 | |||||
| chrX:21402190
|
A | C | 1 | a0001c0001t0011g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.65-24307A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21402190 | ||||||
| chrX:21402595
|
AAGAG | A | 2 | a0001c0001t0023g0006a0001c0001t0043g0007 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.65-23899_65-23896d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21402595 | |||||
| chrX:21402614
|
A | G | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.65-23883A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21402614 | ||||||
| chrX:21402626
|
T | G | 39 | a0001c0001t0001g0158a0001c0001t0002g0028a0001c0001t0003g0015others(36): Show | 39 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.65-23871T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21402626 | ||||||
| chrX:21402693
|
A | G | 1 | a0001c0001t0003g0101 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.65-23804A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21402693 | ||||||
| chrX:21403015
|
G | T | 47 | a0001c0001t0001g0158a0001c0001t0002g0004a0001c0001t0002g0019others(44): Show | 47 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.65-23482G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403015 | ||||||
| chrX:21403057
|
G | A | 12 | a0001c0001t0001g0158a0001c0001t0003g0151a0001c0001t0006g0155others(9): Show | 12 | HG01081.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.65-23440G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403057 | ||||||
| chrX:21403128
|
A | G | 70 | a0001c0001t0001g0158a0001c0001t0002g0003a0001c0001t0002g0004others(67): Show | 70 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.65-23369A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403128 | ||||||
| chrX:21403543
|
T | C | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.65-22954T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403543 | ||||||
| chrX:21403580
|
A | G | 19 | a0001c0001t0001g0158a0001c0001t0002g0028a0001c0001t0003g0024others(16): Show | 19 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.65-22917A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403580 | ||||||
| chrX:21403850
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.65-22647T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403850 | ||||||
| chrX:21403927
|
C | T | 1 | a0001c0001t0027g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.65-22570C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21403927 | ||||||
| chrX:21404789
|
C | CA | 23 | a0001c0001t0001g0036a0001c0001t0002g0028a0001c0001t0002g0110others(20): Show | 23 | HG00609.hp1 HG00741.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.65-21685dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21404789 | |||||
| chrX:21404789
|
CA | C | 5 | a0001c0001t0001g0137a0001c0001t0002g0019a0001c0001t0002g0047others(2): Show | 5 | HG01106.hp1 HG03490.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-21685delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21404789 | |||||
| chrX:21406148
|
G | A | 1 | a0001c0001t0001g0001 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.65-20349G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21406148 | ||||||
| chrX:21406420
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.65-20077T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21406420 | ||||||
| chrX:21406815
|
G | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.65-19682G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21406815 | ||||||
| chrX:21407002
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.65-19495T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21407002 | ||||||
| chrX:21407528
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.65-18969C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21407528 | ||||||
| chrX:21407555
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-18942G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21407555 | ||||||
| chrX:21407557
|
T | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-18940T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21407557 | ||||||
| chrX:21407558
|
GT | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-18934delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21407558 | |||||
| chrX:21407734
|
G | A | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.65-18763G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21407734 | ||||||
| chrX:21408471
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0036others(156): Show | 159 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.65-18026A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21408471 | ||||||
| chrX:21408759
|
G | GT | 2 | a0001c0001t0001g0060a0001c0006t0028g0059 | 2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.65-17729dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21408759 | |||||
| chrX:21408965
|
A | T | 1 | a0001c0001t0043g0007 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.65-17532A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21408965 | ||||||
| chrX:21409107
|
T | C | 1 | a0001c0001t0003g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.65-17390T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21409107 | ||||||
| chrX:21409226
|
AATTATAT others(4): Show |
A | 1 | a0001c0001t0038g0150 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.65-17268_65-17258d others(13): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409226 | |||||
| chrX:21409228
|
T | TTA | 1 | a0001c0001t0001g0062 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.65-17219_65-17218d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
T | TTATATA | 3 | a0001c0001t0002g0003a0001c0001t0022g0033a0001c0001t0043g0007 | 3 | HG00621.hp1 HG02055.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.65-17223_65-17218d others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
T | TTATATAT others(1): Show |
1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.65-17225_65-17218d others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
T | TTATATAT others(3): Show |
1 | a0001c0003t0014g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.65-17227_65-17218d others(12): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
TTA | T | 7 | a0001c0001t0002g0125a0001c0001t0004g0064a0001c0001t0005g0063others(4): Show | 7 | HG00738.hp1 HG01071.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-17219_65-17218d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
TTATA | T | 8 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0002g0110others(5): Show | 8 | HG00673.hp1 HG01192.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-17221_65-17218d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
TTATATA | T | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(6): Show | 9 | HG01167.hp1 HG02027.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-17223_65-17218d others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
TTATATAT others(1): Show |
T | 13 | a0001c0001t0001g0035a0001c0001t0001g0071a0001c0001t0002g0114others(10): Show | 13 | HG00140.hp1 HG01081.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-17225_65-17218d others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
TTATATAT others(3): Show |
T | 23 | a0001c0001t0001g0051a0001c0001t0001g0073a0001c0001t0001g0074others(20): Show | 23 | HG00609.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.65-17227_65-17218d others(12): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
TTATATAT others(5): Show |
T | 24 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0078others(21): Show | 24 | HG00280.hp1 HG00735.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.65-17229_65-17218d others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
TTATATAT others(7): Show |
T | 48 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0052others(45): Show | 48 | HG00642.hp1 HG01106.hp1 HG01261.hp1 others(45): Show |
intron_variant | MODIFIER | c.65-17231_65-17218d others(16): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
TTATATAT others(9): Show |
T | 12 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0003g0015others(9): Show | 12 | HG01243.hp1 HG02280.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-17233_65-17218d others(18): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
TTATATAT others(11): Show |
T | 4 | a0001c0001t0002g0126a0001c0001t0003g0031a0001c0001t0009g0011others(1): Show | 4 | HG02572.hp1 HG02809.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-17235_65-17218d others(20): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
TTATATAT others(13): Show |
T | 4 | a0001c0001t0002g0004a0001c0001t0005g0099a0001c0001t0008g0005others(1): Show | 4 | HG01069.hp1 HG01071.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-17237_65-17218d others(22): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409228
|
TTATATAT others(19): Show |
T | 2 | a0001c0001t0009g0013a0001c0001t0041g0009 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-17243_65-17218d others(28): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21409228 | |||||
| chrX:21409272
|
A | T | 1 | a0001c0001t0015g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.65-17225A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21409272 | ||||||
| chrX:21409389
|
G | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-17108G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21409389 | ||||||
| chrX:21409555
|
G | C | 2 | a0001c0001t0008g0143a0001c0001t0039g0144 | 2 | NA18986.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.65-16942G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21409555 | ||||||
| chrX:21410032
|
C | CTG | 34 | a0001c0001t0001g0134a0001c0001t0002g0003a0001c0001t0002g0046others(31): Show | 34 | HG00621.hp1 HG00741.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.65-16433_65-16432d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410032 | |||||
| chrX:21410032
|
C | CTGTG | 2 | a0001c0001t0011g0017a0001c0001t0042g0008 | 2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.65-16435_65-16432d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410032 | |||||
| chrX:21410032
|
CTG | C | 10 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0003g0024others(7): Show | 10 | HG01081.hp1 HG01106.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-16433_65-16432d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410032 | |||||
| chrX:21410032
|
CTGTG | C | 13 | a0001c0001t0001g0158a0001c0001t0006g0157a0001c0001t0006g0159others(10): Show | 13 | HG01109.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-16435_65-16432d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410032 | |||||
| chrX:21410046
|
G | GTGTT | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-16448_65-16447i others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410046 | |||||
| chrX:21410645
|
C | A | 3 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.65-15852C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21410645 | ||||||
| chrX:21410790
|
T | TTG | 7 | a0001c0001t0007g0140a0001c0001t0009g0010a0001c0001t0009g0011others(4): Show | 7 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-15681_65-15680d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410790 | |||||
| chrX:21410790
|
TTG | T | 4 | a0001c0001t0001g0069a0001c0003t0014g0147a0001c0003t0014g0149others(1): Show | 4 | HG02615.hp1 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-15681_65-15680d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410790 | |||||
| chrX:21410898
|
T | TTG | 1 | a0001c0001t0038g0150 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.65-15582_65-15581d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21410898 | |||||
| chrX:21410906
|
G | A | 1 | a0001c0001t0027g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.65-15591G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21410906 | ||||||
| chrX:21410964
|
A | G | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65-15533A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21410964 | ||||||
| chrX:21411032
|
ACTTTT | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-15459_65-15455d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21411032 | |||||
| chrX:21411253
|
A | G | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.65-15244A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21411253 | ||||||
| chrX:21411297
|
C | T | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.65-15200C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21411297 | ||||||
| chrX:21411330
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-15167G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21411330 | ||||||
| chrX:21411454
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-15043G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21411454 | ||||||
| chrX:21412034
|
C | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-14463C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21412034 | ||||||
| chrX:21412567
|
T | G | 1 | a0001c0001t0003g0101 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.65-13930T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21412567 | ||||||
| chrX:21412657
|
A | G | 1 | a0001c0001t0009g0012 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.65-13840A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21412657 | ||||||
| chrX:21414305
|
A | C | 1 | a0001c0001t0015g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.65-12192A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21414305 | ||||||
| chrX:21414419
|
A | AT | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(1): Show | 4 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-12067dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21414419 | |||||
| chrX:21414419
|
AT | A | 7 | a0001c0001t0013g0066a0001c0002t0001g0042a0001c0002t0001g0104others(4): Show | 7 | HG01167.hp1 HG01934.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-12067delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21414419 | |||||
| chrX:21414487
|
G | A | 2 | a0001c0001t0002g0004a0001c0001t0008g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.65-12010G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21414487 | ||||||
| chrX:21414548
|
C | G | 2 | a0001c0001t0023g0006a0001c0001t0043g0007 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.65-11949C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21414548 | ||||||
| chrX:21414603
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.65-11894T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21414603 | ||||||
| chrX:21414975
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0029g0023 | 2 | HG00735.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.65-11522C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21414975 | ||||||
| chrX:21415235
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-11262G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415235 | ||||||
| chrX:21415547
|
G | A | 1 | a0001c0001t0003g0024 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.65-10950G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415547 | ||||||
| chrX:21415596
|
C | T | 4 | a0001c0001t0001g0062a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | NA18948.hp1 NA18959.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-10901C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415596 | ||||||
| chrX:21415641
|
T | TG | 2 | a0001c0001t0004g0020a0001c0001t0029g0023 | 2 | HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.65-10850dupG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415641 | |||||
| chrX:21415648
|
A | AG | 1 | a0001c0001t0001g0039 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.65-10843dupG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415648 | |||||
| chrX:21415756
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.65-10741G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415756 | ||||||
| chrX:21415827
|
CAT | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0039others(7): Show | 10 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-10664_65-10663d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415827 | |||||
| chrX:21415831
|
TATAC | T | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.65-10664_65-10661d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415831 | |||||
| chrX:21415833
|
TAC | T | 76 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0048others(73): Show | 76 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.65-10626_65-10625d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415833 | |||||
| chrX:21415833
|
TACAC | T | 27 | a0001c0001t0001g0080a0001c0001t0001g0145a0001c0001t0001g0158others(24): Show | 27 | HG01081.hp1 HG01081.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.65-10628_65-10625d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415833 | |||||
| chrX:21415833
|
TACACAC | T | 8 | a0001c0001t0001g0076a0001c0001t0002g0111a0001c0001t0002g0112others(5): Show | 8 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-10630_65-10625d others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415833 | |||||
| chrX:21415833
|
TACACACA others(1): Show |
T | 16 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0046others(13): Show | 16 | HG00621.hp1 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.65-10632_65-10625d others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415833 | |||||
| chrX:21415833
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0007g0140a0001c0001t0020g0141 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.65-10634_65-10625d others(12): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415833 | |||||
| chrX:21415833
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0131 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.65-10638_65-10625d others(16): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415833 | |||||
| chrX:21415865
|
CACACACA others(1): Show |
C | 2 | a0001c0001t0008g0143a0001c0001t0039g0144 | 2 | NA18986.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.65-10630_65-10623d others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415865 | |||||
| chrX:21415867
|
C | T | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.65-10630C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415867 | ||||||
| chrX:21415869
|
C | T | 14 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(11): Show | 14 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-10628C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415869 | ||||||
| chrX:21415869
|
CACAT | C | 3 | a0001c0001t0004g0064a0001c0001t0022g0033a0001c0001t0027g0034 | 3 | HG00738.hp1 HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.65-10626_65-10623d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415869 | |||||
| chrX:21415871
|
C | T | 20 | a0001c0001t0003g0015a0001c0001t0003g0024a0001c0001t0003g0070others(17): Show | 20 | HG01071.hp2 HG01884.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.65-10626C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21415871 | ||||||
| chrX:21415871
|
CAT | C | 1 | a0001c0001t0001g0073 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.65-10611_65-10610d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21415871 | |||||
| chrX:21416854
|
C | CTTTG | 42 | a0001c0001t0001g0158a0001c0001t0002g0028a0001c0001t0003g0015others(39): Show | 42 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.65-9640_65-9639ins others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21416854 | |||||
| chrX:21416932
|
CTTATCTT others(2): Show |
C | 2 | a0001c0001t0001g0060a0001c0006t0028g0059 | 2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.65-9558_65-9550del others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21416932 | |||||
| chrX:21417056
|
A | G | 1 | a0001c0001t0006g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.65-9441A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21417056 | ||||||
| chrX:21417172
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.65-9325C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21417172 | ||||||
| chrX:21417706
|
T | C | 1 | a0001c0001t0005g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.65-8791T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21417706 | ||||||
| chrX:21418276
|
G | C | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.65-8221G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21418276 | ||||||
| chrX:21418562
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.65-7935A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21418562 | ||||||
| chrX:21418831
|
T | G | 1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.65-7666T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21418831 | ||||||
| chrX:21418938
|
A | G | 3 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.65-7559A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21418938 | ||||||
| chrX:21419623
|
G | A | 1 | a0001c0001t0004g0055 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.65-6874G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21419623 | ||||||
| chrX:21419757
|
A | G | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.65-6740A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21419757 | ||||||
| chrX:21420245
|
A | G | 1 | a0001c0001t0022g0033 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.65-6252A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21420245 | ||||||
| chrX:21420982
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-5515T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21420982 | ||||||
| chrX:21421287
|
G | GT | 2 | a0001c0001t0002g0115a0001c0001t0032g0163 | 2 | NA18974.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.65-5191dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21421287 | |||||
| chrX:21421287
|
G | GTTT | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65-5193_65-5191dup others(3): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21421287 | |||||
| chrX:21421287
|
GT | G | 10 | a0001c0001t0005g0079a0001c0001t0005g0095a0001c0001t0005g0099others(7): Show | 10 | HG01167.hp1 HG02300.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-5191delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21421287 | |||||
| chrX:21421287
|
GTT | G | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-5192_65-5191del others(2): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21421287 | |||||
| chrX:21421431
|
G | T | 4 | a0001c0001t0022g0033a0001c0003t0014g0147a0001c0003t0014g0149others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-5066G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21421431 | ||||||
| chrX:21421812
|
G | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-4685G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21421812 | ||||||
| chrX:21422091
|
C | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-4406C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21422091 | ||||||
| chrX:21422504
|
A | G | 1 | a0001c0001t0022g0033 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.65-3993A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21422504 | ||||||
| chrX:21422706
|
TC | T | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.65-3788delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21422706 | |||||
| chrX:21423189
|
A | C | 1 | a0001c0002t0005g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.65-3308A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21423189 | ||||||
| chrX:21423229
|
A | G | 1 | a0001c0001t0016g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.65-3268A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21423229 | ||||||
| chrX:21423368
|
A | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-3129A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21423368 | ||||||
| chrX:21423723
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0096a0001c0001t0030g0086 | 3 | HG02698.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.65-2774T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21423723 | ||||||
| chrX:21423897
|
T | G | 4 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148others(1): Show | 4 | HG02615.hp1 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-2600T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21423897 | ||||||
| chrX:21424152
|
A | G | 2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | NA18984.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.65-2345A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21424152 | ||||||
| chrX:21424168
|
T | C | 7 | a0001c0001t0007g0140a0001c0001t0020g0141a0001c0001t0042g0008others(4): Show | 7 | HG01243.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-2329T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21424168 | ||||||
| chrX:21424401
|
C | T | 2 | a0001c0001t0007g0140a0001c0001t0020g0141 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.65-2096C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21424401 | ||||||
| chrX:21424482
|
C | G | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.65-2015C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21424482 | ||||||
| chrX:21424805
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.65-1692T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21424805 | ||||||
| chrX:21424877
|
A | G | 1 | a0001c0001t0015g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.65-1620A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21424877 | ||||||
| chrX:21425106
|
ACT | A | 1 | a0001c0001t0003g0136 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.65-1381_65-1380del others(2): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 21425106 | |||||
| chrX:21425121
|
C | G | 5 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-1376C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21425121 | ||||||
| chrX:21425747
|
A | G | 1 | a0001c0001t0031g0065 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.65-750A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21425747 | ||||||
| chrX:21425934
|
A | G | 5 | a0001c0001t0020g0141a0001c0003t0014g0147a0001c0003t0014g0149others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-563A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21425934 | ||||||
| chrX:21426336
|
C | G | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.65-161C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21426336 | ||||||
| chrX:21426358
|
C | T | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-139C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 1/21 | chrX | 21426358 | ||||||
| chrX:21426730
|
TCTC | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | NA18948.hp1 NA18982.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.228+74_228+76delCT others(1): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 21426730 | |||||
| chrX:21426734
|
C | T | 69 | a0001c0001t0001g0158a0001c0001t0002g0004a0001c0001t0002g0019others(66): Show | 69 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.228+74C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21426734 | ||||||
| chrX:21426747
|
C | T | 36 | a0001c0001t0001g0158a0001c0001t0002g0028a0001c0001t0003g0015others(33): Show | 36 | HG01071.hp2 HG01081.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.228+87C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21426747 | ||||||
| chrX:21426772
|
T | C | 37 | a0001c0001t0001g0158a0001c0001t0002g0028a0001c0001t0003g0015others(34): Show | 37 | HG01071.hp2 HG01081.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.228+112T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21426772 | ||||||
| chrX:21427080
|
A | T | 1 | a0001c0001t0002g0003 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.228+420A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21427080 | ||||||
| chrX:21427195
|
T | G | 2 | a0001c0001t0003g0061a0001c0001t0025g0130 | 2 | NA18970.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.228+535T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21427195 | ||||||
| chrX:21427273
|
A | G | 1 | a0001c0001t0031g0065 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.228+613A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21427273 | ||||||
| chrX:21427297
|
A | G | 2 | a0001c0001t0023g0006a0001c0001t0043g0007 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.228+637A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21427297 | ||||||
| chrX:21427601
|
C | T | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.228+941C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21427601 | ||||||
| chrX:21427881
|
A | G | 9 | a0001c0001t0002g0028a0001c0001t0003g0024a0001c0001t0003g0029others(6): Show | 9 | HG01081.hp1 HG01109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.228+1221A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21427881 | ||||||
| chrX:21428209
|
A | G | 1 | a0001c0001t0004g0057 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.228+1549A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21428209 | ||||||
| chrX:21428532
|
A | G | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.228+1872A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21428532 | ||||||
| chrX:21428578
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.228+1918A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21428578 | ||||||
| chrX:21428926
|
T | C | 1 | a0001c0001t0023g0006 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.228+2266T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21428926 | ||||||
| chrX:21429349
|
A | G | 2 | a0001c0001t0001g0134a0001c0001t0003g0133 | 2 | HG02071.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.228+2689A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21429349 | ||||||
| chrX:21429813
|
G | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.229-2799G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21429813 | ||||||
| chrX:21429990
|
G | T | 1 | a0001c0001t0001g0075 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.229-2622G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21429990 | ||||||
| chrX:21430030
|
A | T | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.229-2582A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21430030 | ||||||
| chrX:21430426
|
T | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.229-2186T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21430426 | ||||||
| chrX:21430639
|
A | G | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.229-1973A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21430639 | ||||||
| chrX:21431172
|
T | C | 4 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148others(1): Show | 4 | HG02615.hp1 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-1440T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21431172 | ||||||
| chrX:21431687
|
C | T | 12 | a0001c0001t0001g0039a0001c0001t0001g0082a0001c0001t0001g0083others(9): Show | 12 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.229-925C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21431687 | ||||||
