Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26586 |
| ensemblid | ENSG00000136108.15 |
| hgncid | 1990 |
| symbol | CKAP2 |
| name | cytoskeleton associated protein 2 |
| refseq_nuc | NM_018204.5 |
| refseq_prot | NP_060674.3 |
| ensembl_nuc | ENST00000258607.10 |
| ensembl_prot | ENSP00000258607.5 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 52455478 |
| end | 52476627 |
| strand | + |
| ver | v1.2 |
| region | chr13:52455478-52476627 |
| region5000 | chr13:52450478-52481627 |
| regionname0 | CKAP2_chr13_52455478_52476627 |
| regionname5000 | CKAP2_chr13_52450478_52481627 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 682 | 382 | 88 | 70 | 168 | 13 | 42 | 125 | CKAP2_chr13_52450478_52481627 | CKAP2 | MSTPA others(677): Show |
chr13 | 52450478 | 52481627 |
| a0002 | 0/0 | 682 | 7 | 0 | 1 | 4 | 0 | 2 | 3 | CKAP2_chr13_52450478_52481627 | CKAP2 | MSTPA others(677): Show |
chr13 | 52450478 | 52481627 |
| a0003 | 0/0 | 682 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | MSTPA others(677): Show |
chr13 | 52450478 | 52481627 |
| a0004 | 0/0 | 682 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | MSTPA others(677): Show |
chr13 | 52450478 | 52481627 |
| a0005 | 1/0 | 682 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | MSTPA others(677): Show |
chr13 | 52450478 | 52481627 |
| a0006 | 0/0 | 682 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | MSTPA others(677): Show |
chr13 | 52450478 | 52481627 |
| a0007 | 0/0 | 682 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | MSTPA others(677): Show |
chr13 | 52450478 | 52481627 |
| a0008 | 0/0 | 682 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | MSTPA others(677): Show |
chr13 | 52450478 | 52481627 |
| a0009 | 0/0 | 682 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | MSTPA others(677): Show |
chr13 | 52450478 | 52481627 |
| a0010 | 0/0 | 682 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | MSTPA others(677): Show |
chr13 | 52450478 | 52481627 |
| a0011 | 0/0 | 682 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | MSTPA others(677): Show |
chr13 | 52450478 | 52481627 |
| a0012 | 0/0 | 682 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | MSTPA others(677): Show |
chr13 | 52450478 | 52481627 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2046 | 368 | 86 | 65 | 161 | 13 | 42 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0001c0003 | 0/0 | 2046 | 7 | 0 | 0 | 7 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0001c0004 | 0/0 | 2046 | 5 | 0 | 5 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0001c0013 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0001c0016 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0002c0002 | 0/0 | 2046 | 7 | 0 | 1 | 4 | 0 | 2 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0003c0005 | 0/0 | 2046 | 4 | 3 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0004c0006 | 0/0 | 2046 | 3 | 0 | 2 | 0 | 1 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0005c0007 | 1/0 | 2046 | 2 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0006c0008 | 0/0 | 2046 | 2 | 1 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0007c0011 | 0/0 | 2046 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0008c0015 | 0/0 | 2046 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0009c0009 | 0/0 | 2046 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0010c0014 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0011c0012 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 | ||
| a0012c0010 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | ATGAG others(2041): Show |
chr13 | 52450478 | 52481627 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3614 | 175 | 17 | 41 | 95 | 7 | 15 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0001c0001t0002 | 0/1 | 3614 | 148 | 35 | 19 | 64 | 5 | 24 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0001c0001t0003 | 0/0 | 3614 | 24 | 19 | 2 | 0 | 1 | 2 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0001c0001t0004 | 0/0 | 3614 | 11 | 9 | 2 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0001c0001t0005 | 0/0 | 3614 | 3 | 2 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0001c0001t0006 | 0/0 | 3614 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0001c0001t0007 | 0/0 | 3614 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GTAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0001c0001t0009 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0001c0001t0010 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0001c0001t0011 | 0/0 | 3614 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0001c0003t0001 | 0/0 | 3614 | 7 | 0 | 0 | 7 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0001c0004t0001 | 0/0 | 3614 | 5 | 0 | 5 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0001c0013t0008 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0001c0016t0002 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0002c0002t0001 | 0/0 | 3614 | 7 | 0 | 1 | 4 | 0 | 2 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0003c0005t0001 | 0/0 | 3614 | 4 | 3 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0004c0006t0002 | 0/0 | 3614 | 3 | 0 | 2 | 0 | 1 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0005c0007t0002 | 1/0 | 3614 | 2 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0006c0008t0001 | 0/0 | 3614 | 2 | 1 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0007c0011t0001 | 0/0 | 3614 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0008c0015t0001 | 0/0 | 3614 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0009c0009t0001 | 0/0 | 3614 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0010c0014t0001 | 0/0 | 3614 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0011c0012t0002 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| a0012c0010t0002 | 0/0 | 3614 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | GCAGA others(3609): Show |
chr13 | 52450478 | 52481627 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 26 | 0 | 2 | 21 | 0 | 3 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0003 | 0/0 | 16 | 0 | 8 | 0 | 3 | 5 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0005 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0006 | 0/0 | 8 | 1 | 3 | 3 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0020 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0001 | 0/0 | 40 | 0 | 7 | 26 | 0 | 7 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0004 | 0/1 | 14 | 7 | 2 | 0 | 0 | 4 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0012 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0013 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0014 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0041 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0003g0007 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0003g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0003g0044 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0004g0009 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0005g0035 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0006g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0010g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0001t0011g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0003t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0003t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0004t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0004t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0004t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0013t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0001c0016t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0002c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0003c0005t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0003c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0003c0005t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0004c0006t0002g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0005c0007t0002g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0005c0007t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0006c0008t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0006c0008t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0007c0011t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0008c0015t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0009c0009t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0010c0014t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0011c0012t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| a0012c0010t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0006 | t0002 | g0001 | EUR | GBR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | GBR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0044 | EUR | GBR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | FIN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0171 | EUR | FIN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00735 | hp2 | a0007 | c0011 | t0001 | g0016 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00741 | hp1 | a0008 | c0015 | t0001 | g0105 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01069 | hp1 | a0001 | c0001 | t0011 | g0007 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01074 | hp2 | a0006 | c0008 | t0001 | g0179 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01168 | hp2 | a0004 | c0006 | t0002 | g0001 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01169 | hp1 | a0004 | c0006 | t0002 | g0001 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01243 | hp2 | a0003 | c0005 | t0001 | g0037 | AMR | PUR | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01255 | hp1 | a0001 | c0004 | t0001 | g0021 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01256 | hp1 | a0001 | c0004 | t0001 | g0021 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01361 | hp1 | a0001 | c0004 | t0001 | g0121 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01433 | hp1 | a0001 | c0004 | t0001 | g0032 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0080 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0049 | EUR | IBS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0050 | EUR | IBS | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01891 | hp2 | a0006 | c0008 | t0001 | g0180 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01952 | hp1 | a0001 | c0004 | t0001 | g0032 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | CDX | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CDX | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02273 | hp1 | a0009 | c0009 | t0001 | g0021 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0165 