Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10486 |
| ensemblid | ENSG00000112186.13 |
| hgncid | 20039 |
| symbol | CAP2 |
| name | cyclase associated actin cytoskeleton regulatory protein 2 |
| refseq_nuc | NM_006366.3 |
| refseq_prot | NP_006357.1 |
| ensembl_nuc | ENST00000229922.7 |
| ensembl_prot | ENSP00000229922.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 17393595 |
| end | 17557780 |
| strand | + |
| ver | v1.2 |
| region | chr6:17393595-17557780 |
| region5000 | chr6:17388595-17562780 |
| regionname0 | CAP2_chr6_17393595_17557780 |
| regionname5000 | CAP2_chr6_17388595_17562780 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 477 | 185 | 60 | 40 | 49 | 8 | 26 | 31 | CAP2_chr6_17388595_17562780 | CAP2 | MANMQ others(472): Show |
chr6 | 17388595 | 17562780 |
| a0002 | 0/0 | 477 | 12 | 3 | 1 | 7 | 0 | 1 | 5 | CAP2_chr6_17388595_17562780 | CAP2 | MANMQ others(472): Show |
chr6 | 17388595 | 17562780 |
| a0003 | 0/0 | 477 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | MANMQ others(472): Show |
chr6 | 17388595 | 17562780 |
| a0004 | 0/0 | 477 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | MANMQ others(472): Show |
chr6 | 17388595 | 17562780 |
| a0005 | 0/0 | 477 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | MANMQ others(472): Show |
chr6 | 17388595 | 17562780 |
| a0006 | 0/0 | 477 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | MANMQ others(472): Show |
chr6 | 17388595 | 17562780 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1431 | 98 | 22 | 21 | 35 | 3 | 17 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0001c0002 | 1/1 | 1431 | 62 | 20 | 17 | 9 | 5 | 9 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0001c0003 | 0/0 | 1431 | 12 | 11 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0001c0006 | 0/0 | 1431 | 5 | 0 | 0 | 5 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0001c0008 | 0/0 | 1431 | 3 | 3 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0001c0009 | 0/0 | 1431 | 2 | 2 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0001c0011 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0001c0013 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0001c0014 | 0/0 | 1431 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0002c0004 | 0/0 | 1431 | 6 | 2 | 1 | 3 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0002c0005 | 0/0 | 1431 | 5 | 0 | 0 | 4 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0002c0012 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0003c0007 | 0/0 | 1431 | 5 | 3 | 2 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0004c0010 | 0/0 | 1431 | 2 | 1 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0005c0015 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 | ||
| a0006c0016 | 0/0 | 1431 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | ATGGC others(1426): Show |
chr6 | 17388595 | 17562780 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2925 | 55 | 17 | 10 | 16 | 2 | 10 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0001c0001t0002 | 0/0 | 2924 | 41 | 3 | 11 | 19 | 1 | 7 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2919): Show |
chr6 | 17388595 | 17562780 |
| a0001c0001t0005 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0001c0001t0007 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0001c0002t0001 | 0/1 | 2925 | 48 | 16 | 11 | 7 | 4 | 9 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0001c0002t0002 | 1/0 | 2924 | 13 | 3 | 6 | 2 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2919): Show |
chr6 | 17388595 | 17562780 |
| a0001c0002t0006 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0001c0003t0001 | 0/0 | 2925 | 6 | 5 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0001c0003t0002 | 0/0 | 2924 | 6 | 6 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2919): Show |
chr6 | 17388595 | 17562780 |
| a0001c0006t0001 | 0/0 | 2925 | 5 | 0 | 0 | 5 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0001c0008t0001 | 0/0 | 2925 | 3 | 3 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0001c0009t0001 | 0/0 | 2925 | 2 | 2 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0001c0011t0002 | 0/0 | 2924 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2919): Show |
chr6 | 17388595 | 17562780 |
| a0001c0013t0001 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0001c0014t0008 | 0/0 | 2925 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0002c0004t0001 | 0/0 | 2925 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0002c0004t0002 | 0/0 | 2924 | 5 | 2 | 0 | 3 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2919): Show |
chr6 | 17388595 | 17562780 |
| a0002c0005t0001 | 0/0 | 2925 | 3 | 0 | 0 | 2 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0002c0005t0003 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0002c0005t0004 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0002c0012t0001 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0003c0007t0001 | 0/0 | 2925 | 5 | 3 | 2 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0004c0010t0001 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0004c0010t0002 | 0/0 | 2924 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2919): Show |
chr6 | 17388595 | 17562780 |
| a0005c0015t0001 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| a0006c0016t0001 | 0/0 | 2925 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | GACTC others(2920): Show |
chr6 | 17388595 | 17562780 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0001t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0002g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0002t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0003t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0003t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0003t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0006t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0006t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0006t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0006t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0008t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0008t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0008t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0009t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0009t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0011t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0013t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0001c0014t0008g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0002c0004t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0002c0004t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0002c0004t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0002c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0002c0004t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0002c0004t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0002c0005t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0002c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0002c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0002c0005t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0002c0005t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0002c0012t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0003c0007t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0003c0007t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0003c0007t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0003c0007t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0003c0007t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0004c0010t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0004c0010t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0005c0015t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| a0006c0016t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0107 | EUR | GBR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG00438 | hp2 | a0001 | c0006 | t0001 | g0149 | EAS | CHS | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG00597 | hp1 | a0002 | c0004 | t0002 | g0156 | EAS | CHS | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | CHS | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | CHS | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG00735 | hp2 | a0002 | c0004 | t0001 | g0073 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0187 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01106 | hp2 | a0003 | c0007 | t0001 | g0110 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0129 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01243 | hp2 | a0003 | c0007 | t0001 | g0119 | AMR | PUR | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01255 | hp1 | a0004 | c0010 | t0002 | g0061 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01361 | hp2 | a0001 | c0014 | t0008 | g0016 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0065 | AMR | CLM | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0152 | EUR | IBS | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0191 | EUR | IBS | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0167 | EUR | IBS | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0192 | EUR | IBS | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01884 | hp2 | a0002 | c0012 | t0001 | g0014 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0201 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0114 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0115 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0111 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0135 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0116 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02055 | hp1 | a0001 | c0013 | t0001 | g0076 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02055 | hp2 | a0001 | c0008 | t0001 | g0204 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02135 | hp1 | a0001 | c0006 | t0001 | g0155 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02135 | hp2 | a0002 | c0005 | t0001 | g0004 | EAS | KHV | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02280 | hp2 | a0003 | c0007 | t0001 | g0059 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0108 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0079 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02622 | hp1 | a0005 | c0015 | t0001 | g0070 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0145 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0039 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02717 | hp2 | a0002 | c0004 | t0002 | g0085 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02886 | hp2 | a0001 | c0002 | t0006 | g0133 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02897 | hp2 | a0004 | c0010 | t0001 | g0063 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0188 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02970 | hp1 | a0001 | c0003 | t0002 | g0064 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02976 | hp2 | a0002 | c0004 | t0002 | g0083 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03017 | hp2 | a0002 | c0005 | t0001 | g0104 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0048 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0060 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0144 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0090 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0189 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0131 | AFR | ESN | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0093 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03453 | hp1 | a0001 | c0011 | t0002 | g0087 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03453 | hp2 | a0003 | c0007 | t0001 | g0066 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0106 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03540 | hp1 | a0003 | c0007 | t0001 | g0205 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03540 | hp2 | a0001 | c0009 | t0001 | g0015 | AFR | GWD | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0088 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03579 | hp2 | a0001 | c0008 | t0001 | g0057 | AFR | MSL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03831 | hp2 | a0006 | c0016 | t0001 | g0194 | SAS | BEB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | BEB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0094 | SAS | BEB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | STU | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0056 | SAS | STU | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | YRI | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0072 | AFR | YRI | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | CHB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | CHB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | CHB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | YRI | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18990 | hp1 | a0001 | c0006 | t0001 | g0121 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18990 | hp2 | a0001 | c0006 | t0001 | g0034 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18995 | hp1 | a0002 | c0005 | t0003 | g0171 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA18999 | hp2 | a0001 | c0006 | t0001 | g0018 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19002 | hp2 | a0002 | c0004 | t0002 | g0097 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19003 | hp1 | a0002 | c0005 | t0001 | g0203 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19006 | hp2 | a0002 | c0005 | t0004 | g0025 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19043 | hp1 | a0001 | c0009 | t0001 | g0013 | AFR | LWK | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19057 | hp1 | a0002 | c0004 | t0002 | g0182 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0118 | AFR | ASW | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0113 | AFR | ASW | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0193 | EUR | TSI | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02109 | hp1 | a0001 | c0003 | t0002 | g0071 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02486 | hp1 | a0001 | c0008 | t0001 | g0051 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0075 | AFR | LWK | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| NA21309 | hp2 | a0001 | c0003 | t0002 | g0086 | AFR | LWK | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0183 | REF | REF | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0139 | REF | REF | CAP2_chr6_17388595_17562780 | CAP2 | chr6 | 17388595 | 17562780 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:17513875 | A | C | 1 | a0006 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.557A>C | p.Lys186Thr | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/13 | 710/2925 | 557/1434 | 186/477 | chr6 | 17513875 | |||
| chr6:17513932 | C | T | 1 | a0005 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.614C>T | p.Thr205Met | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/13 | 767/2925 | 614/1434 | 205/477 | chr6 | 17513932 | |||
| chr6:17541074 | C | A | 1 | a0002 | 12 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(9): Show |
missense_variant | MODERATE | c.928C>A | p.Pro310Thr | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/13 | 1081/2925 | 928/1434 | 310/477 | chr6 | 17541074 | |||
| chr6:17541077 | A | G | 1 | a0004 | 2 | HG01255.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.931A>G | p.Thr311Ala | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/13 | 1084/2925 | 931/1434 | 311/477 | chr6 | 17541077 | |||
| chr6:17541093 | A | G | 1 | a0003 | 5 | HG01106.hp2 HG01243.hp2 HG02280.hp2 others(2): Show |
missense_variant | MODERATE | c.947A>G | p.Tyr316Cys | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/13 | 1100/2925 | 947/1434 | 316/477 | chr6 | 17541093 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:17421615 | G | A | 1 | a0001c0011 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.60G>A | p.Ser20Ser | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/13 | 213/2925 | 60/1434 | 20/477 | chr6 | 17421615 | |||
| chr6:17426615 | T | C | 5 | a0001c0008 a0001c0009 a0001c0013 others(2): Show |
8 | HG01361.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
synonymous_variant | LOW | c.147T>C | p.Phe49Phe | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/13 | 300/2925 | 147/1434 | 49/477 | chr6 | 17426615 | |||
| chr6:17542956 | A | C | 3 | a0001c0003 a0001c0014 a0005c0015 |
14 | HG01361.hp2 HG01496.hp2 HG02109.hp1 others(11): Show |
synonymous_variant | LOW | c.1122A>C | p.Ile374Ile | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 10/13 | 1275/2925 | 1122/1434 | 374/477 | chr6 | 17542956 | |||
| chr6:17543071 | A | G | 13 | a0001c0001 a0001c0003 a0001c0006 others(10): Show |
140 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(137): Show |
synonymous_variant | LOW | c.1137A>G | p.Lys379Lys | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/13 | 1290/2925 | 1137/1434 | 379/477 | chr6 | 17543071 | |||
| chr6:17551550 | C | T | 2 | a0001c0006 a0002c0005 |
10 | HG00438.hp2 HG02135.hp1 HG02135.hp2 others(7): Show |
synonymous_variant | LOW | c.1296C>T | p.Ile432Ile | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/13 | 1449/2925 | 1296/1434 | 432/477 | chr6 | 17551550 | |||
| chr6:17556370 | C | T | 1 | a0001c0013 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1362C>T | p.Pro454Pro | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 1515/2925 | 1362/1434 | 454/477 | chr6 | 17556370 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:17393710 | G | C | 1 | a0002c0005t0003 | 1 | NA18995.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/13 | 27846 | chr6 | 17393710 | ||||||
| chr6:17556470 | T | C | 1 | a0002c0005t0004 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*28T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 28 | chr6 | 17556470 | ||||||
| chr6:17556557 | A | T | 1 | a0001c0014t0008 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 115 | chr6 | 17556557 | ||||||
| chr6:17556925 | T | C | 1 | a0001c0001t0005 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 483 | chr6 | 17556925 | ||||||
| chr6:17556996 | A | ATT | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(17): Show |
138 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*554_*555insTT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 555 | chr6 | 17556996 | ||||||
| chr6:17557010 | A | C | 1 | a0001c0001t0007 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*568A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 568 | chr6 | 17557010 | ||||||
| chr6:17557171 | AT | A | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(17): Show |
138 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*737delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 737 | INFO_REALIGN_3_PRIME | chr6 | 17557171 | |||||
| chr6:17557497 | A | G | 1 | a0001c0002t0006 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1055A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 13/13 | 1055 | chr6 | 17557497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:17393872 | T | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+126T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17393872 | |||||||
| chr6:17393999 | C | T | 4 | a0001c0001t0002g0206 a0001c0008t0001g0204 a0002c0005t0001g0203 others(1): Show |
4 | HG01943.hp2 HG02055.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+253C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17393999 | |||||||
| chr6:17394135 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-2+389C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394135 | |||||||
| chr6:17394158 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-2+412T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394158 | |||||||
| chr6:17394162 | G | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-2+416G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394162 | |||||||
| chr6:17394210 | C | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+464C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394210 | |||||||
| chr6:17394537 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+791G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394537 | |||||||
| chr6:17394602 | C | T | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2+856C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394602 | |||||||
| chr6:17394748 | G | GATACAAC others(4): Show |
1 | a0001c0001t0002g0055 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-2+1002_-2+1003ins others(11): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394748 | |||||||
| chr6:17394750 | G | C | 1 | a0001c0001t0002g0055 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-2+1004G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394750 | |||||||
| chr6:17394861 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+1115G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394861 | |||||||
| chr6:17394892 | A | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+1146A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17394892 | |||||||
| chr6:17395069 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(47): Show |
50 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2+1323G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395069 | |||||||
| chr6:17395239 | A | G | 4 | a0001c0001t0001g0202 a0001c0001t0002g0199 a0001c0001t0005g0200 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+1493A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395239 | |||||||
| chr6:17395365 | T | C | 1 | a0001c0002t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-2+1619T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395365 | |||||||
| chr6:17395426 | A | C | 3 | a0001c0001t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
3 | HG02970.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2+1680A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395426 | |||||||
| chr6:17395505 | G | A | 2 | a0001c0002t0001g0058 a0001c0008t0001g0057 |
2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-2+1759G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395505 | |||||||
| chr6:17395581 | A | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+1835A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395581 | |||||||
| chr6:17395626 | C | A | 28 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(25): Show |
28 | HG01167.hp2 HG01255.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.-2+1880C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395626 | |||||||
| chr6:17395701 | T | C | 2 | a0001c0001t0001g0001 a0001c0002t0001g0002 |
2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-2+1955T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395701 | |||||||
| chr6:17395702 | T | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(93): Show |
96 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(93): Show |
intron_variant | MODIFIER | c.-2+1956T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395702 | |||||||
| chr6:17395761 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+2015C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395761 | |||||||
| chr6:17395791 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+2045G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395791 | |||||||
| chr6:17395889 | T | G | 2 | a0001c0001t0001g0196 a0001c0002t0001g0197 |
2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2+2143T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17395889 | |||||||
| chr6:17396208 | T | C | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0002t0001g0062 others(7): Show |
10 | HG01255.hp1 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+2462T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17396208 | |||||||
| chr6:17396291 | T | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+2545T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17396291 | |||||||
| chr6:17396424 | A | G | 3 | a0001c0001t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
3 | HG02970.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2+2678A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17396424 | |||||||
| chr6:17396556 | G | C | 2 | a0001c0002t0001g0093 a0001c0002t0001g0094 |
2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-2+2810G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17396556 | |||||||
| chr6:17396749 | C | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+3003C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17396749 | |||||||
| chr6:17396885 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
98 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(95): Show |
intron_variant | MODIFIER | c.-2+3139T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17396885 | |||||||
| chr6:17397100 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+3354C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397100 | |||||||
| chr6:17397203 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(52): Show |
55 | HG00099.hp1 HG01106.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.-2+3457A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397203 | |||||||
| chr6:17397205 | G | A | 3 | a0001c0001t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
3 | HG02970.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2+3459G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397205 | |||||||
| chr6:17397207 | G | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+3461G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397207 | |||||||
| chr6:17397306 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+3560G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397306 | |||||||
| chr6:17397349 | C | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+3603C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397349 | |||||||
| chr6:17397432 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
51 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2+3686C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397432 | |||||||
| chr6:17397466 | G | A | 4 | a0001c0001t0001g0202 a0001c0001t0002g0199 a0001c0001t0005g0200 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+3720G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397466 | |||||||
| chr6:17397588 | G | C | 4 | a0001c0001t0001g0095 a0001c0001t0002g0096 a0001c0002t0001g0098 others(1): Show |
4 | HG00438.hp1 HG00597.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+3842G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397588 | |||||||
| chr6:17397596 | G | A | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-2+3850G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397596 | |||||||
| chr6:17397694 | C | CA | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(65): Show |
68 | HG00099.hp2 HG01071.hp1 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.-2+3971dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17397694 | ||||||
| chr6:17397694 | C | CAA | 15 | a0001c0001t0001g0069 a0001c0001t0001g0103 a0001c0001t0001g0196 others(12): Show |
15 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2+3970_-2+3971dup others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17397694 | ||||||
| chr6:17397694 | CAAAAAAA others(4): Show |
C | 8 | a0001c0002t0001g0056 a0001c0002t0001g0188 a0001c0002t0001g0189 others(5): Show |
8 | HG00741.hp2 HG01516.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2+3961_-2+3971del others(11): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17397694 | ||||||
| chr6:17397720 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-2+3974A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397720 | |||||||
| chr6:17397800 | G | A | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0002t0001g0062 others(7): Show |
10 | HG01255.hp1 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+4054G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397800 | |||||||
| chr6:17397924 | G | A | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0002t0001g0062 others(7): Show |
10 | HG01255.hp1 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+4178G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397924 | |||||||
| chr6:17397924 | GA | G | 7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0002t0001g0136 others(4): Show |
7 | HG00642.hp2 HG00741.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+4191delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17397924 | ||||||
| chr6:17397925 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-2+4179A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17397925 | |||||||
| chr6:17398141 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-2+4395C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398141 | |||||||
| chr6:17398252 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(53): Show |
56 | HG00099.hp1 HG01106.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.-2+4506A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398252 | |||||||
| chr6:17398288 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-2+4542A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398288 | |||||||
| chr6:17398299 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(174): Show |
177 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.-2+4553A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398299 | |||||||
| chr6:17398519 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-2+4773G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398519 | |||||||
| chr6:17398528 | C | CT | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(49): Show |
52 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.-2+4796dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17398528 | ||||||
| chr6:17398563 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(38): Show |
41 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.-2+4817C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398563 | |||||||
| chr6:17398681 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0002g0043 others(3): Show |
6 | HG00099.hp1 HG01175.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+4935C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398681 | |||||||
| chr6:17398814 | G | A | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-2+5068G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398814 | |||||||
| chr6:17398954 | T | G | 1 | a0001c0002t0001g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-2+5208T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17398954 | |||||||
| chr6:17399122 | G | A | 2 | a0001c0002t0001g0077 a0001c0002t0001g0078 |
2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-2+5376G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17399122 | |||||||
| chr6:17399295 | T | C | 1 | a0001c0003t0002g0060 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-2+5549T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17399295 | |||||||
| chr6:17399333 | G | A | 28 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(25): Show |
28 | HG01167.hp2 HG01255.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.-2+5587G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17399333 | |||||||
| chr6:17399500 | G | A | 6 | a0001c0002t0001g0074 a0001c0003t0001g0072 a0001c0003t0001g0075 others(3): Show |
6 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+5754G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17399500 | |||||||
| chr6:17399505 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-2+5759A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17399505 | |||||||
| chr6:17399655 | A | G | 2 | a0001c0001t0002g0181 a0002c0004t0002g0182 |
2 | NA18939.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-2+5909A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17399655 | |||||||
| chr6:17400064 | C | CA | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(56): Show |
59 | HG00099.hp1 HG01106.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.-2+6330dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17400064 | ||||||
| chr6:17400064 | C | CAA | 7 | a0001c0002t0001g0074 a0001c0003t0001g0072 a0001c0003t0001g0075 others(4): Show |
7 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+6329_-2+6330dup others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17400064 | ||||||
| chr6:17400104 | T | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0017 others(20): Show |
23 | HG01192.hp1 HG02027.hp2 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+6358T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17400104 | |||||||
| chr6:17400141 | G | A | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-2+6395G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17400141 | |||||||
| chr6:17400349 | G | A | 14 | a0001c0001t0001g0202 a0001c0001t0002g0003 a0001c0001t0002g0011 others(11): Show |
14 | HG01109.hp2 HG01361.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2+6603G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17400349 | |||||||
| chr6:17400408 | T | C | 1 | a0001c0001t0002g0137 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-2+6662T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17400408 | |||||||
| chr6:17400411 | A | G | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-2+6665A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17400411 | |||||||
| chr6:17400758 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-2+7012G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17400758 | |||||||
| chr6:17400864 | CA | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(92): Show |
95 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(92): Show |
intron_variant | MODIFIER | c.-2+7134delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17400864 | ||||||
| chr6:17401193 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-2+7447G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17401193 | |||||||
| chr6:17401519 | T | C | 1 | a0001c0001t0001g0017 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-2+7773T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17401519 | |||||||
| chr6:17401568 | T | G | 4 | a0001c0001t0001g0202 a0001c0001t0002g0199 a0001c0001t0005g0200 others(1): Show |
4 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+7822T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17401568 | |||||||
| chr6:17401600 | G | A | 14 | a0001c0001t0001g0202 a0001c0001t0002g0003 a0001c0001t0002g0011 others(11): Show |
14 | HG01109.hp2 HG01361.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2+7854G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17401600 | |||||||
| chr6:17402113 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-2+8367G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17402113 | |||||||
| chr6:17402250 | C | T | 1 | a0001c0008t0001g0204 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-2+8504C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17402250 | |||||||
| chr6:17402358 | CA | C | 3 | a0001c0001t0001g0127 a0001c0002t0001g0128 a0001c0002t0002g0129 |
3 | HG01071.hp1 HG01167.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-2+8618delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17402358 | ||||||
| chr6:17402389 | T | G | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-2+8643T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17402389 | |||||||
| chr6:17402490 | G | C | 1 | a0001c0006t0001g0018 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-2+8744G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17402490 | |||||||
| chr6:17402668 | G | C | 1 | a0001c0001t0002g0148 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-2+8922G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17402668 | |||||||
| chr6:17402786 | C | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
98 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(95): Show |
intron_variant | MODIFIER | c.-2+9040C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17402786 | |||||||
| chr6:17403061 | T | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(39): Show |
42 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.-2+9315T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403061 | |||||||
| chr6:17403370 | G | T | 40 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(37): Show |
40 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.-2+9624G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403370 | |||||||
| chr6:17403471 | A | G | 31 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(28): Show |
31 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-2+9725A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403471 | |||||||
| chr6:17403473 | A | G | 4 | a0001c0003t0002g0060 a0001c0003t0002g0064 a0001c0003t0002g0071 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+9727A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403473 | |||||||
| chr6:17403602 | T | A | 40 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(37): Show |
40 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.-2+9856T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403602 | |||||||
| chr6:17403716 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(189): Show |
192 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.-2+9970A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403716 | |||||||
| chr6:17403735 | A | T | 3 | a0001c0003t0002g0060 a0001c0003t0002g0064 a0001c0003t0002g0071 |
3 | HG02109.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-2+9989A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403735 | |||||||
| chr6:17403934 | G | T | 40 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(37): Show |
40 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.-2+10188G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17403934 | |||||||
| chr6:17404333 | C | T | 4 | a0001c0001t0001g0069 a0001c0002t0001g0062 a0004c0010t0001g0063 others(1): Show |
4 | HG01255.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+10587C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404333 | |||||||
| chr6:17404370 | C | T | 8 | a0001c0001t0001g0069 a0001c0002t0001g0062 a0001c0003t0002g0060 others(5): Show |
8 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+10624C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404370 | |||||||
| chr6:17404408 | A | G | 4 | a0001c0001t0002g0096 a0001c0002t0001g0098 a0001c0002t0001g0146 others(1): Show |
4 | HG00597.hp2 HG00609.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+10662A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404408 | |||||||
| chr6:17404422 | G | A | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-2+10676G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404422 | |||||||
| chr6:17404538 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-2+10792G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404538 | |||||||
| chr6:17404559 | G | A | 32 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(29): Show |
32 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.-2+10813G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404559 | |||||||
| chr6:17404604 | CA | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(55): Show |
58 | HG00099.hp1 HG00609.hp2 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.-2+10874delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17404604 | ||||||
| chr6:17404727 | C | T | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-2+10981C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404727 | |||||||
| chr6:17404770 | C | CA | 15 | a0001c0001t0001g0019 a0001c0001t0001g0202 a0001c0001t0002g0003 others(12): Show |
15 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2+11043dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17404770 | ||||||
| chr6:17404814 | C | T | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-2+11068C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404814 | |||||||
| chr6:17404917 | A | C | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-2+11171A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404917 | |||||||
| chr6:17404918 | C | A | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-2+11172C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404918 | |||||||
| chr6:17404919 | C | A | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-2+11173C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404919 | |||||||
| chr6:17404947 | T | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(53): Show |
56 | HG00099.hp1 HG00438.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.-2+11201T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17404947 | |||||||
| chr6:17405018 | C | G | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-2+11272C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405018 | |||||||
| chr6:17405051 | T | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(86): Show |
89 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.-2+11305T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405051 | |||||||
| chr6:17405079 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-2+11333C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405079 | |||||||
| chr6:17405120 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(40): Show |
43 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.-2+11374C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405120 | |||||||
| chr6:17405267 | A | G | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-2+11521A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405267 | |||||||
| chr6:17405275 | G | A | 1 | a0001c0001t0002g0150 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-2+11529G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405275 | |||||||
| chr6:17405277 | G | T | 1 | a0001c0001t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-2+11531G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405277 | |||||||
| chr6:17405285 | G | A | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-2+11539G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405285 | |||||||
| chr6:17405298 | T | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(98): Show |
101 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(98): Show |
intron_variant | MODIFIER | c.-2+11552T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405298 | |||||||
| chr6:17405299 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(53): Show |
56 | HG00099.hp1 HG00438.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.-2+11553G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405299 | |||||||
| chr6:17405318 | G | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(40): Show |
43 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.-2+11572G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405318 | |||||||
| chr6:17405360 | C | T | 1 | a0001c0002t0001g0007 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-2+11614C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405360 | |||||||
| chr6:17405368 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-2+11622T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405368 | |||||||
| chr6:17405498 | G | GTC | 8 | a0001c0001t0001g0069 a0001c0001t0001g0095 a0001c0001t0001g0202 others(5): Show |
8 | HG00438.hp1 HG01109.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+11783_-2+11784d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17405498 | ||||||
| chr6:17405498 | G | GTCTCTC | 6 | a0001c0002t0001g0062 a0001c0003t0002g0060 a0001c0003t0002g0064 others(3): Show |
6 | HG01255.hp1 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+11779_-2+11784d others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17405498 | ||||||
| chr6:17405498 | GTCTC | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0151 a0001c0001t0001g0195 others(2): Show |
5 | HG01516.hp1 HG01952.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+11781_-2+11784d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17405498 | ||||||
| chr6:17405498 | GTCTCTCT others(1): Show |
G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(52): Show |
55 | HG00099.hp1 HG00438.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2+11777_-2+11784d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17405498 | ||||||
| chr6:17405498 | GTCTCTCT others(5): Show |
G | 30 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(27): Show |
30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-2+11773_-2+11784d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17405498 | ||||||
| chr6:17405683 | G | C | 4 | a0001c0001t0001g0179 a0001c0006t0001g0149 a0001c0008t0001g0051 others(1): Show |
4 | HG00438.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+11937G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405683 | |||||||
| chr6:17405763 | C | T | 30 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(27): Show |
30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-2+12017C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405763 | |||||||
| chr6:17405777 | G | A | 4 | a0001c0003t0002g0060 a0001c0003t0002g0064 a0001c0003t0002g0071 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+12031G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405777 | |||||||
| chr6:17405784 | A | C | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2+12038A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405784 | |||||||
| chr6:17405807 | C | G | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-2+12061C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405807 | |||||||
| chr6:17405815 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
86 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.-2+12069G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405815 | |||||||
| chr6:17405825 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-2+12079C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405825 | |||||||
| chr6:17405857 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(53): Show |
56 | HG00099.hp1 HG00438.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.-2+12111C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405857 | |||||||
| chr6:17405878 | C | T | 30 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(27): Show |
30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-2+12132C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405878 | |||||||
| chr6:17405894 | C | T | 4 | a0001c0002t0001g0074 a0001c0003t0001g0072 a0001c0003t0001g0075 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+12148C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17405894 | |||||||
| chr6:17406128 | C | T | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-2+12382C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406128 | |||||||
| chr6:17406145 | C | G | 4 | a0001c0001t0001g0179 a0001c0006t0001g0149 a0001c0008t0001g0051 others(1): Show |
4 | HG00438.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+12399C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406145 | |||||||
| chr6:17406372 | A | G | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2+12626A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406372 | |||||||
| chr6:17406398 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0002g0050 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-2+12657_-2+12667d others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | ||||||
| chr6:17406398 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0002g0011 a0001c0002t0001g0012 |
2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-2+12656_-2+12667d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | ||||||
| chr6:17406398 | C | CTTTTTTT others(8): Show |
1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2+12653_-2+12667d others(17): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | ||||||
| chr6:17406398 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0005 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-2+12667_-2+12668i others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | ||||||
| chr6:17406398 | C | CTTTTTTT others(10): Show |
15 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0021 others(12): Show |
15 | HG00099.hp1 HG01106.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(19): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | ||||||
| chr6:17406398 | C | CTTTTTTT others(11): Show |
19 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0019 others(16): Show |
19 | HG01192.hp1 HG01361.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(20): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | ||||||
| chr6:17406398 | C | CTTTTTTT others(12): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0041 others(3): Show |
6 | HG01175.hp2 HG02071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(21): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | ||||||
| chr6:17406398 | C | CTTTTTTT others(13): Show |
2 | a0001c0001t0001g0042 a0001c0006t0001g0034 |
2 | HG03209.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | ||||||
| chr6:17406398 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0001g0179 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-2+12667_-2+12668i others(24): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | ||||||
| chr6:17406398 | C | CTTTTTTT others(16): Show |
5 | a0001c0006t0001g0149 a0001c0008t0001g0204 a0001c0009t0001g0013 others(2): Show |
5 | HG00438.hp2 HG01361.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(25): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | ||||||
| chr6:17406398 | C | CTTTTTTT others(17): Show |
1 | a0001c0009t0001g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-2+12667_-2+12668i others(26): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | ||||||
| chr6:17406398 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2+12667_-2+12668i others(27): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406398 | ||||||
| chr6:17406412 | T | TTTTTTTT others(14): Show |
2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG01167.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(23): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406412 | ||||||
| chr6:17406412 | T | TTTTTTTT others(15): Show |
7 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0002t0001g0002 others(4): Show |
7 | HG02258.hp1 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(24): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406412 | ||||||
| chr6:17406412 | T | TTTTTTTT others(16): Show |
10 | a0001c0002t0001g0197 a0001c0002t0006g0133 a0001c0003t0001g0065 others(7): Show |
10 | HG00735.hp2 HG01496.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(25): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406412 | ||||||
| chr6:17406412 | T | TTTTTTTT others(17): Show |