| chrX:21431696
|
A | T | 1 | a0001c0001t0013g0066 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.229-916A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21431696 | ||||||
| chrX:21432337
|
A | C | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.229-275A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21432337 | ||||||
| chrX:21432472
|
G | A | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.229-140G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 2/21 | chrX | 21432472 | ||||||
| chrX:21432909
|
G | A | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.431+95G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21432909 | ||||||
| chrX:21433077
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.431+263G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21433077 | ||||||
| chrX:21433550
|
C | T | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.431+736C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21433550 | ||||||
| chrX:21433653
|
T | TAC | 13 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0075others(10): Show | 13 | HG01071.hp2 HG01074.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.431+880_431+881dup others(2): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | |||||
| chrX:21433653
|
T | TACAC | 3 | a0001c0001t0001g0062a0001c0001t0019g0014a0001c0001t0041g0009 | 3 | HG01884.hp2 HG03098.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.431+878_431+881dup others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | |||||
| chrX:21433653
|
T | TACACAC | 2 | a0001c0001t0001g0076a0001c0001t0009g0013 | 2 | HG03486.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.431+876_431+881dup others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | |||||
| chrX:21433653
|
T | TACACACA others(1): Show |
1 | a0001c0001t0009g0012 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.431+874_431+881dup others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | |||||
| chrX:21433653
|
T | TACACACA others(3): Show |
2 | a0001c0001t0009g0011a0001c0001t0042g0008 | 2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.431+872_431+881dup others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | |||||
| chrX:21433653
|
TAC | T | 16 | a0001c0001t0001g0060a0001c0001t0001g0071a0001c0001t0001g0077others(13): Show | 16 | HG00735.hp2 HG01081.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.431+880_431+881del others(2): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | |||||
| chrX:21433653
|
TACAC | T | 6 | a0001c0001t0001g0053a0001c0001t0002g0118a0001c0001t0002g0119others(3): Show | 6 | HG00280.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+878_431+881del others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | |||||
| chrX:21433653
|
TACACAC | T | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.431+876_431+881del others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21433653 | |||||
| chrX:21434139
|
G | A | 69 | a0001c0001t0001g0158a0001c0001t0002g0003a0001c0001t0002g0004others(66): Show | 69 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.431+1325G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21434139 | ||||||
| chrX:21434183
|
C | T | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.431+1369C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21434183 | ||||||
| chrX:21434634
|
T | G | 9 | a0001c0001t0002g0028a0001c0001t0003g0024a0001c0001t0003g0029others(6): Show | 9 | HG01081.hp1 HG01109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.431+1820T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21434634 | ||||||
| chrX:21435382
|
T | A | 5 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.431+2568T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21435382 | ||||||
| chrX:21435743
|
T | C | 1 | a0001c0001t0002g0050 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.431+2929T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21435743 | ||||||
| chrX:21436044
|
C | A | 4 | a0001c0001t0042g0008a0001c0003t0014g0147a0001c0003t0014g0149others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+3230C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21436044 | ||||||
| chrX:21436171
|
C | T | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.431+3357C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21436171 | ||||||
| chrX:21436358
|
A | G | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.431+3544A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21436358 | ||||||
| chrX:21436558
|
T | C | 1 | a0001c0001t0023g0006 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.431+3744T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21436558 | ||||||
| chrX:21437392
|
C | G | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.432-3302C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21437392 | ||||||
| chrX:21437419
|
G | GT | 17 | a0001c0001t0001g0081a0001c0001t0001g0109a0001c0001t0001g0158others(14): Show | 17 | HG00621.hp1 HG00738.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.432-3255dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21437419 | |||||
| chrX:21437419
|
G | GTT | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.432-3256_432-3255d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21437419 | |||||
| chrX:21437419
|
GT | G | 8 | a0001c0001t0001g0071a0001c0001t0003g0116a0001c0001t0004g0117others(5): Show | 8 | HG02015.hp1 HG02886.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.432-3255delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21437419 | |||||
| chrX:21437551
|
C | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-3143C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21437551 | ||||||
| chrX:21437609
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.432-3085G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21437609 | ||||||
| chrX:21437715
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.432-2979G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21437715 | ||||||
| chrX:21437751
|
G | T | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.432-2943G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21437751 | ||||||
| chrX:21438097
|
T | A | 1 | a0001c0001t0035g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2597T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438097 | ||||||
| chrX:21438098
|
G | C | 1 | a0001c0001t0035g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2596G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438098 | ||||||
| chrX:21438100
|
T | C | 1 | a0001c0001t0035g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2594T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438100 | ||||||
| chrX:21438101
|
A | T | 1 | a0001c0001t0035g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2593A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438101 | ||||||
| chrX:21438102
|
AG | A | 1 | a0001c0001t0035g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2590delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21438102 | |||||
| chrX:21438107
|
T | C | 1 | a0001c0001t0035g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2587T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438107 | ||||||
| chrX:21438108
|
G | GC | 1 | a0001c0001t0035g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2586_432-2585i others(3): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438108 | ||||||
| chrX:21438110
|
C | T | 1 | a0001c0001t0035g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2584C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438110 | ||||||
| chrX:21438111
|
A | G | 1 | a0001c0001t0035g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2583A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438111 | ||||||
| chrX:21438112
|
A | T | 1 | a0001c0001t0035g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.432-2582A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438112 | ||||||
| chrX:21438338
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.432-2356A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438338 | ||||||
| chrX:21438426
|
G | C | 1 | a0001c0001t0007g0022 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.432-2268G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438426 | ||||||
| chrX:21438580
|
T | G | 1 | a0001c0001t0002g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.432-2114T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438580 | ||||||
| chrX:21438806
|
CAT | C | 1 | a0001c0003t0014g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.432-1885_432-1884d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 21438806 | |||||
| chrX:21438860
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-1834G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438860 | ||||||
| chrX:21438862
|
G | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-1832G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438862 | ||||||
| chrX:21438919
|
A | G | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.432-1775A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21438919 | ||||||
| chrX:21439416
|
C | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-1278C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439416 | ||||||
| chrX:21439544
|
C | T | 1 | a0001c0001t0002g0121 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.432-1150C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439544 | ||||||
| chrX:21439554
|
A | C | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.432-1140A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439554 | ||||||
| chrX:21439616
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.432-1078A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439616 | ||||||
| chrX:21439633
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-1061A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439633 | ||||||
| chrX:21439702
|
C | T | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.432-992C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439702 | ||||||
| chrX:21439748
|
A | G | 1 | a0001c0001t0003g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.432-946A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439748 | ||||||
| chrX:21439952
|
A | C | 1 | a0001c0001t0008g0124 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.432-742A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21439952 | ||||||
| chrX:21440277
|
A | G | 17 | a0001c0001t0003g0015a0001c0001t0003g0024a0001c0001t0009g0010others(14): Show | 17 | HG01071.hp2 HG01081.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.432-417A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21440277 | ||||||
| chrX:21440371
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.432-323G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21440371 | ||||||
| chrX:21440575
|
G | C | 1 | a0001c0001t0016g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.432-119G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 3/21 | chrX | 21440575 | ||||||
| chrX:21440846
|
T | A | 1 | a0001c0001t0025g0130 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.519+65T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21440846 | ||||||
| chrX:21441035
|
G | T | 1 | a0001c0002t0001g0105 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.519+254G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21441035 | ||||||
| chrX:21441037
|
T | G | 1 | a0001c0001t0011g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.519+256T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21441037 | ||||||
| chrX:21441172
|
A | G | 1 | a0001c0001t0003g0029 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.519+391A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21441172 | ||||||
| chrX:21441568
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0002g0003a0001c0001t0002g0046others(19): Show | 22 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.519+787C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21441568 | ||||||
| chrX:21441765
|
A | G | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.519+984A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21441765 | ||||||
| chrX:21441928
|
A | T | 1 | a0001c0001t0003g0101 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.519+1147A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21441928 | ||||||
| chrX:21442223
|
C | T | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+1442C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21442223 | ||||||
| chrX:21442256
|
TGA | T | 1 | a0001c0001t0001g0131 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.519+1476_519+1477d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21442256 | ||||||
| chrX:21442257
|
G | GA | 1 | a0001c0001t0006g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.519+1487dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21442257 | |||||
| chrX:21442257
|
GA | G | 2 | a0001c0001t0006g0160a0001c0001t0007g0127 | 2 | HG02615.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.519+1487delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21442257 | |||||
| chrX:21442425
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | NA18948.hp1 NA18982.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.519+1644C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21442425 | ||||||
| chrX:21442501
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+1720C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21442501 | ||||||
| chrX:21442643
|
G | T | 1 | a0001c0001t0043g0007 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.519+1862G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21442643 | ||||||
| chrX:21442684
|
T | G | 7 | a0001c0001t0001g0039a0001c0001t0001g0078a0001c0001t0001g0081others(4): Show | 7 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+1903T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21442684 | ||||||
| chrX:21442895
|
A | G | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.519+2114A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21442895 | ||||||
| chrX:21443583
|
C | T | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.519+2802C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21443583 | ||||||
| chrX:21443765
|
C | A | 1 | a0001c0001t0043g0007 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.519+2984C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21443765 | ||||||
| chrX:21444301
|
T | C | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.519+3520T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21444301 | ||||||
| chrX:21444759
|
A | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.519+3978A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21444759 | ||||||
| chrX:21444762
|
TA | T | 5 | a0001c0001t0002g0004a0001c0001t0008g0005a0001c0001t0012g0045others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+3995delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21444762 | |||||
| chrX:21445038
|
A | G | 1 | a0001c0001t0023g0006 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.519+4257A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445038 | ||||||
| chrX:21445148
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+4367G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445148 | ||||||
| chrX:21445413
|
C | T | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+4632C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445413 | ||||||
| chrX:21445527
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.519+4746T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445527 | ||||||
| chrX:21445635
|
A | G | 13 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(10): Show | 13 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.519+4854A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445635 | ||||||
| chrX:21445676
|
G | A | 2 | a0001c0001t0002g0004a0001c0001t0008g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.519+4895G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445676 | ||||||
| chrX:21445772
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.519+4991T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21445772 | ||||||
| chrX:21446240
|
A | G | 3 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0162 | 3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.519+5459A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21446240 | ||||||
| chrX:21446305
|
CA | C | 1 | a0001c0001t0001g0060 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.519+5528delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21446305 | |||||
| chrX:21446423
|
A | G | 1 | a0001c0001t0024g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.519+5642A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21446423 | ||||||
| chrX:21446610
|
T | A | 2 | a0001c0001t0002g0004a0001c0001t0008g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.519+5829T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21446610 | ||||||
| chrX:21446619
|
A | T | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+5838A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21446619 | ||||||
| chrX:21446690
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+5909G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21446690 | ||||||
| chrX:21446901
|
T | C | 1 | a0001c0001t0008g0135 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.519+6120T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21446901 | ||||||
| chrX:21447201
|
G | T | 3 | a0001c0001t0001g0068a0001c0001t0031g0065a0001c0001t0033g0002 | 3 | HG02040.hp1 NA18989.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.519+6420G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21447201 | ||||||
| chrX:21448395
|
C | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+7614C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21448395 | ||||||
| chrX:21448857
|
A | T | 1 | a0001c0001t0031g0065 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.519+8076A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21448857 | ||||||
| chrX:21449158
|
G | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+8377G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21449158 | ||||||
| chrX:21449303
|
C | CA | 7 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0082others(4): Show | 7 | HG01928.hp1 HG01934.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+8541dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21449303 | |||||
| chrX:21449303
|
CA | C | 57 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0002g0003others(54): Show | 57 | HG00140.hp1 HG00621.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.519+8541delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21449303 | |||||
| chrX:21449303
|
CAA | C | 3 | a0001c0001t0003g0151a0001c0001t0011g0017a0001c0007t0036g0026 | 3 | HG01081.hp1 HG01081.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.519+8540_519+8541d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21449303 | |||||
| chrX:21449841
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+9060C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21449841 | ||||||
| chrX:21450033
|
C | T | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.519+9252C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21450033 | ||||||
| chrX:21450065
|
C | CTG | 8 | a0001c0001t0003g0015a0001c0001t0003g0024a0001c0001t0003g0029others(5): Show | 8 | HG01081.hp1 HG02280.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+9303_519+9304d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21450065 | |||||
| chrX:21450065
|
CTG | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+9303_519+9304d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21450065 | |||||
| chrX:21450180
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.519+9399G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21450180 | ||||||
| chrX:21450717
|
G | A | 1 | a0001c0001t0027g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.519+9936G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21450717 | ||||||
| chrX:21450726
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.519+9945C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21450726 | ||||||
| chrX:21451381
|
A | G | 2 | a0001c0001t0006g0155a0003c0004t0006g0154 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.519+10600A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21451381 | ||||||
| chrX:21451703
|
T | TG | 1 | a0001c0001t0001g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.519+10928dupG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21451703 | |||||
| chrX:21451710
|
A | AG | 1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.519+10935dupG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21451710 | |||||
| chrX:21451754
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.519+10973C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21451754 | ||||||
| chrX:21451795
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.519+11014G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21451795 | ||||||
| chrX:21451874
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+11093G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21451874 | ||||||
| chrX:21451917
|
C | A | 1 | a0001c0001t0002g0046 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.519+11136C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21451917 | ||||||
| chrX:21452157
|
C | A | 1 | a0001c0001t0003g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.519+11376C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452157 | ||||||
| chrX:21452264
|
G | T | 33 | a0001c0001t0001g0158a0001c0001t0003g0015a0001c0001t0003g0151others(30): Show | 33 | HG01071.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.519+11483G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452264 | ||||||
| chrX:21452282
|
C | T | 1 | a0001c0001t0004g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.519+11501C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452282 | ||||||
| chrX:21452283
|
G | A | 1 | a0001c0001t0030g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.519+11502G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452283 | ||||||
| chrX:21452290
|
C | T | 1 | a0001c0001t0043g0007 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.519+11509C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452290 | ||||||
| chrX:21452300
|
A | T | 1 | a0001c0001t0002g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.519+11519A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452300 | ||||||
| chrX:21452306
|
T | C | 16 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(13): Show | 16 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.519+11525T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452306 | ||||||
| chrX:21452363
|
AT | A | 1 | a0001c0001t0003g0029 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.519+11584delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452363 | |||||
| chrX:21452372
|
A | G | 1 | a0001c0001t0031g0065 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.519+11591A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452372 | ||||||
| chrX:21452578
|
C | T | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.519+11797C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452578 | ||||||
| chrX:21452702
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+11921G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452702 | ||||||
| chrX:21452753
|
C | CTTATT | 22 | a0001c0001t0001g0071a0001c0001t0001g0074a0001c0001t0001g0158others(19): Show | 22 | HG00735.hp1 HG01433.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.519+12035_519+1203 others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | |||||
| chrX:21452753
|
C | CTTATTTT others(3): Show |
6 | a0001c0001t0001g0036a0001c0001t0002g0019a0001c0001t0002g0111others(3): Show | 6 | HG00140.hp1 HG00741.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+12030_519+1203 others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | |||||
| chrX:21452753
|
C | CTTATTTT others(8): Show |
1 | a0001c0001t0006g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.519+12025_519+1203 others(19): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | |||||
| chrX:21452753
|
C | CTTATTTT others(13): Show |
1 | a0001c0001t0017g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.519+12020_519+1203 others(24): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | |||||
| chrX:21452753
|
CTTATT | C | 27 | a0001c0001t0001g0073a0001c0001t0001g0102a0001c0001t0001g0103others(24): Show | 27 | HG00609.hp1 HG01071.hp2 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.519+12035_519+1203 others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | |||||
| chrX:21452753
|
CTTATTTT others(3): Show |
C | 13 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0053others(10): Show | 13 | HG00280.hp1 HG00673.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.519+12030_519+1203 others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | |||||
| chrX:21452753
|
CTTATTTT others(8): Show |
C | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+12025_519+1203 others(19): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | |||||
| chrX:21452753
|
CTTATTTT others(13): Show |
C | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0033g0002 | 3 | NA18989.hp1 NA19006.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.519+12020_519+1203 others(24): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452753 | |||||
| chrX:21452756
|
A | ATTTTATT others(15): Show |
3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+11978_519+1199 others(26): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21452756 | |||||
| chrX:21452830
|
A | C | 1 | a0001c0001t0004g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.519+12049A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21452830 | ||||||
| chrX:21453137
|
G | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+12356G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21453137 | ||||||
| chrX:21453137
|
GA | G | 1 | a0001c0001t0001g0051 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.519+12357delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21453137 | ||||||
| chrX:21453394
|
TA | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0078a0001c0001t0001g0081others(4): Show | 7 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+12615delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21453394 | |||||
| chrX:21453693
|
T | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+12912T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21453693 | ||||||
| chrX:21453859
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+13078G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21453859 | ||||||
| chrX:21453860
|
G | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519+13079G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21453860 | ||||||
| chrX:21454415
|
A | G | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.519+13634A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21454415 | ||||||
| chrX:21454469
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.519+13688C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21454469 | ||||||
| chrX:21454785
|
C | T | 2 | a0001c0001t0003g0116a0001c0001t0004g0117 | 2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.519+14004C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21454785 | ||||||
| chrX:21454884
|
G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+14103G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21454884 | ||||||
| chrX:21455403
|
G | C | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.519+14622G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21455403 | ||||||
| chrX:21456017
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-14749C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21456017 | ||||||
| chrX:21456025
|
A | C | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.520-14741A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21456025 | ||||||
| chrX:21456361
|
T | C | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.520-14405T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21456361 | ||||||
| chrX:21456685
|
G | C | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.520-14081G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21456685 | ||||||
| chrX:21456965
|
G | A | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.520-13801G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21456965 | ||||||
| chrX:21456968
|
A | G | 2 | a0001c0001t0007g0140a0001c0001t0020g0141 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.520-13798A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21456968 | ||||||
| chrX:21456977
|
A | AT | 1 | a0001c0001t0001g0036 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.520-13783dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21456977 | |||||
| chrX:21457110
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-13656T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21457110 | ||||||
| chrX:21457247
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.520-13519G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21457247 | ||||||
| chrX:21457508
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-13258T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21457508 | ||||||
| chrX:21457658
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-13108T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21457658 | ||||||
| chrX:21457925
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.520-12841A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21457925 | ||||||
| chrX:21458010
|
G | A | 1 | a0001c0001t0002g0126 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.520-12756G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21458010 | ||||||
| chrX:21458215
|
A | G | 3 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0138 | 3 | HG02717.hp1 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.520-12551A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21458215 | ||||||
| chrX:21458426
|
G | T | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.520-12340G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21458426 | ||||||
| chrX:21459018
|
C | CT | 8 | a0001c0001t0009g0010a0001c0001t0009g0012a0001c0001t0009g0013others(5): Show | 8 | HG01358.hp1 HG01884.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.520-11727dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21459018 | |||||
| chrX:21459018
|
C | CTTT | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-11729_520-1172 others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21459018 | |||||
| chrX:21459018
|
CT | C | 8 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0090others(5): Show | 8 | HG02015.hp1 NA18960.hp1 NA19005.hp1 others(5): Show |