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0192 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02886 | hp1 | a0003 | c0005 | t0001 | g0127 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0200 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02970 | hp2 | a0001 | c0013 | t0008 | g0130 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0185 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | MSL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03486 | hp1 | a0003 | c0005 | t0001 | g0037 | AFR | MSL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | MSL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03540 | hp2 | a0001 | c0016 | t0002 | g0158 | AFR | GWD | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | MSL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | MSL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | STU | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0186 | SAS | STU | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | BEB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | BEB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | STU | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0169 | SAS | STU | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | YRI | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0129 | AFR | YRI | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | YRI | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18906 | hp2 | a0003 | c0005 | t0001 | g0126 | AFR | YRI | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18980 | hp2 | a0010 | c0014 | t0001 | g0018 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | LWK | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19043 | hp2 | a0011 | c0012 | t0002 | g0008 | AFR | LWK | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19056 | hp1 | a0012 | c0010 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19062 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19075 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19085 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | YRI | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | YRI | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA20129 | hp2 | a0005 | c0007 | t0002 | g0173 | AFR | ASW | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0144 | EUR | TSI | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | GIH | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0035 | SAS | GIH | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | CLM | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | ACB | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | USA | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | USA | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0136 | AFR | USA | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | USA | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0004 | REF | REF | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| homoSapiens | grch38p0 | a0005 | c0007 | t0002 | g0172 | REF | REF | CKAP2_chr13_52450478_52481627 | CKAP2 | chr13 | 52450478 | 52481627 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52461092 | G | C | 1 | a0009 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.266G>C | p.Ser89Thr | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/9 | 345/3614 | 266/2049 | 89/682 | chr13 | 52461092 | |||
| chr13:52461530 | T | A | 1 | a0002 | 7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
missense_variant | MODERATE | c.704T>A | p.Met235Lys | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/9 | 783/3614 | 704/2049 | 235/682 | chr13 | 52461530 | |||
| chr13:52461604 | C | T | 1 | a0006 | 2 | HG01074.hp2 HG01891.hp2 |
missense_variant | MODERATE | c.778C>T | p.His260Tyr | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/9 | 857/3614 | 778/2049 | 260/682 | chr13 | 52461604 | |||
| chr13:52461790 | A | G | 11 | a0001 a0002 a0003 others(8): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
missense_variant | MODERATE | c.964A>G | p.Ile322Val | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/9 | 1043/3614 | 964/2049 | 322/682 | chr13 | 52461790 | |||
| chr13:52461881 | T | C | 1 | a0012 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.1055T>C | p.Val352Ala | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/9 | 1134/3614 | 1055/2049 | 352/682 | chr13 | 52461881 | |||
| chr13:52462418 | A | G | 1 | a0003 | 4 | HG01243.hp2 HG02886.hp1 HG03486.hp1 others(1): Show |
missense_variant | MODERATE | c.1156A>G | p.Asn386Asp | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/9 | 1235/3614 | 1156/2049 | 386/682 | chr13 | 52462418 | |||
| chr13:52465302 | C | T | 1 | a0008 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1313C>T | p.Pro438Leu | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/9 | 1392/3614 | 1313/2049 | 438/682 | chr13 | 52465302 | |||
| chr13:52465316 | C | G | 1 | a0010 | 1 | NA18980.hp2 | missense_variant | MODERATE | c.1327C>G | p.Leu443Val | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/9 | 1406/3614 | 1327/2049 | 443/682 | chr13 | 52465316 | |||
| chr13:52465412 | C | T | 1 | a0004 | 3 | HG00099.hp1 HG01168.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.1423C>T | p.Pro475Ser | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/9 | 1502/3614 | 1423/2049 | 475/682 | chr13 | 52465412 | |||
| chr13:52474978 | G | A | 1 | a0007 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1886G>A | p.Arg629His | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 1965/3614 | 1886/2049 | 629/682 | chr13 | 52474978 | |||
| chr13:52475091 | C | T | 1 | a0011 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1999C>T | p.Arg667Cys | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 2078/3614 | 1999/2049 | 667/682 | chr13 | 52475091 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52461648 | T | C | 14 | a0001c0001 a0001c0003 a0001c0004 others(11): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
synonymous_variant | LOW | c.822T>C | p.Thr274Thr | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/9 | 901/3614 | 822/2049 | 274/682 | chr13 | 52461648 | |||
| chr13:52461762 | T | A | 1 | a0003c0005 | 4 | HG01243.hp2 HG02886.hp1 HG03486.hp1 others(1): Show |
synonymous_variant | LOW | c.936T>A | p.Thr312Thr | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/9 | 1015/3614 | 936/2049 | 312/682 | chr13 | 52461762 | |||
| chr13:52461825 | G | A | 1 | a0001c0003 | 7 | HG02074.hp1 NA18994.hp1 NA19065.hp1 others(4): Show |
synonymous_variant | LOW | c.999G>A | p.Leu333Leu | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/9 | 1078/3614 | 999/2049 | 333/682 | chr13 | 52461825 | |||
| chr13:52468316 | A | G | 1 | a0001c0013 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.1515A>G | p.Leu505Leu | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/9 | 1594/3614 | 1515/2049 | 505/682 | chr13 | 52468316 | |||
| chr13:52475132 | T | C | 2 | a0001c0004 a0009c0009 |
6 | HG01255.hp1 HG01256.hp1 HG01361.hp1 others(3): Show |
synonymous_variant | LOW | c.2040T>C | p.Asp680Asp | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 2119/3614 | 2040/2049 | 680/682 | chr13 | 52475132 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52455479 | C | T | 1 | a0001c0001t0007 | 2 | HG02559.hp2 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-78C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/9 | 78 | chr13 | 52455479 | ||||||
| chr13:52455516 | T | C | 1 | a0001c0013t0008 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-41T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/9 | 41 | chr13 | 52455516 | ||||||
| chr13:52475299 | C | A | 1 | a0001c0001t0009 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*158C>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 158 | chr13 | 52475299 | ||||||
| chr13:52475351 | A | G | 2 | a0001c0001t0005 a0001c0013t0008 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*210A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 210 | chr13 | 52475351 | ||||||
| chr13:52475357 | G | A | 1 | a0001c0001t0004 | 11 | HG01106.hp1 HG01496.hp2 HG01884.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*216G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 216 | chr13 | 52475357 | ||||||
| chr13:52475497 | T | C | 1 | a0001c0001t0010 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*356T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 356 | chr13 | 52475497 | ||||||
| chr13:52475559 | A | C | 1 | a0001c0001t0006 | 2 | NA18940.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*418A>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 418 | chr13 | 52475559 | ||||||
| chr13:52475607 | C | G | 2 | a0001c0001t0005 a0001c0013t0008 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*466C>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 466 | chr13 | 52475607 | ||||||
| chr13:52475884 | T | C | 2 | a0001c0001t0005 a0001c0013t0008 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*743T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 743 | chr13 | 52475884 | ||||||
| chr13:52476116 | T | C | 2 | a0001c0001t0005 a0001c0013t0008 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*975T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 975 | chr13 | 52476116 | ||||||
| chr13:52476187 | G | A | 1 | a0001c0001t0011 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1046G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 1046 | chr13 | 52476187 | ||||||
| chr13:52476344 | G | A | 14 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(11): Show |
221 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*1203G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 1203 | chr13 | 52476344 | ||||||
| chr13:52476488 | A | G | 2 | a0001c0001t0003 a0001c0001t0011 |
25 | HG00140.hp2 HG01069.hp1 HG01169.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1347A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 9/9 | 1347 | chr13 | 52476488 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52455635 | C | CGCGGTG | 12 | a0001c0001t0002g0047 a0001c0001t0002g0190 a0001c0001t0002g0191 others(9): Show |
13 | HG01109.hp1 HG02040.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.70+44_70+49dupTGGC others(2): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 52455635 | ||||||
| chr13:52455635 | C | CGCGGTGG others(5): Show |
1 | a0001c0001t0002g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.70+38_70+49dupTGGC others(8): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 52455635 | ||||||
| chr13:52455635 | CGCGGTG | C | 5 | a0001c0001t0002g0128 a0001c0001t0005g0035 a0001c0001t0005g0129 others(2): Show |