8 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0091 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(26): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406412 | ||||||
| chr6:17406412 | T | TTTTTTTT others(18): Show |
3 | a0001c0001t0001g0068 a0001c0001t0001g0092 a0005c0015t0001g0070 |
3 | HG02622.hp1 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-2+12667_-2+12668i others(27): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17406412 | ||||||
| chr6:17406454 | T | G | 1 | a0001c0002t0001g0106 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-2+12708T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406454 | |||||||
| chr6:17406479 | C | T | 11 | a0001c0001t0001g0069 a0001c0001t0001g0202 a0001c0001t0002g0199 others(8): Show |
11 | HG01109.hp2 HG01255.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2+12733C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406479 | |||||||
| chr6:17406583 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(98): Show |
101 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(98): Show |
intron_variant | MODIFIER | c.-2+12837A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406583 | |||||||
| chr6:17406677 | C | T | 13 | a0001c0001t0001g0179 a0001c0001t0002g0003 a0001c0001t0002g0011 others(10): Show |
13 | HG00438.hp2 HG01361.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-2+12931C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406677 | |||||||
| chr6:17406771 | C | T | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-2+13025C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406771 | |||||||
| chr6:17406795 | A | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(40): Show |
43 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.-2+13049A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406795 | |||||||
| chr6:17406843 | C | G | 4 | a0001c0003t0002g0060 a0001c0003t0002g0064 a0001c0003t0002g0071 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+13097C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406843 | |||||||
| chr6:17406925 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-2+13179G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406925 | |||||||
| chr6:17406942 | A | C | 4 | a0001c0003t0002g0060 a0001c0003t0002g0064 a0001c0003t0002g0071 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+13196A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17406942 | |||||||
| chr6:17407394 | G | A | 4 | a0001c0001t0001g0179 a0001c0002t0001g0198 a0001c0006t0001g0149 others(1): Show |
4 | HG00438.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+13648G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17407394 | |||||||
| chr6:17407479 | G | GA | 10 | a0001c0001t0001g0179 a0001c0001t0002g0011 a0001c0001t0002g0027 others(7): Show |
10 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+13747dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17407479 | ||||||
| chr6:17407514 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-2+13768C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17407514 | |||||||
| chr6:17407563 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2+13817G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17407563 | |||||||
| chr6:17407778 | CA | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.-1-13753delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17407778 | ||||||
| chr6:17407778 | CAA | C | 10 | a0001c0001t0001g0026 a0001c0001t0001g0068 a0001c0001t0002g0176 others(7): Show |
10 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-13754_-1-13753d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17407778 | ||||||
| chr6:17407778 | CAAA | C | 29 | a0001c0001t0001g0067 a0001c0001t0001g0080 a0001c0001t0001g0081 others(26): Show |
29 | HG00438.hp2 HG00735.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1-13755_-1-13753d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17407778 | ||||||
| chr6:17408032 | T | C | 1 | a0002c0004t0002g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-1-13523T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408032 | |||||||
| chr6:17408160 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(86): Show |
89 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.-1-13395G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408160 | |||||||
| chr6:17408272 | C | T | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-1-13283C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408272 | |||||||
| chr6:17408273 | G | A | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-13282G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408273 | |||||||
| chr6:17408275 | C | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(41): Show |
44 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.-1-13280C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408275 | |||||||
| chr6:17408385 | C | T | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-13170C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408385 | |||||||
| chr6:17408470 | T | C | 33 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(30): Show |
33 | HG00438.hp2 HG00735.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1-13085T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408470 | |||||||
| chr6:17408551 | C | T | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-13004C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408551 | |||||||
| chr6:17408567 | G | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(40): Show |
43 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.-1-12988G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408567 | |||||||
| chr6:17408602 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(86): Show |
89 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.-1-12953G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408602 | |||||||
| chr6:17408660 | C | CT | 25 | a0001c0001t0001g0068 a0001c0001t0001g0082 a0001c0001t0001g0089 others(22): Show |
25 | HG00735.hp2 HG01243.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.-1-12876dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17408660 | ||||||
| chr6:17408660 | C | CTT | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(57): Show |
60 | HG00099.hp1 HG01106.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-1-12877_-1-12876d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17408660 | ||||||
| chr6:17408660 | CT | C | 10 | a0001c0001t0001g0052 a0001c0001t0001g0159 a0001c0001t0002g0157 others(7): Show |
10 | HG01891.hp2 HG01943.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-12876delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17408660 | ||||||
| chr6:17408685 | G | A | 30 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(27): Show |
30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-12870G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408685 | |||||||
| chr6:17408818 | C | A | 6 | a0001c0001t0001g0202 a0001c0001t0002g0199 a0001c0001t0005g0200 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-12737C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408818 | |||||||
| chr6:17408818 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-1-12737C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408818 | |||||||
| chr6:17408836 | A | AT | 8 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0050 others(5): Show |
8 | HG01361.hp2 HG01884.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-12713dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17408836 | ||||||
| chr6:17408841 | T | G | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-12714T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408841 | |||||||
| chr6:17408859 | C | T | 3 | a0001c0001t0001g0179 a0001c0006t0001g0149 a0001c0008t0001g0204 |
3 | HG00438.hp2 HG02055.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.-1-12696C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408859 | |||||||
| chr6:17408862 | G | T | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-12693G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408862 | |||||||
| chr6:17408904 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(50): Show |
53 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.-1-12651T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408904 | |||||||
| chr6:17408968 | C | A | 1 | a0001c0001t0002g0199 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-1-12587C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17408968 | |||||||
| chr6:17409025 | T | C | 30 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(27): Show |
30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-12530T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409025 | |||||||
| chr6:17409035 | G | A | 1 | a0001c0001t0002g0027 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-1-12520G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409035 | |||||||
| chr6:17409109 | C | T | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-12446C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409109 | |||||||
| chr6:17409241 | A | G | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-12314A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409241 | |||||||
| chr6:17409264 | C | T | 1 | a0002c0004t0002g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-1-12291C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409264 | |||||||
| chr6:17409265 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(49): Show |
52 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.-1-12290G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409265 | |||||||
| chr6:17409294 | C | T | 2 | a0001c0002t0001g0144 a0001c0002t0001g0145 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-12261C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409294 | |||||||
| chr6:17409334 | T | C | 1 | a0001c0002t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-1-12221T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409334 | |||||||
| chr6:17409562 | G | A | 33 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(30): Show |
33 | HG00438.hp2 HG00735.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1-11993G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409562 | |||||||
| chr6:17409747 | G | A | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-11808G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409747 | |||||||
| chr6:17409960 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-1-11595G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409960 | |||||||
| chr6:17409998 | G | A | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-11557G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17409998 | |||||||
| chr6:17410046 | C | G | 1 | a0001c0008t0001g0204 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-1-11509C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410046 | |||||||
| chr6:17410113 | C | G | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-11442C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410113 | |||||||
| chr6:17410142 | T | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-1-11413T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410142 | |||||||
| chr6:17410440 | T | A | 1 | a0001c0002t0001g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-1-11115T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410440 | |||||||
| chr6:17410537 | C | T | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-11018C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410537 | |||||||
| chr6:17410572 | AT | A | 5 | a0001c0001t0001g0005 a0001c0001t0002g0206 a0001c0002t0001g0006 others(2): Show |
5 | HG01943.hp2 HG02486.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-10968delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17410572 | ||||||
| chr6:17410597 | T | TCTCGCTC others(6): Show |
1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-10957_-1-10956i others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17410597 | ||||||
| chr6:17410626 | C | T | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-10929C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410626 | |||||||
| chr6:17410658 | C | T | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-10897C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410658 | |||||||
| chr6:17410701 | G | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-1-10854G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410701 | |||||||
| chr6:17410703 | G | A | 1 | a0001c0002t0001g0161 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-1-10852G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410703 | |||||||
| chr6:17410801 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(103): Show |
106 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(103): Show |
intron_variant | MODIFIER | c.-1-10754T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410801 | |||||||
| chr6:17410802 | G | A | 2 | a0001c0008t0001g0051 a0001c0013t0001g0076 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-1-10753G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17410802 | |||||||
| chr6:17411046 | TAC | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(51): Show |
54 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(51): Show |
intron_variant | MODIFIER | c.-1-10505_-1-10504d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17411046 | ||||||
| chr6:17411133 | C | G | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-1-10422C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411133 | |||||||
| chr6:17411354 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(92): Show |
95 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(92): Show |
intron_variant | MODIFIER | c.-1-10201C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411354 | |||||||
| chr6:17411483 | A | C | 30 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(27): Show |
30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-10072A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411483 | |||||||
| chr6:17411555 | C | T | 6 | a0001c0001t0001g0069 a0001c0002t0001g0062 a0001c0002t0001g0144 others(3): Show |
6 | HG01255.hp1 HG02109.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-10000C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411555 | |||||||
| chr6:17411728 | C | T | 2 | a0001c0001t0002g0126 a0001c0001t0002g0175 |
2 | NA18747.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-1-9827C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411728 | |||||||
| chr6:17411798 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-1-9757C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411798 | |||||||
| chr6:17411799 | G | C | 1 | a0001c0002t0001g0020 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-1-9756G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411799 | |||||||
| chr6:17411841 | T | A | 30 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(27): Show |
30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-9714T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411841 | |||||||
| chr6:17411897 | A | G | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-9658A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17411897 | |||||||
| chr6:17412028 | T | C | 30 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(27): Show |
30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-9527T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412028 | |||||||
| chr6:17412076 | T | C | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-9479T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412076 | |||||||
| chr6:17412134 | A | G | 30 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(27): Show |
30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-9421A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412134 | |||||||
| chr6:17412328 | T | C | 30 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(27): Show |
30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-9227T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412328 | |||||||
| chr6:17412498 | A | G | 30 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(27): Show |
30 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-9057A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412498 | |||||||
| chr6:17412545 | T | C | 5 | a0001c0001t0001g0202 a0001c0001t0002g0199 a0001c0001t0005g0200 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-9010T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412545 | |||||||
| chr6:17412954 | A | G | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-8601A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17412954 | |||||||
| chr6:17413055 | G | T | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-1-8500G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413055 | |||||||
| chr6:17413062 | A | G | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-8493A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413062 | |||||||
| chr6:17413114 | C | A | 1 | a0001c0002t0001g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-1-8441C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413114 | |||||||
| chr6:17413149 | A | C | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-8406A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413149 | |||||||
| chr6:17413332 | T | C | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-8223T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413332 | |||||||
| chr6:17413371 | C | T | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-8184C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413371 | |||||||
| chr6:17413416 | C | T | 2 | a0001c0001t0001g0091 a0001c0002t0006g0133 |
2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-1-8139C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413416 | |||||||
| chr6:17413757 | G | A | 3 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0002g0131 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-1-7798G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413757 | |||||||
| chr6:17413875 | G | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0107 |
2 | HG00099.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-1-7680G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413875 | |||||||
| chr6:17413922 | A | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(103): Show |
106 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(103): Show |
intron_variant | MODIFIER | c.-1-7633A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413922 | |||||||
| chr6:17413926 | C | T | 2 | a0001c0002t0001g0188 a0001c0002t0001g0189 |
2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-1-7629C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413926 | |||||||
| chr6:17413927 | G | A | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-1-7628G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17413927 | |||||||
| chr6:17414053 | CA | C | 39 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(36): Show |
39 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.-1-7487delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17414053 | ||||||
| chr6:17414261 | C | CT | 28 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(25): Show |
28 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1-7284dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17414261 | ||||||
| chr6:17414284 | T | C | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-7271T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414284 | |||||||
| chr6:17414285 | TA | T | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-7262delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17414285 | ||||||
| chr6:17414299 | T | A | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-7256T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414299 | |||||||
| chr6:17414342 | A | G | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-7213A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414342 | |||||||
| chr6:17414344 | G | T | 1 | a0002c0004t0002g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-1-7211G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414344 | |||||||
| chr6:17414461 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(103): Show |
106 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(103): Show |
intron_variant | MODIFIER | c.-1-7094A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414461 | |||||||
| chr6:17414468 | A | G | 7 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0002t0001g0012 others(4): Show |
7 | HG01361.hp2 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-7087A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414468 | |||||||
| chr6:17414485 | A | G | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-7070A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414485 | |||||||
| chr6:17414597 | C | T | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-6958C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414597 | |||||||
| chr6:17414993 | C | T | 2 | a0001c0009t0001g0013 a0002c0012t0001g0014 |
2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-1-6562C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17414993 | |||||||
| chr6:17415054 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-1-6501T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415054 | |||||||
| chr6:17415209 | A | G | 2 | a0001c0002t0001g0132 a0001c0003t0002g0131 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-1-6346A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415209 | |||||||
| chr6:17415286 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(83): Show |
86 | HG00099.hp1 HG00735.hp2 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.-1-6269T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415286 | |||||||
| chr6:17415677 | G | A | 12 | a0001c0001t0001g0069 a0001c0001t0001g0202 a0001c0001t0002g0199 others(9): Show |
12 | HG01109.hp2 HG01255.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-5878G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415677 | |||||||
| chr6:17415758 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-1-5797G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415758 | |||||||
| chr6:17415822 | A | G | 2 | a0001c0001t0002g0126 a0001c0001t0002g0175 |
2 | NA18747.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-1-5733A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415822 | |||||||
| chr6:17415825 | G | T | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-5730G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415825 | |||||||
| chr6:17415832 | C | T | 1 | a0001c0002t0001g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-1-5723C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415832 | |||||||
| chr6:17415833 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(52): Show |
55 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.-1-5722G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415833 | |||||||
| chr6:17415931 | A | C | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-5624A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17415931 | |||||||
| chr6:17416027 | T | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(52): Show |
55 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.-1-5528T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416027 | |||||||
| chr6:17416070 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-1-5485A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416070 | |||||||
| chr6:17416153 | T | TGAGAAAA others(316): Show |
1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(323): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | ||||||
| chr6:17416153 | T | TGAGAAAA others(317): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0002g0038 |
3 | HG02258.hp2 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(324): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | ||||||
| chr6:17416153 | T | TGAGAAAA others(318): Show |
14 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0040 others(11): Show |
14 | HG01106.hp1 HG01361.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(325): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | ||||||
| chr6:17416153 | T | TGAGAAAA others(319): Show |
20 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(17): Show |
20 | HG00099.hp1 HG01175.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(326): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | ||||||
| chr6:17416153 | T | TGAGAAAA others(320): Show |
14 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0029 others(11): Show |
14 | HG01496.hp1 HG02027.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(327): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | ||||||
| chr6:17416153 | T | TGAGAAAA others(321): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0030 |
2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(328): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | ||||||
| chr6:17416153 | T | TGAGAAAA others(323): Show |
1 | a0001c0001t0002g0031 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-1-5388_-1-5387ins others(330): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17416153 | ||||||
| chr6:17416212 | G | T | 1 | a0003c0007t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-1-5343G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416212 | |||||||
| chr6:17416359 | G | T | 3 | a0001c0009t0001g0015 a0001c0013t0001g0076 a0001c0014t0008g0016 |
3 | HG01361.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-5196G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416359 | |||||||
| chr6:17416528 | G | A | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-1-5027G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416528 | |||||||
| chr6:17416554 | G | A | 2 | a0001c0002t0001g0036 a0001c0003t0001g0039 |
2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-1-5001G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416554 | |||||||
| chr6:17416560 | G | A | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-4995G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416560 | |||||||
| chr6:17416895 | C | A | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-1-4660C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416895 | |||||||
| chr6:17416976 | A | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(114): Show |
117 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(114): Show |
intron_variant | MODIFIER | c.-1-4579A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416976 | |||||||
| chr6:17416996 | A | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(56): Show |
59 | HG00099.hp1 HG01071.hp1 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.-1-4559A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17416996 | |||||||
| chr6:17417145 | GA | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(65): Show |
68 | HG00099.hp1 HG01071.hp1 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.-1-4399delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17417145 | ||||||
| chr6:17417247 | A | C | 20 | a0001c0001t0001g0052 a0001c0001t0001g0068 a0001c0001t0001g0202 others(17): Show |
20 | HG00741.hp2 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1-4308A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17417247 | |||||||
| chr6:17417274 | A | AT | 39 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0035 others(36): Show |
39 | HG00735.hp1 HG00741.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.-1-4264dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17417274 | ||||||
| chr6:17417274 | AT | A | 7 | a0001c0001t0001g0052 a0001c0002t0001g0130 a0001c0002t0001g0132 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-4264delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17417274 | ||||||
| chr6:17417326 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-1-4229A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17417326 | |||||||
| chr6:17417413 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(116): Show |
119 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(116): Show |
intron_variant | MODIFIER | c.-1-4142T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17417413 | |||||||
| chr6:17417420 | C | T | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-4135C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17417420 | |||||||
| chr6:17417521 | C | T | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-4034C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17417521 | |||||||
| chr6:17417963 | G | A | 1 | a0001c0008t0001g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1-3592G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17417963 | |||||||
| chr6:17418085 | G | C | 1 | a0001c0002t0001g0190 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-1-3470G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418085 | |||||||
| chr6:17418158 | G | C | 2 | a0001c0002t0001g0144 a0001c0002t0001g0145 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-3397G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418158 | |||||||
| chr6:17418176 | C | T | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-3379C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418176 | |||||||
| chr6:17418177 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(60): Show |
63 | HG00099.hp1 HG01071.hp1 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.-1-3378G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418177 | |||||||
| chr6:17418669 | A | AT | 30 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(27): Show |
30 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.-1-2876dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17418669 | ||||||
| chr6:17418682 | A | G | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-2873A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418682 | |||||||
| chr6:17418756 | G | A | 1 | a0001c0002t0001g0058 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-1-2799G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418756 | |||||||
| chr6:17418803 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-2752C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17418803 | |||||||
| chr6:17419381 | G | A | 5 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0002t0001g0012 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-2174G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419381 | |||||||
| chr6:17419426 | G | A | 1 | a0001c0001t0002g0162 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-1-2129G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419426 | |||||||
| chr6:17419468 | T | C | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-1-2087T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419468 | |||||||
| chr6:17419480 | G | A | 5 | a0001c0002t0001g0197 a0001c0003t0001g0065 a0003c0007t0001g0059 others(2): Show |
5 | HG01496.hp2 HG02280.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-2075G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419480 | |||||||
| chr6:17419548 | A | T | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-2007A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419548 | |||||||
| chr6:17419899 | G | C | 2 | a0001c0002t0001g0093 a0001c0002t0001g0094 |
2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-1-1656G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419899 | |||||||
| chr6:17419964 | T | C | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-1591T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17419964 | |||||||
| chr6:17420025 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(114): Show |
117 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(114): Show |
intron_variant | MODIFIER | c.-1-1530T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420025 | |||||||
| chr6:17420060 | C | T | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-1495C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420060 | |||||||
| chr6:17420166 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.-1-1389A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420166 | |||||||
| chr6:17420311 | C | T | 1 | a0001c0008t0001g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1-1244C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420311 | |||||||
| chr6:17420570 | C | T | 2 | a0001c0002t0001g0144 a0001c0002t0001g0145 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-985C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420570 | |||||||
| chr6:17420882 | G | T | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-1-673G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420882 | |||||||
| chr6:17420973 | C | T | 2 | a0001c0001t0002g0126 a0001c0001t0002g0175 |
2 | NA18747.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-1-582C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17420973 | |||||||
| chr6:17420983 | G | GT | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1-570dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 17420983 | ||||||
| chr6:17421072 | A | G | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1-483A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17421072 | |||||||
| chr6:17421218 | C | T | 1 | a0001c0001t0001g0017 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-1-337C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17421218 | |||||||
| chr6:17421251 | G | A | 15 | a0001c0001t0001g0052 a0001c0001t0002g0055 a0001c0002t0001g0056 others(12): Show |
15 | HG00741.hp2 HG01168.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1-304G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 1/12 | chr6 | 17421251 | |||||||
| chr6:17421793 | C | T | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.121+117C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17421793 | |||||||
| chr6:17421838 | A | G | 5 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0002t0001g0012 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+162A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17421838 | |||||||
| chr6:17421855 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0084 |
2 | HG01167.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.121+179C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17421855 | |||||||
| chr6:17421981 | C | G | 5 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0002t0001g0012 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+305C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17421981 | |||||||
| chr6:17422008 | G | A | 1 | a0001c0008t0001g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.121+332G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17422008 | |||||||
| chr6:17422305 | C | T | 15 | a0001c0001t0001g0052 a0001c0001t0002g0055 a0001c0002t0001g0056 others(12): Show |
15 | HG00741.hp2 HG01168.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.121+629C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17422305 | |||||||
| chr6:17422346 | CT | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(98): Show |
101 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(98): Show |
intron_variant | MODIFIER | c.121+691delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 17422346 | ||||||
| chr6:17422498 | C | T | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.121+822C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17422498 | |||||||
| chr6:17422628 | C | T | 1 | a0001c0002t0001g0173 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.121+952C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17422628 | |||||||
| chr6:17422912 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.121+1236T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17422912 | |||||||
| chr6:17422974 | A | G | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.121+1298A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17422974 | |||||||
| chr6:17423044 | T | C | 2 | a0001c0002t0001g0144 a0001c0002t0001g0145 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.121+1368T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17423044 | |||||||
| chr6:17423704 | T | C | 1 | a0001c0002t0001g0193 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.121+2028T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17423704 | |||||||
| chr6:17423845 | A | G | 4 | a0001c0001t0001g0069 a0001c0002t0001g0144 a0001c0002t0001g0145 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+2169A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17423845 | |||||||
| chr6:17424018 | C | A | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.121+2342C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424018 | |||||||
| chr6:17424126 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(119): Show |
122 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(119): Show |
intron_variant | MODIFIER | c.121+2450A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424126 | |||||||
| chr6:17424177 | G | A | 1 | a0001c0009t0001g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.122-2413G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424177 | |||||||
| chr6:17424225 | T | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122-2365T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424225 | |||||||
| chr6:17424228 | G | A | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122-2362G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424228 | |||||||
| chr6:17424243 | G | A | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122-2347G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424243 | |||||||
| chr6:17424244 | A | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122-2346A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424244 | |||||||
| chr6:17424256 | T | C | 2 | a0001c0008t0001g0051 a0001c0013t0001g0076 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.122-2334T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424256 | |||||||
| chr6:17424262 | T | C | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122-2328T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424262 | |||||||
| chr6:17424263 | G | A | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122-2327G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424263 | |||||||
| chr6:17424269 | G | A | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.122-2321G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424269 | |||||||
| chr6:17424306 | A | G | 26 | a0001c0001t0001g0154 a0001c0001t0001g0159 a0001c0001t0001g0179 others(23): Show |
26 | HG00438.hp2 HG00609.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.122-2284A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424306 | |||||||
| chr6:17424365 | A | T | 13 | a0001c0001t0001g0052 a0001c0001t0002g0055 a0001c0002t0001g0056 others(10): Show |
13 | HG00741.hp2 HG01168.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-2225A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424365 | |||||||
| chr6:17424381 | C | A | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122-2209C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424381 | |||||||
| chr6:17424426 | G | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(50): Show |
53 | HG00099.hp1 HG01071.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.122-2164G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424426 | |||||||
| chr6:17424587 | C | T | 1 | a0001c0008t0001g0204 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.122-2003C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17424587 | |||||||
| chr6:17425067 | A | T | 1 | a0001c0008t0001g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.122-1523A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425067 | |||||||
| chr6:17425323 | G | A | 1 | a0001c0003t0002g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.122-1267G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425323 | |||||||
| chr6:17425387 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.122-1203T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425387 | |||||||
| chr6:17425395 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.122-1195C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425395 | |||||||
| chr6:17425587 | C | A | 44 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(41): Show |
44 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.122-1003C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425587 | |||||||
| chr6:17425745 | G | A | 8 | a0001c0001t0001g0069 a0001c0002t0001g0144 a0001c0002t0001g0145 others(5): Show |
8 | HG01496.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.122-845G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425745 | |||||||
| chr6:17425811 | A | G | 1 | a0001c0002t0001g0094 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.122-779A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425811 | |||||||
| chr6:17425815 | C | A | 2 | a0001c0009t0001g0013 a0002c0012t0001g0014 |
2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.122-775C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425815 | |||||||
| chr6:17425870 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.122-720C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425870 | |||||||
| chr6:17425936 | A | T | 1 | a0001c0001t0002g0024 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.122-654A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17425936 | |||||||
| chr6:17426051 | C | T | 1 | a0001c0002t0001g0058 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.122-539C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426051 | |||||||
| chr6:17426099 | C | A | 2 | a0001c0002t0001g0058 a0001c0013t0001g0076 |
2 | HG00642.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.122-491C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426099 | |||||||
| chr6:17426103 | C | A | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122-487C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426103 | |||||||
| chr6:17426115 | C | A | 2 | a0001c0001t0002g0011 a0001c0002t0001g0012 |
2 | HG02738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.122-475C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426115 | |||||||
| chr6:17426231 | CT | C | 16 | a0001c0001t0001g0052 a0001c0001t0001g0142 a0001c0001t0002g0055 others(13): Show |
16 | HG00642.hp1 HG00741.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.122-343delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 17426231 | ||||||
| chr6:17426232 | T | G | 1 | a0001c0001t0001g0026 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.122-358T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426232 | |||||||
| chr6:17426370 | G | T | 29 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(26): Show |
29 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.122-220G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426370 | |||||||
| chr6:17426491 | T | C | 13 | a0001c0001t0001g0052 a0001c0001t0002g0055 a0001c0002t0001g0056 others(10): Show |
13 | HG00741.hp2 HG01168.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-99T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426491 | |||||||
| chr6:17426555 | C | T | 2 | a0001c0001t0001g0095 a0001c0002t0001g0002 |
2 | HG00438.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.122-35C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 2/12 | chr6 | 17426555 | |||||||
| chr6:17426902 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(55): Show |
58 | HG00099.hp1 HG01071.hp1 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.222+212G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17426902 | |||||||
| chr6:17426935 | A | T | 34 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(31): Show |
34 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.222+245A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17426935 | |||||||
| chr6:17426984 | T | A | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+294T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17426984 | |||||||
| chr6:17427043 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.222+353C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427043 | |||||||
| chr6:17427308 | C | T | 34 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(31): Show |
34 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.222+618C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427308 | |||||||
| chr6:17427350 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.222+660C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427350 | |||||||
| chr6:17427548 | G | A | 29 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0068 others(26): Show |
29 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.222+858G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427548 | |||||||
| chr6:17427608 | C | CA | 22 | a0001c0001t0001g0052 a0001c0001t0001g0069 a0001c0001t0002g0055 others(19): Show |
22 | HG00741.hp2 HG01168.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.222+933dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17427608 | ||||||
| chr6:17427608 | CA | C | 35 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(32): Show |
35 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.222+933delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17427608 | ||||||
| chr6:17427625 | G | A | 61 | a0001c0001t0001g0052 a0001c0001t0001g0067 a0001c0001t0001g0068 others(58): Show |
61 | HG00735.hp2 HG00741.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.222+935G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427625 | |||||||
| chr6:17427634 | G | A | 56 | a0001c0001t0001g0052 a0001c0001t0001g0067 a0001c0001t0001g0068 others(53): Show |
56 | HG00735.hp2 HG00741.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.222+944G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427634 | |||||||
| chr6:17427970 | T | C | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.222+1280T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17427970 | |||||||
| chr6:17428012 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.222+1322C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428012 | |||||||
| chr6:17428023 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+1333G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428023 | |||||||
| chr6:17428393 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.222+1703C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428393 | |||||||
| chr6:17428476 | A | G | 8 | a0001c0001t0001g0069 a0001c0002t0001g0144 a0001c0002t0001g0145 others(5): Show |
8 | HG01496.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+1786A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428476 | |||||||
| chr6:17428540 | C | T | 1 | a0001c0003t0001g0090 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.222+1850C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428540 | |||||||
| chr6:17428628 | A | G | 2 | a0001c0002t0001g0144 a0001c0002t0001g0145 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.222+1938A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428628 | |||||||
| chr6:17428630 | G | C | 2 | a0001c0002t0001g0144 a0001c0002t0001g0145 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.222+1940G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428630 | |||||||
| chr6:17428774 | T | TA | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(55): Show |
58 | HG00099.hp1 HG01071.hp1 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.222+2095dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17428774 | ||||||
| chr6:17428896 | G | A | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.222+2206G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17428896 | |||||||
| chr6:17429135 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.222+2445T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429135 | |||||||
| chr6:17429325 | T | C | 5 | a0001c0008t0001g0051 a0001c0009t0001g0013 a0001c0009t0001g0015 others(2): Show |
5 | HG01361.hp2 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+2635T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429325 | |||||||
| chr6:17429379 | G | T | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+2689G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429379 | |||||||
| chr6:17429380 | G | A | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+2690G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429380 | |||||||
| chr6:17429381 | A | ACATCATA others(12): Show |
1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+2691_222+2692i others(21): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429381 | |||||||
| chr6:17429382 | G | A | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+2692G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429382 | |||||||
| chr6:17429385 | T | A | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+2695T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429385 | |||||||
| chr6:17429497 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.222+2807G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429497 | |||||||
| chr6:17429505 | A | G | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.222+2815A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429505 | |||||||
| chr6:17429632 | C | T | 3 | a0001c0008t0001g0051 a0001c0009t0001g0015 a0001c0014t0008g0016 |
3 | HG01361.hp2 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.222+2942C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429632 | |||||||
| chr6:17429947 | C | T | 28 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(25): Show |
28 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.222+3257C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429947 | |||||||
| chr6:17429983 | A | G | 1 | a0001c0002t0002g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.222+3293A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17429983 | |||||||
| chr6:17430167 | A | G | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+3477A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430167 | |||||||
| chr6:17430212 | A | G | 2 | a0001c0009t0001g0013 a0002c0012t0001g0014 |
2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.222+3522A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430212 | |||||||
| chr6:17430507 | C | A | 1 | a0001c0008t0001g0204 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.222+3817C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430507 | |||||||
| chr6:17430540 | G | GT | 32 | a0001c0001t0001g0019 a0001c0001t0001g0052 a0001c0001t0002g0003 others(29): Show |
32 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.222+3865dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17430540 | ||||||
| chr6:17430607 | G | C | 3 | a0001c0008t0001g0051 a0001c0009t0001g0015 a0001c0014t0008g0016 |
3 | HG01361.hp2 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.222+3917G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430607 | |||||||