intron_variant | MODIFIER | c.520-11727delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21459018 | |||||
| chrX:21459108
|
C | T | 1 | a0001c0001t0029g0023 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.520-11658C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459108 | ||||||
| chrX:21459182
|
C | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-11584C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459182 | ||||||
| chrX:21459213
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-11553A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459213 | ||||||
| chrX:21459244
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.520-11522G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459244 | ||||||
| chrX:21459375
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.520-11391G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459375 | ||||||
| chrX:21459523
|
G | T | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-11243G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459523 | ||||||
| chrX:21459541
|
G | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0110a0001c0001t0008g0124 | 3 | HG00621.hp1 HG02074.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.520-11225G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21459541 | ||||||
| chrX:21460540
|
C | T | 67 | a0001c0001t0001g0158a0001c0001t0002g0003a0001c0001t0002g0004others(64): Show | 67 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.520-10226C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21460540 | ||||||
| chrX:21460672
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-10094C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21460672 | ||||||
| chrX:21460865
|
A | G | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.520-9901A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21460865 | ||||||
| chrX:21461074
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0036others(159): Show | 162 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.520-9692A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21461074 | ||||||
| chrX:21461233
|
G | A | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-9533G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21461233 | ||||||
| chrX:21461478
|
T | G | 2 | a0001c0001t0007g0140a0001c0001t0020g0141 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.520-9288T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21461478 | ||||||
| chrX:21461490
|
C | G | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-9276C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21461490 | ||||||
| chrX:21461699
|
A | G | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.520-9067A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21461699 | ||||||
| chrX:21461938
|
A | G | 1 | a0001c0001t0023g0006 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.520-8828A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21461938 | ||||||
| chrX:21462121
|
G | T | 1 | a0001c0001t0002g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.520-8645G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21462121 | ||||||
| chrX:21462211
|
A | G | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.520-8555A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21462211 | ||||||
| chrX:21462714
|
A | AT | 42 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0158others(39): Show | 42 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.520-8035dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21462714 | |||||
| chrX:21462714
|
AT | A | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.520-8035delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21462714 | |||||
| chrX:21462881
|
T | G | 3 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.520-7885T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21462881 | ||||||
| chrX:21462969
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-7797G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21462969 | ||||||
| chrX:21463001
|
C | T | 1 | a0001c0001t0011g0016 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.520-7765C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21463001 | ||||||
| chrX:21463313
|
G | A | 2 | a0001c0001t0023g0006a0001c0001t0043g0007 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.520-7453G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21463313 | ||||||
| chrX:21463807
|
T | C | 3 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.520-6959T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21463807 | ||||||
| chrX:21464241
|
C | G | 41 | a0001c0001t0001g0158a0001c0001t0002g0028a0001c0001t0003g0015others(38): Show | 41 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.520-6525C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21464241 | ||||||
| chrX:21464662
|
G | A | 1 | a0001c0001t0003g0024 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.520-6104G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21464662 | ||||||
| chrX:21464905
|
A | G | 7 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(4): Show | 7 | HG02615.hp1 HG02717.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-5861A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21464905 | ||||||
| chrX:21465358
|
A | AT | 1 | a0001c0001t0041g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.520-5407dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21465358 | |||||
| chrX:21465701
|
A | G | 1 | a0001c0001t0004g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.520-5065A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21465701 | ||||||
| chrX:21466105
|
T | A | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.520-4661T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21466105 | ||||||
| chrX:21466216
|
A | G | 1 | a0001c0001t0002g0050 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.520-4550A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21466216 | ||||||
| chrX:21466286
|
A | T | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.520-4480A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21466286 | ||||||
| chrX:21466680
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0036others(159): Show | 162 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.520-4086A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21466680 | ||||||
| chrX:21466709
|
C | T | 1 | a0001c0001t0006g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.520-4057C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21466709 | ||||||
| chrX:21466861
|
AG | A | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.520-3903delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21466861 | |||||
| chrX:21467289
|
TG | T | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.520-3474delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21467289 | |||||
| chrX:21467682
|
G | GTAAGTTC others(336): Show |
1 | a0001c0001t0002g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.520-3069_520-3068i others(345): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21467682 | |||||
| chrX:21467954
|
T | C | 12 | a0001c0001t0001g0158a0001c0001t0006g0155a0001c0001t0006g0157others(9): Show | 12 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.520-2812T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21467954 | ||||||
| chrX:21468059
|
A | T | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.520-2707A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21468059 | ||||||
| chrX:21468078
|
T | C | 23 | a0001c0001t0001g0158a0001c0001t0003g0015a0001c0001t0006g0155others(20): Show | 23 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.520-2688T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21468078 | ||||||
| chrX:21468282
|
A | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-2484A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21468282 | ||||||
| chrX:21468434
|
AG | A | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.520-2327delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21468434 | |||||
| chrX:21468470
|
T | G | 1 | a0001c0001t0004g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.520-2296T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21468470 | ||||||
| chrX:21468716
|
T | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0036others(156): Show | 159 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.520-2050T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21468716 | ||||||
| chrX:21468838
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-1928T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21468838 | ||||||
| chrX:21469030
|
A | AT | 1 | a0001c0001t0040g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.520-1731dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21469030 | |||||
| chrX:21469108
|
ATGTTTAC others(2): Show |
A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-1647_520-1639d others(11): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21469108 | |||||
| chrX:21469159
|
AT | A | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.520-1602delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21469159 | |||||
| chrX:21469295
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0033g0002 | 2 | NA18989.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.520-1471G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21469295 | ||||||
| chrX:21469479
|
A | G | 2 | a0001c0001t0001g0060a0001c0006t0028g0059 | 2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.520-1287A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21469479 | ||||||
| chrX:21469546
|
TG | T | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-1219delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21469546 | ||||||
| chrX:21469547
|
G | GT | 3 | a0001c0001t0006g0155a0001c0001t0006g0160a0003c0004t0006g0154 | 3 | HG01884.hp1 HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.520-1209dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21469547 | |||||
| chrX:21469577
|
AT | A | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.520-1187delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21469577 | |||||
| chrX:21469626
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520-1140A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21469626 | ||||||
| chrX:21469637
|
G | A | 1 | a0001c0001t0003g0044 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.520-1129G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21469637 | ||||||
| chrX:21469837
|
AG | A | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.520-924delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chrX | 21469837 | |||||
| chrX:21470165
|
AG | A | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.520-600delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21470165 | ||||||
| chrX:21470353
|
ATGTT | A | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.520-412_520-409del others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21470353 | ||||||
| chrX:21470583
|
T | A | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-183T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 4/21 | chrX | 21470583 | ||||||
| chrX:21471039
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.561+232G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471039 | ||||||
| chrX:21471062
|
T | C | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+255T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471062 | ||||||
| chrX:21471247
|
T | C | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.561+440T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471247 | ||||||
| chrX:21471318
|
G | A | 6 | a0001c0001t0002g0028a0001c0001t0003g0024a0001c0001t0012g0025others(3): Show | 6 | HG01081.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.561+511G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471318 | ||||||
| chrX:21471341
|
C | T | 2 | a0001c0001t0002g0112a0001c0001t0002g0113 | 2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.561+534C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471341 | ||||||
| chrX:21471451
|
A | G | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.561+644A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471451 | ||||||
| chrX:21471631
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.561+824G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471631 | ||||||
| chrX:21471727
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.561+920C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471727 | ||||||
| chrX:21471847
|
C | T | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.561+1040C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471847 | ||||||
| chrX:21471934
|
A | G | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.561+1127A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21471934 | ||||||
| chrX:21472021
|
C | T | 1 | a0001c0001t0038g0150 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.561+1214C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21472021 | ||||||
| chrX:21472129
|
G | A | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.561+1322G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21472129 | ||||||
| chrX:21472382
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.561+1575T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21472382 | ||||||
| chrX:21472441
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.561+1634C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21472441 | ||||||
| chrX:21472989
|
T | G | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.561+2182T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21472989 | ||||||
| chrX:21473745
|
G | GT | 12 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0082others(9): Show | 12 | HG00735.hp2 HG01192.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.561+2957dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
G | GTTTTTTT | 4 | a0001c0001t0042g0008a0001c0003t0014g0147a0001c0003t0014g0149others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+2951_561+2957d others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
G | GTTTTTTT others(7): Show |
1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.561+2944_561+2957d others(16): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
G | GTTTTTTT others(12): Show |
4 | a0001c0001t0003g0029a0001c0001t0043g0007a0001c0007t0036g0026others(1): Show | 4 | HG01081.hp1 HG01884.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+2939_561+2957d others(21): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
G | GTTTTTTT others(13): Show |
7 | a0001c0001t0002g0028a0001c0001t0003g0024a0001c0001t0010g0152others(4): Show | 7 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.561+2957_561+2958i others(22): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
G | GTTTTTTT others(14): Show |
4 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0010g0162others(1): Show | 4 | HG02615.hp2 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+2957_561+2958i others(23): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
G | GTTTTTTT others(15): Show |
1 | a0001c0001t0010g0153 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.561+2957_561+2958i others(24): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
G | GTTTTTTT others(16): Show |
5 | a0001c0001t0007g0140a0001c0001t0009g0011a0001c0001t0017g0018others(2): Show | 5 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.561+2957_561+2958i others(25): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
G | GTTTTTTT others(17): Show |
2 | a0001c0001t0009g0010a0001c0001t0009g0012 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.561+2957_561+2958i others(26): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
G | GTTTTTTT others(19): Show |
2 | a0001c0001t0006g0155a0001c0001t0006g0157 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.561+2957_561+2958i others(28): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
G | GTTTTTTT others(20): Show |
3 | a0001c0001t0006g0159a0001c0001t0009g0013a0001c0001t0041g0009 | 3 | HG02886.hp1 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.561+2957_561+2958i others(29): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
GT | G | 6 | a0001c0001t0002g0004a0001c0001t0002g0019a0001c0001t0004g0021others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.561+2957delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
GTT | G | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.561+2956_561+2957d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
GTTTT | G | 1 | a0001c0001t0001g0158 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.561+2954_561+2957d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473745
|
GTTTTTT | G | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.561+2952_561+2957d others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21473745 | |||||
| chrX:21473872
|
G | A | 1 | a0001c0001t0017g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.561+3065G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21473872 | ||||||
| chrX:21474526
|
A | G | 2 | a0001c0001t0023g0006a0001c0001t0043g0007 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.561+3719A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21474526 | ||||||
| chrX:21474860
|
GTATT | G | 1 | a0001c0001t0001g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.561+4057_561+4060d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21474860 | |||||
| chrX:21475180
|
C | T | 1 | a0001c0001t0013g0100 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.561+4373C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21475180 | ||||||
| chrX:21475319
|
A | G | 20 | a0001c0001t0001g0158a0001c0001t0002g0028a0001c0001t0003g0024others(17): Show | 20 | HG01071.hp2 HG01081.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.561+4512A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21475319 | ||||||
| chrX:21475621
|
T | C | 33 | a0001c0001t0001g0158a0001c0001t0002g0028a0001c0001t0003g0015others(30): Show | 33 | HG01071.hp2 HG01081.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.561+4814T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21475621 | ||||||
| chrX:21475837
|
A | AT | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.561+5037dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21475837 | |||||
| chrX:21475967
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.561+5160T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21475967 | ||||||
| chrX:21475993
|
G | A | 1 | a0002c0005t0003g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.561+5186G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21475993 | ||||||
| chrX:21476114
|
G | T | 40 | a0001c0001t0001g0158a0001c0001t0002g0028a0001c0001t0003g0015others(37): Show | 40 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.561+5307G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21476114 | ||||||
| chrX:21476272
|
A | G | 1 | a0001c0001t0004g0064 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.561+5465A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21476272 | ||||||
| chrX:21476295
|
T | C | 13 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(10): Show | 13 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.561+5488T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21476295 | ||||||
| chrX:21476493
|
C | T | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.561+5686C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21476493 | ||||||
| chrX:21477067
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.561+6260C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21477067 | ||||||
| chrX:21477151
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.561+6344C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21477151 | ||||||
| chrX:21477756
|
AGGATGTG others(6): Show |
A | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.561+6950_561+6962d others(15): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21477756 | ||||||
| chrX:21477855
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.561+7048A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21477855 | ||||||
| chrX:21478624
|
G | A | 3 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.561+7817G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21478624 | ||||||
| chrX:21478851
|
C | T | 40 | a0001c0001t0001g0158a0001c0001t0002g0028a0001c0001t0003g0015others(37): Show | 40 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.561+8044C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21478851 | ||||||
| chrX:21478864
|
A | G | 5 | a0001c0001t0022g0033a0001c0001t0027g0034a0001c0003t0014g0147others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.561+8057A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21478864 | ||||||
| chrX:21478909
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.561+8102T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21478909 | ||||||
| chrX:21479101
|
A | G | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.561+8294A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21479101 | ||||||
| chrX:21479172
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0029g0023 | 2 | HG00735.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.561+8365C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21479172 | ||||||
| chrX:21479459
|
TA | T | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.561+8653delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21479459 | ||||||
| chrX:21479772
|
A | G | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+8965A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21479772 | ||||||
| chrX:21480145
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.561+9338C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21480145 | ||||||
| chrX:21480185
|
C | T | 1 | a0001c0001t0035g0054 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.561+9378C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21480185 | ||||||
| chrX:21480276
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0002g0003a0001c0001t0002g0046others(20): Show | 23 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.561+9469C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21480276 | ||||||
| chrX:21480310
|
T | G | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.561+9503T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21480310 | ||||||
| chrX:21480427
|
A | G | 1 | a0001c0001t0005g0072 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.561+9620A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21480427 | ||||||
| chrX:21480547
|
C | T | 16 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0067others(13): Show | 16 | HG00673.hp1 HG02040.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.561+9740C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21480547 | ||||||
| chrX:21481465
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.562-8994C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21481465 | ||||||
| chrX:21481493
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.562-8966C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21481493 | ||||||
| chrX:21482050
|
C | T | 1 | a0001c0001t0037g0092 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.562-8409C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21482050 | ||||||
| chrX:21482233
|
A | G | 12 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(9): Show | 12 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.562-8226A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21482233 | ||||||
| chrX:21482235
|
T | G | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.562-8224T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21482235 | ||||||
| chrX:21482318
|
A | G | 16 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(13): Show | 16 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.562-8141A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21482318 | ||||||
| chrX:21482383
|
A | ACTTGTGC others(4): Show |
18 | a0001c0001t0003g0015a0001c0001t0007g0140a0001c0001t0009g0010others(15): Show | 18 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-8075_562-8074i others(13): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21482383 | |||||
| chrX:21482618
|
C | T | 6 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0055others(3): Show | 6 | HG00609.hp1 HG00741.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.562-7841C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21482618 | ||||||
| chrX:21482939
|
C | A | 1 | a0001c0001t0002g0050 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.562-7520C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21482939 | ||||||
| chrX:21483086
|
G | A | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.562-7373G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483086 | ||||||
| chrX:21483117
|
G | A | 1 | a0001c0001t0005g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.562-7342G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483117 | ||||||
| chrX:21483343
|
A | G | 2 | a0001c0001t0003g0116a0001c0001t0004g0117 | 2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.562-7116A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483343 | ||||||
| chrX:21483593
|
A | AAT | 3 | a0001c0001t0001g0001a0001c0001t0002g0043a0001c0001t0023g0006 | 3 | HG02809.hp2 HG03654.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.562-6844_562-6843d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21483593 | |||||
| chrX:21483593
|
A | AATAT | 7 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(4): Show | 7 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.562-6846_562-6843d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21483593 | |||||
| chrX:21483593
|
A | AATATAT | 1 | a0001c0001t0018g0123 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.562-6848_562-6843d others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21483593 | |||||
| chrX:21483593
|
AAT | A | 45 | a0001c0001t0001g0158a0001c0001t0002g0003a0001c0001t0002g0004others(42): Show | 45 | HG00621.hp1 HG01069.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.562-6844_562-6843d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21483593 | |||||
| chrX:21483773
|
A | G | 3 | a0001c0001t0003g0070a0001c0001t0003g0101a0001c0001t0035g0054 | 3 | NA18967.hp1 NA18994.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.562-6686A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483773 | ||||||
| chrX:21483797
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.562-6662C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483797 | ||||||
| chrX:21483871
|
A | G | 1 | a0001c0001t0007g0127 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.562-6588A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483871 | ||||||
| chrX:21483899
|
C | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.562-6560C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21483899 | ||||||
| chrX:21484289
|
T | TCAAAA | 3 | a0001c0001t0003g0151a0001c0001t0030g0086a0001c0002t0001g0108 | 3 | HG01081.hp2 HG04199.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.562-6134_562-6130d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21484289 | |||||
| chrX:21484289
|
TCAAAA | T | 2 | a0001c0001t0001g0053a0001c0002t0001g0104 | 2 | HG00280.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.562-6134_562-6130d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21484289 | |||||
| chrX:21484331
|
C | T | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.562-6128C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21484331 | ||||||
| chrX:21484751
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.562-5708C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21484751 | ||||||
| chrX:21485141
|
C | G | 1 | a0001c0001t0041g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.562-5318C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485141 | ||||||
| chrX:21485166
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.562-5293A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485166 | ||||||
| chrX:21485303
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0005g0063a0001c0001t0005g0072others(1): Show | 4 | NA18945.hp1 NA18962.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.562-5156T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485303 | ||||||
| chrX:21485380
|
ATGCTC | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.562-5071_562-5067d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21485380 | |||||
| chrX:21485473
|
G | A | 1 | a0001c0001t0038g0150 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.562-4986G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485473 | ||||||
| chrX:21485495
|
T | G | 1 | a0001c0001t0002g0113 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.562-4964T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485495 | ||||||
| chrX:21485540
|
G | A | 1 | a0001c0001t0003g0044 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.562-4919G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485540 | ||||||
| chrX:21485579
|
G | GA | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.562-4872dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21485579 | |||||
| chrX:21485764
|
G | T | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.562-4695G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485764 | ||||||
| chrX:21485834
|
TA | T | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.562-4623delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21485834 | |||||
| chrX:21485887
|
A | C | 15 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.562-4572A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485887 | ||||||
| chrX:21485920
|
A | C | 1 | a0001c0001t0001g0062 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.562-4539A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485920 | ||||||
| chrX:21485951
|
AT | A | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.562-4507delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21485951 | ||||||
| chrX:21486004
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.562-4455G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486004 | ||||||
| chrX:21486016
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.562-4443T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486016 | ||||||
| chrX:21486103
|
A | G | 41 | a0001c0001t0001g0158a0001c0001t0002g0028a0001c0001t0003g0015others(38): Show | 41 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.562-4356A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486103 | ||||||
| chrX:21486135
|
TA | T | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.562-4320delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21486135 | |||||
| chrX:21486265
|
GC | G | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.562-4192delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21486265 | |||||
| chrX:21486314
|