6 | HG02738.hp1 HG02886.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+44_70+49delTGGC others(2): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 52455635 | ||||||
| chr13:52455635 | CGCGGTGG others(5): Show |
C | 11 | a0001c0001t0001g0022 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
17 | HG01255.hp1 HG01256.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.70+38_70+49delTGGC others(8): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 52455635 | ||||||
| chr13:52455635 | CGCGGTGG others(11): Show |
C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
185 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.70+32_70+49delTGGC others(14): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 52455635 | ||||||
| chr13:52455635 | CGCGGTGG others(17): Show |
C | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.70+26_70+49delTGGC others(20): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 52455635 | ||||||
| chr13:52455635 | CGCGGTGG others(23): Show |
C | 1 | a0001c0001t0001g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.70+20_70+49delTGGC others(26): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 52455635 | ||||||
| chr13:52455676 | G | T | 1 | a0001c0001t0002g0189 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.70+50G>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52455676 | |||||||
| chr13:52455677 | C | G | 1 | a0001c0001t0002g0189 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.70+51C>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52455677 | |||||||
| chr13:52455704 | C | T | 1 | a0001c0001t0005g0129 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70+78C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52455704 | |||||||
| chr13:52455723 | C | T | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+97C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52455723 | |||||||
| chr13:52455729 | C | G | 1 | a0001c0001t0010g0200 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.70+103C>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52455729 | |||||||
| chr13:52455731 | C | G | 1 | a0001c0001t0003g0183 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.70+105C>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52455731 | |||||||
| chr13:52455744 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0124 a0001c0001t0001g0125 |
5 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+118C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52455744 | |||||||
| chr13:52455845 | G | A | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+219G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52455845 | |||||||
| chr13:52455861 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0120 |
3 | HG00323.hp1 HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.70+235C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52455861 | |||||||
| chr13:52455913 | T | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+287T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52455913 | |||||||
| chr13:52455985 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.70+359G>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52455985 | |||||||
| chr13:52455991 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0118 |
3 | HG00735.hp1 HG00741.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.70+365C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52455991 | |||||||
| chr13:52456036 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0124 a0001c0001t0001g0125 |
5 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+410T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52456036 | |||||||
| chr13:52456242 | A | T | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-281A>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52456242 | |||||||
| chr13:52456310 | T | C | 4 | a0001c0004t0001g0021 a0001c0004t0001g0032 a0001c0004t0001g0121 others(1): Show |
6 | HG01255.hp1 HG01256.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-213T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52456310 | |||||||
| chr13:52456385 | A | G | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-138A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52456385 | |||||||
| chr13:52456415 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.71-108G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52456415 | |||||||
| chr13:52456430 | G | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(82): Show |
168 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.71-93G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52456430 | |||||||
| chr13:52456452 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.71-71C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 1/8 | chr13 | 52456452 | |||||||
| chr13:52456657 | G | C | 2 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
2 | HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.155+50G>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52456657 | |||||||
| chr13:52456778 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.155+171T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52456778 | |||||||
| chr13:52456791 | G | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.155+184G>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52456791 | |||||||
| chr13:52456898 | A | AT | 12 | a0001c0001t0002g0181 a0001c0001t0005g0035 a0001c0001t0005g0129 others(9): Show |
14 | HG00544.hp1 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.155+304dupT | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52456898 | ||||||
| chr13:52456902 | T | G | 1 | a0001c0001t0002g0047 | 2 | NA18941.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.155+295T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52456902 | |||||||
| chr13:52456942 | G | C | 1 | a0001c0013t0008g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.155+335G>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52456942 | |||||||
| chr13:52456954 | G | A | 2 | a0006c0008t0001g0179 a0006c0008t0001g0180 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.155+347G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52456954 | |||||||
| chr13:52456983 | T | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.155+376T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52456983 | |||||||
| chr13:52457045 | T | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.155+438T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457045 | |||||||
| chr13:52457115 | T | C | 1 | a0001c0001t0004g0051 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.155+508T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457115 | |||||||
| chr13:52457204 | G | T | 4 | a0001c0004t0001g0021 a0001c0004t0001g0032 a0001c0004t0001g0121 others(1): Show |
6 | HG01255.hp1 HG01256.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.155+597G>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457204 | |||||||
| chr13:52457236 | G | A | 22 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0124 others(19): Show |
27 | HG00544.hp1 HG01099.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.155+629G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457236 | |||||||
| chr13:52457237 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.155+630A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457237 | |||||||
| chr13:52457348 | A | G | 1 | a0003c0005t0001g0037 | 2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.155+741A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457348 | |||||||
| chr13:52457367 | A | G | 14 | a0001c0001t0002g0014 a0001c0001t0002g0045 a0001c0001t0002g0047 others(11): Show |
20 | HG00609.hp1 HG00673.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.155+760A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457367 | |||||||
| chr13:52457434 | T | C | 1 | a0002c0002t0001g0184 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.155+827T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457434 | |||||||
| chr13:52457457 | C | T | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.155+850C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457457 | |||||||
| chr13:52457501 | T | G | 1 | a0001c0001t0001g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.155+894T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457501 | |||||||
| chr13:52457713 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.155+1106G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457713 | |||||||
| chr13:52457758 | G | A | 2 | a0006c0008t0001g0179 a0006c0008t0001g0180 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.155+1151G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457758 | |||||||
| chr13:52457829 | G | A | 1 | a0001c0001t0002g0138 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.155+1222G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457829 | |||||||
| chr13:52457840 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.155+1233C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457840 | |||||||
| chr13:52457853 | C | CA | 2 | a0001c0001t0003g0011 a0001c0001t0003g0139 |
6 | HG02055.hp2 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.155+1260dupA | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52457853 | ||||||
| chr13:52457853 | CA | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(93): Show |
187 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.155+1260delA | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52457853 | ||||||
| chr13:52457869 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.155+1262T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457869 | |||||||
| chr13:52457930 | A | G | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0134 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+1323A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52457930 | |||||||
| chr13:52458126 | T | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.155+1519T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52458126 | |||||||
| chr13:52458188 | G | A | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+1581G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52458188 | |||||||
| chr13:52458206 | T | A | 3 | a0001c0001t0002g0023 a0001c0001t0002g0140 a0001c0001t0002g0141 |
5 | NA18950.hp2 NA18982.hp1 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.155+1599T>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52458206 | |||||||
| chr13:52458327 | TG | T | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+1724delG | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52458327 | ||||||
| chr13:52458330 | G | T | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+1723G>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52458330 | |||||||