| chr6:17430621 | C | T | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+3931C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430621 | |||||||
| chr6:17430683 | C | T | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+3993C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430683 | |||||||
| chr6:17430719 | C | T | 8 | a0001c0001t0001g0069 a0001c0002t0001g0144 a0001c0002t0001g0145 others(5): Show |
8 | HG01496.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+4029C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430719 | |||||||
| chr6:17430819 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.222+4129G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430819 | |||||||
| chr6:17430898 | A | T | 11 | a0001c0001t0001g0069 a0001c0002t0001g0144 a0001c0002t0001g0145 others(8): Show |
11 | HG01361.hp2 HG01496.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.222+4208A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430898 | |||||||
| chr6:17430926 | A | G | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.222+4236A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17430926 | |||||||
| chr6:17431194 | C | G | 1 | a0001c0001t0001g0005 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.222+4504C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431194 | |||||||
| chr6:17431290 | C | T | 1 | a0004c0010t0001g0063 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.222+4600C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431290 | |||||||
| chr6:17431324 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+4634G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431324 | |||||||
| chr6:17431371 | A | G | 5 | a0001c0008t0001g0051 a0001c0009t0001g0013 a0001c0009t0001g0015 others(2): Show |
5 | HG01361.hp2 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+4681A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431371 | |||||||
| chr6:17431390 | A | C | 4 | a0001c0001t0001g0069 a0001c0002t0001g0144 a0001c0002t0001g0145 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+4700A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431390 | |||||||
| chr6:17431478 | A | G | 28 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(25): Show |
28 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.222+4788A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431478 | |||||||
| chr6:17431655 | G | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(121): Show |
124 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(121): Show |
intron_variant | MODIFIER | c.222+4965G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431655 | |||||||
| chr6:17431851 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.222+5161T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431851 | |||||||
| chr6:17431856 | G | A | 1 | a0001c0003t0002g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.222+5166G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431856 | |||||||
| chr6:17431931 | G | A | 1 | a0001c0001t0002g0162 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.222+5241G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17431931 | |||||||
| chr6:17432057 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+5367G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432057 | |||||||
| chr6:17432142 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(121): Show |
124 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(121): Show |
intron_variant | MODIFIER | c.222+5452G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432142 | |||||||
| chr6:17432178 | A | C | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+5488A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432178 | |||||||
| chr6:17432604 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(50): Show |
53 | HG00099.hp1 HG00741.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.222+5914C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432604 | |||||||
| chr6:17432633 | A | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+5943A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432633 | |||||||
| chr6:17432664 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(50): Show |
53 | HG00099.hp1 HG00741.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.222+5974T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432664 | |||||||
| chr6:17432719 | C | CCTTG | 169 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.222+6041_222+6044d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17432719 | ||||||
| chr6:17432886 | G | A | 1 | a0001c0003t0001g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.222+6196G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432886 | |||||||
| chr6:17432962 | T | TC | 8 | a0001c0001t0001g0040 a0001c0001t0001g0154 a0001c0001t0001g0185 others(5): Show |
8 | HG00642.hp2 HG01192.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+6278dupC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17432962 | ||||||
| chr6:17432969 | T | C | 3 | a0001c0002t0001g0058 a0001c0008t0001g0057 a0002c0004t0001g0073 |
3 | HG00642.hp1 HG00735.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.222+6279T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17432969 | |||||||
| chr6:17433046 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.222+6356A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433046 | |||||||
| chr6:17433090 | G | A | 3 | a0001c0002t0001g0058 a0001c0008t0001g0057 a0002c0004t0001g0073 |
3 | HG00642.hp1 HG00735.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.222+6400G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433090 | |||||||
| chr6:17433142 | G | A | 24 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(21): Show |
24 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.222+6452G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433142 | |||||||
| chr6:17433166 | A | G | 14 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0001c0002t0001g0062 others(11): Show |
14 | HG01255.hp1 HG01361.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.222+6476A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433166 | |||||||
| chr6:17433333 | G | A | 12 | a0001c0001t0001g0069 a0001c0002t0001g0058 a0001c0002t0001g0144 others(9): Show |
12 | HG00642.hp1 HG01361.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.222+6643G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433333 | |||||||
| chr6:17433572 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(72): Show |
75 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.222+6882A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433572 | |||||||
| chr6:17433661 | C | T | 1 | a0001c0001t0007g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.222+6971C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433661 | |||||||
| chr6:17433720 | G | A | 16 | a0001c0001t0001g0069 a0001c0001t0002g0011 a0001c0002t0001g0012 others(13): Show |
16 | HG00642.hp1 HG01255.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.222+7030G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433720 | |||||||
| chr6:17433759 | T | C | 4 | a0001c0001t0002g0011 a0001c0002t0001g0012 a0001c0002t0001g0062 others(1): Show |
4 | HG01255.hp1 HG02109.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+7069T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433759 | |||||||
| chr6:17433828 | A | G | 2 | a0001c0001t0002g0181 a0001c0002t0001g0098 |
2 | NA18939.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.222+7138A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433828 | |||||||
| chr6:17433924 | C | T | 23 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(20): Show |
23 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.222+7234C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17433924 | |||||||
| chr6:17434046 | C | T | 7 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0001g0065 others(4): Show |
7 | HG01496.hp2 HG02280.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+7356C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434046 | |||||||
| chr6:17434231 | C | CT | 5 | a0001c0003t0002g0060 a0001c0003t0002g0064 a0001c0003t0002g0071 others(2): Show |
5 | HG01361.hp2 HG02109.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+7544dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17434231 | ||||||
| chr6:17434231 | C | CTT | 5 | a0001c0001t0001g0069 a0001c0002t0001g0002 a0001c0002t0001g0144 others(2): Show |
5 | HG02258.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+7543_222+7544d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17434231 | ||||||
| chr6:17434235 | C | CT | 22 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0084 others(19): Show |
22 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.222+7556dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17434235 | ||||||
| chr6:17434235 | C | CTT | 8 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
8 | HG01167.hp2 HG01884.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+7555_222+7556d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17434235 | ||||||
| chr6:17434235 | C | T | 11 | a0001c0001t0001g0069 a0001c0002t0001g0002 a0001c0002t0001g0144 others(8): Show |
11 | HG01361.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+7545C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434235 | |||||||
| chr6:17434235 | CT | C | 7 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0001g0065 others(4): Show |
7 | HG01496.hp2 HG02280.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+7556delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17434235 | ||||||
| chr6:17434417 | C | G | 23 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(20): Show |
23 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.222+7727C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434417 | |||||||
| chr6:17434481 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.222+7791G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434481 | |||||||
| chr6:17434636 | A | G | 25 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(22): Show |
25 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.222+7946A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434636 | |||||||
| chr6:17434646 | A | G | 11 | a0001c0001t0001g0069 a0001c0002t0001g0002 a0001c0002t0001g0144 others(8): Show |
11 | HG01361.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+7956A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434646 | |||||||
| chr6:17434848 | AC | A | 11 | a0001c0001t0001g0069 a0001c0002t0001g0002 a0001c0002t0001g0144 others(8): Show |
11 | HG01361.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+8162delC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17434848 | ||||||
| chr6:17434867 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.222+8177G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434867 | |||||||
| chr6:17434976 | A | G | 9 | a0001c0001t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0130 others(6): Show |
9 | HG01496.hp2 HG02280.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+8286A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434976 | |||||||
| chr6:17434977 | T | G | 11 | a0001c0001t0001g0069 a0001c0002t0001g0002 a0001c0002t0001g0144 others(8): Show |
11 | HG01361.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+8287T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17434977 | |||||||
| chr6:17435051 | G | A | 11 | a0001c0001t0001g0069 a0001c0002t0001g0002 a0001c0002t0001g0144 others(8): Show |
11 | HG01361.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+8361G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435051 | |||||||
| chr6:17435206 | A | G | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.222+8516A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435206 | |||||||
| chr6:17435211 | G | T | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+8521G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435211 | |||||||
| chr6:17435545 | G | C | 9 | a0001c0001t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0130 others(6): Show |
9 | HG01496.hp2 HG02280.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+8855G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435545 | |||||||
| chr6:17435605 | G | A | 4 | a0001c0001t0002g0011 a0001c0002t0001g0012 a0001c0002t0001g0062 others(1): Show |
4 | HG01255.hp1 HG02109.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+8915G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435605 | |||||||
| chr6:17435673 | G | A | 2 | a0001c0001t0002g0181 a0001c0002t0001g0098 |
2 | NA18939.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.222+8983G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435673 | |||||||
| chr6:17435681 | TA | T | 90 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0052 others(87): Show |
90 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.222+9014delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435681 | ||||||
| chr6:17435681 | TAA | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(71): Show |
74 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.222+9013_222+9014d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435681 | ||||||
| chr6:17435681 | TAAA | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0030 others(4): Show |
7 | HG02083.hp1 HG02486.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+9012_222+9014d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435681 | ||||||
| chr6:17435681 | TAAAA | T | 27 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(24): Show |
27 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.222+9011_222+9014d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435681 | ||||||
| chr6:17435702 | A | G | 15 | a0001c0001t0001g0069 a0001c0001t0002g0011 a0001c0002t0001g0002 others(12): Show |
15 | HG01255.hp1 HG01361.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.222+9012A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435702 | |||||||
| chr6:17435717 | T | TA | 7 | a0001c0001t0001g0035 a0001c0001t0001g0127 a0001c0001t0002g0024 others(4): Show |
7 | HG01175.hp1 HG02027.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+9042dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435717 | ||||||
| chr6:17435717 | TA | T | 7 | a0001c0001t0001g0140 a0001c0001t0002g0003 a0001c0002t0001g0191 others(4): Show |
7 | HG00735.hp2 HG01516.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+9042delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435717 | ||||||
| chr6:17435717 | TAAA | T | 9 | a0001c0001t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0130 others(6): Show |
9 | HG01496.hp2 HG02280.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+9040_222+9042d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435717 | ||||||
| chr6:17435727 | AAAAAAC | A | 9 | a0001c0001t0001g0069 a0001c0002t0001g0144 a0001c0002t0001g0145 others(6): Show |
9 | HG01361.hp2 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+9043_222+9048d others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17435727 | ||||||
| chr6:17435732 | A | C | 6 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0002g0199 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+9042A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435732 | |||||||
| chr6:17435733 | C | A | 7 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0002g0011 others(4): Show |
7 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+9043C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435733 | |||||||
| chr6:17435742 | A | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(64): Show |
67 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.222+9052A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17435742 | |||||||
| chr6:17436061 | T | C | 11 | a0001c0001t0001g0069 a0001c0002t0001g0002 a0001c0002t0001g0144 others(8): Show |
11 | HG01361.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+9371T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436061 | |||||||
| chr6:17436067 | A | ATCTTTCT others(1): Show |
4 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0144 others(1): Show |
4 | HG01255.hp1 HG02258.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+9392_222+9399d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436067 | ||||||
| chr6:17436067 | A | ATCTTTCT others(5): Show |
1 | a0001c0001t0002g0011 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.222+9388_222+9399d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436067 | ||||||
| chr6:17436067 | A | ATCTTTCT others(9): Show |
1 | a0001c0002t0001g0145 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.222+9384_222+9399d others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436067 | ||||||
| chr6:17436078 | T | TTTCCTTC others(5): Show |
1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.222+9391_222+9392i others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436078 | ||||||
| chr6:17436078 | T | TTTCCTTC others(9): Show |
3 | a0001c0001t0001g0202 a0001c0001t0002g0199 a0001c0001t0007g0201 |
3 | HG01109.hp2 HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.222+9391_222+9392i others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436078 | ||||||
| chr6:17436078 | T | TTTCCTTC others(13): Show |
2 | a0001c0001t0001g0196 a0001c0001t0005g0200 |
2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.222+9391_222+9392i others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436078 | ||||||
| chr6:17436082 | T | C | 6 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0002g0199 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+9392T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436082 | |||||||
| chr6:17436082 | T | TTTCCTTC others(5): Show |
7 | a0001c0001t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0130 others(4): Show |
7 | HG01496.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+9395_222+9396i others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436082 | ||||||
| chr6:17436082 | T | TTTCCTTC others(9): Show |
1 | a0001c0002t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.222+9395_222+9396i others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436082 | ||||||
| chr6:17436082 | T | TTTCCTTC others(13): Show |
1 | a0003c0007t0001g0059 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.222+9395_222+9396i others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436082 | ||||||
| chr6:17436086 | T | C | 16 | a0001c0001t0001g0099 a0001c0001t0001g0196 a0001c0001t0001g0202 others(13): Show |
16 | HG01109.hp2 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.222+9396T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436086 | |||||||
| chr6:17436086 | T | TTTCC | 13 | a0001c0001t0001g0095 a0001c0001t0002g0147 a0001c0001t0002g0162 others(10): Show |
13 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.222+9429_222+9432d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | ||||||
| chr6:17436086 | T | TTTCCTTC others(1): Show |
17 | a0001c0001t0001g0067 a0001c0001t0001g0080 a0001c0001t0001g0081 others(14): Show |
17 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.222+9425_222+9432d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | ||||||
| chr6:17436086 | T | TTTCCTTC others(5): Show |
4 | a0001c0001t0001g0068 a0001c0003t0001g0075 a0002c0004t0002g0083 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+9421_222+9432d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | ||||||
| chr6:17436086 | T | TTTCTTTC others(1): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0002t0001g0020 |
3 | HG01978.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.222+9399_222+9400i others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | ||||||
| chr6:17436086 | T | TTTCTTTC others(5): Show |
49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.222+9399_222+9400i others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | ||||||
| chr6:17436086 | T | TTTCTTTC others(9): Show |
4 | a0001c0001t0001g0042 a0001c0001t0002g0038 a0001c0002t0002g0129 others(1): Show |
4 | HG01167.hp1 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+9399_222+9400i others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | ||||||
| chr6:17436086 | T | TTTCTTTC others(13): Show |
1 | a0001c0001t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.222+9399_222+9400i others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | ||||||
| chr6:17436086 | TTTCC | T | 3 | a0002c0012t0001g0014 a0003c0007t0001g0110 a0003c0007t0001g0119 |
3 | HG01106.hp2 HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.222+9429_222+9432d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436086 | ||||||
| chr6:17436090 | C | T | 15 | a0001c0001t0001g0069 a0001c0001t0002g0011 a0001c0002t0001g0002 others(12): Show |
15 | HG01255.hp1 HG01361.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.222+9400C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436090 | |||||||
| chr6:17436094 | C | T | 14 | a0001c0001t0001g0069 a0001c0001t0002g0011 a0001c0002t0001g0012 others(11): Show |
14 | HG01255.hp1 HG01361.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.222+9404C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436094 | |||||||
| chr6:17436098 | C | T | 4 | a0001c0001t0001g0069 a0001c0002t0001g0062 a0001c0002t0001g0198 others(1): Show |
4 | HG02109.hp2 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+9408C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436098 | |||||||
| chr6:17436119 | T | C | 11 | a0001c0001t0002g0011 a0001c0002t0001g0002 a0001c0002t0001g0012 others(8): Show |
11 | HG01255.hp1 HG01361.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+9429T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436119 | |||||||
| chr6:17436123 | C | CTCCT | 8 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0069 others(5): Show |
8 | HG01168.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+9447_222+9450d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17436123 | ||||||
| chr6:17436123 | C | T | 11 | a0001c0001t0002g0011 a0001c0002t0001g0002 a0001c0002t0001g0012 others(8): Show |
11 | HG01255.hp1 HG01361.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+9433C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436123 | |||||||
| chr6:17436284 | A | G | 25 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(22): Show |
25 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.222+9594A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436284 | |||||||
| chr6:17436585 | G | A | 4 | a0001c0003t0002g0060 a0001c0003t0002g0064 a0001c0003t0002g0071 others(1): Show |
4 | HG02109.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+9895G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17436585 | |||||||
| chr6:17437002 | G | A | 6 | a0001c0001t0001g0069 a0001c0002t0001g0002 a0001c0002t0001g0144 others(3): Show |
6 | HG02258.hp1 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+10312G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437002 | |||||||
| chr6:17437261 | CTGGTCTA others(3): Show |
C | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 |
3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.222+10572_222+1058 others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437261 | |||||||
| chr6:17437433 | A | G | 2 | a0001c0002t0001g0062 a0004c0010t0002g0061 |
2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.222+10743A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437433 | |||||||
| chr6:17437504 | T | C | 2 | a0001c0002t0001g0144 a0001c0002t0001g0145 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.222+10814T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437504 | |||||||
| chr6:17437649 | C | T | 1 | a0001c0002t0001g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.222+10959C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437649 | |||||||
| chr6:17437650 | G | A | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+10960G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437650 | |||||||
| chr6:17437737 | C | T | 2 | a0001c0002t0001g0058 a0001c0008t0001g0057 |
2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.222+11047C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437737 | |||||||
| chr6:17437803 | G | C | 3 | a0001c0001t0002g0157 a0001c0002t0001g0056 a0001c0002t0001g0153 |
3 | HG03491.hp2 HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.222+11113G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437803 | |||||||
| chr6:17437834 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.222+11144G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437834 | |||||||
| chr6:17437856 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0002g0055 |
3 | HG01168.hp1 HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.222+11166G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437856 | |||||||
| chr6:17437870 | G | A | 15 | a0001c0001t0001g0069 a0001c0001t0002g0011 a0001c0002t0001g0002 others(12): Show |
15 | HG01255.hp1 HG01361.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.222+11180G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437870 | |||||||
| chr6:17437964 | G | C | 2 | a0001c0002t0001g0062 a0004c0010t0002g0061 |
2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.222+11274G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17437964 | |||||||
| chr6:17438011 | C | T | 2 | a0001c0002t0001g0062 a0004c0010t0002g0061 |
2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.222+11321C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438011 | |||||||
| chr6:17438053 | A | C | 9 | a0001c0001t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0130 others(6): Show |
9 | HG01496.hp2 HG02280.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+11363A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438053 | |||||||
| chr6:17438064 | A | AGTG | 5 | a0001c0001t0001g0069 a0001c0002t0001g0144 a0001c0002t0001g0145 others(2): Show |
5 | HG02486.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+11374_222+1137 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438064 | |||||||
| chr6:17438066 | G | C | 5 | a0001c0001t0001g0069 a0001c0002t0001g0144 a0001c0002t0001g0145 others(2): Show |
5 | HG02486.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+11376G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438066 | |||||||
| chr6:17438069 | T | TG | 5 | a0001c0001t0001g0069 a0001c0002t0001g0144 a0001c0002t0001g0145 others(2): Show |
5 | HG02486.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+11379_222+1138 others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438069 | |||||||
| chr6:17438071 | GATTATAA others(3602): Show |
G | 5 | a0001c0001t0001g0069 a0001c0002t0001g0144 a0001c0002t0001g0145 others(2): Show |
5 | HG02486.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+11382_222+1499 others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438071 | |||||||
| chr6:17438121 | G | T | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+11431G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438121 | |||||||
| chr6:17438173 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.222+11483T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438173 | |||||||
| chr6:17438194 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0002g0003 |
2 | HG02486.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.222+11504C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438194 | |||||||
| chr6:17438355 | GATT | G | 141 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(138): Show |
141 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.222+11666_222+1166 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438355 | |||||||
| chr6:17438393 | A | T | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+11703A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438393 | |||||||
| chr6:17438401 | T | G | 97 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(94): Show |
97 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.222+11711T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438401 | |||||||
| chr6:17438404 | T | G | 140 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(137): Show |
140 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.222+11714T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438404 | |||||||
| chr6:17438431 | G | GTAT | 3 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0002g0131 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.222+11742_222+1174 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438431 | ||||||
| chr6:17438431 | G | GTGTTT | 74 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(71): Show |
74 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.222+11743_222+1174 others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438431 | ||||||
| chr6:17438433 | G | GT | 19 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(16): Show |
19 | HG00642.hp2 HG01106.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.222+11766dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | ||||||
| chr6:17438433 | G | GTTT | 5 | a0001c0001t0001g0099 a0001c0002t0001g0058 a0001c0002t0001g0100 others(2): Show |
5 | HG00642.hp1 HG01496.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+11764_222+1176 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | ||||||
| chr6:17438433 | G | GTTTTGT | 19 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0103 others(16): Show |
19 | HG00597.hp1 HG00597.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.222+11747_222+1174 others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | ||||||
| chr6:17438433 | G | GTTTTGTT others(4): Show |
8 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0084 others(5): Show |
8 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+11747_222+1174 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | ||||||
| chr6:17438433 | G | GTTTTGTT others(5): Show |
8 | a0001c0001t0001g0082 a0001c0003t0001g0088 a0001c0003t0002g0060 others(5): Show |
8 | HG01361.hp2 HG02897.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+11747_222+1174 others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | ||||||
| chr6:17438433 | G | GTTTTGTT others(6): Show |
1 | a0001c0003t0002g0071 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.222+11747_222+1174 others(17): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | ||||||
| chr6:17438433 | G | GTTTTTTT others(1): Show |
6 | a0001c0001t0001g0068 a0001c0001t0001g0092 a0001c0003t0001g0072 others(3): Show |
6 | HG02622.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+11759_222+1176 others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | ||||||
| chr6:17438433 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0001g0067 a0001c0002t0001g0197 |
2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.222+11757_222+1176 others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | ||||||
| chr6:17438433 | G | GTTTTTTT others(4): Show |
1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+11756_222+1176 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438433 | ||||||
| chr6:17438433 | G | T | 3 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0002g0131 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.222+11743G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438433 | |||||||
| chr6:17438584 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.222+11894G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438584 | |||||||
| chr6:17438600 | A | G | 141 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(138): Show |
141 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.222+11910A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438600 | |||||||
| chr6:17438640 | A | C | 10 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0002g0199 others(7): Show |
10 | HG01109.hp2 HG01361.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+11950A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438640 | |||||||
| chr6:17438641 | G | A | 5 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0002g0199 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+11951G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438641 | |||||||
| chr6:17438643 | G | A | 94 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(91): Show |
94 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.222+11953G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438643 | |||||||
| chr6:17438674 | T | C | 2 | a0001c0001t0001g0127 a0001c0002t0001g0128 |
2 | HG01071.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.222+11984T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438674 | |||||||
| chr6:17438681 | C | T | 2 | a0001c0001t0001g0127 a0001c0002t0001g0128 |
2 | HG01071.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.222+11991C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438681 | |||||||
| chr6:17438686 | A | G | 2 | a0001c0001t0001g0127 a0001c0002t0001g0128 |
2 | HG01071.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.222+11996A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438686 | |||||||
| chr6:17438690 | C | T | 2 | a0001c0001t0001g0127 a0001c0002t0001g0128 |
2 | HG01071.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.222+12000C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438690 | |||||||
| chr6:17438714 | T | C | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0092 others(7): Show |
10 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+12024T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438714 | |||||||
| chr6:17438718 | T | C | 142 | a0001c0001t0001g0035 a0001c0001t0001g0045 a0001c0001t0001g0049 others(139): Show |
142 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.222+12028T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438718 | |||||||
| chr6:17438745 | T | G | 119 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(116): Show |
119 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.222+12055T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438745 | |||||||
| chr6:17438779 | CTT | C | 140 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(137): Show |
140 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.222+12098_222+1209 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17438779 | ||||||
| chr6:17438802 | A | G | 140 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(137): Show |
140 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.222+12112A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438802 | |||||||
| chr6:17438850 | C | T | 140 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(137): Show |
140 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.222+12160C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438850 | |||||||
| chr6:17438930 | G | A | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.222+12240G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438930 | |||||||
| chr6:17438968 | G | A | 1 | a0001c0002t0001g0007 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.222+12278G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17438968 | |||||||
| chr6:17439147 | A | G | 5 | a0001c0003t0002g0060 a0001c0003t0002g0064 a0001c0003t0002g0071 others(2): Show |
5 | HG01361.hp2 HG02109.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+12457A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17439147 | |||||||
| chr6:17439255 | G | GT | 134 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(131): Show |
134 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.222+12577dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17439255 | ||||||
| chr6:17439255 | G | GTT | 9 | a0001c0001t0001g0124 a0001c0001t0002g0199 a0001c0002t0001g0134 others(6): Show |
9 | HG01361.hp2 HG02109.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+12576_222+1257 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17439255 | ||||||
| chr6:17439728 | T | G | 22 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(19): Show |
22 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.222+13038T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17439728 | |||||||
| chr6:17439760 | T | C | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+13070T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17439760 | |||||||
| chr6:17439775 | G | A | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+13085G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17439775 | |||||||
| chr6:17439847 | T | G | 1 | a0001c0014t0008g0016 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.222+13157T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17439847 | |||||||
| chr6:17439974 | A | G | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+13284A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17439974 | |||||||
| chr6:17440021 | T | C | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+13331T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440021 | |||||||
| chr6:17440150 | T | C | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+13460T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440150 | |||||||
| chr6:17440527 | A | T | 2 | a0001c0001t0001g0091 a0002c0004t0001g0073 |
2 | HG00735.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.222+13837A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440527 | |||||||
| chr6:17440606 | C | CTGTGTGG | 16 | a0001c0001t0001g0142 a0001c0001t0001g0180 a0001c0001t0001g0196 others(13): Show |
16 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.222+13922_222+1392 others(11): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440606 | ||||||
| chr6:17440606 | C | CTGTGTGG others(2): Show |
3 | a0001c0001t0002g0105 a0001c0001t0002g0120 a0001c0001t0002g0157 |
3 | HG01928.hp2 HG01952.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.222+13922_222+1392 others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440606 | ||||||
| chr6:17440606 | C | CTGTGTGG others(4): Show |
1 | a0001c0002t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.222+13922_222+1392 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440606 | ||||||
| chr6:17440606 | CTG | C | 17 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(14): Show |
17 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.222+13923_222+1392 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440606 | ||||||
| chr6:17440607 | T | TGTGTG | 59 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(56): Show |
59 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.222+13918_222+1392 others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440607 | ||||||
| chr6:17440609 | T | TGTG | 17 | a0001c0001t0001g0068 a0001c0001t0001g0095 a0001c0001t0002g0150 others(14): Show |
17 | HG00438.hp1 HG00609.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.222+13920_222+1392 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440609 | ||||||
| chr6:17440611 | T | TG | 17 | a0001c0001t0001g0099 a0001c0001t0002g0122 a0001c0001t0002g0172 others(14): Show |
17 | HG00642.hp1 HG01243.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.222+13922dupG | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440611 | ||||||
| chr6:17440613 | T | G | 8 | a0001c0001t0001g0067 a0001c0002t0001g0130 a0001c0002t0001g0132 others(5): Show |
8 | HG02109.hp1 HG02145.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+13923T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440613 | |||||||
| chr6:17440614 | G | GGTGT | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(30): Show |
33 | HG01071.hp1 HG01192.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.222+13952_222+1395 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440614 | ||||||
| chr6:17440614 | G | GGTGTGT | 4 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0002g0022 others(1): Show |
4 | HG02027.hp2 HG02083.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+13950_222+1395 others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17440614 | ||||||
| chr6:17440614 | G | GT | 113 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(110): Show |
113 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.222+13924_222+1392 others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440614 | |||||||
| chr6:17440614 | G | T | 8 | a0001c0001t0001g0067 a0001c0002t0001g0130 a0001c0002t0001g0132 others(5): Show |
8 | HG02109.hp1 HG02145.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+13924G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440614 | |||||||
| chr6:17440667 | G | A | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+13977G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440667 | |||||||
| chr6:17440719 | A | G | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+14029A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440719 | |||||||
| chr6:17440726 | T | C | 6 | a0001c0002t0001g0058 a0001c0002t0001g0074 a0001c0008t0001g0057 others(3): Show |
6 | HG00642.hp1 HG01243.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+14036T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440726 | |||||||
| chr6:17440751 | G | A | 1 | a0001c0009t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.222+14061G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440751 | |||||||
| chr6:17440777 | C | T | 1 | a0001c0009t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.222+14087C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440777 | |||||||
| chr6:17440818 | A | T | 1 | a0001c0001t0001g0005 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.222+14128A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440818 | |||||||
| chr6:17440882 | C | G | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+14192C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440882 | |||||||
| chr6:17440976 | C | T | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+14286C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17440976 | |||||||
| chr6:17441005 | CT | C | 5 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0002g0199 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+14321delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17441005 | ||||||
| chr6:17441170 | T | A | 1 | a0001c0001t0001g0005 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.222+14480T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441170 | |||||||
| chr6:17441171 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+14481G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441171 | |||||||
| chr6:17441188 | T | C | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+14498T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441188 | |||||||
| chr6:17441546 | A | C | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+14856A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441546 | |||||||
| chr6:17441672 | A | G | 1 | a0001c0002t0001g0077 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.222+14982A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441672 | |||||||
| chr6:17441688 | T | C | 1 | a0001c0001t0002g0031 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.222+14998T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441688 | |||||||
| chr6:17441733 | C | T | 2 | a0001c0002t0001g0058 a0001c0008t0001g0057 |
2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.222+15043C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441733 | |||||||
| chr6:17441741 | T | C | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+15051T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441741 | |||||||
| chr6:17441828 | G | A | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+15138G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441828 | |||||||
| chr6:17441874 | T | G | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+15184T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441874 | |||||||
| chr6:17441959 | A | G | 138 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(135): Show |
138 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.222+15269A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17441959 | |||||||
| chr6:17442095 | A | G | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+15405A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17442095 | |||||||
| chr6:17442152 | A | C | 1 | a0001c0002t0001g0108 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.222+15462A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17442152 | |||||||
| chr6:17442407 | C | T | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+15717C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17442407 | |||||||
| chr6:17442654 | A | G | 139 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(136): Show |
139 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.222+15964A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17442654 | |||||||
| chr6:17442723 | A | AT | 97 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(94): Show |
97 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.222+16045dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17442723 | ||||||
| chr6:17442723 | A | ATT | 40 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(37): Show |
40 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.222+16044_222+1604 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17442723 | ||||||
| chr6:17442866 | C | T | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.222+16176C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17442866 | |||||||
| chr6:17442867 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+16177G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17442867 | |||||||
| chr6:17443112 | C | T | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222+16422C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443112 | |||||||
| chr6:17443145 | G | A | 2 | a0001c0002t0001g0132 a0001c0003t0002g0131 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.222+16455G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443145 | |||||||
| chr6:17443155 | A | C | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.222+16465A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443155 | |||||||
| chr6:17443209 | G | A | 13 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(10): Show |
13 | HG00735.hp2 HG01167.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.222+16519G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443209 | |||||||
| chr6:17443394 | C | G | 106 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(103): Show |
106 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.222+16704C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443394 | |||||||
| chr6:17443521 | G | A | 7 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(4): Show |
7 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+16831G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443521 | |||||||
| chr6:17443574 | G | GACAC | 9 | a0001c0001t0001g0099 a0001c0002t0001g0100 a0001c0002t0002g0079 others(6): Show |
9 | HG01106.hp2 HG01361.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+16901_222+1690 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17443574 | ||||||
| chr6:17443574 | G | GACACAC | 77 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(74): Show |
77 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.222+16899_222+1690 others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17443574 | ||||||
| chr6:17443574 | G | GACACACA others(1): Show |
50 | a0001c0001t0001g0035 a0001c0001t0001g0080 a0001c0001t0001g0081 others(47): Show |
50 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.222+16897_222+1690 others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17443574 | ||||||
| chr6:17443595 | G | T | 1 | a0001c0001t0001g0008 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.222+16905G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443595 | |||||||
| chr6:17443864 | T | C | 138 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(135): Show |
138 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.222+17174T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443864 | |||||||
| chr6:17443874 | T | C | 2 | a0001c0002t0001g0144 a0001c0002t0001g0145 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.222+17184T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443874 | |||||||
| chr6:17443943 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.222+17253G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443943 | |||||||
| chr6:17443945 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.222+17255G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17443945 | |||||||
| chr6:17444020 | G | C | 1 | a0001c0002t0001g0078 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.222+17330G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444020 | |||||||
| chr6:17444072 | A | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222+17382A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444072 | |||||||
| chr6:17444097 | A | G | 138 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(135): Show |
138 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.222+17407A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444097 | |||||||
| chr6:17444234 | C | T | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+17544C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444234 | |||||||
| chr6:17444377 | G | A | 1 | a0001c0011t0002g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.222+17687G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444377 | |||||||
| chr6:17444429 | G | A | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+17739G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444429 | |||||||
| chr6:17444510 | T | C | 4 | a0001c0001t0002g0152 a0001c0002t0001g0188 a0001c0002t0001g0189 others(1): Show |
4 | HG00741.hp2 HG01516.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+17820T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444510 | |||||||
| chr6:17444618 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0002g0105 |
2 | HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.222+17928C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444618 | |||||||
| chr6:17444639 | C | CA | 111 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0035 others(108): Show |
111 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.222+17968dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444639 | ||||||
| chr6:17444639 | C | CAA | 5 | a0001c0001t0001g0124 a0001c0001t0001g0140 a0001c0001t0001g0196 others(2): Show |
5 | HG01255.hp1 HG01978.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+17967_222+1796 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444639 | ||||||
| chr6:17444639 | CA | C | 7 | a0001c0001t0001g0069 a0001c0001t0002g0102 a0001c0002t0001g0144 others(4): Show |
7 | HG01496.hp1 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+17968delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444639 | ||||||