T | C | 3 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.562-4145T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486314 | ||||||
| chrX:21486349
|
AT | A | 1 | a0001c0001t0001g0069 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.562-4106delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21486349 | |||||
| chrX:21486719
|
T | C | 12 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(9): Show | 12 | HG01071.hp2 HG01243.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.562-3740T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486719 | ||||||
| chrX:21486760
|
T | C | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.562-3699T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486760 | ||||||
| chrX:21486824
|
T | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.562-3635T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21486824 | ||||||
| chrX:21487026
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.562-3433C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21487026 | ||||||
| chrX:21487043
|
AG | A | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.562-3414delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21487043 | |||||
| chrX:21487195
|
CA | C | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.562-3260delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21487195 | |||||
| chrX:21487259
|
AT | A | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.562-3196delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21487259 | |||||
| chrX:21487652
|
A | AT | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.562-2807_562-2806i others(3): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21487652 | ||||||
| chrX:21487657
|
AG | A | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.562-2799delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21487657 | |||||
| chrX:21487693
|
A | G | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.562-2766A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21487693 | ||||||
| chrX:21487715
|
G | C | 2 | a0001c0001t0002g0112a0001c0001t0002g0113 | 2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.562-2744G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21487715 | ||||||
| chrX:21487715
|
G | T | 57 | a0001c0001t0001g0158a0001c0001t0002g0003a0001c0001t0002g0004others(54): Show | 57 | HG00140.hp1 HG00621.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.562-2744G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21487715 | ||||||
| chrX:21487801
|
AT | A | 1 | a0001c0001t0002g0115 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.562-2653delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21487801 | |||||
| chrX:21487868
|
G | GA | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.562-2587dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21487868 | |||||
| chrX:21487933
|
AC | A | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.562-2524delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21487933 | |||||
| chrX:21488678
|
A | G | 1 | a0001c0001t0021g0088 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.562-1781A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21488678 | ||||||
| chrX:21488780
|
G | A | 1 | a0001c0001t0004g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.562-1679G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21488780 | ||||||
| chrX:21489449
|
C | CA | 1 | a0001c0001t0003g0136 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.562-1000dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21489449 | |||||
| chrX:21490104
|
ATTT | A | 1 | a0001c0001t0009g0013 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.562-351_562-349del others(3): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 21490104 | |||||
| chrX:21490384
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0005g0063a0001c0001t0005g0072 | 3 | NA18945.hp1 NA18962.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.562-75G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 5/21 | chrX | 21490384 | ||||||
| chrX:21490616
|
A | G | 2 | a0001c0001t0002g0119a0001c0001t0002g0122 | 2 | NA18966.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.681+38A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21490616 | ||||||
| chrX:21490696
|
A | AT | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.681+125dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21490696 | |||||
| chrX:21490934
|
G | T | 2 | a0001c0001t0002g0004a0001c0001t0008g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.681+356G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21490934 | ||||||
| chrX:21492200
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.681+1622A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21492200 | ||||||
| chrX:21492250
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.681+1672C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21492250 | ||||||
| chrX:21492551
|
C | CT | 1 | a0001c0001t0025g0130 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.681+1980dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21492551 | |||||
| chrX:21492591
|
C | CAG | 16 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(13): Show | 16 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.681+2014_681+2015d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21492591 | |||||
| chrX:21492677
|
TG | T | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.681+2102delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21492677 | |||||
| chrX:21493023
|
G | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.681+2445G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21493023 | ||||||
| chrX:21493146
|
T | C | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+2568T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21493146 | ||||||
| chrX:21493238
|
T | G | 1 | a0001c0001t0016g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.681+2660T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21493238 | ||||||
| chrX:21493386
|
A | G | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+2808A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21493386 | ||||||
| chrX:21493499
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.681+2921A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21493499 | ||||||
| chrX:21494221
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.682-3566C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21494221 | ||||||
| chrX:21494279
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0036others(159): Show | 162 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.682-3508G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21494279 | ||||||
| chrX:21495113
|
T | A | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.682-2674T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21495113 | ||||||
| chrX:21495149
|
G | A | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.682-2638G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21495149 | ||||||
| chrX:21495178
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.682-2609T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21495178 | ||||||
| chrX:21495608
|
A | AC | 30 | a0001c0001t0001g0060a0001c0001t0001g0158a0001c0001t0003g0015others(27): Show | 30 | HG01071.hp2 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.682-2176dupC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495608 | |||||
| chrX:21495628
|
CA | C | 2 | a0001c0001t0023g0006a0001c0001t0043g0007 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.682-2154delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495628 | |||||
| chrX:21495666
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.682-2121C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21495666 | ||||||
| chrX:21495783
|
C | CA | 13 | a0001c0001t0001g0083a0001c0001t0001g0128a0001c0001t0001g0131others(10): Show | 13 | HG01256.hp1 HG01258.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.682-1965dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
C | CAA | 3 | a0001c0001t0003g0101a0001c0001t0004g0129a0001c0001t0041g0009 | 3 | HG00609.hp1 HG03098.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.682-1966_682-1965d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
C | CAAAA | 1 | a0001c0001t0003g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.682-1968_682-1965d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
C | CAAAAA | 1 | a0001c0001t0006g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.682-1969_682-1965d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
C | CAAAAAA | 5 | a0001c0001t0010g0153a0001c0001t0016g0032a0001c0001t0017g0018others(2): Show | 5 | HG01071.hp2 HG02602.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-1970_682-1965d others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
C | CAAAAAAA | 8 | a0001c0001t0001g0158a0001c0001t0003g0061a0001c0001t0004g0117others(5): Show | 8 | HG02015.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.682-1971_682-1965d others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
C | CAAAAAAA others(2): Show |
1 | a0001c0001t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.682-1973_682-1965d others(11): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
C | CAAAAAAA others(10): Show |
1 | a0003c0004t0006g0154 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.682-1981_682-1965d others(19): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0004g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.682-1989_682-1965d others(27): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CA | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0051others(38): Show | 41 | HG00741.hp1 HG01074.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.682-1965delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAA | C | 17 | a0001c0001t0002g0049a0001c0001t0002g0111a0001c0001t0002g0113others(14): Show | 17 | HG00735.hp1 HG00741.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.682-1966_682-1965d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAAA | C | 9 | a0001c0001t0001g0060a0001c0001t0002g0028a0001c0001t0002g0112others(6): Show | 9 | HG01433.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-1967_682-1965d others(5): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAAAA | C | 3 | a0001c0001t0002g0114a0001c0001t0011g0016a0001c0003t0026g0148 | 3 | HG00140.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.682-1968_682-1965d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAAAAA | C | 2 | a0001c0003t0014g0147a0001c0003t0014g0149 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.682-1969_682-1965d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAAAAAA | C | 1 | a0001c0001t0043g0007 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.682-1970_682-1965d others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAAAAAAA | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0067a0001c0001t0031g0065 | 3 | HG00673.hp1 HG02040.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.682-1971_682-1965d others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0001g0037a0001c0001t0001g0069a0001c0001t0002g0004others(2): Show | 5 | HG01071.hp1 HG02135.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-1972_682-1965d others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAAAAAAA others(2): Show |
C | 2 | a0001c0001t0001g0068a0001c0001t0008g0005 | 2 | HG01069.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.682-1973_682-1965d others(11): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0015g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.682-1975_682-1965d others(13): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0001g0042 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.682-1976_682-1965d others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0006g0155 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.682-1980_682-1965d others(18): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.682-1981_682-1965d others(19): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAAAAAAA others(11): Show |
C | 4 | a0001c0001t0002g0003a0001c0001t0002g0110a0001c0001t0002g0118others(1): Show | 4 | HG00621.hp1 HG02074.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.682-1982_682-1965d others(20): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495783
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0001g0137 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.682-1983_682-1965d others(21): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495783 | |||||
| chrX:21495822
|
A | AC | 1 | a0001c0001t0004g0064 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.682-1964dupC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 21495822 | |||||
| chrX:21495822
|
A | C | 9 | a0001c0001t0002g0028a0001c0001t0003g0024a0001c0001t0003g0029others(6): Show | 9 | HG01081.hp1 HG01109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-1965A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21495822 | ||||||
| chrX:21495911
|
T | C | 17 | a0001c0001t0001g0158a0001c0001t0006g0155a0001c0001t0006g0157others(14): Show | 17 | HG01071.hp2 HG01884.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.682-1876T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21495911 | ||||||
| chrX:21496492
|
T | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0097a0001c0001t0018g0123 | 3 | HG01358.hp1 HG04228.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.682-1295T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21496492 | ||||||
| chrX:21496757
|
G | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.682-1030G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21496757 | ||||||
| chrX:21497528
|
T | A | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.682-259T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21497528 | ||||||
| chrX:21497553
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.682-234T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21497553 | ||||||
| chrX:21497748
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.682-39A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 6/21 | chrX | 21497748 | ||||||
| chrX:21497898
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0002g0003a0001c0001t0002g0046others(20): Show | 23 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.741+52T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21497898 | ||||||
| chrX:21498017
|
C | CT | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.741+180dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 21498017 | |||||
| chrX:21498483
|
CT | C | 69 | a0001c0001t0001g0158a0001c0001t0002g0003a0001c0001t0002g0004others(66): Show | 69 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.741+640delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 21498483 | |||||
| chrX:21498530
|
A | G | 2 | a0001c0001t0002g0049a0001c0001t0008g0135 | 2 | NA19000.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.741+684A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21498530 | ||||||
| chrX:21498815
|
A | AT | 11 | a0001c0001t0001g0158a0001c0001t0006g0155a0001c0001t0006g0157others(8): Show | 11 | HG01884.hp1 HG02886.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.741+979dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 21498815 | |||||
| chrX:21499112
|
C | T | 1 | a0002c0005t0003g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.741+1266C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21499112 | ||||||
| chrX:21499173
|
A | C | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.741+1327A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21499173 | ||||||
| chrX:21499902
|
A | G | 1 | a0001c0001t0005g0079 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.742-1618A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21499902 | ||||||
| chrX:21499922
|
A | G | 1 | a0001c0001t0003g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.742-1598A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21499922 | ||||||
| chrX:21500554
|
A | G | 13 | a0001c0001t0001g0158a0001c0001t0006g0155a0001c0001t0006g0157others(10): Show | 13 | HG01071.hp2 HG01081.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.742-966A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21500554 | ||||||
| chrX:21500614
|
A | T | 13 | a0001c0001t0001g0158a0001c0001t0003g0151a0001c0001t0006g0155others(10): Show | 13 | HG01071.hp2 HG01081.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.742-906A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21500614 | ||||||
| chrX:21501150
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.742-370A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21501150 | ||||||
| chrX:21501205
|
T | C | 13 | a0001c0001t0001g0158a0001c0001t0003g0151a0001c0001t0006g0155others(10): Show | 13 | HG01071.hp2 HG01081.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.742-315T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21501205 | ||||||
| chrX:21501220
|
C | T | 1 | a0002c0005t0003g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.742-300C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21501220 | ||||||
| chrX:21501314
|
TTTTC | T | 3 | a0001c0001t0004g0132a0001c0001t0016g0032a0001c0001t0018g0123 | 3 | HG01358.hp1 HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.742-200_742-197del others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 21501314 | |||||
| chrX:21501326
|
GTTTA | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.742-189_742-186del others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 21501326 | |||||
| chrX:21501407
|
T | G | 12 | a0001c0001t0001g0158a0001c0001t0003g0151a0001c0001t0006g0155others(9): Show | 12 | HG01081.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.742-113T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 7/21 | chrX | 21501407 | ||||||
| chrX:21501883
|
A | G | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.810+295A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21501883 | ||||||
| chrX:21502002
|
A | T | 5 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG01255.hp1 NA19005.hp1 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.810+414A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21502002 | ||||||
| chrX:21502286
|
T | G | 1 | a0001c0001t0022g0033 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.810+698T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21502286 | ||||||
| chrX:21502378
|
A | G | 4 | a0001c0001t0003g0151a0001c0003t0014g0147a0001c0003t0014g0149others(1): Show | 4 | HG01081.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.810+790A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21502378 | ||||||
| chrX:21502644
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.810+1056C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21502644 | ||||||
| chrX:21503554
|
A | G | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.810+1966A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21503554 | ||||||
| chrX:21504658
|
G | C | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.810+3070G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21504658 | ||||||
| chrX:21504785
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.810+3197T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21504785 | ||||||
| chrX:21505640
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.810+4052C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21505640 | ||||||
| chrX:21505666
|
C | A | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.810+4078C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21505666 | ||||||
| chrX:21506222
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.810+4634G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21506222 | ||||||
| chrX:21506279
|
A | G | 1 | a0001c0001t0004g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.810+4691A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21506279 | ||||||
| chrX:21506439
|
T | C | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.810+4851T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21506439 | ||||||
| chrX:21506987
|
G | GT | 15 | a0001c0001t0001g0158a0001c0001t0003g0151a0001c0001t0006g0155others(12): Show | 15 | HG01071.hp2 HG01081.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.810+5411dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chrX | 21506987 | |||||
| chrX:21507210
|
C | G | 1 | a0001c0001t0015g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.810+5622C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507210 | ||||||
| chrX:21507297
|
C | T | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.810+5709C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507297 | ||||||
| chrX:21507403
|
A | T | 16 | a0001c0001t0001g0158a0001c0001t0003g0151a0001c0001t0006g0155others(13): Show | 16 | HG01071.hp2 HG01081.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.810+5815A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507403 | ||||||
| chrX:21507452
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.810+5864G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507452 | ||||||
| chrX:21507562
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.810+5974A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507562 | ||||||
| chrX:21507800
|
G | A | 16 | a0001c0001t0001g0158a0001c0001t0003g0151a0001c0001t0006g0155others(13): Show | 16 | HG01071.hp2 HG01081.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.810+6212G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507800 | ||||||
| chrX:21507832
|
A | G | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.810+6244A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21507832 | ||||||
| chrX:21508156
|
C | T | 1 | a0001c0001t0004g0064 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.810+6568C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21508156 | ||||||
| chrX:21509026
|
T | C | 2 | a0001c0001t0004g0132a0001c0001t0016g0032 | 2 | HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.810+7438T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21509026 | ||||||
| chrX:21509052
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.811-7433G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21509052 | ||||||
| chrX:21509276
|
C | G | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-7209C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21509276 | ||||||
| chrX:21509324
|
C | A | 2 | a0001c0001t0002g0112a0001c0001t0002g0113 | 2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.811-7161C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21509324 | ||||||
| chrX:21509495
|
T | C | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.811-6990T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21509495 | ||||||
| chrX:21509581
|
A | AC | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.811-6903dupC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chrX | 21509581 | |||||
| chrX:21510357
|
T | TA | 7 | a0001c0001t0002g0028a0001c0001t0003g0029a0001c0001t0017g0146others(4): Show | 7 | HG01081.hp1 HG01109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.811-6119dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chrX | 21510357 | |||||
| chrX:21511027
|
A | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.811-5458A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21511027 | ||||||
| chrX:21511099
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.811-5386C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21511099 | ||||||
| chrX:21511100
|
A | G | 4 | a0001c0001t0042g0008a0001c0003t0014g0147a0001c0003t0014g0149others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-5385A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21511100 | ||||||
| chrX:21511772
|
C | G | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.811-4713C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21511772 | ||||||
| chrX:21511993
|
T | C | 1 | a0002c0005t0003g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.811-4492T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21511993 | ||||||
| chrX:21512191
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.811-4294A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21512191 | ||||||
| chrX:21512410
|
A | T | 1 | a0001c0001t0005g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.811-4075A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21512410 | ||||||
| chrX:21512441
|
T | C | 4 | a0001c0001t0007g0140a0001c0003t0014g0147a0001c0003t0014g0149others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-4044T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21512441 | ||||||
| chrX:21512754
|
T | TTTTTG | 15 | a0001c0001t0003g0015a0001c0001t0003g0024a0001c0001t0009g0010others(12): Show | 15 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.811-3711_811-3707d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chrX | 21512754 | |||||
| chrX:21513051
|
T | TA | 1 | a0001c0001t0001g0035 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.811-3433dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chrX | 21513051 | |||||
| chrX:21513109
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.811-3376G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21513109 | ||||||
| chrX:21513113
|
A | T | 2 | a0001c0001t0009g0011a0001c0001t0009g0012 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.811-3372A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21513113 | ||||||
| chrX:21514403
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.811-2082A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21514403 | ||||||
| chrX:21514475
|
T | C | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.811-2010T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21514475 | ||||||
| chrX:21514636
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.811-1849T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21514636 | ||||||
| chrX:21514682
|
G | A | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.811-1803G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21514682 | ||||||
| chrX:21515041
|
T | TA | 5 | a0001c0001t0004g0064a0001c0001t0042g0008a0001c0003t0014g0147others(2): Show | 5 | HG00738.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.811-1433dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chrX | 21515041 | |||||
| chrX:21515557
|
T | A | 8 | a0001c0001t0009g0013a0001c0001t0010g0162a0001c0001t0022g0033others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.811-928T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21515557 | ||||||
| chrX:21515932
|
T | G | 1 | a0001c0001t0004g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.811-553T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21515932 | ||||||
| chrX:21516037
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.811-448G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21516037 | ||||||
| chrX:21516049
|
C | G | 2 | a0001c0001t0002g0119a0001c0001t0002g0122 | 2 | NA18966.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.811-436C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21516049 | ||||||
| chrX:21516308
|
A | G | 1 | a0001c0001t0004g0056 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.811-177A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | chrX | 21516308 | ||||||
| chrX:21516391
|
A | AC | 22 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0062others(19): Show | 22 | HG00673.hp1 HG00738.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.811-93dupC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chrX | 21516391 | |||||
| chrX:21516943
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.957+312A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21516943 | ||||||
| chrX:21516993
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.957+362A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21516993 | ||||||
| chrX:21516993
|
A | T | 1 | a0001c0001t0015g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.957+362A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21516993 | ||||||
| chrX:21517724
|
T | TA | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.957+1102dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chrX | 21517724 | |||||
| chrX:21517776
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0018g0123 | 2 | HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.957+1145A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21517776 | ||||||
| chrX:21517851
|
A | C | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.957+1220A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21517851 | ||||||
| chrX:21518048
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.957+1417T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21518048 | ||||||
| chrX:21518196
|
TA | T | 1 | a0001c0001t0002g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.957+1566delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21518196 | ||||||
| chrX:21518282
|
G | A | 1 | a0001c0001t0030g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.957+1651G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21518282 | ||||||
| chrX:21518339
|
C | G | 12 | a0001c0001t0001g0158a0001c0001t0006g0155a0001c0001t0006g0157others(9): Show | 12 | HG01071.hp2 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.957+1708C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21518339 | ||||||
| chrX:21518462
|
A | G | 2 | a0001c0001t0023g0006a0001c0001t0043g0007 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.957+1831A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21518462 | ||||||
| chrX:21519228
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.957+2597C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21519228 | ||||||
| chrX:21519390
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.957+2759C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21519390 | ||||||
| chrX:21519926
|
A | G | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.957+3295A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21519926 | ||||||
| chrX:21520405
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.957+3774C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21520405 | ||||||
| chrX:21520479
|
G | GA | 69 | a0001c0001t0001g0158a0001c0001t0002g0003a0001c0001t0002g0004others(66): Show | 69 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.957+3857dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chrX | 21520479 | |||||
| chrX:21520689
|
C | CT | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.957+4071dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chrX | 21520689 | |||||
| chrX:21520692
|
T | C | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.957+4061T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21520692 | ||||||
| chrX:21520923
|
A | G | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.957+4292A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21520923 | ||||||
| chrX:21521353
|