| chr13:52458600 | T | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(82): Show |
168 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.155+1993T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52458600 | |||||||
| chr13:52458601 | G | A | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+1994G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52458601 | |||||||
| chr13:52458604 | T | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.155+1997T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52458604 | |||||||
| chr13:52458659 | T | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0048 a0001c0001t0001g0055 |
6 | HG01175.hp2 HG01934.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.155+2052T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52458659 | |||||||
| chr13:52458776 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.156-2123G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52458776 | |||||||
| chr13:52458857 | C | CA | 18 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0052 others(15): Show |
21 | HG01109.hp2 HG02257.hp1 HG02300.hp2 others(18): Show |
intron_variant | MODIFIER | c.156-2028dupA | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52458857 | ||||||
| chr13:52458985 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0124 a0001c0001t0001g0125 |
5 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-1914A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52458985 | |||||||
| chr13:52459040 | T | TAAG | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.156-1857_156-1855d others(5): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52459040 | ||||||
| chr13:52459381 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.156-1518G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52459381 | |||||||
| chr13:52459392 | A | G | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.156-1507A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52459392 | |||||||
| chr13:52459426 | G | A | 1 | a0001c0001t0002g0144 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.156-1473G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52459426 | |||||||
| chr13:52459480 | G | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(30): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.156-1419G>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52459480 | |||||||
| chr13:52459501 | T | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0018 others(9): Show |
25 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.156-1398T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52459501 | |||||||
| chr13:52459519 | C | T | 10 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0124 others(7): Show |
12 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.156-1380C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52459519 | |||||||
| chr13:52459523 | G | A | 12 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 others(9): Show |
15 | HG00544.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.156-1376G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52459523 | |||||||
| chr13:52459591 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.156-1308A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52459591 | |||||||
| chr13:52459895 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(207): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.156-1004T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52459895 | |||||||
| chr13:52460079 | G | T | 2 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
2 | HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.156-820G>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52460079 | |||||||
| chr13:52460099 | TC | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0124 a0001c0001t0001g0125 |
5 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-794delC | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460099 | ||||||
| chr13:52460159 | G | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.156-740G>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52460159 | |||||||
| chr13:52460228 | C | T | 3 | a0003c0005t0001g0037 a0003c0005t0001g0126 a0003c0005t0001g0127 |
4 | HG01243.hp2 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-671C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52460228 | |||||||
| chr13:52460506 | T | G | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.156-393T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52460506 | |||||||
| chr13:52460538 | G | A | 1 | a0001c0001t0010g0200 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.156-361G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52460538 | |||||||
| chr13:52460564 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.156-335C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52460564 | |||||||
| chr13:52460613 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.156-286C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52460613 | |||||||
| chr13:52460703 | C | CGGCCTCC others(655): Show |
1 | a0001c0001t0001g0058 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.156-168_156-167ins others(662): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460703 | C | CGGCCTCC others(655): Show |
3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.156-168_156-167ins others(662): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460703 | C | CGGCCTCC others(655): Show |
5 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(2): Show |
6 | HG01099.hp2 HG03017.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.156-168_156-167ins others(662): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460703 | C | CGGCCTCC others(656): Show |
3 | a0002c0002t0001g0188 a0003c0005t0001g0037 a0003c0005t0001g0126 |
4 | HG00544.hp1 HG01243.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-168_156-167ins others(663): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460703 | C | CGGCCTCC others(658): Show |
1 | a0003c0005t0001g0127 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.156-168_156-167ins others(665): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460703 | C | CGGCCTCC others(656): Show |
2 | a0001c0001t0002g0038 a0001c0001t0002g0145 |
3 | HG01891.hp1 HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.156-168_156-167ins others(663): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460703 | C | CGGCCTCC others(656): Show |
8 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0092 others(5): Show |
10 | HG00741.hp2 HG01261.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.156-168_156-167ins others(663): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460703 | C | CGGCCTCC others(657): Show |
3 | a0001c0001t0001g0061 a0001c0001t0002g0175 a0001c0001t0003g0123 |
3 | HG02818.hp2 NA18972.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.156-168_156-167ins others(664): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460703 | C | CGGCCTCC others(658): Show |
1 | a0001c0001t0002g0195 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.156-168_156-167ins others(665): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460703 | C | CGGCCTCC others(645): Show |
1 | a0001c0001t0001g0093 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.156-168_156-167ins others(652): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460703 | C | CGGCCTCC others(655): Show |
142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(139): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.156-168_156-167ins others(662): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460703 | C | CGGCCTCC others(656): Show |
38 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(35): Show |
56 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.156-168_156-167ins others(663): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460703 | C | CGGCCTCC others(657): Show |
1 | a0001c0001t0001g0090 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.156-168_156-167ins others(664): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460703 | C | CGGCCTCC others(656): Show |
1 | a0001c0001t0001g0091 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.156-168_156-167ins others(663): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460703 | ||||||
| chr13:52460717 | G | GCTGGGAT others(655): Show |
1 | a0001c0001t0001g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.156-168_156-167ins others(662): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 52460717 | ||||||
| chr13:52460741 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.156-158C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 2/8 | chr13 | 52460741 | |||||||
| chr13:52462028 | G | A | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1100+102G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/8 | chr13 | 52462028 | |||||||
| chr13:52462043 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1100+117T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/8 | chr13 | 52462043 | |||||||
| chr13:52462176 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | NA18956.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1101-187C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/8 | chr13 | 52462176 | |||||||
| chr13:52462214 | G | C | 12 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 others(9): Show |
15 | HG00544.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1101-149G>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/8 | chr13 | 52462214 | |||||||
| chr13:52462263 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
221 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1101-100A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/8 | chr13 | 52462263 | |||||||
| chr13:52462287 | T | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1101-76T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/8 | chr13 | 52462287 | |||||||
| chr13:52462302 | T | TTTTCTC | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1101-60_1101-59ins others(6): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr13 | 52462302 | ||||||
| chr13:52462728 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1305+161C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52462728 | |||||||
| chr13:52462776 | T | TG | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+210dupG | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 52462776 | ||||||
| chr13:52462810 | C | T | 1 | a0001c0001t0002g0034 | 2 | NA18969.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1305+243C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52462810 | |||||||
| chr13:52462813 | G | T | 2 | a0001c0001t0005g0035 a0001c0001t0005g0129 |