| chr6:17444655 | A | AG | 2 | a0001c0002t0001g0058 a0001c0008t0001g0057 |
2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.222+17965_222+1796 others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444655 | |||||||
| chr6:17444674 | G | T | 115 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(112): Show |
115 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.222+17984G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444674 | |||||||
| chr6:17444740 | A | T | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222+18050A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444740 | |||||||
| chr6:17444804 | C | A | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222+18114C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444804 | |||||||
| chr6:17444804 | C | CCA | 25 | a0001c0001t0001g0049 a0001c0001t0001g0068 a0001c0001t0001g0080 others(22): Show |
25 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.222+18153_223-1815 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | ||||||
| chr6:17444804 | C | CCACA | 13 | a0001c0001t0001g0103 a0001c0001t0001g0123 a0001c0001t0001g0124 others(10): Show |
13 | HG01978.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.222+18151_223-1815 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | ||||||
| chr6:17444804 | C | CCACACA | 41 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0095 others(38): Show |
41 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.222+18149_223-1815 others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | ||||||
| chr6:17444804 | C | CCACACAC others(1): Show |
22 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0142 others(19): Show |
22 | HG01516.hp1 HG01975.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.222+18147_223-1815 others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | ||||||
| chr6:17444804 | C | CCACACAC others(3): Show |
6 | a0001c0001t0002g0126 a0001c0001t0002g0162 a0001c0002t0002g0135 others(3): Show |
6 | HG01106.hp2 HG01981.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+18145_223-1815 others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | ||||||
| chr6:17444804 | C | CCACACAC others(5): Show |
2 | a0001c0001t0002g0003 a0001c0002t0001g0198 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.222+18143_223-1815 others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | ||||||
| chr6:17444804 | CCA | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(59): Show |
62 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.222+18153_223-1815 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | ||||||
| chr6:17444804 | CCACA | C | 4 | a0001c0002t0001g0002 a0001c0003t0002g0060 a0001c0003t0002g0064 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+18151_223-1815 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | ||||||
| chr6:17444804 | CCACACA | C | 10 | a0001c0001t0001g0099 a0001c0002t0001g0058 a0001c0002t0001g0074 others(7): Show |
10 | HG00642.hp1 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.222+18149_223-1815 others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | ||||||
| chr6:17444804 | CCACACAC others(7): Show |
C | 1 | a0001c0002t0001g0007 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.222+18141_223-1815 others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | ||||||
| chr6:17444804 | CCACACAC others(9): Show |
C | 1 | a0001c0002t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.222+18139_223-1815 others(20): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17444804 | ||||||
| chr6:17444911 | C | T | 2 | a0002c0004t0002g0083 a0002c0004t0002g0085 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.223-18085C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444911 | |||||||
| chr6:17444977 | A | G | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.223-18019A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444977 | |||||||
| chr6:17444994 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.223-18002T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17444994 | |||||||
| chr6:17445010 | T | A | 98 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(95): Show |
98 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.223-17986T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445010 | |||||||
| chr6:17445021 | T | C | 115 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(112): Show |
115 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.223-17975T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445021 | |||||||
| chr6:17445273 | G | A | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-17723G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445273 | |||||||
| chr6:17445354 | A | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-17642A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445354 | |||||||
| chr6:17445491 | C | A | 1 | a0001c0002t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.223-17505C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445491 | |||||||
| chr6:17445496 | C | T | 100 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(97): Show |
100 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.223-17500C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445496 | |||||||
| chr6:17445550 | G | A | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-17446G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445550 | |||||||
| chr6:17445551 | A | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-17445A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445551 | |||||||
| chr6:17445596 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.223-17400G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445596 | |||||||
| chr6:17445757 | C | T | 4 | a0001c0001t0001g0069 a0001c0002t0001g0144 a0001c0002t0001g0145 others(1): Show |
4 | HG02486.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-17239C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445757 | |||||||
| chr6:17445850 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.223-17146G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17445850 | |||||||
| chr6:17446032 | C | T | 121 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(118): Show |
121 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.223-16964C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446032 | |||||||
| chr6:17446196 | C | G | 8 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0074 others(5): Show |
8 | HG00642.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-16800C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446196 | |||||||
| chr6:17446212 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.223-16784A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446212 | |||||||
| chr6:17446292 | G | A | 98 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(95): Show |
98 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.223-16704G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446292 | |||||||
| chr6:17446353 | C | T | 1 | a0001c0002t0001g0138 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.223-16643C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446353 | |||||||
| chr6:17446367 | A | T | 109 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(106): Show |
109 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.223-16629A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446367 | |||||||
| chr6:17446425 | G | T | 1 | a0003c0007t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.223-16571G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446425 | |||||||
| chr6:17446433 | A | G | 24 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(21): Show |
24 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.223-16563A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446433 | |||||||
| chr6:17446451 | T | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0023 others(2): Show |
5 | HG02027.hp2 HG02083.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-16545T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446451 | |||||||
| chr6:17446551 | T | C | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 |
3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.223-16445T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446551 | |||||||
| chr6:17446569 | G | T | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-16427G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446569 | |||||||
| chr6:17446582 | T | C | 6 | a0001c0002t0001g0058 a0001c0002t0001g0074 a0001c0008t0001g0057 others(3): Show |
6 | HG00642.hp1 HG01243.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.223-16414T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446582 | |||||||
| chr6:17446584 | T | C | 2 | a0001c0002t0001g0191 a0001c0002t0001g0192 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.223-16412T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446584 | |||||||
| chr6:17446594 | T | C | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 |
3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.223-16402T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446594 | |||||||
| chr6:17446610 | C | T | 3 | a0001c0001t0001g0099 a0001c0002t0001g0100 a0004c0010t0002g0061 |
3 | HG01255.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-16386C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446610 | |||||||
| chr6:17446831 | G | A | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-16165G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446831 | |||||||
| chr6:17446864 | G | A | 98 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(95): Show |
98 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.223-16132G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446864 | |||||||
| chr6:17446904 | C | T | 15 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(12): Show |
15 | HG00735.hp2 HG01167.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.223-16092C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446904 | |||||||
| chr6:17446975 | G | A | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-16021G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17446975 | |||||||
| chr6:17447020 | G | A | 111 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(108): Show |
111 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.223-15976G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17447020 | |||||||
| chr6:17447034 | A | T | 132 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(129): Show |
132 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.223-15962A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17447034 | |||||||
| chr6:17447175 | TA | T | 128 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(125): Show |
128 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.223-15803delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17447175 | ||||||
| chr6:17447228 | C | G | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-15768C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17447228 | |||||||
| chr6:17447504 | A | G | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 |
3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.223-15492A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17447504 | |||||||
| chr6:17447754 | T | C | 1 | a0001c0002t0006g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.223-15242T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17447754 | |||||||
| chr6:17447784 | T | C | 1 | a0001c0009t0001g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.223-15212T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17447784 | |||||||
| chr6:17448057 | A | G | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 |
3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.223-14939A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448057 | |||||||
| chr6:17448072 | C | G | 131 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(128): Show |
131 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.223-14924C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448072 | |||||||
| chr6:17448149 | C | T | 3 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0002g0131 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.223-14847C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448149 | |||||||
| chr6:17448346 | T | C | 1 | a0001c0002t0001g0012 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.223-14650T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448346 | |||||||
| chr6:17448679 | T | C | 1 | a0001c0001t0002g0024 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.223-14317T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448679 | |||||||
| chr6:17448712 | C | T | 31 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(28): Show |
31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-14284C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448712 | |||||||
| chr6:17448731 | G | A | 1 | a0001c0009t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223-14265G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448731 | |||||||
| chr6:17448768 | CT | C | 107 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0049 others(104): Show |
107 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.223-14215delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17448768 | ||||||
| chr6:17448825 | G | C | 31 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(28): Show |
31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-14171G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448825 | |||||||
| chr6:17448841 | A | C | 1 | a0001c0009t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223-14155A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448841 | |||||||
| chr6:17448860 | C | G | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-14136C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448860 | |||||||
| chr6:17448892 | C | G | 131 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(128): Show |
131 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.223-14104C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17448892 | |||||||
| chr6:17449053 | C | T | 31 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(28): Show |
31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-13943C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449053 | |||||||
| chr6:17449057 | C | A | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(7): Show |
10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-13939C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449057 | |||||||
| chr6:17449413 | A | T | 17 | a0001c0001t0001g0053 a0001c0001t0001g0080 a0001c0001t0001g0081 others(14): Show |
17 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.223-13583A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449413 | |||||||
| chr6:17449416 | T | A | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-13580T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449416 | |||||||
| chr6:17449449 | C | T | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-13547C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449449 | |||||||
| chr6:17449516 | C | T | 6 | a0001c0002t0001g0058 a0001c0002t0001g0074 a0001c0008t0001g0057 others(3): Show |
6 | HG00642.hp1 HG01243.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.223-13480C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449516 | |||||||
| chr6:17449545 | TA | T | 4 | a0001c0002t0001g0074 a0003c0007t0001g0059 a0003c0007t0001g0066 others(1): Show |
4 | HG01243.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-13450delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449545 | |||||||
| chr6:17449611 | G | A | 100 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(97): Show |
100 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.223-13385G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449611 | |||||||
| chr6:17449664 | C | G | 1 | a0001c0002t0001g0128 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.223-13332C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17449664 | |||||||
| chr6:17450054 | C | A | 1 | a0001c0002t0001g0128 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.223-12942C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17450054 | |||||||
| chr6:17450055 | CT | C | 5 | a0001c0001t0001g0026 a0001c0001t0002g0163 a0001c0002t0002g0160 others(2): Show |
5 | HG03017.hp2 HG03041.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-12927delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17450055 | ||||||
| chr6:17450104 | T | A | 21 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(18): Show |
21 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.223-12892T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17450104 | |||||||
| chr6:17450134 | C | T | 1 | a0002c0004t0001g0073 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.223-12862C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17450134 | |||||||
| chr6:17450244 | G | T | 31 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(28): Show |
31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-12752G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17450244 | |||||||
| chr6:17450496 | G | C | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-12500G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17450496 | |||||||
| chr6:17450885 | G | A | 2 | a0001c0002t0001g0109 a0001c0002t0001g0164 |
2 | HG02027.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.223-12111G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17450885 | |||||||
| chr6:17451221 | ATCT | A | 14 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0002t0001g0144 others(11): Show |
14 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.223-11771_223-1176 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17451221 | ||||||
| chr6:17451231 | CA | C | 112 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(109): Show |
112 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.223-11753delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17451231 | ||||||
| chr6:17451232 | A | T | 1 | a0002c0004t0001g0073 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.223-11764A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451232 | |||||||
| chr6:17451241 | A | T | 5 | a0001c0001t0001g0054 a0001c0001t0002g0055 a0001c0002t0001g0058 others(2): Show |
5 | HG00642.hp1 HG01168.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-11755A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451241 | |||||||
| chr6:17451242 | AAT | A | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-11752_223-1175 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17451242 | ||||||
| chr6:17451412 | C | T | 1 | a0002c0012t0001g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.223-11584C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451412 | |||||||
| chr6:17451569 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0002g0055 |
3 | HG01168.hp1 HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.223-11427G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451569 | |||||||
| chr6:17451667 | G | A | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-11329G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451667 | |||||||
| chr6:17451819 | C | G | 2 | a0001c0002t0001g0191 a0001c0002t0001g0192 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.223-11177C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451819 | |||||||
| chr6:17451850 | CT | C | 31 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(28): Show |
31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-11145delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17451850 | |||||||
| chr6:17452111 | G | A | 31 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(28): Show |
31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-10885G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452111 | |||||||
| chr6:17452154 | T | G | 31 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(28): Show |
31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-10842T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452154 | |||||||
| chr6:17452345 | C | T | 1 | a0001c0009t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223-10651C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452345 | |||||||
| chr6:17452374 | C | T | 1 | a0002c0004t0001g0073 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.223-10622C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452374 | |||||||
| chr6:17452469 | G | T | 131 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(128): Show |
131 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.223-10527G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452469 | |||||||
| chr6:17452508 | G | A | 37 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(34): Show |
37 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.223-10488G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452508 | |||||||
| chr6:17452526 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.223-10470C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452526 | |||||||
| chr6:17452609 | A | T | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-10387A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452609 | |||||||
| chr6:17452680 | T | G | 31 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(28): Show |
31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-10316T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452680 | |||||||
| chr6:17452692 | C | G | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-10304C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452692 | |||||||
| chr6:17452730 | G | A | 32 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(29): Show |
32 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.223-10266G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452730 | |||||||
| chr6:17452730 | G | C | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-10266G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452730 | |||||||
| chr6:17452770 | GTTTCACT others(4): Show |
G | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 |
3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.223-10221_223-1021 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17452770 | ||||||
| chr6:17452854 | G | A | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-10142G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17452854 | |||||||
| chr6:17453266 | AAC | A | 2 | a0001c0001t0002g0163 a0001c0002t0002g0135 |
2 | HG01981.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.223-9727_223-9726d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17453266 | ||||||
| chr6:17453552 | C | T | 32 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(29): Show |
32 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.223-9444C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453552 | |||||||
| chr6:17453603 | A | C | 17 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(14): Show |
17 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.223-9393A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453603 | |||||||
| chr6:17453705 | C | T | 2 | a0001c0002t0001g0093 a0001c0002t0001g0094 |
2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.223-9291C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453705 | |||||||
| chr6:17453793 | G | A | 1 | a0001c0002t0002g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.223-9203G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453793 | |||||||
| chr6:17453839 | C | T | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-9157C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453839 | |||||||
| chr6:17453884 | CTCTT | C | 2 | a0001c0002t0001g0062 a0001c0002t0002g0079 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.223-9108_223-9105d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17453884 | ||||||
| chr6:17453901 | CT | C | 97 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(94): Show |
97 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.223-9077delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17453901 | ||||||
| chr6:17453902 | T | TTTC | 31 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(28): Show |
31 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-9092_223-9091i others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17453902 | ||||||
| chr6:17453906 | T | C | 4 | a0001c0001t0001g0091 a0001c0003t0002g0060 a0001c0003t0002g0064 others(1): Show |
4 | HG02109.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-9090T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453906 | |||||||
| chr6:17453919 | T | C | 1 | a0001c0011t0002g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.223-9077T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453919 | |||||||
| chr6:17453941 | A | G | 121 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(118): Show |
121 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.223-9055A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17453941 | |||||||
| chr6:17453990 | CCCTCCCA others(6): Show |
C | 16 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(13): Show |
16 | HG00735.hp2 HG01167.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.223-8973_223-8961d others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17453990 | ||||||
| chr6:17454419 | C | A | 33 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(30): Show |
33 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.223-8577C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454419 | |||||||
| chr6:17454545 | C | T | 3 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0002g0131 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.223-8451C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454545 | |||||||
| chr6:17454614 | T | C | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.223-8382T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454614 | |||||||
| chr6:17454618 | G | T | 33 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(30): Show |
33 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.223-8378G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454618 | |||||||
| chr6:17454920 | C | T | 2 | a0001c0002t0001g0193 a0006c0016t0001g0194 |
2 | HG03831.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.223-8076C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454920 | |||||||
| chr6:17454921 | G | A | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(7): Show |
10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-8075G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454921 | |||||||
| chr6:17454977 | T | C | 8 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0074 others(5): Show |
8 | HG00642.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-8019T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454977 | |||||||
| chr6:17454980 | A | G | 33 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(30): Show |
33 | HG00735.hp2 HG01167.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.223-8016A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17454980 | |||||||
| chr6:17455034 | C | T | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-7962C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455034 | |||||||
| chr6:17455283 | G | GA | 5 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0023 others(2): Show |
5 | HG02027.hp2 HG02083.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-7701dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17455283 | ||||||
| chr6:17455283 | GA | G | 110 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(107): Show |
110 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.223-7701delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17455283 | ||||||
| chr6:17455314 | G | A | 3 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0002g0131 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.223-7682G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455314 | |||||||
| chr6:17455600 | A | G | 17 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(14): Show |
17 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.223-7396A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455600 | |||||||
| chr6:17455677 | A | G | 22 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(19): Show |
22 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.223-7319A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455677 | |||||||
| chr6:17455680 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.223-7316C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455680 | |||||||
| chr6:17455725 | T | C | 142 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(139): Show |
142 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.223-7271T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455725 | |||||||
| chr6:17455814 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.223-7182C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455814 | |||||||
| chr6:17455819 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.223-7177G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455819 | |||||||
| chr6:17455824 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.223-7172C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455824 | |||||||
| chr6:17455831 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.223-7165A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455831 | |||||||
| chr6:17455931 | A | G | 2 | a0001c0002t0001g0077 a0001c0002t0001g0078 |
2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.223-7065A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455931 | |||||||
| chr6:17455958 | T | TA | 2 | a0001c0002t0001g0125 a0001c0002t0002g0129 |
2 | HG01167.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.223-7037dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17455958 | ||||||
| chr6:17455999 | C | T | 1 | a0001c0009t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223-6997C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17455999 | |||||||
| chr6:17456019 | A | T | 3 | a0001c0002t0001g0058 a0001c0002t0001g0074 a0001c0008t0001g0057 |
3 | HG00642.hp1 HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.223-6977A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456019 | |||||||
| chr6:17456046 | G | A | 5 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0074 others(2): Show |
5 | HG00642.hp1 HG01243.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-6950G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456046 | |||||||
| chr6:17456186 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.223-6810G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456186 | |||||||
| chr6:17456269 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0084 |
2 | HG01167.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.223-6727C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456269 | |||||||
| chr6:17456361 | G | C | 18 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(15): Show |
18 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.223-6635G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456361 | |||||||
| chr6:17456463 | T | A | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-6533T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456463 | |||||||
| chr6:17456504 | G | C | 9 | a0001c0001t0002g0102 a0001c0002t0001g0108 a0001c0002t0002g0111 others(6): Show |
9 | HG01496.hp1 HG01928.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-6492G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456504 | |||||||
| chr6:17456584 | C | T | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-6412C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456584 | |||||||
| chr6:17456595 | C | T | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-6401C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456595 | |||||||
| chr6:17456669 | T | C | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-6327T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456669 | |||||||
| chr6:17456670 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.223-6326T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456670 | |||||||
| chr6:17456825 | C | G | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.223-6171C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456825 | |||||||
| chr6:17456826 | C | A | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-6170C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456826 | |||||||
| chr6:17456876 | T | G | 141 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(138): Show |
141 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.223-6120T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456876 | |||||||
| chr6:17456966 | G | C | 1 | a0001c0001t0001g0017 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.223-6030G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17456966 | |||||||
| chr6:17457195 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.223-5801C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457195 | |||||||
| chr6:17457318 | G | A | 3 | a0001c0002t0001g0107 a0001c0002t0001g0136 a0001c0002t0001g0184 |
3 | HG00099.hp2 HG01175.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.223-5678G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457318 | |||||||
| chr6:17457399 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.223-5597C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457399 | |||||||
| chr6:17457440 | G | A | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-5556G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457440 | |||||||
| chr6:17457473 | A | T | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-5523A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457473 | |||||||
| chr6:17457547 | G | T | 1 | a0001c0009t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223-5449G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457547 | |||||||
| chr6:17457637 | G | C | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-5359G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457637 | |||||||
| chr6:17457677 | C | A | 3 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0002g0131 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.223-5319C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457677 | |||||||
| chr6:17457906 | A | G | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.223-5090A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17457906 | |||||||
| chr6:17458030 | C | G | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0002g0055 others(3): Show |
6 | HG01168.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-4966C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458030 | |||||||
| chr6:17458128 | T | G | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.223-4868T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458128 | |||||||
| chr6:17458234 | A | G | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-4762A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458234 | |||||||
| chr6:17458349 | A | G | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-4647A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458349 | |||||||
| chr6:17458359 | A | G | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-4637A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458359 | |||||||
| chr6:17458513 | A | G | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(7): Show |
10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-4483A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458513 | |||||||
| chr6:17458621 | T | C | 1 | a0002c0004t0001g0073 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.223-4375T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458621 | |||||||
| chr6:17458722 | C | T | 1 | a0001c0002t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.223-4274C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458722 | |||||||
| chr6:17458814 | T | C | 36 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(33): Show |
36 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.223-4182T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458814 | |||||||
| chr6:17458885 | G | A | 36 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(33): Show |
36 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.223-4111G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17458885 | |||||||
| chr6:17458886 | C | CA | 12 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0002g0137 others(9): Show |
12 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.223-4095dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17458886 | ||||||
| chr6:17458886 | C | CAA | 11 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0074 others(8): Show |
11 | HG00642.hp1 HG01243.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-4096_223-4095d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17458886 | ||||||
| chr6:17458886 | C | CAAA | 25 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(22): Show |
25 | HG00735.hp2 HG01167.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.223-4097_223-4095d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17458886 | ||||||
| chr6:17459055 | C | A | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.223-3941C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459055 | |||||||
| chr6:17459099 | T | G | 9 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0074 others(6): Show |
9 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-3897T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459099 | |||||||
| chr6:17459214 | C | T | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-3782C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459214 | |||||||
| chr6:17459302 | T | C | 3 | a0001c0001t0002g0003 a0001c0009t0001g0015 a0001c0014t0008g0016 |
3 | HG01361.hp2 HG02486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.223-3694T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459302 | |||||||
| chr6:17459486 | G | A | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-3510G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459486 | |||||||
| chr6:17459522 | G | T | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-3474G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459522 | |||||||
| chr6:17459739 | AATG | A | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(7): Show |
10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-3254_223-3252d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17459739 | ||||||
| chr6:17459815 | G | A | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-3181G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459815 | |||||||
| chr6:17459850 | C | T | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-3146C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459850 | |||||||
| chr6:17459930 | G | A | 98 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(95): Show |
98 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.223-3066G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459930 | |||||||
| chr6:17459934 | C | T | 100 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(97): Show |
100 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.223-3062C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459934 | |||||||
| chr6:17459945 | C | T | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-3051C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459945 | |||||||
| chr6:17459994 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.223-3002T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17459994 | |||||||
| chr6:17460026 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.223-2970G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460026 | |||||||
| chr6:17460150 | T | C | 1 | a0001c0009t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.223-2846T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460150 | |||||||
| chr6:17460153 | C | T | 28 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(25): Show |
28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-2843C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460153 | |||||||
| chr6:17460168 | C | T | 95 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(92): Show |
95 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.223-2828C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460168 | |||||||
| chr6:17460284 | C | CTT | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-2711_223-2710i others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17460284 | ||||||
| chr6:17460320 | G | A | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-2676G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460320 | |||||||
| chr6:17460617 | C | G | 18 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(15): Show |
18 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.223-2379C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460617 | |||||||
| chr6:17460620 | G | A | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-2376G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460620 | |||||||
| chr6:17460738 | C | T | 7 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(4): Show |
7 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-2258C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460738 | |||||||
| chr6:17460847 | A | T | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-2149A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460847 | |||||||
| chr6:17460928 | G | A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0002g0055 others(3): Show |
6 | HG01168.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-2068G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460928 | |||||||
| chr6:17460994 | C | T | 136 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(133): Show |
136 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.223-2002C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17460994 | |||||||
| chr6:17461005 | C | T | 2 | a0001c0002t0001g0193 a0006c0016t0001g0194 |
2 | HG03831.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.223-1991C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461005 | |||||||
| chr6:17461013 | G | A | 1 | a0001c0002t0002g0167 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.223-1983G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461013 | |||||||
| chr6:17461188 | CAA | C | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-1798_223-1797d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461188 | ||||||
| chr6:17461191 | A | C | 2 | a0001c0001t0002g0032 a0001c0002t0001g0134 |
2 | HG02071.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.223-1805A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461191 | |||||||
| chr6:17461199 | A | C | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(7): Show |
10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-1797A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461199 | |||||||
| chr6:17461218 | C | G | 26 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(23): Show |
26 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.223-1778C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461218 | |||||||
| chr6:17461218 | C | T | 1 | a0001c0002t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.223-1778C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461218 | |||||||
| chr6:17461218 | CT | C | 108 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0052 others(105): Show |
108 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.223-1767delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461218 | ||||||
| chr6:17461219 | T | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.223-1777T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461219 | |||||||
| chr6:17461238 | G | T | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(7): Show |
10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-1758G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461238 | |||||||
| chr6:17461239 | A | T | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(7): Show |
10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-1757A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461239 | |||||||
| chr6:17461240 | G | A | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(7): Show |
10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-1756G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461240 | |||||||
| chr6:17461242 | C | T | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.223-1754C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461242 | |||||||
| chr6:17461428 | T | G | 28 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(25): Show |
28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-1568T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461428 | |||||||
| chr6:17461476 | T | C | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0080 others(35): Show |
38 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.223-1520T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461476 | |||||||
| chr6:17461638 | G | A | 97 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(94): Show |
97 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.223-1358G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461638 | |||||||
| chr6:17461709 | A | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0041 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.223-1287A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461709 | |||||||
| chr6:17461737 | G | A | 134 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(131): Show |
134 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.223-1259G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461737 | |||||||
| chr6:17461776 | A | T | 28 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(25): Show |
28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-1220A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461776 | |||||||
| chr6:17461793 | C | T | 5 | a0001c0001t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0130 others(2): Show |
5 | HG03130.hp2 HG03195.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-1203C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461793 | |||||||
| chr6:17461795 | A | G | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.223-1201A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461795 | |||||||
| chr6:17461803 | G | T | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.223-1193G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461803 | |||||||
| chr6:17461809 | T | G | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.223-1187T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461809 | |||||||
| chr6:17461861 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.223-1135C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461861 | |||||||
| chr6:17461882 | A | C | 97 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0049 others(94): Show |
97 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.223-1114A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461882 | |||||||
| chr6:17461917 | T | C | 28 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(25): Show |
28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-1079T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461917 | |||||||
| chr6:17461950 | A | G | 134 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(131): Show |
134 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.223-1046A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461950 | |||||||
| chr6:17461950 | A | T | 3 | a0001c0001t0001g0099 a0001c0001t0002g0003 a0001c0002t0001g0100 |
3 | HG02486.hp2 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223-1046A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461950 | |||||||
| chr6:17461954 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.223-1042T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461954 | |||||||
| chr6:17461976 | G | C | 27 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(24): Show |
27 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.223-1020G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461976 | |||||||
| chr6:17461977 | G | A | 1 | a0001c0003t0002g0086 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.223-1019G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17461977 | |||||||
| chr6:17461992 | C | CA | 18 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0019 others(15): Show |
18 | HG00642.hp2 HG00735.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.223-973dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0002g0172 a0001c0006t0001g0155 a0002c0005t0001g0004 others(1): Show |
4 | HG02135.hp1 HG02135.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-982_223-973dup others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0002t0001g0112 others(1): Show |
4 | HG02735.hp1 HG02976.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-985_223-973dup others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0103 a0001c0001t0001g0123 |
2 | HG03130.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.223-986_223-973dup others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(8): Show |
10 | a0001c0001t0002g0126 a0001c0001t0002g0163 a0001c0001t0002g0175 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-987_223-973dup others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(9): Show |
5 | a0001c0001t0001g0165 a0001c0001t0002g0206 a0001c0002t0001g0093 others(2): Show |
5 | HG00609.hp1 HG01943.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-988_223-973dup others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(10): Show |
8 | a0001c0001t0001g0174 a0001c0001t0002g0050 a0001c0001t0002g0162 others(5): Show |
8 | HG00438.hp2 HG01517.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-989_223-973dup others(17): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(11): Show |
4 | a0001c0001t0001g0143 a0001c0001t0002g0031 a0001c0001t0002g0150 others(1): Show |
4 | HG01168.hp2 NA18990.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-990_223-973dup others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0052 a0001c0001t0001g0142 |
2 | HG01891.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.223-991_223-973dup others(19): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0140 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.223-992_223-973dup others(20): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.223-993_223-973dup others(21): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(15): Show |
3 | a0001c0001t0001g0053 a0001c0001t0002g0105 a0001c0002t0001g0078 |
3 | HG01952.hp2 HG02896.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.223-994_223-973dup others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(16): Show |