A | T | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.957+4722A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21521353 | ||||||
| chrX:21521798
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.958-5069C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21521798 | ||||||
| chrX:21522192
|
T | C | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.958-4675T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21522192 | ||||||
| chrX:21523741
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.958-3126G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21523741 | ||||||
| chrX:21524269
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.958-2598A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21524269 | ||||||
| chrX:21524502
|
G | T | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.958-2365G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21524502 | ||||||
| chrX:21524718
|
C | G | 1 | a0001c0001t0043g0007 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.958-2149C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21524718 | ||||||
| chrX:21525674
|
A | G | 2 | a0001c0001t0010g0162a0001c0001t0042g0008 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.958-1193A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21525674 | ||||||
| chrX:21525849
|
A | C | 1 | a0001c0001t0003g0029 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.958-1018A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21525849 | ||||||
| chrX:21526143
|
G | GA | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.958-720dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chrX | 21526143 | |||||
| chrX:21526206
|
T | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0033g0002 | 3 | NA18989.hp1 NA19006.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.958-661T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21526206 | ||||||
| chrX:21526660
|
C | T | 1 | a0001c0001t0003g0029 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.958-207C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21526660 | ||||||
| chrX:21526766
|
T | A | 1 | a0001c0001t0002g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.958-101T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | chrX | 21526766 | ||||||
| chrX:21526786
|
A | ATTG | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0010g0162others(2): Show | 5 | HG02486.hp1 HG02647.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.958-51_958-49dupGT others(1): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chrX | 21526786 | |||||
| chrX:21526786
|
ATTG | A | 5 | a0001c0001t0003g0031a0001c0001t0017g0018a0001c0003t0014g0147others(2): Show | 5 | HG01071.hp2 HG02615.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.958-51_958-49delGT others(1): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chrX | 21526786 | |||||
| chrX:21526786
|
ATTGTTG | A | 1 | a0001c0001t0001g0001 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.958-54_958-49delGT others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chrX | 21526786 | |||||
| chrX:21527227
|
ATC | A | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1091+230_1091+231d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chrX | 21527227 | |||||
| chrX:21527230
|
T | C | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1091+230T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21527230 | ||||||
| chrX:21527370
|
A | T | 5 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+370A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21527370 | ||||||
| chrX:21527617
|
T | C | 1 | a0001c0001t0005g0063 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1091+617T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21527617 | ||||||
| chrX:21527624
|
A | T | 4 | a0001c0001t0042g0008a0001c0003t0014g0147a0001c0003t0014g0149others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091+624A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21527624 | ||||||
| chrX:21527759
|
C | CA | 1 | a0001c0001t0009g0013 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1091+766dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chrX | 21527759 | |||||
| chrX:21527806
|
ATAATT | A | 21 | a0001c0001t0002g0003a0001c0001t0002g0046a0001c0001t0002g0047others(18): Show | 21 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1091+810_1091+814d others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chrX | 21527806 | |||||
| chrX:21527852
|
C | A | 1 | a0001c0001t0011g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1091+852C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21527852 | ||||||
| chrX:21527872
|
A | G | 5 | a0001c0001t0010g0162a0001c0001t0042g0008a0001c0003t0014g0147others(2): Show | 5 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+872A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21527872 | ||||||
| chrX:21528002
|
A | G | 2 | a0001c0001t0003g0015a0001c0001t0003g0031 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1091+1002A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21528002 | ||||||
| chrX:21528049
|
T | C | 16 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(13): Show | 16 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1091+1049T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21528049 | ||||||
| chrX:21528259
|
A | G | 1 | a0001c0001t0004g0055 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1091+1259A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21528259 | ||||||
| chrX:21528865
|
C | G | 4 | a0001c0001t0002g0115a0001c0001t0003g0070a0001c0001t0003g0101others(1): Show | 4 | NA18967.hp1 NA18974.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091+1865C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21528865 | ||||||
| chrX:21528937
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1091+1937T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21528937 | ||||||
| chrX:21529017
|
T | C | 6 | a0001c0001t0002g0019a0001c0001t0010g0162a0001c0001t0042g0008others(3): Show | 6 | HG01106.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1091+2017T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21529017 | ||||||
| chrX:21529328
|
A | G | 1 | a0001c0001t0043g0007 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1091+2328A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21529328 | ||||||
| chrX:21529405
|
A | G | 2 | a0001c0001t0010g0162a0001c0001t0042g0008 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1091+2405A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21529405 | ||||||
| chrX:21529503
|
AG | A | 1 | a0001c0002t0005g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1092-2352delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21529503 | ||||||
| chrX:21529659
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1092-2197A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21529659 | ||||||
| chrX:21530465
|
C | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1092-1391C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | chrX | 21530465 | ||||||
| chrX:21531674
|
ACT | A | 1 | a0001c0001t0004g0117 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1092-180_1092-179d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chrX | 21531674 | |||||
| chrX:21532213
|
TG | T | 1 | a0001c0001t0002g0115 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1303+148delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21532213 | |||||
| chrX:21532657
|
AC | A | 1 | a0001c0001t0002g0115 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1303+592delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21532657 | |||||
| chrX:21532887
|
A | G | 4 | a0001c0001t0001g0071a0001c0001t0005g0063a0001c0001t0005g0072others(1): Show | 4 | NA18945.hp1 NA18962.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303+820A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21532887 | ||||||
| chrX:21533383
|
A | G | 5 | a0001c0001t0010g0162a0001c0001t0042g0008a0001c0003t0014g0147others(2): Show | 5 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303+1316A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21533383 | ||||||
| chrX:21533463
|
A | T | 1 | a0001c0002t0007g0041 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1303+1396A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21533463 | ||||||
| chrX:21533659
|
A | G | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(1): Show | 4 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.1303+1592A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21533659 | ||||||
| chrX:21533824
|
A | G | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1303+1757A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21533824 | ||||||
| chrX:21534068
|
A | G | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1303+2001A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534068 | ||||||
| chrX:21534117
|
G | GT | 2 | a0001c0001t0010g0162a0001c0001t0042g0008 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1303+2051dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21534117 | |||||
| chrX:21534123
|
A | G | 14 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(11): Show | 14 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1303+2056A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534123 | ||||||
| chrX:21534295
|
G | A | 5 | a0001c0001t0010g0162a0001c0001t0042g0008a0001c0003t0014g0147others(2): Show | 5 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303+2228G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534295 | ||||||
| chrX:21534295
|
G | GAT | 2 | a0001c0001t0001g0093a0001c0001t0018g0123 | 2 | HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1303+2241_1303+224 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21534295 | |||||
| chrX:21534410
|
T | C | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1303+2343T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534410 | ||||||
| chrX:21534418
|
A | G | 12 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(9): Show | 12 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1303+2351A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534418 | ||||||
| chrX:21534734
|
T | C | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1303+2667T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534734 | ||||||
| chrX:21534739
|
C | T | 2 | a0001c0001t0002g0112a0001c0001t0002g0113 | 2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1303+2672C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534739 | ||||||
| chrX:21534966
|
C | A | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1303+2899C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21534966 | ||||||
| chrX:21535389
|
A | AT | 9 | a0001c0001t0002g0028a0001c0001t0003g0024a0001c0001t0003g0029others(6): Show | 9 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1303+3330dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21535389 | |||||
| chrX:21535514
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1303+3447A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21535514 | ||||||
| chrX:21536116
|
A | G | 2 | a0001c0001t0002g0004a0001c0001t0008g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1303+4049A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21536116 | ||||||
| chrX:21536829
|
G | GT | 19 | a0001c0001t0002g0115a0001c0001t0003g0015a0001c0001t0003g0070others(16): Show | 19 | HG01071.hp2 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1303+4776dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21536829 | |||||
| chrX:21536829
|
G | GTTT | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1303+4774_1303+477 others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21536829 | |||||
| chrX:21536829
|
GT | G | 3 | a0001c0001t0001g0073a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG01515.hp1 NA18984.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1303+4776delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21536829 | |||||
| chrX:21537255
|
T | C | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1303+5188T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21537255 | ||||||
| chrX:21537399
|
TAA | T | 2 | a0001c0001t0003g0116a0001c0001t0004g0117 | 2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1303+5333_1303+533 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21537399 | ||||||
| chrX:21537731
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0002g0019a0001c0001t0005g0063others(2): Show | 5 | HG01106.hp1 NA18945.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303+5664G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21537731 | ||||||
| chrX:21537786
|
G | GT | 3 | a0001c0001t0001g0074a0001c0001t0003g0044a0001c0003t0026g0148 | 3 | HG02965.hp1 HG03942.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1303+5735dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21537786 | |||||
| chrX:21537786
|
GT | G | 5 | a0001c0001t0001g0096a0001c0001t0002g0047a0001c0001t0005g0095others(2): Show | 5 | HG02647.hp1 HG03710.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303+5735delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21537786 | |||||
| chrX:21537793
|
T | G | 1 | a0001c0001t0001g0094 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1303+5726T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21537793 | ||||||
| chrX:21537804
|
T | G | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303+5737T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21537804 | ||||||
| chrX:21538124
|
A | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1303+6057A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21538124 | ||||||
| chrX:21538229
|
T | G | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1303+6162T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21538229 | ||||||
| chrX:21539502
|
G | GT | 34 | a0001c0001t0001g0158a0001c0001t0003g0015a0001c0001t0006g0155others(31): Show | 34 | HG01071.hp2 HG01081.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.1303+7444dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21539502 | |||||
| chrX:21539596
|
A | G | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1303+7529A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21539596 | ||||||
| chrX:21539622
|
ACTT | A | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1303+7559_1303+756 others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21539622 | |||||
| chrX:21540073
|
A | T | 1 | a0001c0001t0004g0055 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1303+8006A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540073 | ||||||
| chrX:21540077
|
A | G | 1 | a0001c0001t0004g0055 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1303+8010A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540077 | ||||||
| chrX:21540141
|
G | T | 1 | a0001c0001t0007g0022 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1303+8074G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540141 | ||||||
| chrX:21540311
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1303+8244G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540311 | ||||||
| chrX:21540460
|
G | T | 1 | a0001c0001t0043g0007 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1303+8393G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540460 | ||||||
| chrX:21540659
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1303+8592A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540659 | ||||||
| chrX:21540970
|
A | G | 3 | a0001c0001t0001g0058a0001c0001t0001g0096a0001c0001t0030g0086 | 3 | HG02698.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1303+8903A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21540970 | ||||||
| chrX:21540988
|
G | GT | 4 | a0001c0001t0001g0036a0001c0001t0007g0140a0001c0001t0020g0141others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303+8933dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21540988 | |||||
| chrX:21541046
|
G | A | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1303+8979G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21541046 | ||||||
| chrX:21541076
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1303+9009G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21541076 | ||||||
| chrX:21541132
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1303+9065G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21541132 | ||||||
| chrX:21541583
|
A | G | 4 | a0001c0001t0002g0003a0001c0001t0002g0110a0001c0001t0002g0118others(1): Show | 4 | HG00621.hp1 HG02074.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303+9516A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21541583 | ||||||
| chrX:21541617
|
C | A | 4 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0056others(1): Show | 4 | HG00741.hp1 HG01192.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303+9550C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21541617 | ||||||
| chrX:21542249
|
G | T | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1303+10182G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21542249 | ||||||
| chrX:21542384
|
G | A | 1 | a0001c0001t0007g0127 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1303+10317G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21542384 | ||||||
| chrX:21542515
|
A | G | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303+10448A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21542515 | ||||||
| chrX:21542729
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1303+10662G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21542729 | ||||||
| chrX:21542937
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1303+10870T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21542937 | ||||||
| chrX:21543057
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1303+10990A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21543057 | ||||||
| chrX:21543336
|
G | A | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1303+11269G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21543336 | ||||||
| chrX:21543492
|
G | A | 1 | a0001c0003t0014g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1303+11425G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21543492 | ||||||
| chrX:21544172
|
A | G | 3 | a0001c0001t0003g0044a0001c0001t0034g0091a0001c0001t0037g0092 | 3 | HG02735.hp1 HG03942.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1303+12105A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544172 | ||||||
| chrX:21544316
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1303+12249G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544316 | ||||||
| chrX:21544480
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1303+12413T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544480 | ||||||
| chrX:21544486
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1303+12419G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544486 | ||||||
| chrX:21544555
|
G | C | 7 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(4): Show | 7 | HG01071.hp2 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1303+12488G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544555 | ||||||
| chrX:21544586
|
T | C | 1 | a0001c0001t0016g0085 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1303+12519T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544586 | ||||||
| chrX:21544792
|
G | A | 1 | a0001c0001t0007g0127 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1303+12725G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544792 | ||||||
| chrX:21544830
|
A | G | 2 | a0001c0001t0010g0162a0001c0001t0042g0008 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1303+12763A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544830 | ||||||
| chrX:21544909
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1303+12842C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21544909 | ||||||
| chrX:21545815
|
G | C | 3 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0162 | 3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1303+13748G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21545815 | ||||||
| chrX:21546014
|
T | G | 1 | a0001c0001t0041g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1303+13947T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21546014 | ||||||
| chrX:21546063
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1303+13996G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21546063 | ||||||
| chrX:21546438
|
C | T | 27 | a0001c0001t0003g0015a0001c0001t0006g0155a0001c0001t0006g0157others(24): Show | 27 | HG01071.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1303+14371C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21546438 | ||||||
| chrX:21546655
|
A | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0096a0001c0001t0030g0086 | 3 | HG02698.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1303+14588A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21546655 | ||||||
| chrX:21546767
|
G | C | 7 | a0001c0001t0010g0162a0001c0001t0022g0033a0001c0001t0027g0034others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303+14700G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21546767 | ||||||
| chrX:21546895
|
T | C | 2 | a0001c0001t0010g0162a0001c0001t0042g0008 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1304-14576T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21546895 | ||||||
| chrX:21547323
|
A | G | 2 | a0001c0001t0002g0004a0001c0001t0008g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1304-14148A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21547323 | ||||||
| chrX:21547365
|
A | T | 1 | a0001c0001t0010g0153 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1304-14106A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21547365 | ||||||
| chrX:21547366
|
C | T | 1 | a0001c0001t0010g0153 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1304-14105C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21547366 | ||||||
| chrX:21547847
|
T | G | 1 | a0001c0001t0043g0007 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1304-13624T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21547847 | ||||||
| chrX:21547914
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1304-13557G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21547914 | ||||||
| chrX:21548053
|
G | A | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1304-13418G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21548053 | ||||||
| chrX:21548133
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-13338A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21548133 | ||||||
| chrX:21548493
|
C | G | 1 | a0001c0001t0024g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1304-12978C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21548493 | ||||||
| chrX:21548784
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1304-12687C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21548784 | ||||||
| chrX:21549026
|
C | G | 12 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(9): Show | 12 | HG01081.hp1 HG01884.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1304-12445C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21549026 | ||||||
| chrX:21549324
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1304-12147A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21549324 | ||||||
| chrX:21549520
|
C | T | 2 | a0001c0001t0006g0155a0003c0004t0006g0154 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1304-11951C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21549520 | ||||||
| chrX:21549672
|
A | G | 26 | a0001c0001t0003g0015a0001c0001t0006g0155a0001c0001t0006g0157others(23): Show | 26 | HG01071.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1304-11799A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21549672 | ||||||
| chrX:21549813
|
T | C | 14 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(11): Show | 14 | HG01071.hp2 HG01884.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1304-11658T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21549813 | ||||||
| chrX:21550233
|
G | A | 32 | a0001c0001t0003g0015a0001c0001t0006g0155a0001c0001t0006g0157others(29): Show | 32 | HG01071.hp2 HG01081.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1304-11238G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21550233 | ||||||
| chrX:21550362
|
G | A | 2 | a0001c0001t0004g0129a0001c0001t0013g0066 | 2 | HG00609.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1304-11109G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21550362 | ||||||
| chrX:21550618
|
G | A | 1 | a0001c0001t0004g0064 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1304-10853G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21550618 | ||||||
| chrX:21550971
|
G | C | 1 | a0001c0001t0017g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1304-10500G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21550971 | ||||||
| chrX:21551030
|
CA | C | 26 | a0001c0001t0002g0003a0001c0001t0002g0046a0001c0001t0002g0047others(23): Show | 26 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1304-10426delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21551030 | |||||
| chrX:21551218
|
G | A | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(1): Show | 4 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304-10253G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21551218 | ||||||
| chrX:21551322
|
A | T | 1 | a0001c0001t0041g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1304-10149A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21551322 | ||||||
| chrX:21551369
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1304-10102G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21551369 | ||||||
| chrX:21551505
|
G | A | 21 | a0001c0001t0002g0003a0001c0001t0002g0046a0001c0001t0002g0047others(18): Show | 21 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1304-9966G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21551505 | ||||||
| chrX:21551802
|
A | G | 22 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0062others(19): Show | 22 | HG00673.hp1 HG00738.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.1304-9669A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21551802 | ||||||
| chrX:21551948
|
A | G | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0031g0065others(1): Show | 4 | HG02040.hp1 NA18989.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304-9523A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21551948 | ||||||
| chrX:21552099
|
G | GA | 1 | a0001c0001t0025g0130 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1304-9358dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21552099 | |||||
| chrX:21552099
|
GA | G | 5 | a0001c0001t0001g0131a0001c0001t0011g0016a0001c0003t0014g0147others(2): Show | 5 | HG02615.hp1 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1304-9358delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21552099 | |||||
| chrX:21552212
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0033g0002 | 2 | NA18989.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1304-9259G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21552212 | ||||||
| chrX:21552598
|
A | C | 4 | a0001c0001t0019g0014a0001c0003t0014g0147a0001c0003t0014g0149others(1): Show | 4 | HG01884.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304-8873A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21552598 | ||||||
| chrX:21552617
|
G | A | 5 | a0001c0001t0007g0022a0001c0001t0042g0008a0001c0003t0014g0147others(2): Show | 5 | HG02132.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1304-8854G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21552617 | ||||||
| chrX:21552875
|
G | A | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1304-8596G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21552875 | ||||||
| chrX:21553161
|
CA | C | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1304-8301delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21553161 | |||||
| chrX:21553215
|
T | G | 1 | a0001c0001t0029g0023 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1304-8256T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21553215 | ||||||
| chrX:21553479
|
CT | C | 8 | a0001c0001t0002g0028a0001c0001t0003g0024a0001c0001t0003g0029others(5): Show | 8 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1304-7991delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21553479 | ||||||
| chrX:21553497
|
G | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-7974G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21553497 | ||||||
| chrX:21553534
|
C | CA | 4 | a0001c0001t0005g0079a0001c0001t0005g0095a0001c0001t0005g0099others(1): Show | 4 | HG02300.hp1 NA18747.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304-7924dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21553534 | |||||
| chrX:21553534
|
CA | C | 11 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(8): Show | 11 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1304-7924delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21553534 | |||||
| chrX:21553571
|
A | G | 1 | a0001c0001t0013g0100 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1304-7900A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21553571 | ||||||
| chrX:21553691
|
CT | C | 4 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304-7778delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21553691 | |||||
| chrX:21554478
|
C | T | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1304-6993C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21554478 | ||||||
| chrX:21554782
|
T | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0039others(32): Show | 35 | HG00642.hp1 HG01255.hp1 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.1304-6689T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21554782 | ||||||
| chrX:21555007
|
C | CT | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1304-6449dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21555007 | |||||
| chrX:21555400
|
C | G | 17 | a0001c0001t0003g0015a0001c0001t0009g0010a0001c0001t0009g0011others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1304-6071C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21555400 | ||||||
| chrX:21555424
|
C | G | 1 | a0001c0001t0007g0127 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1304-6047C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21555424 | ||||||
| chrX:21555443
|
A | G | 1 | a0001c0001t0007g0127 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1304-6028A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21555443 | ||||||
| chrX:21555457
|
T | C | 1 | a0001c0001t0011g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1304-6014T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21555457 | ||||||
| chrX:21557645
|
G | A | 69 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0019others(66): Show | 69 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.1304-3826G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21557645 | ||||||