3 | HG06807.hp1 NA18522.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1305+246G>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52462813 | |||||||
| chr13:52462974 | C | G | 4 | a0001c0004t0001g0021 a0001c0004t0001g0032 a0001c0004t0001g0121 others(1): Show |
6 | HG01255.hp1 HG01256.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1305+407C>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52462974 | |||||||
| chr13:52463225 | A | G | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+658A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52463225 | |||||||
| chr13:52463233 | C | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0170 a0001c0001t0002g0193 others(2): Show |
11 | HG02258.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+666C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52463233 | |||||||
| chr13:52463234 | G | A | 3 | a0003c0005t0001g0037 a0003c0005t0001g0126 a0003c0005t0001g0127 |
4 | HG01243.hp2 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305+667G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52463234 | |||||||
| chr13:52463234 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1305+667G>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52463234 | |||||||
| chr13:52463448 | C | T | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1305+881C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52463448 | |||||||
| chr13:52463510 | T | G | 2 | a0006c0008t0001g0179 a0006c0008t0001g0180 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1305+943T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52463510 | |||||||
| chr13:52463572 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0064 |
4 | NA18962.hp2 NA18975.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+1005T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52463572 | |||||||
| chr13:52463607 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1305+1040A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52463607 | |||||||
| chr13:52463702 | T | G | 3 | a0001c0001t0002g0146 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG00597.hp2 HG02040.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1305+1135T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52463702 | |||||||
| chr13:52463707 | T | C | 12 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 others(9): Show |
15 | HG00544.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1305+1140T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52463707 | |||||||
| chr13:52463823 | G | C | 1 | a0003c0005t0001g0126 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1305+1256G>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52463823 | |||||||
| chr13:52463900 | G | C | 3 | a0003c0005t0001g0037 a0003c0005t0001g0126 a0003c0005t0001g0127 |
4 | HG01243.hp2 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305+1333G>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52463900 | |||||||
| chr13:52464062 | C | A | 1 | a0001c0001t0002g0034 | 2 | NA18969.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1306-1233C>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464062 | |||||||
| chr13:52464069 | C | A | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306-1226C>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464069 | |||||||
| chr13:52464085 | A | G | 1 | a0001c0001t0010g0200 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1306-1210A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464085 | |||||||
| chr13:52464086 | C | T | 2 | a0001c0001t0004g0080 a0001c0001t0004g0088 |
2 | HG01496.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1306-1209C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464086 | |||||||
| chr13:52464107 | C | T | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306-1188C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464107 | |||||||
| chr13:52464137 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1306-1158T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464137 | |||||||
| chr13:52464240 | A | G | 1 | a0001c0001t0002g0033 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1306-1055A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464240 | |||||||
| chr13:52464343 | A | G | 2 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
2 | HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1306-952A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464343 | |||||||
| chr13:52464345 | G | A | 1 | a0001c0013t0008g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1306-950G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464345 | |||||||
| chr13:52464371 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1306-924G>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464371 | |||||||
| chr13:52464501 | C | T | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306-794C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464501 | |||||||
| chr13:52464553 | C | CA | 11 | a0001c0001t0001g0134 a0001c0001t0002g0140 a0001c0001t0002g0147 others(8): Show |
11 | HG00280.hp2 HG01109.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1306-721dupA | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 52464553 | ||||||
| chr13:52464553 | CA | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(95): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1306-721delA | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 52464553 | ||||||
| chr13:52464570 | A | C | 1 | a0001c0001t0001g0079 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1306-725A>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464570 | |||||||
| chr13:52464576 | A | C | 2 | a0001c0001t0002g0159 a0001c0001t0002g0191 |
2 | HG01109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1306-719A>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464576 | |||||||
| chr13:52464678 | A | G | 2 | a0001c0001t0002g0042 a0001c0001t0002g0189 |
3 | HG01243.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1306-617A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464678 | |||||||
| chr13:52464678 | A | T | 1 | a0008c0015t0001g0105 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1306-617A>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464678 | |||||||
| chr13:52464723 | C | A | 1 | a0001c0013t0008g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1306-572C>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464723 | |||||||
| chr13:52464725 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1306-570T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464725 | |||||||
| chr13:52464994 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1306-301T>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52464994 | |||||||
| chr13:52465012 | T | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0064 |
4 | NA18962.hp2 NA18975.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306-283T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52465012 | |||||||
| chr13:52465045 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1306-250C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52465045 | |||||||
| chr13:52465089 | A | T | 10 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0124 others(7): Show |
12 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1306-206A>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52465089 | |||||||
| chr13:52465123 | C | T | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1306-172C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52465123 | |||||||
| chr13:52465201 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1306-94A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 5/8 | chr13 | 52465201 | |||||||
| chr13:52465493 | A | G | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476+28A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465493 | |||||||
| chr13:52465600 | G | A | 2 | a0001c0001t0003g0039 a0001c0001t0003g0164 |
3 | HG02717.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1476+135G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465600 | |||||||
| chr13:52465613 | A | G | 8 | a0001c0001t0002g0047 a0001c0001t0002g0190 a0001c0001t0002g0195 others(5): Show |
9 | HG00673.hp2 HG02040.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1476+148A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465613 | |||||||
| chr13:52465840 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1476+375G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465840 | |||||||
| chr13:52465880 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1476+415A>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465880 | |||||||
| chr13:52465906 | T | TATATATA others(7): Show |
97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(94): Show |
183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1476+469_1476+482d others(16): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52465906 | ||||||
| chr13:52465906 | TATATATA others(7): Show |
T | 1 | a0001c0001t0003g0169 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1476+469_1476+482d others(16): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52465906 | ||||||
| chr13:52465914 | T | C | 1 | a0002c0002t0001g0185 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1476+449T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465914 | |||||||
| chr13:52465920 | C | CAT | 3 | a0001c0001t0001g0022 a0001c0001t0001g0124 a0001c0001t0001g0125 |
5 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1476+463_1476+464d others(4): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52465920 | ||||||
| chr13:52465930 | CACACATA others(5): Show |
C | 3 | a0003c0005t0001g0037 a0003c0005t0001g0126 a0003c0005t0001g0127 |
4 | HG01243.hp2 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1476+478_1476+489d others(14): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52465930 | ||||||
| chr13:52465935 | A | G | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1476+470A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465935 | |||||||
| chr13:52465940 | T | TATACACA others(7): Show |
1 | a0001c0001t0001g0078 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1476+482_1476+483i others(16): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52465940 | ||||||
| chr13:52465945 | ACATATAT others(3): Show |
A | 2 | a0001c0001t0002g0043 a0001c0001t0009g0165 |
3 | HG01192.hp2 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1476+483_1476+492d others(12): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52465945 | ||||||
| chr13:52465946 | C | CACATATA others(9): Show |
2 | a0006c0008t0001g0179 a0006c0008t0001g0180 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1476+482_1476+483i others(18): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52465946 | ||||||