1 | a0001c0002t0001g0077 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.223-995_223-973dup others(23): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(19): Show |
1 | a0001c0002t0001g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.223-998_223-973dup others(26): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | C | CAAAAAAA others(31): Show |
1 | a0001c0008t0001g0204 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.223-973_223-972ins others(38): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | CA | C | 10 | a0001c0001t0002g0120 a0001c0001t0002g0158 a0001c0001t0002g0170 others(7): Show |
10 | HG01261.hp1 HG01928.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-973delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | CAA | C | 5 | a0001c0001t0001g0099 a0001c0001t0002g0147 a0001c0001t0002g0169 others(2): Show |
5 | HG01255.hp2 HG01261.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-974_223-973del others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | CAAAAA | C | 8 | a0001c0001t0001g0069 a0001c0001t0001g0159 a0001c0001t0001g0196 others(5): Show |
8 | HG00741.hp2 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.223-977_223-973del others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | CAAAAAAA others(1): Show |
C | 25 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0084 others(22): Show |
25 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.223-980_223-973del others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | CAAAAAAA others(2): Show |
C | 10 | a0001c0001t0001g0082 a0001c0001t0001g0179 a0001c0001t0001g0180 others(7): Show |
10 | HG02083.hp2 HG02897.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-981_223-973del others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0002g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.223-984_223-973del others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | CAAAAAAA others(7): Show |
C | 1 | a0003c0007t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.223-986_223-973del others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | CAAAAAAA others(10): Show |
C | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-989_223-973del others(17): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17461992 | CAAAAAAA others(11): Show |
C | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.223-990_223-973del others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17461992 | ||||||
| chr6:17462085 | A | T | 28 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(25): Show |
28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-911A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462085 | |||||||
| chr6:17462089 | A | G | 28 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(25): Show |
28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-907A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462089 | |||||||
| chr6:17462114 | T | C | 28 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(25): Show |
28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-882T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462114 | |||||||
| chr6:17462214 | G | C | 2 | a0001c0002t0001g0093 a0001c0002t0001g0094 |
2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.223-782G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462214 | |||||||
| chr6:17462243 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.223-753C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462243 | |||||||
| chr6:17462302 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.223-694G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462302 | |||||||
| chr6:17462418 | CAT | C | 5 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0002g0199 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-577_223-576del others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462418 | |||||||
| chr6:17462568 | GC | G | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(7): Show |
10 | HG01255.hp1 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-424delC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 17462568 | ||||||
| chr6:17462815 | G | A | 28 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(25): Show |
28 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.223-181G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 3/12 | chr6 | 17462815 | |||||||
| chr6:17463250 | C | G | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.300+177C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463250 | |||||||
| chr6:17463268 | G | GT | 15 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(12): Show |
15 | HG00735.hp2 HG01167.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.300+207dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17463268 | ||||||
| chr6:17463268 | G | GTT | 10 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0074 others(7): Show |
10 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+206_300+207dup others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17463268 | ||||||
| chr6:17463295 | C | T | 1 | a0001c0001t0002g0027 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.300+222C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463295 | |||||||
| chr6:17463319 | G | A | 18 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(15): Show |
18 | HG00735.hp2 HG01167.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.300+246G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463319 | |||||||
| chr6:17463362 | C | G | 1 | a0001c0002t0001g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.300+289C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463362 | |||||||
| chr6:17463365 | A | G | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+292A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463365 | |||||||
| chr6:17463435 | C | T | 94 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(91): Show |
94 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.300+362C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463435 | |||||||
| chr6:17463472 | T | A | 10 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0074 others(7): Show |
10 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+399T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463472 | |||||||
| chr6:17463573 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.300+500C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463573 | |||||||
| chr6:17463574 | G | A | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.300+501G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463574 | |||||||
| chr6:17463613 | T | C | 10 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0074 others(7): Show |
10 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+540T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463613 | |||||||
| chr6:17463698 | C | G | 132 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(129): Show |
132 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.300+625C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463698 | |||||||
| chr6:17463816 | A | G | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(6): Show |
9 | HG01496.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+743A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17463816 | |||||||
| chr6:17464043 | T | C | 140 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(137): Show |
140 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.300+970T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464043 | |||||||
| chr6:17464111 | G | A | 3 | a0001c0001t0002g0003 a0001c0009t0001g0015 a0001c0014t0008g0016 |
3 | HG01361.hp2 HG02486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+1038G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464111 | |||||||
| chr6:17464195 | G | A | 3 | a0001c0002t0001g0058 a0001c0002t0001g0074 a0001c0008t0001g0057 |
3 | HG00642.hp1 HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.300+1122G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464195 | |||||||
| chr6:17464269 | G | A | 1 | a0001c0003t0002g0086 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.300+1196G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464269 | |||||||
| chr6:17464456 | A | G | 132 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(129): Show |
132 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.300+1383A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464456 | |||||||
| chr6:17464535 | A | G | 3 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0002g0131 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.300+1462A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464535 | |||||||
| chr6:17464565 | G | C | 134 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(131): Show |
134 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.300+1492G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464565 | |||||||
| chr6:17464574 | T | C | 88 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(85): Show |
88 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.300+1501T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464574 | |||||||
| chr6:17464661 | A | G | 10 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0074 others(7): Show |
10 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+1588A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464661 | |||||||
| chr6:17464784 | A | G | 113 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(110): Show |
113 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.300+1711A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464784 | |||||||
| chr6:17464829 | G | A | 10 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0002g0137 others(7): Show |
10 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+1756G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464829 | |||||||
| chr6:17464848 | G | A | 2 | a0001c0002t0001g0074 a0004c0010t0002g0061 |
2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.300+1775G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464848 | |||||||
| chr6:17464867 | G | A | 10 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0074 others(7): Show |
10 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+1794G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464867 | |||||||
| chr6:17464884 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.300+1811G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17464884 | |||||||
| chr6:17465034 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0174 |
2 | HG02071.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.300+1961A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465034 | |||||||
| chr6:17465097 | A | G | 13 | a0001c0002t0001g0002 a0001c0002t0001g0058 a0001c0002t0001g0074 others(10): Show |
13 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.300+2024A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465097 | |||||||
| chr6:17465268 | T | C | 1 | a0006c0016t0001g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.300+2195T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465268 | |||||||
| chr6:17465343 | C | A | 8 | a0001c0001t0001g0069 a0001c0001t0001g0196 a0001c0001t0001g0202 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+2270C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465343 | |||||||
| chr6:17465365 | C | A | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.300+2292C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465365 | |||||||
| chr6:17465513 | C | T | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+2440C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465513 | |||||||
| chr6:17465690 | A | G | 6 | a0001c0001t0002g0038 a0001c0002t0001g0144 a0001c0002t0001g0145 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+2617A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465690 | |||||||
| chr6:17465691 | A | G | 6 | a0001c0001t0002g0038 a0001c0002t0001g0144 a0001c0002t0001g0145 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+2618A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465691 | |||||||
| chr6:17465697 | T | C | 8 | a0001c0001t0001g0069 a0001c0001t0001g0196 a0001c0001t0001g0202 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+2624T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465697 | |||||||
| chr6:17465732 | C | T | 1 | a0001c0002t0001g0062 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.300+2659C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465732 | |||||||
| chr6:17465750 | A | G | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.300+2677A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465750 | |||||||
| chr6:17465911 | G | T | 1 | a0001c0001t0002g0120 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.300+2838G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17465911 | |||||||
| chr6:17466056 | G | A | 12 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(9): Show |
12 | HG01496.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+2983G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466056 | |||||||
| chr6:17466223 | T | A | 9 | a0001c0001t0001g0099 a0001c0001t0002g0003 a0001c0002t0001g0100 others(6): Show |
9 | HG02280.hp2 HG02486.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+3150T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466223 | |||||||
| chr6:17466430 | C | A | 8 | a0001c0001t0001g0069 a0001c0001t0001g0196 a0001c0001t0001g0202 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+3357C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466430 | |||||||
| chr6:17466491 | G | C | 15 | a0001c0001t0001g0099 a0001c0001t0002g0003 a0001c0001t0002g0038 others(12): Show |
15 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.300+3418G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466491 | |||||||
| chr6:17466493 | A | G | 6 | a0001c0001t0002g0038 a0001c0002t0001g0144 a0001c0002t0001g0145 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+3420A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466493 | |||||||
| chr6:17466666 | C | T | 6 | a0001c0001t0002g0038 a0001c0002t0001g0144 a0001c0002t0001g0145 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+3593C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466666 | |||||||
| chr6:17466678 | T | C | 136 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0049 others(133): Show |
136 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.300+3605T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466678 | |||||||
| chr6:17466691 | C | T | 1 | a0001c0002t0001g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.300+3618C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466691 | |||||||
| chr6:17466750 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.300+3677T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466750 | |||||||
| chr6:17466860 | C | T | 6 | a0001c0001t0002g0038 a0001c0002t0001g0144 a0001c0002t0001g0145 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+3787C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466860 | |||||||
| chr6:17466928 | A | G | 6 | a0001c0001t0002g0038 a0001c0002t0001g0144 a0001c0002t0001g0145 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+3855A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17466928 | |||||||
| chr6:17467050 | T | C | 1 | a0001c0001t0002g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.300+3977T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467050 | |||||||
| chr6:17467110 | C | T | 9 | a0001c0001t0001g0099 a0001c0001t0002g0003 a0001c0002t0001g0100 others(6): Show |
9 | HG02280.hp2 HG02486.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+4037C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467110 | |||||||
| chr6:17467112 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.300+4039C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467112 | |||||||
| chr6:17467232 | A | G | 2 | a0001c0002t0001g0144 a0001c0002t0001g0145 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+4159A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467232 | |||||||
| chr6:17467533 | T | G | 3 | a0001c0001t0001g0091 a0002c0004t0001g0073 a0004c0010t0002g0061 |
3 | HG00735.hp2 HG01255.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.300+4460T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467533 | |||||||
| chr6:17467611 | C | A | 1 | a0001c0001t0002g0163 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.300+4538C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467611 | |||||||
| chr6:17467636 | G | C | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+4563G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467636 | |||||||
| chr6:17467775 | G | T | 3 | a0001c0001t0001g0091 a0002c0004t0001g0073 a0004c0010t0002g0061 |
3 | HG00735.hp2 HG01255.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.300+4702G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467775 | |||||||
| chr6:17467803 | A | G | 1 | a0001c0002t0002g0115 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.300+4730A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467803 | |||||||
| chr6:17467815 | A | C | 35 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(32): Show |
35 | HG01109.hp2 HG01167.hp2 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.300+4742A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467815 | |||||||
| chr6:17467830 | C | T | 5 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0002g0199 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+4757C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17467830 | |||||||
| chr6:17468300 | G | A | 3 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0002g0131 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.300+5227G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17468300 | |||||||
| chr6:17468467 | C | G | 16 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(13): Show |
16 | HG01167.hp2 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.300+5394C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17468467 | |||||||
| chr6:17468631 | C | T | 1 | a0002c0005t0003g0171 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.300+5558C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17468631 | |||||||
| chr6:17468809 | T | C | 6 | a0001c0001t0002g0038 a0001c0002t0001g0144 a0001c0002t0001g0145 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+5736T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17468809 | |||||||
| chr6:17468906 | C | T | 1 | a0001c0014t0008g0016 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.300+5833C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17468906 | |||||||
| chr6:17469030 | CCACCT | C | 6 | a0001c0001t0002g0038 a0001c0002t0001g0144 a0001c0002t0001g0145 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+5973_300+5977d others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17469030 | ||||||
| chr6:17469090 | A | G | 1 | a0001c0002t0001g0007 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.300+6017A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469090 | |||||||
| chr6:17469270 | C | T | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 |
3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+6197C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469270 | |||||||
| chr6:17469285 | T | C | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.300+6212T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469285 | |||||||
| chr6:17469416 | C | CTGTGTGT others(1): Show |
2 | a0001c0001t0002g0126 a0001c0001t0002g0175 |
2 | NA18747.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.300+6353_300+6360d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17469416 | ||||||
| chr6:17469416 | CTG | C | 4 | a0001c0001t0001g0092 a0001c0002t0001g0144 a0001c0002t0001g0145 others(1): Show |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+6359_300+6360d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17469416 | ||||||
| chr6:17469558 | A | G | 5 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0002g0199 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+6485A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469558 | |||||||
| chr6:17469593 | G | C | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.300+6520G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469593 | |||||||
| chr6:17469618 | G | A | 3 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0002g0131 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.300+6545G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469618 | |||||||
| chr6:17469624 | A | G | 5 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+6551A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469624 | |||||||
| chr6:17469957 | A | G | 3 | a0001c0001t0001g0099 a0001c0001t0002g0003 a0001c0002t0001g0100 |
3 | HG02486.hp2 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.300+6884A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17469957 | |||||||
| chr6:17470183 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0002g0003 a0001c0002t0001g0100 |
3 | HG02486.hp2 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.300+7110G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470183 | |||||||
| chr6:17470208 | A | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+7135A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470208 | |||||||
| chr6:17470295 | G | A | 3 | a0001c0001t0001g0091 a0002c0004t0001g0073 a0004c0010t0002g0061 |
3 | HG00735.hp2 HG01255.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.300+7222G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470295 | |||||||
| chr6:17470336 | G | C | 7 | a0001c0001t0001g0099 a0001c0001t0002g0003 a0001c0001t0002g0038 others(4): Show |
7 | HG02486.hp2 HG02630.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.300+7263G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470336 | |||||||
| chr6:17470406 | T | G | 1 | a0001c0001t0002g0032 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.300+7333T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470406 | |||||||
| chr6:17470462 | A | G | 126 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(123): Show |
126 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.300+7389A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470462 | |||||||
| chr6:17470466 | A | T | 3 | a0001c0001t0001g0099 a0001c0001t0002g0003 a0001c0002t0001g0100 |
3 | HG02486.hp2 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.300+7393A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470466 | |||||||
| chr6:17470769 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.300+7696A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470769 | |||||||
| chr6:17470797 | G | T | 2 | a0001c0002t0001g0062 a0001c0002t0002g0079 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.300+7724G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470797 | |||||||
| chr6:17470840 | T | C | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+7767T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17470840 | |||||||
| chr6:17471362 | T | C | 3 | a0001c0001t0001g0091 a0002c0004t0001g0073 a0004c0010t0002g0061 |
3 | HG00735.hp2 HG01255.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.300+8289T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471362 | |||||||
| chr6:17471561 | G | A | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+8488G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471561 | |||||||
| chr6:17471603 | C | G | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+8530C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471603 | |||||||
| chr6:17471615 | G | A | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+8542G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471615 | |||||||
| chr6:17471645 | A | C | 1 | a0001c0003t0001g0088 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.300+8572A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471645 | |||||||
| chr6:17471659 | G | A | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+8586G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471659 | |||||||
| chr6:17471788 | G | A | 5 | a0001c0002t0001g0036 a0001c0002t0001g0188 a0001c0002t0001g0189 others(2): Show |
5 | HG00741.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+8715G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471788 | |||||||
| chr6:17471830 | CA | C | 79 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(76): Show |
79 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.300+8772delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17471830 | ||||||
| chr6:17471830 | CAA | C | 46 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(43): Show |
46 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.300+8771_300+8772d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17471830 | ||||||
| chr6:17471997 | G | A | 6 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 others(3): Show |
6 | HG01255.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+8924G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17471997 | |||||||
| chr6:17472035 | T | C | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 |
3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+8962T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17472035 | |||||||
| chr6:17472038 | TAATAGTG others(306): Show |
T | 126 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(123): Show |
126 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.300+8982_300+9294d others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17472038 | ||||||
| chr6:17472207 | G | A | 3 | a0001c0002t0001g0101 a0001c0002t0001g0112 a0001c0008t0001g0204 |
3 | HG02055.hp2 HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.300+9134G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17472207 | |||||||
| chr6:17472333 | C | CA | 6 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0030 others(3): Show |
6 | HG00438.hp1 HG02055.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+9280dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17472333 | ||||||
| chr6:17472661 | C | T | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+9588C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17472661 | |||||||
| chr6:17472872 | T | C | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+9799T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17472872 | |||||||
| chr6:17472972 | C | G | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.300+9899C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17472972 | |||||||
| chr6:17473023 | T | G | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+9950T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473023 | |||||||
| chr6:17473037 | CT | C | 19 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(16): Show |
19 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.300+9977delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17473037 | ||||||
| chr6:17473039 | T | G | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+9966T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473039 | |||||||
| chr6:17473253 | G | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.300+10180G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473253 | |||||||
| chr6:17473515 | C | T | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+10442C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473515 | |||||||
| chr6:17473599 | G | T | 1 | a0002c0004t0001g0073 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.300+10526G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473599 | |||||||
| chr6:17473696 | T | G | 76 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(73): Show |
76 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.300+10623T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473696 | |||||||
| chr6:17473953 | A | G | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+10880A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17473953 | |||||||
| chr6:17474151 | T | A | 1 | a0001c0001t0002g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.300+11078T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474151 | |||||||
| chr6:17474184 | TC | T | 4 | a0001c0008t0001g0051 a0001c0009t0001g0013 a0001c0009t0001g0015 others(1): Show |
4 | HG01361.hp2 HG02486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+11112delC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474184 | |||||||
| chr6:17474185 | C | CT | 15 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0095 others(12): Show |
15 | HG00438.hp1 HG00741.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.300+11137dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474185 | ||||||
| chr6:17474185 | CT | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0068 others(22): Show |
25 | HG00642.hp1 HG01071.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.300+11137delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474185 | ||||||
| chr6:17474185 | CTT | C | 84 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(81): Show |
84 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.300+11136_300+1113 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474185 | ||||||
| chr6:17474185 | CTTT | C | 12 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0001c0001t0001g0196 others(9): Show |
12 | HG00735.hp2 HG01109.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+11135_300+1113 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474185 | ||||||
| chr6:17474185 | CTTTT | C | 5 | a0001c0001t0002g0038 a0001c0002t0001g0002 a0001c0002t0001g0130 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+11134_300+1113 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474185 | ||||||
| chr6:17474186 | T | G | 4 | a0001c0008t0001g0051 a0001c0009t0001g0013 a0001c0009t0001g0015 others(1): Show |
4 | HG01361.hp2 HG02486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+11113T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474186 | |||||||
| chr6:17474187 | T | C | 1 | a0001c0009t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.300+11114T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474187 | |||||||
| chr6:17474187 | T | G | 2 | a0001c0002t0001g0144 a0001c0002t0001g0145 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+11114T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474187 | |||||||
| chr6:17474188 | T | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+11115T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474188 | |||||||
| chr6:17474193 | T | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+11120T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474193 | |||||||
| chr6:17474322 | GA | G | 12 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(9): Show |
12 | HG01496.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+11259delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474322 | ||||||
| chr6:17474569 | C | T | 5 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+11496C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474569 | |||||||
| chr6:17474724 | A | AT | 12 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0065 others(9): Show |
12 | HG01496.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+11658dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17474724 | ||||||
| chr6:17474808 | G | A | 2 | a0001c0001t0001g0091 a0002c0004t0001g0073 |
2 | HG00735.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.300+11735G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474808 | |||||||
| chr6:17474970 | G | A | 1 | a0002c0005t0001g0004 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.300+11897G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17474970 | |||||||
| chr6:17475054 | A | G | 2 | a0001c0002t0001g0107 a0001c0002t0001g0184 |
2 | HG00099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.300+11981A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475054 | |||||||
| chr6:17475150 | G | A | 5 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0002g0199 others(2): Show |
5 | HG01109.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+12077G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475150 | |||||||
| chr6:17475153 | C | T | 5 | a0001c0001t0001g0091 a0001c0002t0001g0130 a0001c0002t0001g0132 others(2): Show |
5 | HG00735.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+12080C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475153 | |||||||
| chr6:17475194 | C | CA | 20 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0103 others(17): Show |
20 | HG01109.hp2 HG01255.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.300+12136dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17475194 | ||||||
| chr6:17475194 | CA | C | 13 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0002t0001g0112 others(10): Show |
13 | HG01496.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.300+12136delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17475194 | ||||||
| chr6:17475206 | A | AG | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+12133_300+1213 others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475206 | |||||||
| chr6:17475227 | C | A | 1 | a0001c0002t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.300+12154C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475227 | |||||||
| chr6:17475557 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.300+12484C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475557 | |||||||
| chr6:17475851 | C | G | 1 | a0001c0001t0002g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.300+12778C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475851 | |||||||
| chr6:17475851 | C | T | 1 | a0001c0001t0002g0172 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.300+12778C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17475851 | |||||||
| chr6:17476230 | T | C | 38 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(35): Show |
38 | HG00735.hp2 HG01109.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.300+13157T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476230 | |||||||
| chr6:17476360 | T | C | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 |
3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+13287T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476360 | |||||||
| chr6:17476382 | G | A | 18 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(15): Show |
18 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+13309G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476382 | |||||||
| chr6:17476525 | C | T | 11 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0002g0003 others(8): Show |
11 | HG00735.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+13452C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476525 | |||||||
| chr6:17476528 | C | G | 2 | a0001c0009t0001g0015 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+13455C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476528 | |||||||
| chr6:17476794 | T | G | 1 | a0001c0001t0002g0150 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.300+13721T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476794 | |||||||
| chr6:17476864 | C | CT | 5 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0095 others(2): Show |
5 | HG00438.hp1 HG01175.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+13816dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17476864 | ||||||
| chr6:17476864 | CT | C | 51 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0068 others(48): Show |
51 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.300+13816delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17476864 | ||||||
| chr6:17476864 | CTT | C | 74 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(71): Show |
74 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(71): Show |
intron_variant | MODIFIER | c.300+13815_300+1381 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17476864 | ||||||
| chr6:17476864 | CTTT | C | 5 | a0001c0001t0001g0123 a0001c0002t0001g0098 a0001c0002t0001g0146 others(2): Show |
5 | HG00609.hp1 HG00609.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+13814_300+1381 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17476864 | ||||||
| chr6:17476864 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0040 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.300+13807_300+1381 others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17476864 | ||||||
| chr6:17476909 | C | T | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.300+13836C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476909 | |||||||
| chr6:17476936 | A | G | 1 | a0002c0005t0004g0025 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.300+13863A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17476936 | |||||||
| chr6:17477194 | C | G | 76 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(73): Show |
76 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.300+14121C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477194 | |||||||
| chr6:17477266 | G | C | 2 | a0001c0001t0002g0046 a0001c0001t0002g0152 |
2 | HG01516.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.300+14193G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477266 | |||||||
| chr6:17477307 | C | T | 2 | a0001c0002t0001g0132 a0001c0003t0002g0131 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.300+14234C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477307 | |||||||
| chr6:17477346 | G | A | 1 | a0001c0002t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.300+14273G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477346 | |||||||
| chr6:17477453 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.300+14380A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477453 | |||||||
| chr6:17477541 | C | T | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.300+14468C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477541 | |||||||
| chr6:17477956 | C | T | 117 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(114): Show |
117 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.300+14883C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17477956 | |||||||
| chr6:17478003 | A | G | 1 | a0002c0012t0001g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.300+14930A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478003 | |||||||
| chr6:17478195 | C | T | 5 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+15122C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478195 | |||||||
| chr6:17478242 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.300+15169C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478242 | |||||||
| chr6:17478297 | C | CT | 36 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(33): Show |
36 | HG01109.hp2 HG01167.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.300+15244dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17478297 | ||||||
| chr6:17478297 | C | CTT | 5 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+15243_300+1524 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17478297 | ||||||
| chr6:17478297 | CT | C | 9 | a0001c0001t0001g0154 a0001c0001t0002g0027 a0001c0002t0001g0107 others(6): Show |
9 | HG00099.hp2 HG01261.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+15244delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17478297 | ||||||
| chr6:17478312 | T | C | 1 | a0001c0001t0002g0050 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.300+15239T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478312 | |||||||
| chr6:17478540 | C | G | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+15467C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478540 | |||||||
| chr6:17478832 | A | C | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.300+15759A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478832 | |||||||
| chr6:17478868 | T | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+15795T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478868 | |||||||
| chr6:17478999 | C | T | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+15926C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17478999 | |||||||
| chr6:17479070 | G | A | 1 | a0001c0002t0001g0193 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.300+15997G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479070 | |||||||
| chr6:17479357 | G | C | 113 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0052 others(110): Show |
113 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.300+16284G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479357 | |||||||
| chr6:17479433 | C | T | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+16360C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479433 | |||||||
| chr6:17479435 | T | A | 11 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0003t0001g0072 others(8): Show |
11 | HG02109.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+16362T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479435 | |||||||
| chr6:17479526 | G | C | 18 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(15): Show |
18 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+16453G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479526 | |||||||
| chr6:17479594 | G | C | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+16521G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479594 | |||||||
| chr6:17479607 | A | AT | 11 | a0001c0001t0001g0026 a0001c0001t0001g0052 a0001c0001t0001g0091 others(8): Show |
11 | HG00735.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+16556dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17479607 | ||||||
| chr6:17479607 | AT | A | 41 | a0001c0001t0001g0045 a0001c0001t0001g0067 a0001c0001t0001g0068 others(38): Show |
41 | HG00099.hp1 HG00642.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.300+16556delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17479607 | ||||||
| chr6:17479607 | ATTT | A | 9 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0084 others(6): Show |
9 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+16554_300+1655 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17479607 | ||||||
| chr6:17479635 | A | G | 5 | a0001c0001t0001g0091 a0001c0002t0001g0130 a0001c0002t0001g0132 others(2): Show |
5 | HG00735.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+16562A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479635 | |||||||
| chr6:17479697 | C | T | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+16624C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479697 | |||||||
| chr6:17479758 | C | T | 1 | a0001c0001t0002g0181 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.300+16685C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479758 | |||||||
| chr6:17479761 | G | A | 1 | a0001c0003t0002g0086 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.300+16688G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479761 | |||||||
| chr6:17479802 | A | G | 1 | a0001c0001t0002g0158 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.300+16729A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479802 | |||||||
| chr6:17479858 | G | A | 115 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(112): Show |
115 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.300+16785G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479858 | |||||||
| chr6:17479866 | C | T | 2 | a0001c0002t0001g0062 a0001c0002t0002g0079 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.300+16793C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479866 | |||||||
| chr6:17479867 | G | A | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+16794G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17479867 | |||||||
| chr6:17480144 | C | G | 1 | a0002c0004t0001g0073 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.300+17071C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480144 | |||||||
| chr6:17480156 | G | A | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.300+17083G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480156 | |||||||
| chr6:17480294 | G | T | 3 | a0001c0002t0001g0101 a0001c0002t0001g0112 a0001c0008t0001g0204 |
3 | HG02055.hp2 HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.300+17221G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480294 | |||||||
| chr6:17480639 | T | A | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.300+17566T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480639 | |||||||
| chr6:17480761 | G | A | 1 | a0002c0004t0001g0073 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.300+17688G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480761 | |||||||
| chr6:17480771 | T | G | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.300+17698T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480771 | |||||||
| chr6:17480771 | T | TG | 11 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0099 others(8): Show |
11 | HG02027.hp1 HG02109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+17700dupG | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17480771 | ||||||
| chr6:17480773 | GT | G | 28 | a0001c0001t0001g0091 a0001c0001t0002g0003 a0001c0001t0002g0038 others(25): Show |
28 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.300+17719delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17480773 | ||||||
| chr6:17480774 | T | G | 132 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0017 others(129): Show |
132 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.300+17701T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480774 | |||||||
| chr6:17480775 | T | G | 28 | a0001c0001t0001g0091 a0001c0001t0002g0003 a0001c0001t0002g0038 others(25): Show |
28 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.300+17702T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480775 | |||||||
| chr6:17480806 | C | T | 3 | a0001c0002t0001g0058 a0001c0002t0001g0074 a0001c0008t0001g0057 |
3 | HG00642.hp1 HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.300+17733C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480806 | |||||||
| chr6:17480848 | C | T | 8 | a0001c0001t0001g0069 a0001c0001t0001g0196 a0001c0001t0001g0202 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+17775C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480848 | |||||||
| chr6:17480860 | C | A | 1 | a0001c0002t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.300+17787C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480860 | |||||||
| chr6:17480884 | C | A | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.300+17811C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480884 | |||||||
| chr6:17480908 | A | T | 1 | a0001c0002t0002g0114 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.300+17835A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480908 | |||||||
| chr6:17480921 | G | C | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.300+17848G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480921 | |||||||
| chr6:17480923 | T | G | 7 | a0001c0001t0002g0038 a0001c0002t0001g0002 a0001c0002t0001g0058 others(4): Show |
7 | HG00642.hp1 HG01243.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+17850T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17480923 | |||||||
| chr6:17480952 | A | AT | 7 | a0001c0001t0001g0040 a0001c0001t0001g0099 a0001c0001t0001g0202 others(4): Show |
7 | HG01106.hp1 HG01109.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+17905dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17480952 | ||||||
| chr6:17480952 | A | ATT | 7 | a0001c0001t0001g0068 a0001c0003t0001g0072 a0001c0003t0001g0075 others(4): Show |
7 | HG02109.hp1 HG02622.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+17904_300+1790 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17480952 | ||||||
| chr6:17480952 | AT | A | 121 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0017 others(118): Show |
121 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.300+17905delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17480952 | ||||||
| chr6:17480952 | ATT | A | 9 | a0001c0002t0001g0078 a0001c0003t0001g0065 a0001c0003t0002g0086 others(6): Show |
9 | HG01361.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+17904_300+1790 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17480952 | ||||||
| chr6:17481031 | T | A | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+17958T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481031 | |||||||
| chr6:17481141 | A | G | 32 | a0001c0001t0001g0049 a0001c0001t0001g0140 a0001c0001t0001g0142 others(29): Show |
32 | HG00438.hp2 HG00597.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.300+18068A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481141 | |||||||
| chr6:17481273 | C | A | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+18200C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481273 | |||||||
| chr6:17481452 | A | AT | 171 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(168): Show |
171 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.300+18379_300+1838 others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481452 | |||||||
| chr6:17481453 | C | A | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+18380C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481453 | |||||||
| chr6:17481644 | T | C | 3 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0002g0131 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.300+18571T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481644 | |||||||
| chr6:17481672 | A | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.300+18599A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481672 | |||||||
| chr6:17481741 | C | T | 3 | a0001c0003t0001g0065 a0001c0009t0001g0015 a0001c0014t0008g0016 |
3 | HG01361.hp2 HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+18668C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481741 | |||||||
| chr6:17481816 | C | T | 53 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(50): Show |
53 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.300+18743C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481816 | |||||||
| chr6:17481851 | G | C | 6 | a0001c0003t0001g0065 a0001c0009t0001g0015 a0001c0014t0008g0016 others(3): Show |
6 | HG01361.hp2 HG01496.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.300+18778G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17481851 | |||||||
| chr6:17482086 | G | A | 54 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(51): Show |
54 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.300+19013G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482086 | |||||||
| chr6:17482146 | C | T | 6 | a0001c0001t0002g0038 a0001c0002t0001g0002 a0001c0002t0001g0058 others(3): Show |