| chrX:21557758
|
T | A | 4 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304-3713T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21557758 | ||||||
| chrX:21557818
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-3653T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21557818 | ||||||
| chrX:21557943
|
G | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1304-3528G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21557943 | ||||||
| chrX:21558103
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-3368C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21558103 | ||||||
| chrX:21558381
|
T | A | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1304-3090T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21558381 | ||||||
| chrX:21558552
|
T | TA | 4 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304-2908dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21558552 | |||||
| chrX:21558677
|
T | G | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1304-2794T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21558677 | ||||||
| chrX:21558885
|
AT | A | 1 | a0001c0001t0001g0075 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1304-2580delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21558885 | |||||
| chrX:21559112
|
G | A | 3 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0162 | 3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1304-2359G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21559112 | ||||||
| chrX:21559255
|
A | G | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1304-2216A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21559255 | ||||||
| chrX:21559302
|
T | C | 7 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1304-2169T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21559302 | ||||||
| chrX:21559520
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-1951A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21559520 | ||||||
| chrX:21559523
|
G | A | 6 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1304-1948G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21559523 | ||||||
| chrX:21559668
|
T | G | 6 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1304-1803T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21559668 | ||||||
| chrX:21560241
|
G | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-1230G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21560241 | ||||||
| chrX:21560380
|
A | G | 1 | a0001c0001t0008g0124 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1304-1091A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21560380 | ||||||
| chrX:21560403
|
C | T | 1 | a0001c0001t0010g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1304-1068C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21560403 | ||||||
| chrX:21560883
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1304-588T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21560883 | ||||||
| chrX:21561167
|
T | C | 1 | a0001c0001t0007g0022 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1304-304T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21561167 | ||||||
| chrX:21561182
|
T | TA | 3 | a0001c0001t0001g0071a0001c0001t0003g0024a0001c0001t0004g0055 | 3 | HG01258.hp1 HG02280.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1304-271dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21561182 | |||||
| chrX:21561182
|
TA | T | 36 | a0001c0001t0001g0060a0001c0001t0001g0102a0001c0001t0001g0103others(33): Show | 36 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1304-271delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21561182 | |||||
| chrX:21561182
|
TAA | T | 28 | a0001c0001t0002g0019a0001c0001t0003g0015a0001c0001t0004g0129others(25): Show | 28 | HG00609.hp1 HG01071.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1304-272_1304-271d others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21561182 | |||||
| chrX:21561182
|
TAAA | T | 1 | a0001c0001t0010g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1304-273_1304-271d others(5): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 21561182 | |||||
| chrX:21561270
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG03491.hp1 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1304-201C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 11/21 | chrX | 21561270 | ||||||
| chrX:21562003
|
T | G | 1 | a0001c0001t0006g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1393+443T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | chrX | 21562003 | ||||||
| chrX:21562028
|
G | GA | 6 | a0001c0001t0002g0112a0001c0001t0006g0155a0001c0001t0007g0140others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1393+480dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 21562028 | |||||
| chrX:21562028
|
GA | G | 1 | a0001c0001t0006g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1393+480delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 21562028 | |||||
| chrX:21562219
|
ATGG | A | 1 | a0001c0001t0001g0131 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1393+663_1393+665d others(5): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 21562219 | |||||
| chrX:21562268
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1393+708A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | chrX | 21562268 | ||||||
| chrX:21562365
|
G | A | 1 | a0001c0006t0028g0059 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1393+805G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | chrX | 21562365 | ||||||
| chrX:21562718
|
A | G | 2 | a0001c0001t0003g0116a0001c0001t0004g0117 | 2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1394-520A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | chrX | 21562718 | ||||||
| chrX:21563158
|
C | CTAA | 7 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1394-77_1394-75dup others(3): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 21563158 | |||||
| chrX:21563663
|
T | A | 6 | a0001c0001t0001g0035a0001c0001t0001g0052a0001c0001t0001g0058others(3): Show | 6 | HG02056.hp1 HG02698.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1608+211T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21563663 | ||||||
| chrX:21564162
|
G | GA | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1608+713dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21564162 | |||||
| chrX:21564178
|
A | G | 70 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0019others(67): Show | 70 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.1608+726A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21564178 | ||||||
| chrX:21564186
|
A | AG | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1608+735dupG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21564186 | |||||
| chrX:21564206
|
G | T | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1608+754G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21564206 | ||||||
| chrX:21564231
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1608+779G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21564231 | ||||||
| chrX:21564381
|
A | G | 4 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0004g0020others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+929A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21564381 | ||||||
| chrX:21564425
|
A | AC | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1608+973_1608+974i others(3): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21564425 | ||||||
| chrX:21564430
|
GT | G | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1608+980delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21564430 | |||||
| chrX:21564454
|
A | C | 1 | a0001c0001t0015g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1608+1002A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21564454 | ||||||
| chrX:21564502
|
C | CT | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1608+1051dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21564502 | |||||
| chrX:21564601
|
A | AT | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1608+1153dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21564601 | |||||
| chrX:21564652
|
T | TG | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1608+1201dupG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21564652 | |||||
| chrX:21564732
|
T | TA | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1608+1284dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21564732 | |||||
| chrX:21564754
|
GT | G | 25 | a0001c0001t0003g0015a0001c0001t0006g0155a0001c0001t0006g0157others(22): Show | 25 | HG01081.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1608+1313delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21564754 | |||||
| chrX:21564833
|
T | TC | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1608+1382dupC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21564833 | |||||
| chrX:21565123
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1608+1671C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21565123 | ||||||
| chrX:21565371
|
G | A | 3 | a0001c0001t0002g0004a0001c0001t0004g0020a0001c0001t0008g0005 | 3 | HG01069.hp1 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1608+1919G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21565371 | ||||||
| chrX:21565608
|
T | C | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1608+2156T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21565608 | ||||||
| chrX:21566099
|
A | AT | 36 | a0001c0001t0002g0004a0001c0001t0003g0015a0001c0001t0003g0031others(33): Show | 36 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1608+2650dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21566099 | |||||
| chrX:21566145
|
G | A | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1608+2693G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21566145 | ||||||
| chrX:21566169
|
A | T | 3 | a0001c0001t0005g0079a0001c0001t0005g0095a0001c0001t0005g0099 | 3 | NA18747.hp1 NA18960.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1608+2717A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21566169 | ||||||
| chrX:21566263
|
G | C | 4 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+2811G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21566263 | ||||||
| chrX:21566499
|
T | G | 2 | a0001c0001t0009g0010a0001c0001t0041g0009 | 2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1608+3047T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21566499 | ||||||
| chrX:21567067
|
G | T | 1 | a0001c0001t0012g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1608+3615G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21567067 | ||||||
| chrX:21567359
|
T | C | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1608+3907T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21567359 | ||||||
| chrX:21567792
|
TGTG | T | 1 | a0001c0001t0001g0134 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1608+4344_1608+434 others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567792 | |||||
| chrX:21567795
|
G | GGT | 1 | a0001c0001t0041g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1608+4388_1608+438 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | |||||
| chrX:21567795
|
G | GGTGT | 4 | a0001c0001t0001g0096a0001c0001t0009g0013a0001c0001t0019g0014others(1): Show | 4 | HG01884.hp2 HG03486.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+4386_1608+438 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | |||||
| chrX:21567795
|
G | GGTGTGT | 1 | a0001c0001t0002g0126 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1608+4384_1608+438 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | |||||
| chrX:21567795
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0011g0016 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1608+4380_1608+438 others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | |||||
| chrX:21567795
|
G | GGTT | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+4345_1608+434 others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | |||||
| chrX:21567795
|
GGT | G | 29 | a0001c0001t0001g0048a0001c0001t0001g0062a0001c0001t0001g0069others(26): Show | 29 | HG00673.hp1 HG00735.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1608+4388_1608+438 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | |||||
| chrX:21567795
|
GGTGT | G | 57 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(54): Show | 57 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1608+4386_1608+438 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | |||||
| chrX:21567795
|
GGTGTGT | G | 35 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0052others(32): Show | 35 | HG00642.hp1 HG01255.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.1608+4384_1608+438 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | |||||
| chrX:21567795
|
GGTGTGTG others(1): Show |
G | 7 | a0001c0001t0002g0019a0001c0001t0002g0111a0001c0001t0002g0112others(4): Show | 7 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.1608+4382_1608+438 others(12): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | |||||
| chrX:21567795
|
GGTGTGTG others(3): Show |
G | 8 | a0001c0001t0002g0028a0001c0001t0003g0024a0001c0001t0003g0101others(5): Show | 8 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1608+4380_1608+438 others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21567795 | |||||
| chrX:21567891
|
T | C | 1 | a0001c0001t0043g0007 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1608+4439T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21567891 | ||||||
| chrX:21567899
|
A | T | 1 | a0001c0001t0010g0153 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1608+4447A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21567899 | ||||||
| chrX:21567922
|
T | C | 1 | a0001c0001t0017g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1608+4470T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21567922 | ||||||
| chrX:21568205
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1608+4753T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21568205 | ||||||
| chrX:21568351
|
C | T | 2 | a0001c0001t0002g0112a0001c0001t0002g0113 | 2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1608+4899C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21568351 | ||||||
| chrX:21568585
|
G | A | 2 | a0001c0001t0002g0004a0001c0001t0008g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1608+5133G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21568585 | ||||||
| chrX:21568646
|
TA | T | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1608+5195delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21568646 | ||||||
| chrX:21569114
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+5662T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21569114 | ||||||
| chrX:21569210
|
G | GTTA | 4 | a0001c0001t0042g0008a0001c0003t0014g0147a0001c0003t0014g0149others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+5779_1608+578 others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21569210 | |||||
| chrX:21569210
|
GTTA | G | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1608+5779_1608+578 others(7): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21569210 | |||||
| chrX:21569218
|
T | G | 1 | a0001c0001t0002g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1608+5766T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21569218 | ||||||
| chrX:21569508
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1608+6056C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21569508 | ||||||
| chrX:21569515
|
A | G | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1608+6063A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21569515 | ||||||
| chrX:21570271
|
C | G | 1 | a0001c0001t0016g0085 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1608+6819C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21570271 | ||||||
| chrX:21570706
|
G | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+7254G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21570706 | ||||||
| chrX:21570767
|
C | T | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1608+7315C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21570767 | ||||||
| chrX:21570974
|
T | C | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1608+7522T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21570974 | ||||||
| chrX:21571313
|
A | G | 1 | a0001c0001t0038g0150 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1608+7861A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21571313 | ||||||
| chrX:21571467
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1608+8015A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21571467 | ||||||
| chrX:21571684
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1608+8232A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21571684 | ||||||
| chrX:21572131
|
A | G | 1 | a0001c0001t0024g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1608+8679A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21572131 | ||||||
| chrX:21572329
|
A | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+8877A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21572329 | ||||||
| chrX:21572624
|
C | G | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+9172C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21572624 | ||||||
| chrX:21572792
|
A | G | 11 | a0001c0001t0003g0031a0001c0001t0006g0157a0001c0001t0006g0159others(8): Show | 11 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1608+9340A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21572792 | ||||||
| chrX:21573050
|
C | G | 2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | NA18984.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1608+9598C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21573050 | ||||||
| chrX:21573436
|
C | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+9984C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21573436 | ||||||
| chrX:21573497
|
G | A | 2 | a0001c0001t0002g0125a0001c0001t0002g0126 | 2 | NA18943.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1608+10045G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21573497 | ||||||
| chrX:21574555
|
G | T | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+11103G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21574555 | ||||||
| chrX:21574764
|
G | A | 11 | a0001c0001t0006g0157a0001c0001t0006g0159a0001c0001t0006g0160others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1608+11312G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21574764 | ||||||
| chrX:21575222
|
A | G | 2 | a0001c0001t0007g0140a0001c0001t0020g0141 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1608+11770A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21575222 | ||||||
| chrX:21575279
|
T | C | 1 | a0001c0002t0007g0040 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1608+11827T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21575279 | ||||||
| chrX:21575364
|
TC | T | 1 | a0001c0001t0008g0005 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1608+11918delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21575364 | |||||
| chrX:21575518
|
A | G | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1608+12066A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21575518 | ||||||
| chrX:21575523
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+12071T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21575523 | ||||||
| chrX:21575968
|
C | G | 2 | a0001c0001t0007g0140a0001c0001t0020g0141 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1608+12516C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21575968 | ||||||
| chrX:21576268
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1608+12816G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21576268 | ||||||
| chrX:21576753
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1608+13301G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21576753 | ||||||
| chrX:21576876
|
T | C | 3 | a0001c0003t0014g0147a0001c0003t0014g0149a0001c0003t0026g0148 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+13424T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21576876 | ||||||
| chrX:21577112
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0158 | 2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1609-13460C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21577112 | ||||||
| chrX:21577139
|
A | C | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-13433A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21577139 | ||||||
| chrX:21577624
|
C | CT | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-12939dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21577624 | |||||
| chrX:21578370
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1609-12202A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21578370 | ||||||
| chrX:21578549
|
G | GT | 12 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0080others(9): Show | 12 | HG00280.hp1 HG01074.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1609-12007dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21578549 | |||||
| chrX:21578549
|
G | GTT | 1 | a0001c0001t0027g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1609-12008_1609-12 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21578549 | |||||
| chrX:21578549
|
GT | G | 27 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0067others(24): Show | 27 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1609-12007delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21578549 | |||||
| chrX:21578549
|
GTT | G | 3 | a0001c0001t0006g0161a0001c0001t0009g0010a0001c0001t0041g0009 | 3 | HG02280.hp2 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1609-12008_1609-12 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21578549 | |||||
| chrX:21578930
|
G | A | 2 | a0001c0001t0003g0116a0001c0001t0004g0117 | 2 | HG02015.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1609-11642G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21578930 | ||||||
| chrX:21579718
|
G | C | 8 | a0001c0001t0002g0028a0001c0001t0003g0024a0001c0001t0003g0029others(5): Show | 8 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1609-10854G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21579718 | ||||||
| chrX:21581004
|
C | T | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1609-9568C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21581004 | ||||||
| chrX:21581245
|
T | C | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-9327T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21581245 | ||||||
| chrX:21581521
|
G | A | 1 | a0001c0002t0001g0042 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1609-9051G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21581521 | ||||||
| chrX:21581657
|
A | G | 4 | a0001c0001t0042g0008a0001c0003t0014g0147a0001c0003t0014g0149others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-8915A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21581657 | ||||||
| chrX:21581770
|
T | C | 5 | a0001c0001t0003g0015a0001c0001t0011g0016a0001c0001t0011g0017others(2): Show | 5 | HG02717.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1609-8802T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21581770 | ||||||
| chrX:21582396
|
T | C | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-8176T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21582396 | ||||||
| chrX:21582958
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1609-7614T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21582958 | ||||||
| chrX:21583313
|
T | C | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1609-7259T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21583313 | ||||||
| chrX:21584360
|
T | C | 1 | a0001c0001t0007g0022 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1609-6212T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21584360 | ||||||
| chrX:21584933
|
C | G | 1 | a0001c0001t0001g0093 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1609-5639C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21584933 | ||||||
| chrX:21585621
|
G | A | 1 | a0001c0001t0005g0095 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1609-4951G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21585621 | ||||||
| chrX:21585667
|
T | G | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-4905T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21585667 | ||||||
| chrX:21585707
|
T | C | 2 | a0001c0003t0014g0147a0001c0003t0014g0149 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1609-4865T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21585707 | ||||||
| chrX:21586185
|
G | C | 1 | a0001c0001t0030g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1609-4387G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586185 | ||||||
| chrX:21586251
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1609-4321G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586251 | ||||||
| chrX:21586332
|
G | T | 2 | a0001c0001t0002g0112a0001c0001t0013g0066 | 2 | HG01167.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1609-4240G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586332 | ||||||
| chrX:21586413
|
G | C | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1609-4159G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586413 | ||||||
| chrX:21586472
|
G | T | 1 | a0001c0001t0013g0066 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1609-4100G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586472 | ||||||
| chrX:21586847
|
C | A | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-3725C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586847 | ||||||
| chrX:21586877
|
G | C | 2 | a0001c0003t0014g0147a0001c0003t0014g0149 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1609-3695G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586877 | ||||||
| chrX:21586904
|
G | A | 4 | a0001c0001t0002g0115a0001c0001t0003g0070a0001c0001t0003g0101others(1): Show | 4 | NA18967.hp1 NA18974.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-3668G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21586904 | ||||||
| chrX:21587111
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1609-3461C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21587111 | ||||||
| chrX:21587156
|
T | G | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0031g0065others(1): Show | 4 | HG02040.hp1 NA18989.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-3416T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21587156 | ||||||
| chrX:21587493
|
T | C | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1609-3079T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21587493 | ||||||
| chrX:21587597
|
T | G | 5 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0162others(2): Show | 5 | HG01071.hp2 HG01884.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1609-2975T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21587597 | ||||||
| chrX:21587887
|
G | GA | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1609-2683dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21587887 | |||||
| chrX:21587943
|
G | A | 3 | a0001c0001t0002g0115a0001c0001t0003g0070a0001c0001t0035g0054 | 3 | NA18967.hp1 NA18974.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1609-2629G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21587943 | ||||||
| chrX:21588773
|
GT | G | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1609-1797delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 21588773 | |||||
| chrX:21588844
|
A | G | 6 | a0001c0001t0003g0029a0001c0001t0007g0140a0001c0001t0010g0152others(3): Show | 6 | HG01071.hp2 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1609-1728A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21588844 | ||||||
| chrX:21589168
|
A | G | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1609-1404A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21589168 | ||||||
| chrX:21589685
|
A | G | 1 | a0001c0001t0024g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1609-887A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21589685 | ||||||
| chrX:21589777
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1609-795C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21589777 | ||||||
| chrX:21590503
|
G | A | 2 | a0001c0003t0014g0147a0001c0003t0014g0149 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1609-69G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 13/21 | chrX | 21590503 | ||||||
| chrX:21591383
|
T | TTG | 5 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(2): Show | 5 | HG01071.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1830+189_1830+190i others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21591383 | ||||||
| chrX:21591384
|
A | T | 5 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(2): Show | 5 | HG01071.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1830+190A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21591384 | ||||||
| chrX:21591558
|
G | GT | 1 | a0001c0001t0001g0035 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1830+374dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chrX | 21591558 | |||||
| chrX:21591558
|
G | T | 1 | a0001c0001t0003g0029 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1830+364G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21591558 | ||||||
| chrX:21591704
|
C | T | 3 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1830+510C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21591704 | ||||||
| chrX:21591710
|
G | T | 3 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1830+516G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21591710 | ||||||
| chrX:21591728
|
A | G | 6 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1830+534A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21591728 | ||||||
| chrX:21592027
|
A | G | 29 | a0001c0001t0003g0029a0001c0001t0006g0155a0001c0001t0006g0157others(26): Show | 29 | HG01071.hp2 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1830+833A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21592027 | ||||||
| chrX:21592775
|
A | T | 2 | a0001c0001t0002g0112a0001c0001t0013g0066 | 2 | HG01167.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1830+1581A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21592775 | ||||||
| chrX:21593184
|
A | C | 1 | a0001c0001t0001g0074 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1831-1790A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21593184 | ||||||
| chrX:21593650
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0036others(159): Show | 162 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.1831-1324G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21593650 | ||||||
| chrX:21593772
|
G | A | 7 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(4): Show | 7 | HG01243.hp1 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1831-1202G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21593772 | ||||||