| chr13:52465948 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1476+483T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465948 | |||||||
| chr13:52465951 | ATATG | A | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476+487_1476+490d others(6): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465951 | |||||||
| chr13:52465955 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1476+490G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465955 | |||||||
| chr13:52465955 | GCACACAT others(5): Show |
G | 2 | a0001c0001t0002g0042 a0001c0001t0002g0189 |
3 | HG01243.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1476+502_1476+513d others(14): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52465955 | ||||||
| chr13:52465960 | C | T | 6 | a0001c0001t0001g0060 a0001c0001t0002g0043 a0001c0001t0005g0035 others(3): Show |
8 | HG01192.hp2 HG02135.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1476+495C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465960 | |||||||
| chr13:52465966 | T | C | 34 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(31): Show |
88 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1476+501T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465966 | |||||||
| chr13:52465967 | A | G | 4 | a0001c0001t0001g0060 a0001c0001t0005g0035 a0001c0001t0005g0129 others(1): Show |
5 | HG02135.hp1 HG02970.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1476+502A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465967 | |||||||
| chr13:52465972 | C | T | 2 | a0001c0001t0002g0043 a0001c0001t0009g0165 |
3 | HG01192.hp2 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1476+507C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465972 | |||||||
| chr13:52465972 | CAT | C | 8 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(5): Show |
9 | HG00544.hp1 HG01074.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1476+512_1476+513d others(4): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52465972 | ||||||
| chr13:52465979 | G | A | 5 | a0001c0001t0001g0060 a0001c0001t0001g0137 a0001c0001t0005g0035 others(2): Show |
6 | HG02135.hp1 HG02970.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1476+514G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52465979 | |||||||
| chr13:52466005 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1476+540A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466005 | |||||||
| chr13:52466010 | C | CATACACA others(11): Show |
1 | a0001c0001t0001g0077 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1476+563_1476+580d others(20): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52466010 | ||||||
| chr13:52466039 | A | C | 1 | a0001c0001t0002g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1476+574A>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466039 | |||||||
| chr13:52466040 | TAC | T | 10 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0134 others(7): Show |
11 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1476+585_1476+586d others(4): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52466040 | ||||||
| chr13:52466124 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0067 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1476+659T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466124 | |||||||
| chr13:52466179 | G | A | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476+714G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466179 | |||||||
| chr13:52466187 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1476+722A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466187 | |||||||
| chr13:52466394 | C | T | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476+929C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466394 | |||||||
| chr13:52466523 | G | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0068 a0001c0001t0001g0069 |
3 | NA18972.hp2 NA18999.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1476+1058G>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466523 | |||||||
| chr13:52466572 | C | T | 4 | a0001c0004t0001g0021 a0001c0004t0001g0032 a0001c0004t0001g0121 others(1): Show |
6 | HG01255.hp1 HG01256.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1476+1107C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466572 | |||||||
| chr13:52466687 | A | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(75): Show |
155 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1476+1222A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466687 | |||||||
| chr13:52466776 | C | G | 4 | a0001c0004t0001g0021 a0001c0004t0001g0032 a0001c0004t0001g0121 others(1): Show |
6 | HG01255.hp1 HG01256.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1476+1311C>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466776 | |||||||
| chr13:52466797 | C | T | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476+1332C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466797 | |||||||
| chr13:52466876 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1477-1402G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466876 | |||||||
| chr13:52466876 | G | C | 1 | a0001c0013t0008g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1477-1402G>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466876 | |||||||
| chr13:52466954 | G | GT | 4 | a0001c0001t0002g0038 a0001c0001t0002g0043 a0001c0001t0002g0145 others(1): Show |
6 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1477-1314dupT | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52466954 | ||||||
| chr13:52466964 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1477-1314T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466964 | |||||||
| chr13:52466982 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1477-1296G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52466982 | |||||||
| chr13:52467080 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0083 a0001c0001t0001g0087 |
3 | NA19001.hp1 NA19007.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1477-1198A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467080 | |||||||
| chr13:52467100 | C | CA | 7 | a0001c0001t0002g0040 a0001c0001t0002g0043 a0001c0001t0002g0161 others(4): Show |
9 | HG00438.hp1 HG01192.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1477-1158dupA | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52467100 | ||||||
| chr13:52467100 | CA | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(93): Show |
189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1477-1158delA | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52467100 | ||||||
| chr13:52467100 | CAA | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0036 others(12): Show |
20 | HG00558.hp2 HG01168.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1477-1159_1477-115 others(6): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52467100 | ||||||
| chr13:52467100 | CAAA | C | 9 | a0001c0001t0001g0135 a0001c0001t0005g0035 a0001c0001t0005g0129 others(6): Show |
11 | HG00544.hp1 HG01099.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.1477-1160_1477-115 others(7): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52467100 | ||||||
| chr13:52467100 | CAAAAAAA others(3): Show |
C | 1 | a0001c0016t0002g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1477-1167_1477-115 others(14): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52467100 | ||||||
| chr13:52467220 | G | A | 12 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 others(9): Show |
15 | HG00544.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1477-1058G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467220 | |||||||
| chr13:52467222 | GGA | G | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0134 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1477-1055_1477-105 others(6): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467222 | |||||||
| chr13:52467253 | T | G | 12 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 others(9): Show |
15 | HG00544.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1477-1025T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467253 | |||||||
| chr13:52467402 | A | T | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477-876A>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467402 | |||||||
| chr13:52467452 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1477-826C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467452 | |||||||
| chr13:52467482 | C | T | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477-796C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467482 | |||||||
| chr13:52467522 | G | A | 1 | a0001c0001t0004g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1477-756G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467522 | |||||||
| chr13:52467578 | G | T | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0134 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1477-700G>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467578 | |||||||
| chr13:52467607 | G | A | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477-671G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467607 | |||||||
| chr13:52467674 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1477-604A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467674 | |||||||
| chr13:52467706 | AAAAAAAG | A | 10 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0124 others(7): Show |
12 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1477-558_1477-552d others(9): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52467706 | ||||||
| chr13:52467778 | G | T | 13 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0039 others(10): Show |
25 | HG00140.hp2 HG01069.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1477-500G>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467778 | |||||||
| chr13:52467815 | G | GT | 11 | a0001c0001t0001g0069 a0001c0001t0001g0075 a0001c0001t0001g0114 others(8): Show |
12 | HG01074.hp2 HG01891.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.1477-451dupT | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52467815 | ||||||
| chr13:52467855 | G | A | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1477-423G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467855 | |||||||
| chr13:52467905 | G | A | 4 | a0001c0004t0001g0021 a0001c0004t0001g0032 a0001c0004t0001g0121 others(1): Show |
6 | HG01255.hp1 HG01256.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1477-373G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467905 | |||||||
| chr13:52467967 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0110 others(7): Show |