6 | HG00642.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+19073C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482146 | |||||||
| chr6:17482221 | C | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+19148C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482221 | |||||||
| chr6:17482449 | C | G | 8 | a0001c0001t0001g0069 a0001c0001t0001g0196 a0001c0001t0001g0202 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+19376C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482449 | |||||||
| chr6:17482453 | A | G | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.300+19380A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482453 | |||||||
| chr6:17482507 | C | CA | 13 | a0001c0001t0001g0040 a0001c0001t0001g0092 a0001c0001t0002g0141 others(10): Show |
13 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.300+19466dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | ||||||
| chr6:17482507 | C | CAA | 5 | a0001c0002t0001g0136 a0001c0002t0001g0184 a0001c0014t0008g0016 others(2): Show |
5 | HG01175.hp1 HG01261.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+19465_300+1946 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | ||||||
| chr6:17482507 | CAA | C | 8 | a0001c0001t0001g0067 a0001c0001t0002g0038 a0001c0002t0001g0002 others(5): Show |
8 | HG00642.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.300+19465_300+1946 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | ||||||
| chr6:17482507 | CAAA | C | 9 | a0001c0001t0001g0068 a0001c0003t0001g0072 a0001c0003t0001g0075 others(6): Show |
9 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+19464_300+1946 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | ||||||
| chr6:17482507 | CAAAAAAA others(3): Show |
C | 15 | a0001c0001t0001g0019 a0001c0001t0001g0080 a0001c0001t0001g0081 others(12): Show |
15 | HG00438.hp1 HG01167.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.300+19457_300+1946 others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | ||||||
| chr6:17482507 | CAAAAAAA others(4): Show |
C | 112 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(109): Show |
112 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.300+19456_300+1946 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | ||||||
| chr6:17482507 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.300+19455_300+1946 others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | ||||||
| chr6:17482507 | CAAAAAAA others(8): Show |
C | 14 | a0001c0001t0001g0069 a0001c0001t0001g0091 a0001c0001t0001g0196 others(11): Show |
14 | HG00735.hp2 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.300+19452_300+1946 others(19): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | ||||||
| chr6:17482507 | CAAAAAAA others(9): Show |
C | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+19451_300+1946 others(20): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17482507 | ||||||
| chr6:17482540 | G | A | 6 | a0001c0003t0001g0065 a0001c0009t0001g0015 a0001c0014t0008g0016 others(3): Show |
6 | HG01361.hp2 HG01496.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.300+19467G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482540 | |||||||
| chr6:17482595 | C | T | 3 | a0001c0003t0001g0065 a0001c0009t0001g0015 a0001c0014t0008g0016 |
3 | HG01361.hp2 HG01496.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300+19522C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482595 | |||||||
| chr6:17482868 | T | C | 1 | a0002c0004t0001g0073 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.300+19795T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482868 | |||||||
| chr6:17482889 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.300+19816C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482889 | |||||||
| chr6:17482974 | C | T | 5 | a0001c0001t0001g0091 a0001c0002t0001g0130 a0001c0002t0001g0132 others(2): Show |
5 | HG00735.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+19901C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17482974 | |||||||
| chr6:17483151 | TG | T | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+20082delG | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17483151 | ||||||
| chr6:17483210 | GTGTCT | G | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.300+20141_300+2014 others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17483210 | ||||||
| chr6:17483298 | G | T | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+20225G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483298 | |||||||
| chr6:17483329 | T | C | 5 | a0001c0001t0001g0091 a0001c0002t0001g0130 a0001c0002t0001g0132 others(2): Show |
5 | HG00735.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+20256T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483329 | |||||||
| chr6:17483339 | T | C | 2 | a0001c0002t0001g0191 a0001c0002t0001g0192 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.300+20266T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483339 | |||||||
| chr6:17483420 | G | A | 1 | a0001c0002t0001g0012 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.300+20347G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483420 | |||||||
| chr6:17483437 | A | G | 6 | a0001c0002t0001g0020 a0001c0002t0001g0144 a0001c0002t0001g0145 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.300+20364A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483437 | |||||||
| chr6:17483605 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.300+20532G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483605 | |||||||
| chr6:17483636 | C | T | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.300+20563C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483636 | |||||||
| chr6:17483644 | C | T | 127 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(124): Show |
127 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.300+20571C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483644 | |||||||
| chr6:17483808 | T | G | 4 | a0001c0002t0001g0020 a0001c0002t0001g0144 a0001c0002t0001g0145 others(1): Show |
4 | HG02486.hp1 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+20735T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483808 | |||||||
| chr6:17483850 | A | G | 8 | a0001c0001t0001g0069 a0001c0001t0001g0196 a0001c0001t0001g0202 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+20777A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483850 | |||||||
| chr6:17483906 | C | G | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 |
3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+20833C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483906 | |||||||
| chr6:17483920 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.300+20847C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483920 | |||||||
| chr6:17483961 | C | T | 4 | a0001c0001t0001g0091 a0001c0002t0001g0130 a0001c0002t0001g0132 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+20888C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17483961 | |||||||
| chr6:17484021 | C | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0010 |
2 | HG03831.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.300+20948C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484021 | |||||||
| chr6:17484112 | G | C | 1 | a0001c0001t0002g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.300+21039G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484112 | |||||||
| chr6:17484122 | T | G | 7 | a0001c0001t0001g0069 a0001c0001t0001g0196 a0001c0001t0002g0199 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.300+21049T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484122 | |||||||
| chr6:17484280 | G | A | 14 | a0001c0001t0001g0069 a0001c0001t0001g0196 a0001c0001t0001g0202 others(11): Show |
14 | HG00642.hp1 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.300+21207G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484280 | |||||||
| chr6:17484288 | G | A | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.300+21215G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484288 | |||||||
| chr6:17484322 | C | T | 2 | a0001c0002t0001g0077 a0001c0002t0001g0078 |
2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.300+21249C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484322 | |||||||
| chr6:17484324 | C | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.300+21251C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484324 | |||||||
| chr6:17484326 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.300+21253C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484326 | |||||||
| chr6:17484362 | G | C | 1 | a0001c0002t0002g0114 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.300+21289G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484362 | |||||||
| chr6:17484372 | G | A | 5 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+21299G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484372 | |||||||
| chr6:17484387 | T | C | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.300+21314T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484387 | |||||||
| chr6:17484438 | C | T | 4 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0002g0131 others(1): Show |
4 | HG01255.hp1 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+21365C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484438 | |||||||
| chr6:17484484 | A | C | 1 | a0001c0002t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.300+21411A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484484 | |||||||
| chr6:17484628 | C | T | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.300+21555C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484628 | |||||||
| chr6:17484637 | A | G | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.300+21564A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484637 | |||||||
| chr6:17484904 | T | G | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.300+21831T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484904 | |||||||
| chr6:17484952 | A | T | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.300+21879A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17484952 | |||||||
| chr6:17485014 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.300+21941A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485014 | |||||||
| chr6:17485148 | G | GT | 5 | a0001c0001t0002g0003 a0001c0002t0001g0020 a0001c0002t0001g0144 others(2): Show |
5 | HG02486.hp1 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-22011dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17485148 | ||||||
| chr6:17485148 | G | T | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-22021G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485148 | |||||||
| chr6:17485309 | A | C | 8 | a0001c0003t0001g0065 a0001c0009t0001g0013 a0001c0009t0001g0015 others(5): Show |
8 | HG01361.hp2 HG01496.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-21860A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485309 | |||||||
| chr6:17485439 | A | G | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-21730A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485439 | |||||||
| chr6:17485449 | C | T | 4 | a0001c0001t0001g0091 a0001c0002t0001g0130 a0001c0002t0001g0132 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-21720C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485449 | |||||||
| chr6:17485616 | A | T | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.301-21553A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485616 | |||||||
| chr6:17485673 | A | T | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-21496A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485673 | |||||||
| chr6:17485828 | T | C | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-21341T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485828 | |||||||
| chr6:17485856 | C | T | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-21313C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485856 | |||||||
| chr6:17485890 | G | A | 8 | a0001c0001t0001g0069 a0001c0001t0001g0196 a0001c0001t0002g0038 others(5): Show |
8 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.301-21279G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485890 | |||||||
| chr6:17485915 | G | A | 6 | a0001c0003t0001g0065 a0001c0009t0001g0015 a0001c0014t0008g0016 others(3): Show |
6 | HG01361.hp2 HG01496.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-21254G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17485915 | |||||||
| chr6:17486281 | C | T | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-20888C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486281 | |||||||
| chr6:17486437 | C | T | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-20732C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486437 | |||||||
| chr6:17486457 | T | C | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.301-20712T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486457 | |||||||
| chr6:17486536 | G | A | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.301-20633G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486536 | |||||||
| chr6:17486765 | G | A | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-20404G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486765 | |||||||
| chr6:17486893 | AC | A | 41 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(38): Show |
41 | HG00642.hp1 HG01109.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.301-20271delC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17486893 | ||||||
| chr6:17486912 | A | C | 5 | a0001c0001t0001g0045 a0001c0001t0002g0011 a0001c0001t0002g0043 others(2): Show |
5 | HG00099.hp1 HG01175.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-20257A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486912 | |||||||
| chr6:17486921 | A | G | 2 | a0001c0009t0001g0013 a0001c0013t0001g0076 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-20248A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17486921 | |||||||
| chr6:17487275 | A | G | 56 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(53): Show |
56 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.301-19894A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487275 | |||||||
| chr6:17487340 | T | C | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 |
3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-19829T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487340 | |||||||
| chr6:17487406 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.301-19763T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487406 | |||||||
| chr6:17487452 | GGTTT | G | 39 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0081 others(36): Show |
39 | HG00642.hp1 HG01109.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.301-19688_301-1968 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17487452 | ||||||
| chr6:17487538 | T | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0178 a0001c0001t0002g0172 others(2): Show |
5 | HG02135.hp1 NA18612.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-19631T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487538 | |||||||
| chr6:17487562 | C | T | 2 | a0001c0002t0001g0062 a0001c0002t0002g0079 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.301-19607C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487562 | |||||||
| chr6:17487630 | C | T | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG01167.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.301-19539C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487630 | |||||||
| chr6:17487678 | C | T | 2 | a0001c0002t0001g0144 a0001c0002t0001g0145 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-19491C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17487678 | |||||||
| chr6:17488004 | G | A | 1 | a0001c0001t0005g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.301-19165G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488004 | |||||||
| chr6:17488033 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(38): Show |
41 | HG00438.hp1 HG01192.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.301-19136T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488033 | |||||||
| chr6:17488037 | G | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(38): Show |
41 | HG00438.hp1 HG01192.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.301-19132G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488037 | |||||||
| chr6:17488068 | C | G | 3 | a0001c0002t0001g0198 a0001c0009t0001g0013 a0001c0013t0001g0076 |
3 | HG02055.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.301-19101C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488068 | |||||||
| chr6:17488181 | T | G | 8 | a0001c0001t0001g0091 a0001c0002t0001g0130 a0001c0002t0001g0132 others(5): Show |
8 | HG01255.hp1 HG01361.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.301-18988T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488181 | |||||||
| chr6:17488287 | T | G | 3 | a0001c0002t0001g0198 a0001c0009t0001g0013 a0001c0013t0001g0076 |
3 | HG02055.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.301-18882T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488287 | |||||||
| chr6:17488355 | T | C | 3 | a0001c0002t0001g0198 a0001c0009t0001g0013 a0001c0013t0001g0076 |
3 | HG02055.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.301-18814T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17488355 | |||||||
| chr6:17489001 | C | T | 1 | a0001c0002t0001g0161 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.301-18168C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489001 | |||||||
| chr6:17489002 | G | A | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.301-18167G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489002 | |||||||
| chr6:17489123 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.301-18046C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489123 | |||||||
| chr6:17489204 | C | T | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-17965C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489204 | |||||||
| chr6:17489301 | A | T | 1 | a0001c0002t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.301-17868A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489301 | |||||||
| chr6:17489331 | C | T | 14 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0081 others(11): Show |
14 | HG00735.hp2 HG01167.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.301-17838C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489331 | |||||||
| chr6:17489497 | A | C | 3 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0001c0003t0002g0131 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.301-17672A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489497 | |||||||
| chr6:17489531 | G | C | 1 | a0002c0012t0001g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.301-17638G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489531 | |||||||
| chr6:17489589 | C | T | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.301-17580C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489589 | |||||||
| chr6:17489593 | T | G | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-17576T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489593 | |||||||
| chr6:17489656 | G | C | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-17513G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489656 | |||||||
| chr6:17489687 | G | A | 2 | a0002c0004t0002g0182 a0002c0005t0001g0203 |
2 | NA19003.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.301-17482G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17489687 | |||||||
| chr6:17489748 | G | GA | 2 | a0001c0001t0001g0196 a0001c0001t0005g0200 |
2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.301-17420dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17489748 | ||||||
| chr6:17490247 | A | G | 1 | a0001c0003t0001g0039 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.301-16922A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17490247 | |||||||
| chr6:17490284 | A | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(5): Show |
8 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-16885A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17490284 | |||||||
| chr6:17490614 | G | A | 5 | a0001c0002t0001g0107 a0001c0002t0001g0128 a0001c0002t0001g0136 others(2): Show |
5 | HG00099.hp2 HG01071.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-16555G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17490614 | |||||||
| chr6:17490653 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.301-16516G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17490653 | |||||||
| chr6:17491129 | C | T | 9 | a0001c0001t0002g0102 a0001c0002t0001g0108 a0001c0002t0002g0111 others(6): Show |
9 | HG01496.hp1 HG01928.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-16040C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491129 | |||||||
| chr6:17491172 | A | G | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.301-15997A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491172 | |||||||
| chr6:17491174 | G | A | 1 | a0001c0002t0001g0062 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.301-15995G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491174 | |||||||
| chr6:17491485 | T | C | 1 | a0001c0002t0001g0128 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.301-15684T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491485 | |||||||
| chr6:17491511 | C | T | 17 | a0001c0001t0001g0052 a0001c0002t0001g0020 a0001c0002t0001g0130 others(14): Show |
17 | HG00597.hp1 HG01361.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.301-15658C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491511 | |||||||
| chr6:17491721 | G | A | 1 | a0001c0014t0008g0016 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.301-15448G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491721 | |||||||
| chr6:17491914 | A | G | 2 | a0001c0002t0001g0093 a0001c0002t0001g0094 |
2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.301-15255A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491914 | |||||||
| chr6:17491928 | T | A | 10 | a0001c0001t0001g0068 a0001c0001t0002g0038 a0001c0002t0001g0130 others(7): Show |
10 | HG01255.hp1 HG01361.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.301-15241T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491928 | |||||||
| chr6:17491952 | A | G | 1 | a0001c0002t0001g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.301-15217A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17491952 | |||||||
| chr6:17492022 | T | C | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.301-15147T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492022 | |||||||
| chr6:17492123 | C | A | 4 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0009t0001g0013 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-15046C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492123 | |||||||
| chr6:17492159 | G | A | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0008t0001g0051 |
3 | HG02486.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-15010G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492159 | |||||||
| chr6:17492294 | C | CAA | 6 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-14868_301-1486 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17492294 | ||||||
| chr6:17492529 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.301-14640T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492529 | |||||||
| chr6:17492622 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.301-14547G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492622 | |||||||
| chr6:17492692 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.301-14477G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492692 | |||||||
| chr6:17492862 | A | G | 120 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(117): Show |
120 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.301-14307A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17492862 | |||||||
| chr6:17493077 | A | T | 46 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0049 others(43): Show |
46 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.301-14092A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17493077 | |||||||
| chr6:17493294 | C | CT | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-13873dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17493294 | ||||||
| chr6:17493330 | A | AAGATATG others(9): Show |
3 | a0001c0001t0001g0029 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG01168.hp2 HG01975.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.301-13837_301-1382 others(20): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17493330 | ||||||
| chr6:17493459 | C | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(121): Show |
124 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.301-13710C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17493459 | |||||||
| chr6:17493564 | C | G | 1 | a0001c0001t0001g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.301-13605C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17493564 | |||||||
| chr6:17493775 | C | CA | 15 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(12): Show |
15 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.301-13379dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17493775 | ||||||
| chr6:17493775 | C | CAA | 44 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0017 others(41): Show |
44 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.301-13380_301-1337 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17493775 | ||||||
| chr6:17493860 | G | A | 1 | a0001c0002t0001g0020 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.301-13309G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17493860 | |||||||
| chr6:17493865 | C | T | 1 | a0001c0014t0008g0016 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.301-13304C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17493865 | |||||||
| chr6:17493872 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0042 others(91): Show |
94 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.301-13297G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17493872 | |||||||
| chr6:17494117 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0042 others(92): Show |
95 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.301-13052A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494117 | |||||||
| chr6:17494139 | G | A | 2 | a0001c0002t0001g0093 a0001c0002t0001g0094 |
2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.301-13030G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494139 | |||||||
| chr6:17494232 | T | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(41): Show |
44 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.301-12937T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494232 | |||||||
| chr6:17494334 | G | A | 77 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0049 others(74): Show |
77 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.301-12835G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494334 | |||||||
| chr6:17494507 | C | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0042 others(91): Show |
94 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.301-12662C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494507 | |||||||
| chr6:17494547 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0042 others(93): Show |
96 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.301-12622G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494547 | |||||||
| chr6:17494669 | G | A | 7 | a0001c0003t0001g0039 a0001c0003t0001g0090 a0001c0003t0002g0060 others(4): Show |
7 | HG02109.hp1 HG02647.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.301-12500G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494669 | |||||||
| chr6:17494776 | C | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0042 |
2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301-12393C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494776 | |||||||
| chr6:17494807 | T | C | 1 | a0001c0002t0001g0098 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.301-12362T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494807 | |||||||
| chr6:17494903 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0042 others(91): Show |
94 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.301-12266C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494903 | |||||||
| chr6:17494934 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.301-12235T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494934 | |||||||
| chr6:17494967 | A | T | 1 | a0001c0002t0001g0136 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.301-12202A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17494967 | |||||||
| chr6:17495108 | C | G | 1 | a0001c0006t0001g0121 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.301-12061C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495108 | |||||||
| chr6:17495229 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.301-11940G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495229 | |||||||
| chr6:17495259 | C | G | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-11910C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495259 | |||||||
| chr6:17495371 | C | A | 123 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(120): Show |
123 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.301-11798C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495371 | |||||||
| chr6:17495448 | C | G | 1 | a0001c0001t0002g0011 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.301-11721C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495448 | |||||||
| chr6:17495882 | G | A | 6 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0196 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-11287G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495882 | |||||||
| chr6:17495939 | C | G | 78 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0049 others(75): Show |
78 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.301-11230C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495939 | |||||||
| chr6:17495968 | C | T | 24 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(21): Show |
24 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.301-11201C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17495968 | |||||||
| chr6:17496027 | T | TG | 16 | a0001c0001t0001g0103 a0001c0001t0001g0202 a0001c0001t0002g0038 others(13): Show |
16 | HG01109.hp2 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.301-11130dupG | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496027 | ||||||
| chr6:17496027 | T | TGGCG | 17 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0023 others(14): Show |
17 | HG01071.hp2 HG01168.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.301-11140_301-1113 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496027 | ||||||
| chr6:17496027 | T | TGGCGG | 40 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0019 others(37): Show |
40 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.301-11140_301-1113 others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496027 | ||||||
| chr6:17496027 | T | TGGCGGG | 39 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0140 others(36): Show |
39 | HG00438.hp2 HG00597.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.301-11140_301-1113 others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496027 | ||||||
| chr6:17496027 | T | TGGCGGGG others(4): Show |
1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.301-11140_301-1113 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496027 | ||||||
| chr6:17496030 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.301-11139G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496030 | |||||||
| chr6:17496032 | G | T | 4 | a0001c0002t0001g0036 a0001c0002t0001g0188 a0001c0002t0001g0189 others(1): Show |
4 | HG00741.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-11137G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496032 | |||||||
| chr6:17496033 | G | A | 6 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0196 others(3): Show |
6 | HG01517.hp1 HG01884.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-11136G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496033 | |||||||
| chr6:17496033 | G | GGT | 23 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(20): Show |
23 | HG00735.hp2 HG01167.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.301-11135_301-1113 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496033 | ||||||
| chr6:17496036 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.301-11133G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496036 | |||||||
| chr6:17496036 | G | T | 1 | a0001c0002t0001g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.301-11133G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496036 | |||||||
| chr6:17496037 | G | T | 3 | a0001c0002t0001g0002 a0002c0004t0002g0097 a0002c0005t0003g0171 |
3 | HG02258.hp1 NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.301-11132G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496037 | |||||||
| chr6:17496141 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.301-11028A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496141 | |||||||
| chr6:17496303 | C | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(149): Show |
152 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.301-10866C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496303 | |||||||
| chr6:17496326 | A | AGTATCTT | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0009t0001g0013 |
3 | HG02145.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.301-10840_301-1083 others(11): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17496326 | ||||||
| chr6:17496440 | C | T | 2 | a0001c0002t0001g0020 a0001c0002t0002g0118 |
2 | HG03834.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.301-10729C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496440 | |||||||
| chr6:17496721 | G | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-10448G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496721 | |||||||
| chr6:17496830 | T | C | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-10339T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17496830 | |||||||
| chr6:17497231 | A | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(46): Show |
49 | HG00438.hp1 HG00642.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.301-9938A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17497231 | |||||||
| chr6:17497260 | T | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(149): Show |
152 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.301-9909T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17497260 | |||||||
| chr6:17497361 | C | T | 1 | a0001c0003t0002g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.301-9808C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17497361 | |||||||
| chr6:17497704 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(126): Show |
129 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.301-9465T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17497704 | |||||||
| chr6:17498123 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.301-9046G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17498123 | |||||||
| chr6:17498346 | G | A | 2 | a0001c0003t0002g0064 a0001c0003t0002g0071 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.301-8823G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17498346 | |||||||
| chr6:17498622 | T | C | 84 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(81): Show |
84 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.301-8547T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17498622 | |||||||
| chr6:17498864 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.301-8305G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17498864 | |||||||
| chr6:17498891 | G | A | 1 | a0001c0002t0001g0138 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.301-8278G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17498891 | |||||||
| chr6:17499398 | C | CA | 81 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0029 others(78): Show |
81 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.301-7749dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499398 | ||||||
| chr6:17499398 | C | CAA | 5 | a0001c0001t0001g0069 a0001c0001t0002g0044 a0001c0002t0002g0079 others(2): Show |
5 | HG01175.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-7750_301-7749d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499398 | ||||||
| chr6:17499398 | C | CAAAAAAA others(1): Show |
5 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-7756_301-7749d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499398 | ||||||
| chr6:17499398 | CA | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0159 a0001c0002t0001g0153 others(2): Show |
5 | HG02970.hp1 HG03017.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-7749delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499398 | ||||||
| chr6:17499398 | CAA | C | 16 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(13): Show |
16 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.301-7750_301-7749d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499398 | ||||||
| chr6:17499612 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.301-7557G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17499612 | |||||||
| chr6:17499624 | G | A | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-7545G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17499624 | |||||||
| chr6:17499657 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0042 |
2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301-7512T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17499657 | |||||||
| chr6:17499848 | C | CATAA | 51 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0029 others(48): Show |
51 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.301-7291_301-7288d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499848 | ||||||
| chr6:17499848 | C | CATAAATA others(1): Show |
75 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0019 others(72): Show |
75 | HG00438.hp1 HG00597.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.301-7295_301-7288d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499848 | ||||||
| chr6:17499848 | C | CATAAATA others(5): Show |
23 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0026 others(20): Show |
23 | HG01361.hp1 HG01361.hp2 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.301-7299_301-7288d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499848 | ||||||
| chr6:17499848 | C | CATAAATA others(9): Show |
1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.301-7303_301-7288d others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17499848 | ||||||
| chr6:17500284 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.301-6885G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500284 | |||||||
| chr6:17500340 | A | AAT | 9 | a0001c0001t0001g0123 a0001c0001t0002g0120 a0001c0001t0002g0170 others(6): Show |
9 | HG01928.hp2 HG02027.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-6786_301-6785d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATAT | 12 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0165 others(9): Show |
12 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-6788_301-6785d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATAT | 10 | a0001c0001t0001g0045 a0001c0002t0001g0094 a0001c0002t0001g0098 others(7): Show |
10 | HG00099.hp1 HG00741.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.301-6790_301-6785d others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATATA others(1): Show |
18 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0030 others(15): Show |
18 | HG00609.hp1 HG01071.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.301-6792_301-6785d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATATA others(3): Show |
19 | a0001c0001t0001g0069 a0001c0001t0001g0142 a0001c0001t0002g0024 others(16): Show |
19 | HG00099.hp2 HG01175.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.301-6794_301-6785d others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATATA others(5): Show |
28 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0081 others(25): Show |
28 | HG01106.hp2 HG01109.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.301-6796_301-6785d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATATA others(7): Show |
14 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0095 others(11): Show |
14 | HG00438.hp1 HG00735.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.301-6798_301-6785d others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATATA others(9): Show |
7 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0092 others(4): Show |
7 | HG00741.hp2 HG01168.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-6800_301-6785d others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATATA others(11): Show |
14 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0103 others(11): Show |
14 | HG00735.hp1 HG01109.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.301-6802_301-6785d others(20): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATATA others(13): Show |
7 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0174 others(4): Show |
7 | HG02027.hp2 HG02071.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-6804_301-6785d others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATATA others(15): Show |
4 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0002g0162 others(1): Show |
4 | HG02818.hp2 HG03195.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-6806_301-6785d others(24): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATATA others(17): Show |
2 | a0001c0001t0002g0137 a0001c0002t0001g0125 |
2 | HG01071.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.301-6808_301-6785d others(26): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATATA others(19): Show |
3 | a0001c0001t0001g0008 a0001c0001t0002g0028 a0004c0010t0001g0063 |
3 | HG01192.hp1 HG02897.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.301-6810_301-6785d others(28): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATATA others(21): Show |
1 | a0002c0005t0001g0004 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.301-6812_301-6785d others(30): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATATA others(25): Show |
1 | a0001c0002t0001g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.301-6816_301-6785d others(34): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | AATATATA others(27): Show |
1 | a0001c0001t0002g0126 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.301-6818_301-6785d others(36): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0145 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.301-6829_301-6828i others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500340 | |||||||
| chr6:17500340 | A | ATATATAT others(6): Show |
1 | a0002c0004t0002g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.301-6829_301-6828i others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500340 | |||||||
| chr6:17500340 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.301-6829_301-6828i others(23): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500340 | |||||||
| chr6:17500340 | AAT | A | 11 | a0001c0001t0001g0054 a0001c0001t0001g0180 a0001c0001t0002g0096 others(8): Show |
11 | HG00597.hp2 HG01928.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.301-6786_301-6785d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | AATAT | A | 4 | a0001c0001t0001g0053 a0001c0001t0002g0027 a0001c0002t0001g0056 others(1): Show |
4 | HG03669.hp2 HG04228.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-6788_301-6785d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | AATATAT | A | 4 | a0001c0001t0001g0017 a0001c0002t0001g0006 a0001c0002t0001g0062 others(1): Show |
4 | HG02109.hp2 HG03491.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-6790_301-6785d others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | AATATATA others(3): Show |
A | 1 | a0001c0003t0002g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.301-6794_301-6785d others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | AATATATA others(5): Show |
A | 2 | a0001c0001t0001g0021 a0001c0001t0002g0022 |
2 | HG02083.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.301-6796_301-6785d others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | AATATATA others(9): Show |
A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.301-6800_301-6785d others(18): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | AATATATA others(13): Show |
A | 5 | a0001c0001t0002g0102 a0001c0001t0002g0147 a0001c0001t0002g0169 others(2): Show |
5 | HG01255.hp2 HG01261.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-6804_301-6785d others(22): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | AATATATA others(19): Show |
A | 1 | a0001c0001t0002g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.301-6810_301-6785d others(28): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | AATATATA others(21): Show |
A | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.301-6812_301-6785d others(30): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500340 | AATATATA others(25): Show |
A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0124 |
3 | HG02280.hp1 HG02738.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301-6816_301-6785d others(34): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500340 | ||||||
| chr6:17500368 | T | TATATATA others(21): Show |
1 | a0001c0014t0008g0016 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.301-6785_301-6784i others(30): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17500368 | ||||||
| chr6:17500384 | T | TATATATA others(4): Show |
1 | a0001c0001t0001g0151 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.301-6785_301-6784i others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500384 | |||||||
| chr6:17500384 | T | TATATATA others(14): Show |
1 | a0001c0001t0002g0032 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.301-6785_301-6784i others(23): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500384 | |||||||
| chr6:17500431 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.301-6738C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500431 | |||||||
| chr6:17500762 | A | G | 1 | a0001c0014t0008g0016 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.301-6407A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500762 | |||||||
| chr6:17500846 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.301-6323C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500846 | |||||||
| chr6:17500908 | A | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.301-6261A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17500908 | |||||||
| chr6:17501122 | G | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0042 |
2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301-6047G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501122 | |||||||
| chr6:17501327 | G | A | 1 | a0001c0003t0002g0086 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.301-5842G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501327 | |||||||
| chr6:17501382 | C | G | 1 | a0001c0014t0008g0016 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.301-5787C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501382 | |||||||
| chr6:17501447 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.301-5722T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501447 | |||||||
| chr6:17501476 | G | A | 12 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(9): Show |
12 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-5693G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501476 | |||||||
| chr6:17501836 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.301-5333G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501836 | |||||||
| chr6:17501880 | C | T | 12 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(9): Show |
12 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-5289C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17501880 | |||||||
| chr6:17502039 | T | C | 1 | a0006c0016t0001g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.301-5130T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17502039 | |||||||
| chr6:17502083 | G | A | 1 | a0002c0012t0001g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.301-5086G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17502083 | |||||||
| chr6:17502705 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(150): Show |
153 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.301-4464T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17502705 | |||||||
| chr6:17502891 | C | T | 12 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(9): Show |
12 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-4278C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17502891 | |||||||
| chr6:17503180 | G | A | 2 | a0001c0002t0001g0125 a0001c0002t0002g0129 |
2 | HG01167.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.301-3989G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503180 | |||||||
| chr6:17503275 | C | T | 2 | a0001c0002t0001g0107 a0001c0002t0001g0184 |
2 | HG00099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.301-3894C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503275 | |||||||
| chr6:17503320 | C | G | 1 | a0001c0003t0002g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.301-3849C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503320 | |||||||
| chr6:17503477 | G | A | 1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.301-3692G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503477 | |||||||
| chr6:17503559 | G | A | 12 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(9): Show |
12 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-3610G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503559 | |||||||
| chr6:17503563 | C | T | 12 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(9): Show |
12 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-3606C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503563 | |||||||
| chr6:17503598 | C | G | 84 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(81): Show |
84 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.301-3571C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503598 | |||||||
| chr6:17503604 | C | CA | 15 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0023 others(12): Show |