| chrX:21593914
|
C | T | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1831-1060C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21593914 | ||||||
| chrX:21594025
|
A | T | 4 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(1): Show | 4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1831-949A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21594025 | ||||||
| chrX:21594117
|
T | C | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1831-857T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 15/21 | chrX | 21594117 | ||||||
| chrX:21595082
|
G | GT | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1904+46dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chrX | 21595082 | |||||
| chrX:21595478
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1976+83C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21595478 | ||||||
| chrX:21595555
|
A | G | 2 | a0001c0001t0033g0002a0001c0002t0007g0041 | 2 | NA18977.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1976+160A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21595555 | ||||||
| chrX:21595746
|
C | T | 1 | a0001c0001t0024g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1976+351C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21595746 | ||||||
| chrX:21595902
|
C | CA | 2 | a0001c0001t0009g0011a0001c0001t0009g0012 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1976+508dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21595902 | |||||
| chrX:21596120
|
T | C | 1 | a0001c0001t0027g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1976+725T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21596120 | ||||||
| chrX:21596264
|
G | A | 3 | a0001c0001t0006g0157a0001c0001t0006g0159a0001c0006t0028g0059 | 3 | HG02886.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1976+869G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21596264 | ||||||
| chrX:21596503
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1976+1108T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21596503 | ||||||
| chrX:21596561
|
C | CA | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1976+1170dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21596561 | |||||
| chrX:21596662
|
GT | G | 1 | a0001c0001t0003g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1976+1279delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21596662 | |||||
| chrX:21597015
|
G | A | 4 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(1): Show | 4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1976+1620G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21597015 | ||||||
| chrX:21597033
|
C | A | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1976+1638C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21597033 | ||||||
| chrX:21597404
|
T | G | 4 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(1): Show | 4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1976+2009T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21597404 | ||||||
| chrX:21598008
|
C | CAT | 3 | a0001c0001t0001g0036a0001c0001t0020g0141a0001c0001t0042g0008 | 3 | HG01243.hp1 HG02647.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1976+2631_1976+263 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21598008 | |||||
| chrX:21598008
|
C | CATAT | 3 | a0001c0001t0001g0074a0001c0003t0014g0147a0001c0003t0014g0149 | 3 | HG02615.hp1 HG03471.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1976+2629_1976+263 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21598008 | |||||
| chrX:21598008
|
CAT | C | 7 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0009g0010others(4): Show | 7 | HG00673.hp1 HG01109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1976+2631_1976+263 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21598008 | |||||
| chrX:21598008
|
CATAT | C | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1976+2629_1976+263 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21598008 | |||||
| chrX:21598024
|
TATAC | T | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1976+2631_1976+263 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21598024 | |||||
| chrX:21598025
|
A | G | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1976+2630A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21598025 | ||||||
| chrX:21598026
|
T | TAC | 1 | a0001c0001t0006g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1976+2647_1976+264 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21598026 | |||||
| chrX:21598042
|
C | A | 2 | a0001c0001t0011g0016a0001c0001t0011g0138 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1976+2647C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21598042 | ||||||
| chrX:21598242
|
G | C | 30 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(27): Show | 30 | HG01071.hp2 HG01081.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1976+2847G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21598242 | ||||||
| chrX:21598252
|
A | G | 6 | a0001c0001t0002g0047a0001c0001t0002g0049a0001c0001t0002g0050others(3): Show | 6 | NA18943.hp1 NA18944.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.1976+2857A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21598252 | ||||||
| chrX:21598356
|
G | GA | 3 | a0001c0001t0020g0141a0001c0003t0014g0147a0001c0003t0014g0149 | 3 | HG01243.hp1 HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1977-2925dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21598356 | |||||
| chrX:21598969
|
C | T | 4 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(1): Show | 4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1977-2313C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21598969 | ||||||
| chrX:21598974
|
T | C | 1 | a0001c0001t0031g0065 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1977-2308T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21598974 | ||||||
| chrX:21599324
|
G | GT | 4 | a0001c0001t0001g0081a0001c0001t0002g0047a0001c0001t0022g0033others(1): Show | 4 | HG02055.hp1 HG02486.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1977-1949dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599324 | |||||
| chrX:21599339
|
G | GGT | 15 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0158others(12): Show | 15 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1977-1899_1977-189 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599339 | |||||
| chrX:21599339
|
G | GGTGT | 3 | a0001c0001t0002g0043a0001c0001t0002g0125a0001c0001t0042g0008 | 3 | HG02647.hp1 HG02809.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1977-1901_1977-189 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599339 | |||||
| chrX:21599339
|
G | GGTGTGT | 1 | a0001c0001t0023g0006 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1977-1903_1977-189 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599339 | |||||
| chrX:21599339
|
G | GT | 1 | a0001c0001t0025g0130 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1977-1943_1977-194 others(5): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21599339 | ||||||
| chrX:21599339
|
GGT | G | 61 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0039others(58): Show | 61 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.1977-1899_1977-189 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599339 | |||||
| chrX:21599339
|
GGTGT | G | 39 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0067others(36): Show | 39 | HG00280.hp1 HG00673.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1977-1901_1977-189 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599339 | |||||
| chrX:21599339
|
GGTGTGT | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0058a0001c0001t0004g0129others(1): Show | 4 | HG00609.hp1 HG02486.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1977-1903_1977-189 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599339 | |||||
| chrX:21599348
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1977-1934G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21599348 | ||||||
| chrX:21599381
|
TGTGA | T | 1 | a0001c0001t0038g0150 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1977-1899_1977-189 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599381 | |||||
| chrX:21599383
|
T | TGA | 1 | a0001c0002t0001g0042 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1977-1896_1977-189 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599383 | |||||
| chrX:21599383
|
TGA | T | 6 | a0001c0001t0002g0028a0001c0001t0003g0015a0001c0001t0003g0024others(3): Show | 6 | HG01081.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1977-1896_1977-189 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 21599383 | |||||
| chrX:21599896
|
A | G | 1 | a0001c0001t0017g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1977-1386A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21599896 | ||||||
| chrX:21600039
|
A | C | 2 | a0001c0001t0012g0045a0001c0001t0020g0141 | 2 | HG01243.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1977-1243A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21600039 | ||||||
| chrX:21600112
|
C | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0082a0001c0001t0001g0084 | 3 | HG00642.hp1 HG01261.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.1977-1170C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21600112 | ||||||
| chrX:21600427
|
C | T | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1977-855C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21600427 | ||||||
| chrX:21600880
|
C | T | 1 | a0001c0001t0017g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1977-402C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 17/21 | chrX | 21600880 | ||||||
| chrX:21601450
|
AT | A | 1 | a0001c0001t0001g0078 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2044+106delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chrX | 21601450 | |||||
| chrX:21601563
|
A | AC | 1 | a0001c0001t0002g0003 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2044+219dupC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chrX | 21601563 | |||||
| chrX:21601949
|
G | A | 3 | a0001c0001t0011g0016a0001c0001t0011g0017a0001c0001t0011g0138 | 3 | HG03041.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2044+600G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21601949 | ||||||
| chrX:21602125
|
T | TTTTG | 1 | a0001c0001t0004g0021 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2044+800_2044+803d others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chrX | 21602125 | |||||
| chrX:21602129
|
G | T | 7 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(4): Show | 7 | HG01071.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044+780G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602129 | ||||||
| chrX:21602164
|
C | T | 1 | a0001c0003t0014g0149 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2044+815C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602164 | ||||||
| chrX:21602194
|
G | A | 3 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0162 | 3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2044+845G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602194 | ||||||
| chrX:21602229
|
C | T | 2 | a0001c0001t0002g0113a0001c0001t0029g0023 | 2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.2044+880C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602229 | ||||||
| chrX:21602504
|
A | C | 3 | a0001c0001t0011g0016a0001c0001t0011g0017a0001c0001t0011g0138 | 3 | HG03041.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2044+1155A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602504 | ||||||
| chrX:21602736
|
G | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0096a0001c0001t0030g0086 | 3 | HG02698.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2044+1387G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602736 | ||||||
| chrX:21602939
|
C | G | 8 | a0001c0001t0002g0028a0001c0001t0003g0015a0001c0001t0003g0024others(5): Show | 8 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044+1590C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21602939 | ||||||
| chrX:21603100
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2044+1751A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21603100 | ||||||
| chrX:21603372
|
C | A | 6 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(3): Show | 6 | HG02615.hp1 HG02922.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2044+2023C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21603372 | ||||||
| chrX:21603400
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2044+2051A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21603400 | ||||||
| chrX:21604030
|
G | A | 4 | a0001c0001t0011g0016a0001c0001t0011g0017a0001c0001t0011g0138others(1): Show | 4 | HG03041.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2044+2681G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21604030 | ||||||
| chrX:21604470
|
A | AAT | 5 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0162others(2): Show | 5 | HG01071.hp2 HG01884.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2045-2299_2045-229 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chrX | 21604470 | |||||
| chrX:21605313
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0128 | 2 | NA19066.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2045-1466A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605313 | ||||||
| chrX:21605357
|
T | C | 2 | a0001c0003t0014g0147a0001c0003t0014g0149 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2045-1422T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605357 | ||||||
| chrX:21605515
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2045-1264A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605515 | ||||||
| chrX:21605639
|
A | G | 7 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2045-1140A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605639 | ||||||
| chrX:21605646
|
TC | T | 3 | a0001c0001t0005g0079a0001c0001t0005g0095a0001c0001t0005g0099 | 3 | NA18747.hp1 NA18960.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.2045-1132delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605646 | ||||||
| chrX:21605754
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2045-1025G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605754 | ||||||
| chrX:21605769
|
C | T | 9 | a0001c0001t0002g0028a0001c0001t0003g0015a0001c0001t0003g0024others(6): Show | 9 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2045-1010C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605769 | ||||||
| chrX:21605882
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2045-897A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605882 | ||||||
| chrX:21605982
|
T | C | 3 | a0001c0001t0020g0141a0001c0003t0014g0147a0001c0003t0014g0149 | 3 | HG01243.hp1 HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2045-797T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21605982 | ||||||
| chrX:21606228
|
G | A | 2 | a0001c0001t0002g0004a0001c0001t0008g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2045-551G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21606228 | ||||||
| chrX:21606430
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2045-349A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 18/21 | chrX | 21606430 | ||||||
| chrX:21607315
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2145+436G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 19/21 | chrX | 21607315 | ||||||
| chrX:21608603
|
T | C | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2146-468T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 19/21 | chrX | 21608603 | ||||||
| chrX:21608624
|
T | C | 2 | a0001c0003t0014g0147a0001c0003t0014g0149 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2146-447T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 19/21 | chrX | 21608624 | ||||||
| chrX:21608740
|
T | G | 1 | a0001c0001t0017g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2146-331T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 19/21 | chrX | 21608740 | ||||||
| chrX:21609807
|
T | C | 1 | a0001c0001t0023g0006 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2692+190T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21609807 | ||||||
| chrX:21609852
|
T | G | 4 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(1): Show | 4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2692+235T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21609852 | ||||||
| chrX:21609973
|
G | A | 1 | a0001c0001t0017g0018 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2692+356G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21609973 | ||||||
| chrX:21610138
|
G | A | 2 | a0001c0003t0014g0147a0001c0003t0014g0149 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2692+521G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21610138 | ||||||
| chrX:21610250
|
C | T | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2692+633C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21610250 | ||||||
| chrX:21610334
|
T | C | 9 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(6): Show | 9 | HG01071.hp2 HG01884.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2692+717T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21610334 | ||||||
| chrX:21611299
|
T | A | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2692+1682T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21611299 | ||||||
| chrX:21611697
|
G | C | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2692+2080G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21611697 | ||||||
| chrX:21611739
|
C | A | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2692+2122C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21611739 | ||||||
| chrX:21611893
|
ACT | A | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2692+2277_2692+227 others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21611893 | ||||||
| chrX:21612694
|
G | C | 2 | a0001c0001t0023g0006a0001c0001t0043g0007 | 2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2692+3077G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21612694 | ||||||
| chrX:21613484
|
C | T | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2692+3867C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21613484 | ||||||
| chrX:21613821
|
TC | T | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+4207delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21613821 | |||||
| chrX:21613939
|
C | CA | 5 | a0001c0001t0002g0114a0001c0001t0011g0016a0001c0001t0011g0017others(2): Show | 5 | HG00140.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2692+4336dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21613939 | |||||
| chrX:21613939
|
CA | C | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2692+4336delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21613939 | |||||
| chrX:21614121
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2692+4504G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21614121 | ||||||
| chrX:21614585
|
T | TA | 23 | a0001c0001t0003g0024a0001c0001t0003g0029a0001c0001t0006g0155others(20): Show | 23 | HG01071.hp2 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.2692+4976dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21614585 | |||||
| chrX:21614712
|
G | T | 1 | a0001c0001t0022g0033 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2692+5095G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21614712 | ||||||
| chrX:21614716
|
G | C | 1 | a0001c0001t0024g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2692+5099G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21614716 | ||||||
| chrX:21615092
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0036others(159): Show | 162 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.2692+5475A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21615092 | ||||||
| chrX:21615253
|
T | A | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2692+5636T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21615253 | ||||||
| chrX:21615346
|
TG | T | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+5731delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21615346 | |||||
| chrX:21615521
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2692+5904T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21615521 | ||||||
| chrX:21615561
|
A | G | 4 | a0001c0001t0011g0016a0001c0001t0011g0017a0001c0001t0011g0138others(1): Show | 4 | HG03041.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2692+5944A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21615561 | ||||||
| chrX:21615575
|
G | GA | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+5961dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21615575 | |||||
| chrX:21615736
|
A | G | 1 | a0001c0001t0003g0044 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2692+6119A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21615736 | ||||||
| chrX:21616003
|
AC | A | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+6388delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21616003 | |||||
| chrX:21616058
|
T | C | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2692+6441T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21616058 | ||||||
| chrX:21616189
|
TC | T | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+6575delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21616189 | |||||
| chrX:21616359
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2692+6742G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21616359 | ||||||
| chrX:21616762
|
TC | T | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+7148delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21616762 | |||||
| chrX:21616856
|
CTTAA | C | 2 | a0001c0001t0002g0004a0001c0001t0008g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2692+7243_2692+724 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21616856 | |||||
| chrX:21616926
|
GC | G | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+7311delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21616926 | |||||
| chrX:21617099
|
TTTATG | T | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2692+7492_2692+749 others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21617099 | |||||
| chrX:21617382
|
C | T | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2692+7765C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21617382 | ||||||
| chrX:21617527
|
A | AG | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+7911dupG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21617527 | |||||
| chrX:21617695
|
T | G | 5 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(2): Show | 5 | HG01071.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2692+8078T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21617695 | ||||||
| chrX:21617757
|
G | A | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2692+8140G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21617757 | ||||||
| chrX:21617824
|
CA | C | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+8212delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21617824 | |||||
| chrX:21617911
|
A | AC | 4 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0162others(1): Show | 4 | HG01884.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2692+8301dupC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21617911 | |||||
| chrX:21617911
|
AC | A | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+8301delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21617911 | |||||
| chrX:21617932
|
G | A | 2 | a0001c0001t0022g0033a0001c0001t0027g0034 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2692+8315G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21617932 | ||||||
| chrX:21617973
|
CT | C | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+8358delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21617973 | |||||
| chrX:21618109
|
G | C | 5 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(2): Show | 5 | HG01884.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2692+8492G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21618109 | ||||||
| chrX:21618213
|
A | T | 3 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0013 | 3 | HG02572.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2692+8596A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21618213 | ||||||
| chrX:21618364
|
A | G | 9 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2692+8747A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21618364 | ||||||
| chrX:21618366
|
TC | T | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+8752delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21618366 | |||||
| chrX:21618827
|
A | AG | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+9213dupG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21618827 | |||||
| chrX:21619051
|
A | AT | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+9439dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21619051 | |||||
| chrX:21619057
|
A | G | 2 | a0001c0001t0006g0155a0003c0004t0006g0154 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2692+9440A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21619057 | ||||||
| chrX:21619690
|
C | T | 66 | a0001c0001t0001g0077a0001c0001t0002g0003a0001c0001t0002g0004others(63): Show | 66 | HG00621.hp1 HG00735.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.2692+10073C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21619690 | ||||||
| chrX:21619837
|
T | A | 1 | a0001c0001t0012g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2692+10220T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21619837 | ||||||
| chrX:21620003
|
T | TG | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+10389dupG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21620003 | |||||
| chrX:21620016
|
CTTTA | C | 1 | a0001c0001t0001g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2692+10404_2692+10 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21620016 | |||||
| chrX:21620256
|
A | G | 4 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(1): Show | 4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2692+10639A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21620256 | ||||||
| chrX:21620450
|
G | GC | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+10836dupC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21620450 | |||||
| chrX:21620660
|
CA | C | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+11046delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21620660 | |||||
| chrX:21620820
|
G | GA | 3 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0162 | 3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2692+11211dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21620820 | |||||
| chrX:21620871
|
C | A | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2692+11254C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21620871 | ||||||
| chrX:21620926
|
TC | T | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+11312delC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21620926 | |||||
| chrX:21621018
|
C | T | 1 | a0001c0001t0004g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2692+11401C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21621018 | ||||||
| chrX:21621169
|
A | AC | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+11553dupC | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21621169 | |||||
| chrX:21621289
|
T | C | 1 | a0001c0001t0001g0052 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2692+11672T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21621289 | ||||||
| chrX:21621493
|
C | T | 17 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(14): Show | 17 | HG01884.hp1 HG02280.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.2692+11876C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21621493 | ||||||
| chrX:21621508
|
G | A | 6 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(3): Show | 6 | HG02615.hp1 HG02922.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2692+11891G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21621508 | ||||||
| chrX:21622392
|
T | C | 30 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(27): Show | 30 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.2692+12775T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21622392 | ||||||
| chrX:21622593
|
G | GA | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+12982dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21622593 | |||||
| chrX:21622853
|
A | AT | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+13242dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21622853 | |||||
| chrX:21622949
|
A | AG | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+13334dupG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21622949 | |||||
| chrX:21623292
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2692+13675T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21623292 | ||||||
| chrX:21623467
|
AT | A | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+13852delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21623467 | |||||
| chrX:21623542
|
T | C | 10 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(7): Show | 10 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2692+13925T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21623542 | ||||||
| chrX:21624442
|
G | GA | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+14827dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21624442 | |||||
| chrX:21624482
|
A | T | 1 | a0001c0001t0027g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2692+14865A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21624482 | ||||||
| chrX:21624509
|
T | TTTG | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+14892_2692+14 others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21624509 | ||||||
| chrX:21624510
|
G | T | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+14893G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21624510 | ||||||
| chrX:21624518
|
G | GT | 3 | a0001c0001t0001g0036a0001c0001t0032g0163a0001c0001t0042g0008 | 3 | HG02647.hp1 HG04115.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2692+14910dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21624518 | |||||
| chrX:21624565
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2692+14948G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21624565 | ||||||
| chrX:21624906
|
G | T | 1 | a0001c0001t0002g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2692+15289G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21624906 | ||||||
| chrX:21625340
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2692+15723G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21625340 | ||||||
| chrX:21625678
|