18 | HG00323.hp2 HG00408.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.1477-311G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467967 | |||||||
| chr13:52467999 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1477-279A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52467999 | |||||||
| chr13:52468090 | G | A | 1 | a0001c0001t0010g0200 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1477-188G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52468090 | |||||||
| chr13:52468131 | T | G | 1 | a0001c0001t0002g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1477-147T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52468131 | |||||||
| chr13:52468136 | G | A | 1 | a0001c0001t0010g0200 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1477-142G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52468136 | |||||||
| chr13:52468171 | C | CTG | 12 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 others(9): Show |
15 | HG00544.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1477-106_1477-105i others(4): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr13 | 52468171 | ||||||
| chr13:52468189 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1477-89A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52468189 | |||||||
| chr13:52468204 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1477-74C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52468204 | |||||||
| chr13:52468232 | A | T | 1 | a0001c0013t0008g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1477-46A>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 6/8 | chr13 | 52468232 | |||||||
| chr13:52468394 | T | G | 7 | a0001c0013t0008g0130 a0002c0002t0001g0046 a0002c0002t0001g0184 others(4): Show |
8 | HG00544.hp1 HG01099.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1546+47T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52468394 | |||||||
| chr13:52468479 | A | G | 2 | a0006c0008t0001g0179 a0006c0008t0001g0180 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1546+132A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52468479 | |||||||
| chr13:52468492 | G | A | 2 | a0001c0001t0002g0190 a0001c0001t0002g0198 |
2 | HG02040.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1546+145G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52468492 | |||||||
| chr13:52468649 | C | G | 1 | a0001c0001t0002g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1546+302C>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52468649 | |||||||
| chr13:52468650 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0103 |
3 | HG01257.hp1 HG01346.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1546+303C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52468650 | |||||||
| chr13:52468894 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0124 a0001c0001t0001g0125 |
5 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546+547G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52468894 | |||||||
| chr13:52469013 | T | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0101 a0001c0001t0001g0104 others(1): Show |
6 | HG00639.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1546+666T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469013 | |||||||
| chr13:52469198 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(131): Show |
236 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1546+851G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469198 | |||||||
| chr13:52469458 | C | G | 1 | a0001c0001t0003g0155 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1546+1111C>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469458 | |||||||
| chr13:52469461 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1546+1114G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469461 | |||||||
| chr13:52469548 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1546+1201G>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469548 | |||||||
| chr13:52469567 | ATGAAATA others(312): Show |
A | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546+1236_1546+155 others(4): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 52469567 | ||||||
| chr13:52469589 | A | AT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(7): Show |
10 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1546+1245dupT | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 52469589 | ||||||
| chr13:52469589 | A | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
15 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.1546+1242A>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469589 | |||||||
| chr13:52469593 | A | AT | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(5): Show |
9 | HG00323.hp1 HG00733.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1546+1249dupT | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 52469593 | ||||||
| chr13:52469593 | A | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(56): Show |
108 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1546+1246A>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469593 | |||||||
| chr13:52469596 | TA | T | 12 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0124 others(9): Show |
14 | HG01074.hp2 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1546+1250delA | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469596 | |||||||
| chr13:52469597 | A | AT | 5 | a0001c0001t0004g0009 a0001c0001t0004g0051 a0001c0001t0004g0070 others(2): Show |
10 | HG01106.hp1 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1546+1260dupT | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 52469597 | ||||||
| chr13:52469597 | A | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1546+1250A>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469597 | |||||||
| chr13:52469597 | ATT | A | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
6 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1546+1259_1546+126 others(6): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 52469597 | ||||||
| chr13:52469601 | T | A | 2 | a0001c0001t0002g0043 a0001c0001t0009g0165 |
3 | HG01192.hp2 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1546+1254T>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469601 | |||||||
| chr13:52469628 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1546+1281C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469628 | |||||||
| chr13:52469638 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(122): Show |
224 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.1546+1291A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469638 | |||||||
| chr13:52469657 | C | T | 1 | a0001c0001t0002g0038 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1546+1310C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469657 | |||||||
| chr13:52469687 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1546+1340C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469687 | |||||||
| chr13:52469745 | C | T | 1 | a0003c0005t0001g0037 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1546+1398C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469745 | |||||||
| chr13:52469753 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0068 |
2 | NA18972.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1546+1406C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469753 | |||||||
| chr13:52469884 | C | A | 1 | a0001c0001t0001g0027 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1546+1537C>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469884 | |||||||
| chr13:52469984 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1546+1637A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469984 | |||||||
| chr13:52469986 | T | C | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546+1639T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52469986 | |||||||
| chr13:52470046 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1546+1699C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470046 | |||||||
| chr13:52470145 | G | A | 1 | a0001c0001t0010g0200 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1546+1798G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470145 | |||||||
| chr13:52470187 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG00423.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1546+1840C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470187 | |||||||
| chr13:52470217 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1546+1870C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470217 | |||||||
| chr13:52470218 | G | A | 2 | a0001c0001t0002g0159 a0001c0001t0002g0191 |
2 | HG01109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1546+1871G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470218 | |||||||
| chr13:52470348 | G | A | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546+2001G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470348 | |||||||
| chr13:52470362 | T | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546+2015T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470362 | |||||||
| chr13:52470370 | GCT | G | 4 | a0001c0004t0001g0021 a0001c0004t0001g0032 a0001c0004t0001g0121 others(1): Show |
6 | HG01255.hp1 HG01256.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1546+2024_1546+202 others(6): Show |
CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470370 | |||||||
| chr13:52470376 | A | T | 2 | a0001c0001t0002g0038 a0001c0001t0002g0145 |
3 | HG01891.hp1 HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1546+2029A>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470376 | |||||||
| chr13:52470401 | G | A | 1 | a0001c0013t0008g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1546+2054G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470401 | |||||||
| chr13:52470583 | C | T | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546+2236C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470583 | |||||||
| chr13:52470605 | GA | G | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546+2268delA | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 52470605 | ||||||
| chr13:52470741 | A | G | 12 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 others(9): Show |
15 | HG00544.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1546+2394A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470741 | |||||||
| chr13:52470816 | C | G | 1 | a0001c0001t0003g0169 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1546+2469C>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470816 | |||||||
| chr13:52470827 | T | G | 1 | a0001c0001t0002g0145 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1546+2480T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470827 | |||||||