15 | HG01106.hp1 HG01106.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.301-3544dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17503604 | ||||||
| chr6:17503604 | CA | C | 25 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(22): Show |
25 | HG00597.hp1 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.301-3544delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17503604 | ||||||
| chr6:17503698 | A | G | 1 | a0001c0001t0002g0028 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.301-3471A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503698 | |||||||
| chr6:17503971 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.301-3198A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17503971 | |||||||
| chr6:17504177 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.301-2992T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504177 | |||||||
| chr6:17504271 | A | C | 142 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(139): Show |
142 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.301-2898A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504271 | |||||||
| chr6:17504337 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.301-2832T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504337 | |||||||
| chr6:17504344 | T | A | 1 | a0001c0001t0002g0031 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.301-2825T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504344 | |||||||
| chr6:17504345 | G | T | 1 | a0001c0001t0002g0031 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.301-2824G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504345 | |||||||
| chr6:17504346 | G | T | 1 | a0001c0001t0002g0031 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.301-2823G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504346 | |||||||
| chr6:17504347 | T | G | 1 | a0001c0001t0002g0031 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.301-2822T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504347 | |||||||
| chr6:17504537 | G | A | 1 | a0001c0002t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.301-2632G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504537 | |||||||
| chr6:17504861 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.301-2308T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17504861 | |||||||
| chr6:17505073 | C | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0042 |
2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301-2096C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505073 | |||||||
| chr6:17505114 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-2055C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505114 | |||||||
| chr6:17505158 | T | G | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.301-2011T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505158 | |||||||
| chr6:17505326 | C | T | 1 | a0001c0002t0002g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.301-1843C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505326 | |||||||
| chr6:17505518 | T | A | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.301-1651T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505518 | |||||||
| chr6:17505532 | C | T | 1 | a0002c0004t0002g0097 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.301-1637C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505532 | |||||||
| chr6:17505713 | A | G | 134 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
134 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.301-1456A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505713 | |||||||
| chr6:17505841 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.301-1328C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505841 | |||||||
| chr6:17505880 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(150): Show |
153 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.301-1289C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505880 | |||||||
| chr6:17505885 | C | T | 134 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
134 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.301-1284C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17505885 | |||||||
| chr6:17506017 | C | G | 1 | a0006c0016t0001g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.301-1152C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506017 | |||||||
| chr6:17506035 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-1134C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506035 | |||||||
| chr6:17506075 | T | A | 1 | a0002c0004t0002g0182 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.301-1094T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506075 | |||||||
| chr6:17506360 | T | C | 1 | a0002c0012t0001g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.301-809T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506360 | |||||||
| chr6:17506404 | G | A | 1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.301-765G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506404 | |||||||
| chr6:17506490 | A | C | 2 | a0001c0003t0002g0048 a0004c0010t0002g0061 |
2 | HG01255.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.301-679A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506490 | |||||||
| chr6:17506569 | G | A | 4 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | HG01167.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-600G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506569 | |||||||
| chr6:17506596 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0042 |
2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.301-573C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506596 | |||||||
| chr6:17506637 | CA | C | 97 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(94): Show |
97 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.301-520delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 17506637 | ||||||
| chr6:17506717 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.301-452A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506717 | |||||||
| chr6:17506793 | A | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(148): Show |
151 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.301-376A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506793 | |||||||
| chr6:17506817 | T | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.301-352T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506817 | |||||||
| chr6:17506946 | T | C | 2 | a0001c0002t0001g0006 a0001c0002t0001g0153 |
2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.301-223T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17506946 | |||||||
| chr6:17507025 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG02027.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.301-144T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17507025 | |||||||
| chr6:17507035 | G | C | 1 | a0001c0002t0001g0190 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.301-134G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17507035 | |||||||
| chr6:17507042 | A | G | 2 | a0001c0002t0001g0101 a0001c0002t0001g0112 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.301-127A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 4/12 | chr6 | 17507042 | |||||||
| chr6:17507439 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(152): Show |
155 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.444+127A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 5/12 | chr6 | 17507439 | |||||||
| chr6:17507485 | C | A | 2 | a0001c0002t0001g0006 a0001c0002t0001g0153 |
2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.445-156C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 5/12 | chr6 | 17507485 | |||||||
| chr6:17507730 | C | A | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | splice_region_variant&intron_variant | LOW | c.530+4C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17507730 | |||||||
| chr6:17507915 | T | C | 2 | a0001c0002t0001g0130 a0001c0002t0001g0132 |
2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.530+189T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17507915 | |||||||
| chr6:17507992 | T | A | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.530+266T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17507992 | |||||||
| chr6:17508593 | A | G | 145 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(142): Show |
145 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.530+867A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17508593 | |||||||
| chr6:17508755 | C | CT | 105 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0029 others(102): Show |
105 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.530+1042dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 17508755 | ||||||
| chr6:17508755 | C | CTT | 11 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0091 others(8): Show |
11 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.530+1041_530+1042d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 17508755 | ||||||
| chr6:17508755 | C | CTTT | 26 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0017 others(23): Show |
26 | HG00438.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.530+1040_530+1042d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 17508755 | ||||||
| chr6:17508755 | C | CTTTT | 6 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0080 others(3): Show |
6 | HG01167.hp2 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.530+1039_530+1042d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 17508755 | ||||||
| chr6:17508782 | A | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(33): Show |
36 | HG00438.hp1 HG00735.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.530+1056A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17508782 | |||||||
| chr6:17508838 | A | C | 2 | a0001c0002t0001g0191 a0001c0002t0001g0192 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.530+1112A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17508838 | |||||||
| chr6:17508997 | C | T | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.530+1271C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17508997 | |||||||
| chr6:17509161 | A | C | 1 | a0001c0002t0001g0164 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.530+1435A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17509161 | |||||||
| chr6:17509185 | G | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.530+1459G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17509185 | |||||||
| chr6:17509388 | A | G | 2 | a0001c0002t0001g0191 a0001c0002t0001g0192 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.530+1662A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17509388 | |||||||
| chr6:17509532 | G | A | 1 | a0002c0012t0001g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.530+1806G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17509532 | |||||||
| chr6:17509541 | G | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(4): Show |
7 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.530+1815G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17509541 | |||||||
| chr6:17509656 | C | G | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.530+1930C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17509656 | |||||||
| chr6:17510028 | A | T | 1 | a0001c0001t0001g0023 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.530+2302A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17510028 | |||||||
| chr6:17510065 | G | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0124 others(2): Show |
5 | HG02071.hp1 HG02071.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+2339G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17510065 | |||||||
| chr6:17510198 | G | A | 13 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(10): Show |
13 | HG00597.hp1 HG01891.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.530+2472G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17510198 | |||||||
| chr6:17510270 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.530+2544A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17510270 | |||||||
| chr6:17510889 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.531-2960G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17510889 | |||||||
| chr6:17510895 | C | T | 1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.531-2954C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17510895 | |||||||
| chr6:17511100 | A | G | 7 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.531-2749A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511100 | |||||||
| chr6:17511216 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.531-2633G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511216 | |||||||
| chr6:17511256 | C | T | 43 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(40): Show |
43 | HG00438.hp1 HG00735.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.531-2593C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511256 | |||||||
| chr6:17511271 | C | T | 9 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0091 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.531-2578C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511271 | |||||||
| chr6:17511364 | T | C | 1 | a0001c0001t0002g0050 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.531-2485T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511364 | |||||||
| chr6:17511396 | T | C | 11 | a0001c0002t0001g0108 a0001c0002t0001g0166 a0001c0002t0002g0111 others(8): Show |
11 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.531-2453T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511396 | |||||||
| chr6:17511450 | C | T | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.531-2399C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511450 | |||||||
| chr6:17511474 | C | G | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.531-2375C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511474 | |||||||
| chr6:17511517 | T | C | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0002t0001g0198 |
3 | HG02630.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.531-2332T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511517 | |||||||
| chr6:17511537 | T | C | 132 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(129): Show |
132 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.531-2312T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511537 | |||||||
| chr6:17511744 | C | G | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.531-2105C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511744 | |||||||
| chr6:17511821 | G | C | 5 | a0001c0001t0002g0003 a0001c0002t0001g0130 a0001c0002t0001g0132 others(2): Show |
5 | HG01255.hp1 HG02486.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.531-2028G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511821 | |||||||
| chr6:17511823 | C | A | 57 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(54): Show |
57 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.531-2026C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511823 | |||||||
| chr6:17511889 | G | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(21): Show |
24 | HG00438.hp1 HG00741.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.531-1960G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17511889 | |||||||
| chr6:17512225 | T | C | 1 | a0002c0004t0002g0083 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.531-1624T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512225 | |||||||
| chr6:17512401 | A | G | 5 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(2): Show |
5 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-1448A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512401 | |||||||
| chr6:17512411 | G | A | 91 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(88): Show |
91 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.531-1438G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512411 | |||||||
| chr6:17512599 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(151): Show |
154 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.531-1250T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512599 | |||||||
| chr6:17512637 | G | A | 2 | a0001c0002t0001g0098 a0001c0002t0001g0161 |
2 | HG00609.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.531-1212G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512637 | |||||||
| chr6:17512748 | A | T | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531-1101A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512748 | |||||||
| chr6:17512751 | C | G | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.531-1098C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512751 | |||||||
| chr6:17512752 | A | T | 1 | a0002c0005t0003g0171 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.531-1097A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17512752 | |||||||
| chr6:17513100 | A | T | 1 | a0001c0011t0002g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.531-749A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17513100 | |||||||
| chr6:17513424 | C | CT | 8 | a0001c0003t0001g0065 a0001c0003t0001g0072 a0001c0003t0001g0075 others(5): Show |
8 | HG01361.hp2 HG01496.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.531-416dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 17513424 | ||||||
| chr6:17513723 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(151): Show |
154 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.531-126T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17513723 | |||||||
| chr6:17513747 | C | A | 1 | a0001c0002t0002g0129 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.531-102C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 6/12 | chr6 | 17513747 | |||||||
| chr6:17514101 | C | A | 9 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0091 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.636+147C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514101 | |||||||
| chr6:17514174 | C | T | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.636+220C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514174 | |||||||
| chr6:17514231 | C | T | 1 | a0001c0006t0001g0121 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.636+277C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514231 | |||||||
| chr6:17514232 | G | A | 1 | a0001c0002t0002g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.636+278G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514232 | |||||||
| chr6:17514312 | G | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.636+358G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514312 | |||||||
| chr6:17514364 | A | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.636+410A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514364 | |||||||
| chr6:17514406 | G | T | 57 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(54): Show |
57 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.636+452G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514406 | |||||||
| chr6:17514502 | C | A | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0002t0001g0198 |
3 | HG02630.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.636+548C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514502 | |||||||
| chr6:17514582 | T | C | 82 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(79): Show |
82 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.636+628T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514582 | |||||||
| chr6:17514834 | G | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0153 |
2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.636+880G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514834 | |||||||
| chr6:17514863 | T | A | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+909T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514863 | |||||||
| chr6:17514867 | T | C | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+913T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514867 | |||||||
| chr6:17514869 | G | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.636+915G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514869 | |||||||
| chr6:17514877 | TTA | T | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+925_636+926del others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17514877 | ||||||
| chr6:17514983 | C | T | 10 | a0001c0001t0002g0150 a0002c0004t0002g0097 a0002c0004t0002g0156 others(7): Show |
10 | HG00597.hp1 HG01884.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.636+1029C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514983 | |||||||
| chr6:17514995 | C | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(5): Show |
8 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.636+1041C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17514995 | |||||||
| chr6:17515190 | C | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.636+1236C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17515190 | |||||||
| chr6:17515749 | T | C | 10 | a0001c0001t0002g0150 a0002c0004t0002g0097 a0002c0004t0002g0156 others(7): Show |
10 | HG00597.hp1 HG01884.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.636+1795T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17515749 | |||||||
| chr6:17515758 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(93): Show |
96 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.636+1804G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17515758 | |||||||
| chr6:17515931 | C | A | 9 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0091 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.636+1977C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17515931 | |||||||
| chr6:17515991 | G | A | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.636+2037G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17515991 | |||||||
| chr6:17516476 | G | C | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.636+2522G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17516476 | |||||||
| chr6:17516940 | T | G | 53 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(50): Show |
53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.636+2986T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17516940 | |||||||
| chr6:17517216 | A | G | 10 | a0001c0001t0002g0150 a0002c0004t0002g0097 a0002c0004t0002g0156 others(7): Show |
10 | HG00597.hp1 HG01884.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.636+3262A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517216 | |||||||
| chr6:17517425 | T | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.636+3471T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517425 | |||||||
| chr6:17517459 | G | T | 6 | a0001c0003t0001g0065 a0001c0003t0001g0072 a0001c0003t0001g0075 others(3): Show |
6 | HG01361.hp2 HG01496.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.636+3505G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517459 | |||||||
| chr6:17517503 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0029 others(67): Show |
70 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.636+3549C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517503 | |||||||
| chr6:17517508 | A | C | 53 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(50): Show |
53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.636+3554A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517508 | |||||||
| chr6:17517605 | T | A | 1 | a0001c0002t0001g0078 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.636+3651T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517605 | |||||||
| chr6:17517672 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(147): Show |
150 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.636+3718A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517672 | |||||||
| chr6:17517680 | C | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0134 |
2 | HG03239.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.636+3726C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517680 | |||||||
| chr6:17517715 | A | G | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.636+3761A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517715 | |||||||
| chr6:17517844 | T | C | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.636+3890T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517844 | |||||||
| chr6:17517856 | G | A | 54 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(51): Show |
54 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.636+3902G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17517856 | |||||||
| chr6:17517902 | A | AAAAT | 3 | a0001c0003t0002g0048 a0001c0014t0008g0016 a0005c0015t0001g0070 |
3 | HG01361.hp2 HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.636+3970_636+3973d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17517902 | ||||||
| chr6:17517902 | A | AAAATAAA others(1): Show |
5 | a0001c0003t0001g0065 a0001c0003t0001g0072 a0001c0003t0001g0075 others(2): Show |
5 | HG01496.hp2 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+3966_636+3973d others(10): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17517902 | ||||||
| chr6:17518033 | C | T | 2 | a0001c0002t0001g0098 a0001c0002t0001g0161 |
2 | HG00609.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.636+4079C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518033 | |||||||
| chr6:17518244 | T | C | 68 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(65): Show |
68 | HG00438.hp1 HG00735.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.636+4290T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518244 | |||||||
| chr6:17518389 | T | C | 1 | a0001c0002t0001g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.636+4435T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518389 | |||||||
| chr6:17518542 | T | G | 1 | a0001c0002t0001g0062 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.636+4588T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518542 | |||||||
| chr6:17518848 | G | C | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.636+4894G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518848 | |||||||
| chr6:17518861 | C | T | 53 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(50): Show |
53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.636+4907C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518861 | |||||||
| chr6:17518917 | C | T | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.636+4963C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17518917 | |||||||
| chr6:17519024 | C | T | 13 | a0002c0004t0001g0073 a0002c0004t0002g0083 a0002c0004t0002g0085 others(10): Show |
13 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.636+5070C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519024 | |||||||
| chr6:17519035 | C | T | 1 | a0001c0002t0006g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.636+5081C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519035 | |||||||
| chr6:17519104 | G | A | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.636+5150G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519104 | |||||||
| chr6:17519337 | A | G | 2 | a0001c0002t0001g0002 a0001c0002t0001g0062 |
2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.636+5383A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519337 | |||||||
| chr6:17519400 | G | T | 31 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
31 | HG00438.hp1 HG00741.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.636+5446G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519400 | |||||||
| chr6:17519645 | C | G | 1 | a0001c0002t0006g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.636+5691C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519645 | |||||||
| chr6:17519789 | C | G | 1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.636+5835C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519789 | |||||||
| chr6:17519824 | T | C | 56 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(53): Show |
56 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.636+5870T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519824 | |||||||
| chr6:17519877 | G | A | 13 | a0001c0001t0002g0150 a0002c0004t0001g0073 a0002c0004t0002g0083 others(10): Show |
13 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.636+5923G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17519877 | |||||||
| chr6:17520118 | GT | G | 6 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0002g0024 others(3): Show |
6 | HG00642.hp2 HG00735.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.636+6171delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17520118 | ||||||
| chr6:17520252 | C | G | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.636+6298C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520252 | |||||||
| chr6:17520282 | A | AT | 8 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(5): Show |
8 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.636+6336dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17520282 | ||||||
| chr6:17520298 | C | T | 1 | a0001c0011t0002g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.636+6344C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520298 | |||||||
| chr6:17520325 | G | T | 59 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(56): Show |
59 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.636+6371G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520325 | |||||||
| chr6:17520353 | G | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.636+6399G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520353 | |||||||
| chr6:17520575 | A | G | 44 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(41): Show |
44 | HG00438.hp1 HG00741.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.636+6621A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520575 | |||||||
| chr6:17520840 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.636+6886A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520840 | |||||||
| chr6:17520942 | C | G | 1 | a0001c0002t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.636+6988C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17520942 | |||||||
| chr6:17521013 | G | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(4): Show |
7 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.636+7059G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521013 | |||||||
| chr6:17521020 | T | C | 1 | a0001c0002t0001g0078 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.636+7066T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521020 | |||||||
| chr6:17521140 | C | T | 53 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(50): Show |
53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.636+7186C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521140 | |||||||
| chr6:17521165 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(154): Show |
157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.636+7211G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521165 | |||||||
| chr6:17521169 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(154): Show |
157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.636+7215T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521169 | |||||||
| chr6:17521258 | C | CA | 91 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(88): Show |
91 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.636+7315dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17521258 | ||||||
| chr6:17521277 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.636+7323C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521277 | |||||||
| chr6:17521375 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+7421A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521375 | |||||||
| chr6:17521508 | G | T | 56 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(53): Show |
56 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.636+7554G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521508 | |||||||
| chr6:17521724 | TG | T | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+7771delG | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521724 | |||||||
| chr6:17521726 | C | T | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+7772C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521726 | |||||||
| chr6:17521752 | C | T | 53 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(50): Show |
53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.636+7798C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521752 | |||||||
| chr6:17521887 | T | C | 5 | a0001c0001t0002g0003 a0001c0002t0001g0130 a0001c0002t0001g0132 others(2): Show |
5 | HG01255.hp1 HG02486.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.636+7933T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521887 | |||||||
| chr6:17521894 | A | G | 2 | a0001c0002t0001g0108 a0001c0002t0002g0116 |
2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.636+7940A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521894 | |||||||
| chr6:17521906 | C | T | 12 | a0002c0004t0001g0073 a0002c0004t0002g0083 a0002c0004t0002g0085 others(9): Show |
12 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.636+7952C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521906 | |||||||
| chr6:17521920 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.636+7966C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521920 | |||||||
| chr6:17521936 | C | A | 3 | a0001c0002t0001g0107 a0001c0002t0001g0136 a0001c0002t0001g0184 |
3 | HG00099.hp2 HG01175.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.636+7982C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17521936 | |||||||
| chr6:17522065 | C | T | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+8111C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522065 | |||||||
| chr6:17522088 | G | A | 8 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.636+8134G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522088 | |||||||
| chr6:17522137 | A | G | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+8183A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522137 | |||||||
| chr6:17522222 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.636+8268T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522222 | |||||||
| chr6:17522279 | A | T | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.636+8325A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522279 | |||||||
| chr6:17522620 | C | T | 12 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0002g0011 others(9): Show |
12 | HG00642.hp2 HG00735.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.636+8666C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522620 | |||||||
| chr6:17522750 | G | A | 6 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0002g0024 others(3): Show |
6 | HG00642.hp2 HG00735.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.636+8796G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522750 | |||||||
| chr6:17522755 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+8801T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17522755 | |||||||
| chr6:17523016 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.636+9062G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523016 | |||||||
| chr6:17523076 | A | T | 6 | a0001c0003t0001g0065 a0001c0003t0001g0072 a0001c0003t0001g0075 others(3): Show |
6 | HG01361.hp2 HG01496.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.636+9122A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523076 | |||||||
| chr6:17523081 | G | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(64): Show |
67 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.636+9127G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523081 | |||||||
| chr6:17523130 | C | T | 3 | a0001c0002t0001g0074 a0001c0002t0001g0101 a0001c0002t0001g0112 |
3 | HG01243.hp1 HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.636+9176C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523130 | |||||||
| chr6:17523259 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(64): Show |
67 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.636+9305A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523259 | |||||||
| chr6:17523317 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(64): Show |
67 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.636+9363G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523317 | |||||||
| chr6:17523339 | G | A | 4 | a0001c0003t0001g0065 a0001c0003t0001g0072 a0001c0003t0001g0075 others(1): Show |
4 | HG01496.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+9385G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523339 | |||||||
| chr6:17523504 | C | T | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+9550C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523504 | |||||||
| chr6:17523904 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.636+9950T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523904 | |||||||
| chr6:17523941 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(154): Show |
157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.636+9987A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17523941 | |||||||
| chr6:17524012 | G | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(64): Show |
67 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.636+10058G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524012 | |||||||
| chr6:17524074 | C | CA | 8 | a0001c0001t0001g0095 a0001c0002t0001g0101 a0001c0002t0001g0134 others(5): Show |
8 | HG00438.hp1 HG01192.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.636+10142dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17524074 | ||||||
| chr6:17524074 | CA | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(46): Show |
49 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.636+10142delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17524074 | ||||||
| chr6:17524074 | CAA | C | 19 | a0001c0001t0001g0069 a0001c0002t0001g0020 a0001c0002t0001g0077 others(16): Show |
19 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.636+10141_636+1014 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17524074 | ||||||
| chr6:17524074 | CAAAAAAA others(4): Show |
C | 53 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(50): Show |
53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.636+10132_636+1014 others(15): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17524074 | ||||||
| chr6:17524076 | A | G | 5 | a0001c0002t0002g0079 a0001c0003t0002g0048 a0003c0007t0001g0059 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+10122A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524076 | |||||||
| chr6:17524077 | A | G | 18 | a0001c0002t0001g0020 a0001c0002t0001g0077 a0001c0002t0001g0078 others(15): Show |
18 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.636+10123A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524077 | |||||||
| chr6:17524159 | G | A | 13 | a0001c0001t0002g0150 a0002c0004t0001g0073 a0002c0004t0002g0083 others(10): Show |
13 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.636+10205G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524159 | |||||||
| chr6:17524202 | G | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(12): Show |
15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.636+10248G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524202 | |||||||
| chr6:17524301 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(64): Show |
67 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.636+10347A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524301 | |||||||
| chr6:17524338 | A | C | 2 | a0001c0001t0002g0126 a0001c0001t0002g0175 |
2 | NA18747.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.636+10384A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524338 | |||||||
| chr6:17524346 | T | C | 1 | a0001c0002t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.636+10392T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524346 | |||||||
| chr6:17524396 | G | A | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.636+10442G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524396 | |||||||
| chr6:17524506 | C | T | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.636+10552C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524506 | |||||||
| chr6:17524722 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.636+10768A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524722 | |||||||
| chr6:17524893 | C | CTT | 5 | a0001c0003t0002g0048 a0001c0009t0001g0015 a0003c0007t0001g0059 others(2): Show |
5 | HG02280.hp2 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.636+10955_636+1095 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17524893 | ||||||
| chr6:17524893 | CT | C | 174 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.636+10956delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17524893 | ||||||
| chr6:17524899 | T | C | 52 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0001g0049 others(49): Show |
52 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.636+10945T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17524899 | |||||||
| chr6:17525021 | C | T | 31 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
31 | HG00438.hp1 HG00741.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.636+11067C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525021 | |||||||
| chr6:17525044 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.636+11090G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525044 | |||||||
| chr6:17525150 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.636+11196G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525150 | |||||||
| chr6:17525222 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+11268T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525222 | |||||||
| chr6:17525240 | A | G | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.636+11286A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525240 | |||||||
| chr6:17525372 | G | A | 2 | a0001c0003t0002g0048 a0005c0015t0001g0070 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.636+11418G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525372 | |||||||
| chr6:17525388 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+11434T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525388 | |||||||
| chr6:17525394 | G | A | 2 | a0001c0003t0002g0048 a0005c0015t0001g0070 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.636+11440G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525394 | |||||||
| chr6:17525410 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0163 |
2 | NA18992.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.636+11456G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525410 | |||||||
| chr6:17525445 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.636+11491G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525445 | |||||||
| chr6:17525468 | C | CA | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(86): Show |
89 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.636+11526dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17525468 | ||||||
| chr6:17525551 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(170): Show |
173 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.636+11597A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525551 | |||||||
| chr6:17525736 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+11782G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525736 | |||||||
| chr6:17525786 | T | G | 5 | a0001c0001t0002g0003 a0001c0002t0001g0130 a0001c0002t0001g0132 others(2): Show |
5 | HG01255.hp1 HG02486.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.636+11832T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525786 | |||||||
| chr6:17525865 | G | A | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.636+11911G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525865 | |||||||
| chr6:17525869 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0140 a0001c0001t0001g0142 others(2): Show |
5 | HG01168.hp1 HG01168.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+11915G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17525869 | |||||||
| chr6:17526029 | G | T | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.636+12075G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526029 | |||||||
| chr6:17526082 | G | A | 1 | a0001c0002t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.636+12128G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526082 | |||||||
| chr6:17526085 | C | G | 1 | a0001c0001t0001g0154 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.636+12131C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526085 | |||||||
| chr6:17526110 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(154): Show |
157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.636+12156G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526110 | |||||||
| chr6:17526150 | C | T | 1 | a0001c0002t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.636+12196C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526150 | |||||||
| chr6:17526262 | C | T | 1 | a0001c0003t0002g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+12308C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526262 | |||||||
| chr6:17526263 | A | G | 1 | a0001c0003t0002g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+12309A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526263 | |||||||
| chr6:17526264 | C | T | 1 | a0001c0003t0002g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+12310C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526264 | |||||||
| chr6:17526266 | C | T | 1 | a0001c0003t0002g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+12312C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526266 | |||||||
| chr6:17526274 | T | C | 1 | a0001c0003t0002g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+12320T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526274 | |||||||
| chr6:17526280 | A | G | 1 | a0001c0003t0002g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636+12326A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526280 | |||||||
| chr6:17526359 | C | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(12): Show |
15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.636+12405C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526359 | |||||||
| chr6:17526361 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+12407A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526361 | |||||||
| chr6:17526369 | G | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.636+12415G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526369 | |||||||
| chr6:17526639 | A | G | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-12630A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526639 | |||||||
| chr6:17526935 | C | T | 2 | a0001c0003t0002g0048 a0005c0015t0001g0070 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.637-12334C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17526935 | |||||||
| chr6:17526956 | C | CA | 101 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0019 others(98): Show |
101 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.637-12291dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17526956 | ||||||
| chr6:17526956 | C | CAA | 21 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(18): Show |
21 | HG00438.hp1 HG01361.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.637-12292_637-1229 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17526956 | ||||||
| chr6:17526956 | C | CAAA | 19 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(16): Show |
19 | HG01106.hp2 HG01243.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.637-12293_637-1229 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17526956 | ||||||
| chr6:17526956 | CA | C | 5 | a0001c0001t0002g0003 a0001c0002t0001g0130 a0001c0002t0001g0132 others(2): Show |
5 | HG01255.hp1 HG02486.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-12291delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17526956 | ||||||
| chr6:17526969 | A | AAAAG | 15 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(12): Show |
15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.637-12297_637-1229 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17526969 | ||||||
| chr6:17527172 | C | A | 1 | a0001c0006t0001g0121 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.637-12097C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527172 | |||||||
| chr6:17527293 | G | A | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.637-11976G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527293 | |||||||
| chr6:17527597 | C | CT | 61 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0049 others(58): Show |
61 | HG00438.hp2 HG00597.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.637-11655dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17527597 | ||||||
| chr6:17527597 | C | CTT | 43 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(40): Show |
43 | HG00438.hp1 HG00741.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.637-11656_637-1165 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17527597 | ||||||
| chr6:17527597 | C | CTTT | 26 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0002g0150 others(23): Show |
26 | HG00597.hp1 HG00735.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.637-11657_637-1165 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17527597 | ||||||
| chr6:17527597 | C | CTTTT | 6 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG01109.hp2 HG01891.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-11658_637-1165 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17527597 | ||||||
| chr6:17527597 | C | CTTTTT | 19 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(16): Show |
19 | HG01106.hp2 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.637-11659_637-1165 others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17527597 | ||||||
| chr6:17527636 | G | A | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0013t0001g0076 |
3 | HG02055.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.637-11633G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527636 | |||||||
| chr6:17527755 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.637-11514T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527755 | |||||||
| chr6:17527892 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(154): Show |