C | T | 1 | a0001c0001t0018g0123 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2692+16061C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21625678 | ||||||
| chrX:21625996
|
CA | C | 1 | a0001c0001t0006g0155 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2692+16382delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21625996 | |||||
| chrX:21626153
|
T | G | 1 | a0001c0001t0001g0137 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2692+16536T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21626153 | ||||||
| chrX:21626172
|
G | A | 2 | a0001c0003t0014g0147a0001c0003t0014g0149 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2692+16555G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21626172 | ||||||
| chrX:21626244
|
T | TA | 19 | a0001c0001t0001g0035a0001c0001t0001g0082a0001c0001t0002g0004others(16): Show | 19 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2692+16650dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21626244 | |||||
| chrX:21626244
|
T | TAA | 7 | a0001c0001t0002g0028a0001c0001t0003g0015a0001c0001t0012g0025others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2692+16649_2692+16 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21626244 | |||||
| chrX:21626244
|
T | TAAA | 3 | a0001c0001t0003g0024a0001c0001t0003g0029a0001c0001t0003g0151 | 3 | HG01081.hp2 HG02280.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2692+16648_2692+16 others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21626244 | |||||
| chrX:21626244
|
TA | T | 19 | a0001c0001t0001g0037a0001c0001t0001g0093a0001c0001t0003g0044others(16): Show | 19 | HG00738.hp1 HG01884.hp2 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.2692+16650delA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21626244 | |||||
| chrX:21626244
|
TAA | T | 4 | a0001c0001t0009g0010a0001c0001t0009g0012a0001c0001t0009g0013others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.2692+16649_2692+16 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21626244 | |||||
| chrX:21626244
|
TAAA | T | 1 | a0001c0001t0009g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2692+16648_2692+16 others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21626244 | |||||
| chrX:21626267
|
AT | A | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2692+16651delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21626267 | ||||||
| chrX:21626268
|
T | A | 1 | a0001c0001t0003g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2692+16651T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21626268 | ||||||
| chrX:21626735
|
A | G | 9 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(6): Show | 9 | HG01071.hp2 HG01884.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2692+17118A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21626735 | ||||||
| chrX:21626958
|
G | C | 1 | a0001c0001t0018g0123 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2692+17341G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21626958 | ||||||
| chrX:21627220
|
C | T | 11 | a0001c0001t0002g0028a0001c0001t0003g0015a0001c0001t0003g0024others(8): Show | 11 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2692+17603C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21627220 | ||||||
| chrX:21627221
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0158 | 2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2692+17604G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21627221 | ||||||
| chrX:21627250
|
T | G | 2 | a0001c0001t0001g0068a0001c0001t0033g0002 | 2 | NA18989.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2692+17633T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21627250 | ||||||
| chrX:21627336
|
C | CA | 10 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(7): Show | 10 | HG01071.hp2 HG01884.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2692+17732dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21627336 | |||||
| chrX:21627424
|
G | A | 1 | a0001c0001t0024g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2692+17807G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21627424 | ||||||
| chrX:21627454
|
G | A | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2692+17837G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21627454 | ||||||
| chrX:21627522
|
TG | T | 1 | a0001c0001t0039g0144 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2692+17908delG | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21627522 | |||||
| chrX:21628395
|
C | G | 2 | a0001c0001t0007g0022a0001c0001t0025g0130 | 2 | HG02132.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2692+18778C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21628395 | ||||||
| chrX:21628726
|
C | T | 4 | a0001c0001t0002g0111a0001c0001t0004g0020a0001c0001t0004g0021others(1): Show | 4 | HG00741.hp2 HG01192.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.2692+19109C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21628726 | ||||||
| chrX:21628854
|
T | A | 1 | a0001c0001t0041g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2692+19237T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21628854 | ||||||
| chrX:21629422
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2693-19409C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21629422 | ||||||
| chrX:21629677
|
C | T | 5 | a0001c0001t0001g0071a0001c0001t0005g0063a0001c0001t0005g0072others(2): Show | 5 | HG02055.hp1 NA18945.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.2693-19154C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21629677 | ||||||
| chrX:21629772
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2693-19059G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21629772 | ||||||
| chrX:21629815
|
T | A | 1 | a0001c0001t0001g0082 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2693-19016T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21629815 | ||||||
| chrX:21629859
|
G | A | 4 | a0001c0001t0020g0141a0001c0001t0042g0008a0001c0003t0014g0147others(1): Show | 4 | HG01243.hp1 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2693-18972G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21629859 | ||||||
| chrX:21629881
|
G | A | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-18950G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21629881 | ||||||
| chrX:21630122
|
TAAAGTC | T | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2693-18704_2693-18 others(12): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21630122 | |||||
| chrX:21630182
|
T | G | 3 | a0001c0001t0020g0141a0001c0003t0014g0147a0001c0003t0014g0149 | 3 | HG01243.hp1 HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2693-18649T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21630182 | ||||||
| chrX:21630306
|
A | G | 8 | a0001c0001t0002g0028a0001c0001t0003g0015a0001c0001t0003g0024others(5): Show | 8 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2693-18525A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21630306 | ||||||
| chrX:21630469
|
TACA | T | 2 | a0001c0001t0003g0070a0001c0001t0035g0054 | 2 | NA18967.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2693-18356_2693-18 others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21630469 | |||||
| chrX:21630581
|
T | TCAGA | 5 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(2): Show | 5 | HG01071.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2693-18243_2693-18 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21630581 | |||||
| chrX:21630698
|
T | TAC | 10 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(7): Show | 10 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2693-18121_2693-18 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21630698 | |||||
| chrX:21630714
|
C | CATAT | 4 | a0001c0001t0001g0077a0001c0001t0002g0112a0001c0001t0004g0056others(1): Show | 4 | HG00735.hp2 HG00741.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.2693-18106_2693-18 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21630714 | |||||
| chrX:21630840
|
A | C | 10 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(7): Show | 10 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2693-17991A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21630840 | ||||||
| chrX:21630872
|
A | G | 6 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(3): Show | 6 | HG01071.hp2 HG01884.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2693-17959A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21630872 | ||||||
| chrX:21631030
|
T | A | 7 | a0001c0001t0001g0137a0001c0001t0007g0140a0001c0001t0010g0152others(4): Show | 7 | HG01071.hp2 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2693-17801T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631030 | ||||||
| chrX:21631030
|
T | TA | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-17792dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21631030 | |||||
| chrX:21631314
|
G | A | 5 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0012others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2693-17517G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631314 | ||||||
| chrX:21631431
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2693-17400G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631431 | ||||||
| chrX:21631450
|
G | A | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-17381G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631450 | ||||||
| chrX:21631670
|
T | C | 1 | a0001c0002t0001g0042 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2693-17161T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631670 | ||||||
| chrX:21631848
|
A | G | 1 | a0001c0001t0006g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2693-16983A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631848 | ||||||
| chrX:21631874
|
A | G | 3 | a0001c0001t0020g0141a0001c0003t0014g0147a0001c0003t0014g0149 | 3 | HG01243.hp1 HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2693-16957A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21631874 | ||||||
| chrX:21632392
|
T | A | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-16439T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21632392 | ||||||
| chrX:21632812
|
TTAAG | T | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-16018_2693-16 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21632812 | ||||||
| chrX:21632990
|
T | TAC | 16 | a0001c0001t0001g0068a0001c0001t0001g0089a0001c0001t0001g0090others(13): Show | 16 | HG01071.hp2 HG01106.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2693-15807_2693-15 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21632990 | |||||
| chrX:21632990
|
T | TACAC | 2 | a0001c0003t0014g0147a0001c0003t0014g0149 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2693-15809_2693-15 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21632990 | |||||
| chrX:21632990
|
T | TACACAC | 1 | a0001c0001t0022g0033 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2693-15811_2693-15 others(12): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21632990 | |||||
| chrX:21632990
|
TAC | T | 8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0067others(5): Show | 8 | HG00735.hp2 HG00741.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.2693-15807_2693-15 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21632990 | |||||
| chrX:21632990
|
TACAC | T | 6 | a0001c0001t0001g0081a0001c0001t0001g0109a0001c0001t0010g0162others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2693-15809_2693-15 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21632990 | |||||
| chrX:21632990
|
TACACAC | T | 17 | a0001c0001t0002g0003a0001c0001t0002g0046a0001c0001t0002g0047others(14): Show | 17 | HG00621.hp1 HG02074.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.2693-15811_2693-15 others(12): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21632990 | |||||
| chrX:21633350
|
A | G | 3 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2693-15481A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21633350 | ||||||
| chrX:21633417
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0002g0112a0001c0001t0013g0066 | 3 | HG00735.hp2 HG01167.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2693-15414T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21633417 | ||||||
| chrX:21633580
|
A | ACT | 10 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(7): Show | 10 | HG01071.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2693-15249_2693-15 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21633580 | |||||
| chrX:21633631
|
G | A | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2693-15200G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21633631 | ||||||
| chrX:21633758
|
T | C | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-15073T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21633758 | ||||||
| chrX:21634066
|
A | G | 1 | a0001c0001t0021g0088 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2693-14765A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21634066 | ||||||
| chrX:21634075
|
TTTC | T | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2693-14750_2693-14 others(9): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21634075 | |||||
| chrX:21634111
|
CT | C | 2 | a0001c0001t0002g0119a0001c0001t0002g0122 | 2 | NA18966.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2693-14719delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21634111 | ||||||
| chrX:21634227
|
C | G | 7 | a0001c0001t0006g0155a0001c0001t0006g0160a0001c0001t0006g0161others(4): Show | 7 | HG01071.hp2 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2693-14604C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21634227 | ||||||
| chrX:21634491
|
G | T | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-14340G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21634491 | ||||||
| chrX:21634520
|
T | A | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2693-14311T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21634520 | ||||||
| chrX:21634879
|
C | T | 6 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0162others(3): Show | 6 | HG02615.hp1 HG02647.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2693-13952C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21634879 | ||||||
| chrX:21635028
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2693-13803C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635028 | ||||||
| chrX:21635378
|
A | ATG | 2 | a0001c0001t0001g0001a0001c0001t0037g0092 | 2 | HG04204.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2693-13423_2693-13 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21635378 | |||||
| chrX:21635378
|
A | ATGTGTG | 1 | a0001c0001t0013g0100 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2693-13427_2693-13 others(12): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21635378 | |||||
| chrX:21635378
|
ATG | A | 58 | a0001c0001t0001g0077a0001c0001t0002g0003a0001c0001t0002g0004others(55): Show | 58 | HG00621.hp1 HG00735.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.2693-13423_2693-13 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21635378 | |||||
| chrX:21635378
|
ATGTG | A | 8 | a0001c0001t0002g0028a0001c0001t0004g0064a0001c0001t0007g0140others(5): Show | 8 | HG00738.hp1 HG01071.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2693-13425_2693-13 others(10): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21635378 | |||||
| chrX:21635406
|
G | GTATATAT others(23): Show |
1 | a0001c0001t0002g0119 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2693-13424_2693-13 others(36): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21635406 | |||||
| chrX:21635408
|
G | A | 8 | a0001c0001t0002g0119a0001c0001t0007g0140a0001c0001t0010g0152others(5): Show | 8 | HG01071.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2693-13423G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635408 | ||||||
| chrX:21635410
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2693-13421A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635410 | ||||||
| chrX:21635420
|
A | C | 4 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0162others(1): Show | 4 | HG01071.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2693-13411A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635420 | ||||||
| chrX:21635452
|
CTA | C | 1 | a0001c0001t0006g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2693-13371_2693-13 others(8): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21635452 | |||||
| chrX:21635502
|
G | A | 28 | a0001c0001t0003g0029a0001c0001t0006g0155a0001c0001t0006g0157others(25): Show | 28 | HG01071.hp2 HG01081.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.2693-13329G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635502 | ||||||
| chrX:21635503
|
T | A | 28 | a0001c0001t0003g0029a0001c0001t0006g0155a0001c0001t0006g0157others(25): Show | 28 | HG01071.hp2 HG01081.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.2693-13328T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635503 | ||||||
| chrX:21635523
|
T | C | 3 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0162 | 3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2693-13308T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635523 | ||||||
| chrX:21635550
|
GTGTATAT others(1): Show |
G | 5 | a0001c0001t0020g0141a0001c0001t0022g0033a0001c0001t0027g0034others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2693-13263_2693-13 others(14): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21635550 | |||||
| chrX:21635902
|
C | T | 1 | a0001c0001t0013g0066 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2693-12929C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21635902 | ||||||
| chrX:21636277
|
G | GA | 5 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(2): Show | 5 | HG01071.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2693-12550dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21636277 | |||||
| chrX:21636305
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2693-12526C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21636305 | ||||||
| chrX:21636332
|
T | TA | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2693-12488dupA | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21636332 | |||||
| chrX:21636492
|
G | C | 1 | a0001c0001t0021g0088 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2693-12339G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21636492 | ||||||
| chrX:21636902
|
C | T | 1 | a0001c0001t0029g0023 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2693-11929C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21636902 | ||||||
| chrX:21636912
|
A | C | 1 | a0001c0001t0043g0007 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2693-11919A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21636912 | ||||||
| chrX:21637154
|
C | G | 3 | a0001c0001t0010g0152a0001c0001t0010g0153a0001c0001t0010g0162 | 3 | HG03209.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2693-11677C>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21637154 | ||||||
| chrX:21637212
|
G | C | 72 | a0001c0001t0001g0053a0001c0001t0001g0077a0001c0001t0002g0003others(69): Show | 72 | HG00280.hp1 HG00621.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.2693-11619G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21637212 | ||||||
| chrX:21637841
|
G | T | 1 | a0001c0001t0015g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2693-10990G>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21637841 | ||||||
| chrX:21638335
|
A | C | 3 | a0001c0001t0020g0141a0001c0003t0014g0147a0001c0003t0014g0149 | 3 | HG01243.hp1 HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2693-10496A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21638335 | ||||||
| chrX:21638368
|
T | A | 1 | a0001c0001t0002g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2693-10463T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21638368 | ||||||
| chrX:21638896
|
C | A | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2693-9935C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21638896 | ||||||
| chrX:21639152
|
A | G | 1 | a0001c0001t0006g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2693-9679A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21639152 | ||||||
| chrX:21639259
|
T | C | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2693-9572T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21639259 | ||||||
| chrX:21639374
|
C | T | 1 | a0001c0001t0019g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2693-9457C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21639374 | ||||||
| chrX:21639969
|
G | A | 1 | a0001c0001t0015g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2693-8862G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21639969 | ||||||
| chrX:21639976
|
A | G | 4 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(1): Show | 4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2693-8855A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21639976 | ||||||
| chrX:21640638
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2693-8193A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21640638 | ||||||
| chrX:21640652
|
T | C | 5 | a0001c0001t0007g0140a0001c0001t0010g0152a0001c0001t0010g0153others(2): Show | 5 | HG01071.hp2 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2693-8179T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21640652 | ||||||
| chrX:21642148
|
A | C | 1 | a0001c0001t0031g0065 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2693-6683A>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21642148 | ||||||
| chrX:21642170
|
C | A | 5 | a0001c0001t0006g0155a0001c0001t0006g0160a0001c0001t0006g0161others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2693-6661C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21642170 | ||||||
| chrX:21642182
|
C | T | 28 | a0001c0001t0002g0019a0001c0001t0006g0155a0001c0001t0006g0157others(25): Show | 28 | HG01081.hp1 HG01106.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.2693-6649C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21642182 | ||||||
| chrX:21643056
|
G | GT | 1 | a0001c0001t0001g0048 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2693-5765dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21643056 | |||||
| chrX:21643079
|
T | C | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2693-5752T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21643079 | ||||||
| chrX:21643532
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2693-5299A>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21643532 | ||||||
| chrX:21643628
|
G | GT | 1 | a0001c0001t0020g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2693-5197dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21643628 | |||||
| chrX:21643684
|
T | C | 1 | a0001c0001t0029g0023 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2693-5147T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21643684 | ||||||
| chrX:21644379
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2693-4452A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21644379 | ||||||
| chrX:21644665
|
T | A | 1 | a0001c0003t0026g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2693-4166T>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21644665 | ||||||
| chrX:21644850
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0016g0085 | 2 | HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2693-3981T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21644850 | ||||||
| chrX:21645851
|
T | C | 4 | a0001c0001t0011g0016a0001c0001t0011g0017a0001c0001t0011g0138others(1): Show | 4 | HG03041.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2693-2980T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21645851 | ||||||
| chrX:21645863
|
C | A | 1 | a0001c0001t0012g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2693-2968C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21645863 | ||||||
| chrX:21646274
|
A | G | 2 | a0001c0001t0012g0045a0001c0001t0012g0142 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2693-2557A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21646274 | ||||||
| chrX:21646932
|
G | C | 15 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(12): Show | 15 | HG01071.hp2 HG01109.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.2693-1899G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21646932 | ||||||
| chrX:21647077
|
C | T | 1 | a0001c0007t0036g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2693-1754C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21647077 | ||||||
| chrX:21647148
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2693-1683T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21647148 | ||||||
| chrX:21647150
|
T | G | 13 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(10): Show | 13 | HG01109.hp1 HG01884.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2693-1681T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21647150 | ||||||
| chrX:21647753
|
CT | C | 1 | a0001c0001t0002g0125 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2693-1071delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21647753 | |||||
| chrX:21647921
|
T | C | 1 | a0001c0001t0006g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2693-910T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21647921 | ||||||
| chrX:21647922
|
C | T | 1 | a0001c0001t0001g0001 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2693-909C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21647922 | ||||||
| chrX:21648069
|
A | G | 1 | a0001c0002t0001g0042 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2693-762A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648069 | ||||||
| chrX:21648386
|
A | G | 4 | a0001c0001t0002g0004a0001c0001t0003g0031a0001c0001t0008g0005others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.2693-445A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648386 | ||||||
| chrX:21648395
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2693-436C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648395 | ||||||
| chrX:21648616
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2693-215A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648616 | ||||||
| chrX:21648770
|
T | TTC | 1 | a0001c0001t0001g0051 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2693-41_2693-40dup others(2): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21648770 | |||||
| chrX:21648770
|
T | TTCTC | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-43_2693-40dup others(4): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21648770 | |||||
| chrX:21648788
|
C | T | 1 | a0001c0002t0007g0041 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2693-43C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648788 | ||||||
| chrX:21648791
|
TTTC | T | 1 | a0001c0002t0007g0041 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2693-37_2693-35del others(3): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21648791 | |||||
| chrX:21648792
|
T | C | 2 | a0001c0001t0011g0017a0001c0001t0012g0025 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2693-39T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648792 | ||||||
| chrX:21648794
|
C | CT | 99 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0036others(96): Show | 99 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.2693-12dupT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21648794 | |||||
| chrX:21648794
|
C | CTT | 12 | a0001c0001t0001g0039a0001c0001t0001g0052a0001c0001t0001g0158others(9): Show | 12 | HG00642.hp1 HG01192.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2693-13_2693-12dup others(2): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21648794 | |||||
| chrX:21648794
|
C | CTTT | 7 | a0001c0001t0009g0013a0001c0001t0011g0016a0001c0001t0011g0138others(4): Show | 7 | HG01884.hp2 HG02486.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2693-14_2693-12dup others(3): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21648794 | |||||
| chrX:21648794
|
C | CTTTCTT | 2 | a0001c0001t0011g0017a0001c0001t0012g0025 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2693-34_2693-33ins others(6): Show |
CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21648794 | |||||
| chrX:21648794
|
C | T | 1 | a0001c0001t0042g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-37C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | chrX | 21648794 | ||||||
| chrX:21648794
|
CT | C | 1 | a0001c0001t0003g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2693-12delT | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 21648794 | |||||
| chrX:21649865
|
C | T | 7 | a0001c0001t0002g0046a0001c0001t0002g0119a0001c0001t0002g0120others(4): Show | 7 | HG02083.hp1 NA18612.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.2889+838C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21649865 | ||||||
| chrX:21650278
|
G | A | 31 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(28): Show | 31 | HG01071.hp2 HG01081.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.2889+1251G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21650278 | ||||||
| chrX:21650280
|
A | G | 1 | a0001c0001t0021g0088 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2889+1253A>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21650280 | ||||||
| chrX:21650340
|
C | T | 1 | a0001c0001t0007g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2889+1313C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21650340 | ||||||
| chrX:21650425
|
G | A | 1 | a0001c0001t0006g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2889+1398G>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21650425 | ||||||
| chrX:21650695
|
T | G | 15 | a0001c0001t0006g0155a0001c0001t0006g0157a0001c0001t0006g0159others(12): Show | 15 | HG01071.hp2 HG01109.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.2890-1611T>G | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21650695 | ||||||
| chrX:21650724
|
G | C | 1 | a0001c0001t0002g0120 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2890-1582G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21650724 | ||||||
| chrX:21651166
|
T | C | 1 | a0001c0001t0009g0013 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2890-1140T>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21651166 | ||||||
| chrX:21651461
|
C | A | 1 | a0001c0001t0030g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2890-845C>A | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21651461 | ||||||
| chrX:21652095
|
G | C | 1 | a0001c0003t0026g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2890-211G>C | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21652095 | ||||||
| chrX:21652272
|
C | T | 1 | a0001c0001t0011g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2890-34C>T | CNKSR2 | ENSG00000149970.16 | transcript | ENST00000379510.5 | protein_coding | 21/21 | chrX | 21652272 |