| chr13:52470836 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1546+2489A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470836 | |||||||
| chr13:52470917 | T | C | 3 | a0003c0005t0001g0037 a0003c0005t0001g0126 a0003c0005t0001g0127 |
4 | HG01243.hp2 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546+2570T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470917 | |||||||
| chr13:52470974 | A | G | 1 | a0001c0001t0002g0149 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1546+2627A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470974 | |||||||
| chr13:52470982 | A | C | 5 | a0001c0001t0001g0026 a0001c0001t0001g0052 a0001c0001t0001g0054 others(2): Show |
6 | HG00621.hp2 NA18612.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.1546+2635A>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52470982 | |||||||
| chr13:52471035 | G | A | 4 | a0001c0001t0002g0038 a0001c0001t0002g0043 a0001c0001t0002g0145 others(1): Show |
6 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1546+2688G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52471035 | |||||||
| chr13:52471072 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1546+2725C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52471072 | |||||||
| chr13:52471107 | A | G | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-2722A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52471107 | |||||||
| chr13:52471112 | C | T | 7 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0134 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1547-2717C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52471112 | |||||||
| chr13:52471113 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1547-2716G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52471113 | |||||||
| chr13:52471124 | C | T | 2 | a0001c0001t0002g0042 a0001c0001t0002g0189 |
3 | HG01243.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1547-2705C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52471124 | |||||||
| chr13:52471354 | A | G | 1 | a0001c0001t0002g0177 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1547-2475A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52471354 | |||||||
| chr13:52471508 | T | TA | 4 | a0001c0001t0002g0038 a0001c0001t0002g0043 a0001c0001t0002g0145 others(1): Show |
6 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547-2308dupA | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 52471508 | ||||||
| chr13:52471620 | A | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-2209A>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52471620 | |||||||
| chr13:52471785 | A | C | 1 | a0001c0001t0001g0073 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1547-2044A>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52471785 | |||||||
| chr13:52471828 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0067 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1547-2001G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52471828 | |||||||
| chr13:52471989 | T | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-1840T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52471989 | |||||||
| chr13:52472067 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0085 |
2 | HG00597.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1547-1762T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52472067 | |||||||
| chr13:52472099 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0124 a0001c0001t0001g0125 |
5 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1547-1730C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52472099 | |||||||
| chr13:52472193 | T | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-1636T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52472193 | |||||||
| chr13:52472204 | GT | G | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-1618delT | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 52472204 | ||||||
| chr13:52472221 | A | T | 1 | a0001c0001t0010g0200 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1547-1608A>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52472221 | |||||||
| chr13:52472303 | G | T | 1 | a0001c0001t0003g0183 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1547-1526G>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52472303 | |||||||
| chr13:52472453 | T | A | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1547-1376T>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52472453 | |||||||
| chr13:52472503 | C | T | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-1326C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52472503 | |||||||
| chr13:52472658 | T | G | 1 | a0001c0001t0003g0154 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1547-1171T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52472658 | |||||||
| chr13:52472664 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1547-1165G>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52472664 | |||||||
| chr13:52472701 | C | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(92): Show |
186 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1547-1128C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52472701 | |||||||
| chr13:52472895 | T | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-934T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52472895 | |||||||
| chr13:52473047 | TA | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0100 a0001c0001t0001g0112 others(2): Show |
7 | HG01069.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1547-766delA | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 52473047 | ||||||
| chr13:52473055 | A | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-774A>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52473055 | |||||||
| chr13:52473183 | T | A | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-646T>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52473183 | |||||||
| chr13:52473184 | C | A | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-645C>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52473184 | |||||||
| chr13:52473202 | CT | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-624delT | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 52473202 | ||||||
| chr13:52473209 | T | A | 1 | a0001c0001t0002g0177 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1547-620T>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52473209 | |||||||
| chr13:52473383 | C | T | 2 | a0006c0008t0001g0179 a0006c0008t0001g0180 |
2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1547-446C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52473383 | |||||||
| chr13:52473472 | C | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0124 a0001c0001t0001g0125 |
5 | HG02257.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1547-357C>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52473472 | |||||||
| chr13:52473514 | T | C | 34 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(31): Show |
88 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1547-315T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52473514 | |||||||
| chr13:52473574 | G | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
221 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1547-255G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52473574 | |||||||
| chr13:52473720 | C | T | 22 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0124 others(19): Show |
27 | HG00544.hp1 HG01099.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1547-109C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52473720 | |||||||
| chr13:52473784 | T | G | 1 | a0001c0001t0001g0029 | 2 | NA18941.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1547-45T>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52473784 | |||||||
| chr13:52473801 | G | A | 10 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0124 others(7): Show |
12 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1547-28G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 7/8 | chr13 | 52473801 | |||||||
| chr13:52474200 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0079 |
4 | NA18974.hp2 NA18978.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1802+116T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 8/8 | chr13 | 52474200 | |||||||
| chr13:52474223 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1802+139C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 8/8 | chr13 | 52474223 | |||||||
| chr13:52474252 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1802+168G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 8/8 | chr13 | 52474252 | |||||||
| chr13:52474402 | T | C | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1802+318T>C | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 8/8 | chr13 | 52474402 | |||||||
| chr13:52474475 | C | T | 1 | a0002c0002t0001g0184 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1802+391C>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 8/8 | chr13 | 52474475 | |||||||
| chr13:52474509 | A | G | 2 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
2 | HG00544.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1803-386A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 8/8 | chr13 | 52474509 | |||||||
| chr13:52474606 | T | A | 3 | a0001c0001t0002g0153 a0001c0001t0002g0157 a0001c0001t0002g0167 |
3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1803-289T>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 8/8 | chr13 | 52474606 | |||||||
| chr13:52474634 | A | G | 2 | a0001c0001t0005g0035 a0001c0001t0005g0129 |
3 | HG06807.hp1 NA18522.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1803-261A>G | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 8/8 | chr13 | 52474634 | |||||||
| chr13:52474672 | G | A | 6 | a0002c0002t0001g0046 a0002c0002t0001g0184 a0002c0002t0001g0185 others(3): Show |
7 | HG00544.hp1 HG01099.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1803-223G>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 8/8 | chr13 | 52474672 | |||||||
| chr13:52474689 | G | T | 2 | a0001c0001t0005g0035 a0001c0001t0005g0129 |
3 | HG06807.hp1 NA18522.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1803-206G>T | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 8/8 | chr13 | 52474689 | |||||||
| chr13:52474792 | C | A | 3 | a0001c0001t0005g0035 a0001c0001t0005g0129 a0001c0013t0008g0130 |
4 | HG02970.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1803-103C>A | CKAP2 | ENSG00000136108.15 | transcript | ENST00000258607.10 | protein_coding | 8/8 | chr13 | 52474792 |