157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.637-11377T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527892 | |||||||
| chr6:17527919 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
98 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.637-11350C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527919 | |||||||
| chr6:17527958 | A | C | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.637-11311A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17527958 | |||||||
| chr6:17528112 | C | G | 1 | a0002c0004t0001g0073 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.637-11157C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528112 | |||||||
| chr6:17528189 | C | G | 1 | a0001c0009t0001g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.637-11080C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528189 | |||||||
| chr6:17528209 | C | T | 80 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(77): Show |
80 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.637-11060C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528209 | |||||||
| chr6:17528213 | G | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(15): Show |
18 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.637-11056G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528213 | |||||||
| chr6:17528235 | A | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0042 |
2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.637-11034A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528235 | |||||||
| chr6:17528284 | G | A | 1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.637-10985G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528284 | |||||||
| chr6:17528619 | G | T | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.637-10650G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528619 | |||||||
| chr6:17528664 | G | A | 1 | a0001c0002t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.637-10605G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528664 | |||||||
| chr6:17528964 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-10305C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528964 | |||||||
| chr6:17528967 | G | A | 27 | a0001c0001t0001g0069 a0001c0002t0001g0002 a0001c0002t0001g0020 others(24): Show |
27 | HG01361.hp2 HG01496.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.637-10302G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528967 | |||||||
| chr6:17528992 | G | A | 5 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
5 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-10277G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17528992 | |||||||
| chr6:17529052 | CA | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(51): Show |
54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-10207delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529052 | ||||||
| chr6:17529111 | T | C | 7 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
7 | HG01891.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.637-10158T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529111 | |||||||
| chr6:17529176 | T | G | 32 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(29): Show |
32 | HG00438.hp1 HG00741.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.637-10093T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529176 | |||||||
| chr6:17529220 | A | G | 9 | a0001c0002t0001g0058 a0001c0003t0001g0039 a0001c0003t0001g0090 others(6): Show |
9 | HG00642.hp1 HG02109.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-10049A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529220 | |||||||
| chr6:17529223 | T | G | 1 | a0001c0001t0001g0017 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.637-10046T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529223 | |||||||
| chr6:17529357 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(51): Show |
54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-9912T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529357 | |||||||
| chr6:17529361 | T | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(51): Show |
54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-9908T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529361 | |||||||
| chr6:17529416 | C | T | 1 | a0002c0004t0001g0073 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.637-9853C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529416 | |||||||
| chr6:17529417 | G | A | 5 | a0001c0001t0002g0003 a0001c0002t0001g0130 a0001c0002t0001g0132 others(2): Show |
5 | HG01255.hp1 HG02486.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-9852G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529417 | |||||||
| chr6:17529469 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(63): Show |
66 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.637-9800A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529469 | |||||||
| chr6:17529610 | C | T | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.637-9659C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529610 | |||||||
| chr6:17529618 | G | A | 2 | a0001c0003t0002g0048 a0005c0015t0001g0070 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.637-9651G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529618 | |||||||
| chr6:17529638 | C | T | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.637-9631C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529638 | |||||||
| chr6:17529640 | C | CA | 15 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0045 others(12): Show |
15 | HG00099.hp1 HG00597.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.637-9617dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529640 | ||||||
| chr6:17529640 | C | CAA | 26 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0017 others(23): Show |
26 | HG00438.hp1 HG00741.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.637-9618_637-9617d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529640 | ||||||
| chr6:17529640 | C | CAAAAAA | 6 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0003c0007t0001g0059 others(3): Show |
6 | HG01106.hp2 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-9622_637-9617d others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529640 | ||||||
| chr6:17529640 | C | CAAAAAAA | 10 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0068 others(7): Show |
10 | HG01109.hp2 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.637-9623_637-9617d others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529640 | ||||||
| chr6:17529640 | C | CAAAAAAA others(4): Show |
4 | a0001c0003t0001g0065 a0001c0003t0001g0072 a0001c0003t0001g0075 others(1): Show |
4 | HG01496.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-9627_637-9617d others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529640 | ||||||
| chr6:17529640 | CA | C | 11 | a0002c0004t0001g0073 a0002c0004t0002g0083 a0002c0004t0002g0085 others(8): Show |
11 | HG00597.hp1 HG00735.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.637-9617delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529640 | ||||||
| chr6:17529651 | A | AAAAAAAA others(7): Show |
1 | a0001c0002t0001g0062 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.637-9617_637-9616i others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | ||||||
| chr6:17529651 | A | AAAAAAAA others(4): Show |
2 | a0001c0002t0002g0115 a0001c0002t0006g0133 |
2 | HG01952.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.637-9617_637-9616i others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | ||||||
| chr6:17529651 | A | AAAAAAAA others(5): Show |
2 | a0001c0002t0001g0020 a0001c0014t0008g0016 |
2 | HG01361.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.637-9617_637-9616i others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | ||||||
| chr6:17529651 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.637-9617_637-9616i others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | ||||||
| chr6:17529651 | A | AAAAAAAA others(4): Show |
11 | a0001c0002t0001g0078 a0001c0002t0001g0108 a0001c0002t0002g0079 others(8): Show |
11 | HG01517.hp1 HG01928.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.637-9617_637-9616i others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | ||||||
| chr6:17529651 | A | AAAAAAAA others(3): Show |
1 | a0001c0002t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.637-9617_637-9616i others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | ||||||
| chr6:17529651 | A | AAAAAAAA others(5): Show |
2 | a0001c0008t0001g0204 a0006c0016t0001g0194 |
2 | HG02055.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.637-9617_637-9616i others(14): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | ||||||
| chr6:17529651 | A | AAAAAAAT others(4): Show |
1 | a0001c0002t0001g0077 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.637-9617_637-9616i others(13): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | ||||||
| chr6:17529651 | A | AAAAAAAT others(10): Show |
1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.637-9617_637-9616i others(19): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | ||||||
| chr6:17529651 | A | AAAT | 9 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0003t0001g0039 others(6): Show |
9 | HG02109.hp1 HG02647.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-9617_637-9616i others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529651 | ||||||
| chr6:17529651 | A | ATAT | 2 | a0001c0002t0001g0058 a0001c0008t0001g0057 |
2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.637-9618_637-9617i others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529651 | |||||||
| chr6:17529651 | A | T | 4 | a0001c0002t0001g0007 a0001c0002t0001g0109 a0001c0002t0001g0173 others(1): Show |
4 | HG01106.hp1 HG02027.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-9618A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529651 | |||||||
| chr6:17529652 | AT | A | 4 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0002g0176 others(1): Show |
4 | HG01884.hp2 HG03017.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-9616delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529652 | |||||||
| chr6:17529653 | T | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(86): Show |
89 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.637-9616T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529653 | |||||||
| chr6:17529655 | T | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0037 others(58): Show |
61 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.637-9614T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529655 | |||||||
| chr6:17529657 | T | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0003c0007t0001g0110 others(1): Show |
4 | HG01106.hp2 HG01243.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-9612T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529657 | |||||||
| chr6:17529780 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.637-9489C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17529780 | |||||||
| chr6:17529980 | C | CA | 17 | a0001c0001t0002g0003 a0001c0002t0001g0130 a0001c0002t0001g0132 others(14): Show |
17 | HG00597.hp1 HG00735.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.637-9276dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529980 | ||||||
| chr6:17529980 | CA | C | 5 | a0001c0001t0001g0069 a0001c0002t0001g0002 a0001c0002t0001g0062 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-9276delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17529980 | ||||||
| chr6:17530026 | T | C | 1 | a0001c0002t0001g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.637-9243T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530026 | |||||||
| chr6:17530320 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(51): Show |
54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-8949G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530320 | |||||||
| chr6:17530386 | G | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(51): Show |
54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-8883G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530386 | |||||||
| chr6:17530397 | G | A | 29 | a0001c0001t0001g0069 a0001c0002t0001g0002 a0001c0002t0001g0020 others(26): Show |
29 | HG01106.hp2 HG01243.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.637-8872G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530397 | |||||||
| chr6:17530476 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.637-8793G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530476 | |||||||
| chr6:17530635 | T | C | 1 | a0001c0002t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.637-8634T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530635 | |||||||
| chr6:17530721 | G | A | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.637-8548G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530721 | |||||||
| chr6:17530763 | C | A | 1 | a0001c0002t0001g0197 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.637-8506C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530763 | |||||||
| chr6:17530839 | G | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(12): Show |
15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.637-8430G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17530839 | |||||||
| chr6:17531022 | A | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(27): Show |
30 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.637-8247A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531022 | |||||||
| chr6:17531178 | G | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(184): Show |
187 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.637-8091G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531178 | |||||||
| chr6:17531204 | A | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(84): Show |
87 | HG00438.hp1 HG00741.hp1 HG01106.hp2 others(84): Show |
intron_variant | MODIFIER | c.637-8065A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531204 | |||||||
| chr6:17531353 | C | T | 3 | a0001c0001t0002g0022 a0001c0001t0002g0158 a0001c0001t0002g0168 |
3 | HG02083.hp1 HG02132.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.637-7916C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531353 | |||||||
| chr6:17531371 | G | A | 2 | a0001c0003t0001g0090 a0001c0003t0002g0131 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.637-7898G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531371 | |||||||
| chr6:17531430 | T | C | 1 | a0005c0015t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.637-7839T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531430 | |||||||
| chr6:17531590 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(154): Show |
157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.637-7679A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531590 | |||||||
| chr6:17531679 | G | T | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.637-7590G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531679 | |||||||
| chr6:17531710 | A | G | 13 | a0001c0001t0002g0150 a0002c0004t0001g0073 a0002c0004t0002g0083 others(10): Show |
13 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.637-7559A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531710 | |||||||
| chr6:17531733 | G | A | 21 | a0001c0002t0001g0002 a0001c0002t0001g0020 a0001c0002t0001g0062 others(18): Show |
21 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.637-7536G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17531733 | |||||||
| chr6:17532025 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(154): Show |
157 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.637-7244A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532025 | |||||||
| chr6:17532037 | C | T | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.637-7232C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532037 | |||||||
| chr6:17532134 | C | CT | 14 | a0001c0001t0001g0029 a0001c0001t0001g0124 a0001c0001t0001g0179 others(11): Show |
14 | HG00597.hp2 HG00741.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-7112dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17532134 | ||||||
| chr6:17532134 | CT | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0042 others(42): Show |
45 | HG00438.hp1 HG01167.hp1 HG01517.hp1 others(42): Show |
intron_variant | MODIFIER | c.637-7112delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17532134 | ||||||
| chr6:17532163 | CAG | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(51): Show |
54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-7103_637-7102d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17532163 | ||||||
| chr6:17532392 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.637-6877C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532392 | |||||||
| chr6:17532430 | C | G | 21 | a0001c0002t0001g0002 a0001c0002t0001g0020 a0001c0002t0001g0062 others(18): Show |
21 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.637-6839C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532430 | |||||||
| chr6:17532432 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.637-6837C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532432 | |||||||
| chr6:17532511 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(51): Show |
54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-6758C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532511 | |||||||
| chr6:17532670 | C | T | 1 | a0001c0003t0002g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.637-6599C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532670 | |||||||
| chr6:17532703 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(51): Show |
54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-6566A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532703 | |||||||
| chr6:17532704 | C | T | 1 | a0001c0002t0001g0012 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.637-6565C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532704 | |||||||
| chr6:17532727 | G | A | 4 | a0001c0001t0001g0196 a0001c0001t0002g0199 a0001c0001t0005g0200 others(1): Show |
4 | HG01891.hp1 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-6542G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532727 | |||||||
| chr6:17532734 | C | T | 1 | a0001c0002t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.637-6535C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532734 | |||||||
| chr6:17532735 | G | A | 8 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.637-6534G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532735 | |||||||
| chr6:17532740 | T | TC | 56 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0037 others(53): Show |
56 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.637-6529_637-6528i others(3): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532740 | |||||||
| chr6:17532741 | A | C | 89 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(86): Show |
89 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.637-6528A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532741 | |||||||
| chr6:17532750 | A | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG01978.hp2 HG02735.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-6519A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532750 | |||||||
| chr6:17532752 | C | A | 21 | a0001c0002t0001g0002 a0001c0002t0001g0020 a0001c0002t0001g0062 others(18): Show |
21 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.637-6517C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532752 | |||||||
| chr6:17532754 | C | A | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.637-6515C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532754 | |||||||
| chr6:17532764 | A | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(49): Show |
52 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(49): Show |
intron_variant | MODIFIER | c.637-6505A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532764 | |||||||
| chr6:17532802 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(51): Show |
54 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-6467G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532802 | |||||||
| chr6:17532839 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0052 others(11): Show |
14 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-6430A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532839 | |||||||
| chr6:17532922 | G | T | 2 | a0001c0002t0001g0130 a0001c0002t0001g0132 |
2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.637-6347G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532922 | |||||||
| chr6:17532974 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.637-6295A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17532974 | |||||||
| chr6:17533070 | C | A | 1 | a0002c0004t0002g0097 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.637-6199C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17533070 | |||||||
| chr6:17533078 | C | CAAAA | 17 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.637-6174_637-6171d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17533078 | ||||||
| chr6:17533078 | C | CAAAAA | 24 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(21): Show |
24 | HG01517.hp1 HG01952.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.637-6175_637-6171d others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17533078 | ||||||
| chr6:17533078 | C | CAAAAAA | 11 | a0001c0001t0001g0052 a0001c0001t0001g0068 a0001c0002t0001g0002 others(8): Show |
11 | HG01243.hp2 HG01891.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-6176_637-6171d others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17533078 | ||||||
| chr6:17533078 | CA | C | 135 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.637-6171delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17533078 | ||||||
| chr6:17533214 | TTAAA | T | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.637-6052_637-6049d others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17533214 | ||||||
| chr6:17533485 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.637-5784C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17533485 | |||||||
| chr6:17533572 | C | CT | 46 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(43): Show |
46 | HG00438.hp1 HG00741.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.637-5682dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17533572 | ||||||
| chr6:17533672 | G | C | 14 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-5597G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17533672 | |||||||
| chr6:17533846 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.637-5423G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17533846 | |||||||
| chr6:17533895 | C | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0103 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.637-5374C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17533895 | |||||||
| chr6:17534008 | A | G | 2 | a0001c0001t0002g0011 a0001c0001t0002g0044 |
2 | HG01175.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.637-5261A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534008 | |||||||
| chr6:17534117 | C | A | 1 | a0001c0014t0008g0016 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.637-5152C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534117 | |||||||
| chr6:17534220 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(89): Show |
92 | HG00438.hp1 HG00741.hp1 HG01106.hp2 others(89): Show |
intron_variant | MODIFIER | c.637-5049A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534220 | |||||||
| chr6:17534221 | T | G | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.637-5048T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534221 | |||||||
| chr6:17534530 | C | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(161): Show |
164 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.637-4739C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534530 | |||||||
| chr6:17534686 | T | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(199): Show |
202 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.637-4583T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534686 | |||||||
| chr6:17534701 | C | T | 54 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(51): Show |
54 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-4568C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534701 | |||||||
| chr6:17534788 | T | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0052 others(3): Show |
6 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-4481T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534788 | |||||||
| chr6:17534895 | C | T | 19 | a0001c0002t0001g0020 a0001c0002t0001g0077 a0001c0002t0001g0078 others(16): Show |
19 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.637-4374C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534895 | |||||||
| chr6:17534947 | G | A | 31 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
31 | HG00438.hp1 HG00741.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.637-4322G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534947 | |||||||
| chr6:17534953 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(89): Show |
92 | HG00438.hp1 HG00741.hp1 HG01106.hp2 others(89): Show |
intron_variant | MODIFIER | c.637-4316A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534953 | |||||||
| chr6:17534972 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.637-4297G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17534972 | |||||||
| chr6:17535116 | T | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
198 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.637-4153T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535116 | |||||||
| chr6:17535223 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(89): Show |
92 | HG00438.hp1 HG00741.hp1 HG01106.hp2 others(89): Show |
intron_variant | MODIFIER | c.637-4046C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535223 | |||||||
| chr6:17535274 | C | CT | 5 | a0001c0001t0001g0019 a0001c0002t0001g0094 a0001c0002t0001g0128 others(2): Show |
5 | HG00609.hp2 HG01071.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-3978dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17535274 | ||||||
| chr6:17535274 | CT | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0052 others(21): Show |
24 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.637-3978delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17535274 | ||||||
| chr6:17535526 | G | A | 54 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(51): Show |
54 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-3743G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535526 | |||||||
| chr6:17535553 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.637-3716C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535553 | |||||||
| chr6:17535563 | C | T | 1 | a0001c0006t0001g0034 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.637-3706C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535563 | |||||||
| chr6:17535762 | A | G | 52 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(49): Show |
52 | HG00438.hp1 HG00741.hp1 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.637-3507A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535762 | |||||||
| chr6:17535797 | G | A | 13 | a0001c0001t0002g0150 a0002c0004t0001g0073 a0002c0004t0002g0083 others(10): Show |
13 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.637-3472G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535797 | |||||||
| chr6:17535910 | A | C | 4 | a0001c0002t0001g0130 a0001c0002t0001g0132 a0004c0010t0001g0063 others(1): Show |
4 | HG01255.hp1 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-3359A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17535910 | |||||||
| chr6:17536115 | G | A | 1 | a0001c0001t0001g0017 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.637-3154G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536115 | |||||||
| chr6:17536356 | T | C | 8 | a0001c0003t0001g0039 a0001c0003t0001g0090 a0001c0003t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.637-2913T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536356 | |||||||
| chr6:17536569 | C | T | 14 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-2700C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536569 | |||||||
| chr6:17536766 | C | T | 1 | a0001c0002t0006g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.637-2503C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536766 | |||||||
| chr6:17536811 | G | A | 1 | a0006c0016t0001g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.637-2458G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536811 | |||||||
| chr6:17536866 | T | C | 1 | a0002c0004t0002g0182 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.637-2403T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536866 | |||||||
| chr6:17536884 | GA | G | 5 | a0001c0003t0001g0065 a0001c0003t0001g0072 a0001c0003t0001g0075 others(2): Show |
5 | HG01361.hp2 HG01496.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-2384delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17536884 | |||||||
| chr6:17537233 | C | A | 2 | a0001c0002t0001g0188 a0001c0002t0001g0189 |
2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.637-2036C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537233 | |||||||
| chr6:17537237 | GGTACAGT others(3): Show |
G | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.637-2029_637-2020d others(12): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17537237 | ||||||
| chr6:17537253 | C | T | 5 | a0001c0003t0001g0065 a0001c0003t0001g0072 a0001c0003t0001g0075 others(2): Show |
5 | HG01361.hp2 HG01496.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-2016C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537253 | |||||||
| chr6:17537270 | T | G | 21 | a0001c0002t0001g0002 a0001c0002t0001g0020 a0001c0002t0001g0062 others(18): Show |
21 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.637-1999T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537270 | |||||||
| chr6:17537325 | T | C | 1 | a0001c0003t0002g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.637-1944T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537325 | |||||||
| chr6:17537500 | A | ATGTTT | 19 | a0001c0002t0001g0020 a0001c0002t0001g0077 a0001c0002t0001g0078 others(16): Show |
19 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.637-1752_637-1748d others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17537500 | ||||||
| chr6:17537566 | G | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(58): Show |
61 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.637-1703G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537566 | |||||||
| chr6:17537599 | A | G | 14 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-1670A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537599 | |||||||
| chr6:17537602 | CTGT | C | 14 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-1665_637-1663d others(5): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17537602 | ||||||
| chr6:17537668 | G | A | 14 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-1601G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537668 | |||||||
| chr6:17537747 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.637-1522G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537747 | |||||||
| chr6:17537791 | C | T | 2 | a0001c0002t0001g0002 a0001c0002t0001g0062 |
2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.637-1478C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537791 | |||||||
| chr6:17537927 | C | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0153 |
2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.637-1342C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17537927 | |||||||
| chr6:17538023 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(160): Show |
163 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.637-1246T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17538023 | |||||||
| chr6:17538023 | T | G | 1 | a0002c0004t0002g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.637-1246T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17538023 | |||||||
| chr6:17538376 | C | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(58): Show |
61 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.637-893C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17538376 | |||||||
| chr6:17538704 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.637-565G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17538704 | |||||||
| chr6:17538941 | A | G | 14 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-328A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17538941 | |||||||
| chr6:17539018 | AGG | A | 12 | a0002c0004t0001g0073 a0002c0004t0002g0083 a0002c0004t0002g0085 others(9): Show |
12 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.637-249_637-248del others(2): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 17539018 | ||||||
| chr6:17539030 | C | A | 2 | a0001c0002t0001g0093 a0001c0002t0001g0094 |
2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.637-239C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17539030 | |||||||
| chr6:17539047 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(161): Show |
164 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.637-222T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17539047 | |||||||
| chr6:17539090 | G | C | 1 | a0001c0001t0002g0170 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.637-179G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17539090 | |||||||
| chr6:17539187 | G | T | 53 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(50): Show |
53 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.637-82G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17539187 | |||||||
| chr6:17539196 | G | A | 1 | a0001c0002t0001g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.637-73G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17539196 | |||||||
| chr6:17539225 | C | T | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.637-44C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 7/12 | chr6 | 17539225 | |||||||
| chr6:17540212 | A | G | 106 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(103): Show |
106 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.826+754A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540212 | |||||||
| chr6:17540313 | C | T | 19 | a0001c0002t0001g0020 a0001c0002t0001g0077 a0001c0002t0001g0078 others(16): Show |
19 | HG01517.hp1 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.827-660C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540313 | |||||||
| chr6:17540345 | G | A | 1 | a0002c0004t0002g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.827-628G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540345 | |||||||
| chr6:17540447 | TA | T | 7 | a0001c0002t0001g0109 a0001c0002t0001g0164 a0001c0006t0001g0149 others(4): Show |
7 | HG00438.hp2 HG02027.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.827-509delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 17540447 | ||||||
| chr6:17540448 | A | T | 1 | a0001c0003t0002g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.827-525A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540448 | |||||||
| chr6:17540558 | C | T | 15 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(12): Show |
15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.827-415C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540558 | |||||||
| chr6:17540560 | T | C | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.827-413T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540560 | |||||||
| chr6:17540613 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.827-360G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540613 | |||||||
| chr6:17540664 | G | C | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.827-309G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540664 | |||||||
| chr6:17540669 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0052 others(3): Show |
6 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.827-304G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 8/12 | chr6 | 17540669 | |||||||
| chr6:17541246 | A | T | 14 | a0001c0003t0001g0039 a0001c0003t0001g0065 a0001c0003t0001g0072 others(11): Show |
14 | HG01361.hp2 HG01496.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1002+98A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541246 | |||||||
| chr6:17541253 | G | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0029 others(106): Show |
109 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1002+105G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541253 | |||||||
| chr6:17541259 | G | A | 71 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(68): Show |
71 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1002+111G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541259 | |||||||
| chr6:17541362 | C | G | 12 | a0002c0004t0001g0073 a0002c0004t0002g0083 a0002c0004t0002g0085 others(9): Show |
12 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1002+214C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541362 | |||||||
| chr6:17541377 | C | T | 1 | a0001c0002t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1002+229C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541377 | |||||||
| chr6:17541400 | T | G | 1 | a0001c0002t0001g0012 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1002+252T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541400 | |||||||
| chr6:17541436 | C | T | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1002+288C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541436 | |||||||
| chr6:17541529 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1002+381G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541529 | |||||||
| chr6:17541673 | G | C | 5 | a0001c0003t0001g0065 a0001c0003t0001g0072 a0001c0003t0001g0075 others(2): Show |
5 | HG01361.hp2 HG01496.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002+525G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541673 | |||||||
| chr6:17541674 | C | T | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1002+526C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541674 | |||||||
| chr6:17541726 | AC | A | 54 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(51): Show |
54 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1002+581delC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 17541726 | ||||||
| chr6:17541736 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1002+588G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541736 | |||||||
| chr6:17541742 | G | A | 1 | a0001c0002t0002g0111 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1002+594G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541742 | |||||||
| chr6:17541766 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(34): Show |
37 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1002+618T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541766 | |||||||
| chr6:17541774 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0029 others(103): Show |
106 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1002+626C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541774 | |||||||
| chr6:17541934 | G | C | 103 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(100): Show |
103 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1002+786G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541934 | |||||||
| chr6:17541962 | T | C | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1002+814T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541962 | |||||||
| chr6:17541973 | C | G | 1 | a0001c0001t0002g0096 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1002+825C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17541973 | |||||||
| chr6:17542073 | T | G | 100 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
100 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1003-764T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17542073 | |||||||
| chr6:17542156 | G | C | 1 | a0001c0006t0001g0149 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1003-681G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17542156 | |||||||
| chr6:17542385 | T | G | 31 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
31 | HG00438.hp1 HG01167.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.1003-452T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17542385 | |||||||
| chr6:17542437 | C | T | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1003-400C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17542437 | |||||||
| chr6:17542461 | AC | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0041 others(37): Show |
40 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.1003-374delC | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 17542461 | ||||||
| chr6:17542805 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(137): Show |
140 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1003-32A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 9/12 | chr6 | 17542805 | |||||||
| chr6:17543547 | G | A | 1 | a0001c0011t0002g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1209+404G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17543547 | |||||||
| chr6:17543612 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.1209+469A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17543612 | |||||||
| chr6:17543624 | C | CA | 8 | a0001c0001t0001g0082 a0001c0002t0001g0074 a0001c0002t0001g0101 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209+503dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17543624 | ||||||
| chr6:17543624 | CA | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0037 others(28): Show |
31 | HG01109.hp2 HG01243.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.1209+503delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17543624 | ||||||
| chr6:17543624 | CAA | C | 59 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0045 others(56): Show |
59 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1209+502_1209+503d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17543624 | ||||||
| chr6:17543624 | CAAAAAAA others(7): Show |
C | 4 | a0001c0003t0001g0065 a0001c0003t0001g0072 a0001c0003t0001g0075 others(1): Show |
4 | HG01496.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1209+490_1209+503d others(16): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17543624 | ||||||
| chr6:17543715 | T | G | 50 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(47): Show |
50 | HG00438.hp1 HG01167.hp2 HG01192.hp1 others(47): Show |
intron_variant | MODIFIER | c.1209+572T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17543715 | |||||||
| chr6:17543723 | T | G | 1 | a0002c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1209+580T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17543723 | |||||||
| chr6:17544120 | G | A | 3 | a0001c0002t0001g0074 a0001c0002t0001g0101 a0001c0002t0001g0112 |
3 | HG01243.hp1 HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1209+977G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544120 | |||||||
| chr6:17544124 | C | CA | 115 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1209+994dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17544124 | ||||||
| chr6:17544124 | C | CAA | 6 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0151 others(3): Show |
6 | HG00438.hp2 HG02055.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1209+993_1209+994d others(4): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17544124 | ||||||
| chr6:17544138 | G | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(193): Show |
196 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.1209+995G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544138 | |||||||
| chr6:17544508 | A | G | 2 | a0001c0002t0001g0002 a0001c0002t0001g0062 |
2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1209+1365A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544508 | |||||||
| chr6:17544544 | C | CT | 70 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(67): Show |
70 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1209+1414dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17544544 | ||||||
| chr6:17544664 | T | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG01884.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1209+1521T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544664 | |||||||
| chr6:17544693 | C | T | 4 | a0001c0003t0001g0065 a0001c0003t0001g0072 a0001c0003t0001g0075 others(1): Show |
4 | HG01496.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1209+1550C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544693 | |||||||
| chr6:17544696 | G | A | 8 | a0001c0003t0001g0039 a0001c0003t0001g0090 a0001c0003t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209+1553G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544696 | |||||||
| chr6:17544741 | G | T | 3 | a0003c0007t0001g0059 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1209+1598G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544741 | |||||||
| chr6:17544752 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1209+1609G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544752 | |||||||
| chr6:17544980 | A | T | 1 | a0001c0001t0005g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1209+1837A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17544980 | |||||||
| chr6:17545024 | C | G | 27 | a0001c0002t0001g0002 a0001c0002t0001g0020 a0001c0002t0001g0062 others(24): Show |
27 | HG01361.hp2 HG01496.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.1209+1881C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17545024 | |||||||
| chr6:17545278 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(26): Show |
29 | HG00438.hp1 HG01167.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.1209+2135G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17545278 | |||||||
| chr6:17545278 | G | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0029 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1209+2135G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17545278 | |||||||
| chr6:17545376 | T | G | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1209+2233T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17545376 | |||||||
| chr6:17545991 | C | T | 14 | a0001c0001t0002g0003 a0001c0001t0002g0150 a0002c0004t0001g0073 others(11): Show |
14 | HG00597.hp1 HG00735.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1209+2848C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17545991 | |||||||
| chr6:17545995 | A | G | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1209+2852A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17545995 | |||||||
| chr6:17546135 | T | C | 1 | a0001c0008t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1209+2992T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546135 | |||||||
| chr6:17546190 | C | T | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1209+3047C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546190 | |||||||
| chr6:17546243 | T | A | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1209+3100T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546243 | |||||||
| chr6:17546391 | G | A | 1 | a0001c0002t0002g0167 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1209+3248G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546391 | |||||||
| chr6:17546483 | G | A | 2 | a0004c0010t0001g0063 a0004c0010t0002g0061 |
2 | HG01255.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1209+3340G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546483 | |||||||
| chr6:17546498 | T | C | 1 | a0001c0002t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1209+3355T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546498 | |||||||
| chr6:17546550 | T | G | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1209+3407T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546550 | |||||||
| chr6:17546558 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1209+3415A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546558 | |||||||
| chr6:17546567 | T | C | 1 | a0002c0004t0002g0083 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1209+3424T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17546567 | |||||||
| chr6:17547011 | A | T | 17 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(14): Show |
17 | HG01109.hp2 HG01255.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1209+3868A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547011 | |||||||
| chr6:17547116 | A | G | 1 | a0001c0006t0001g0121 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1209+3973A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547116 | |||||||
| chr6:17547182 | G | T | 3 | a0001c0002t0001g0002 a0003c0007t0001g0066 a0003c0007t0001g0205 |
3 | HG02258.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1209+4039G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547182 | |||||||
| chr6:17547280 | A | G | 1 | a0004c0010t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1209+4137A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547280 | |||||||
| chr6:17547357 | C | T | 2 | a0001c0001t0002g0150 a0002c0005t0001g0004 |
2 | HG02135.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1210-4107C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547357 | |||||||
| chr6:17547371 | AT | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0140 a0001c0001t0001g0142 others(1): Show |
4 | HG01168.hp2 HG01975.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210-4091delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17547371 | ||||||
| chr6:17547433 | A | T | 2 | a0001c0002t0001g0077 a0001c0002t0001g0078 |
2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1210-4031A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547433 | |||||||
| chr6:17547503 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1210-3961G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547503 | |||||||
| chr6:17547518 | T | C | 2 | a0003c0007t0001g0110 a0003c0007t0001g0119 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1210-3946T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547518 | |||||||
| chr6:17547557 | A | G | 44 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0045 others(41): Show |
44 | HG00099.hp1 HG00597.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1210-3907A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547557 | |||||||
| chr6:17547568 | A | G | 4 | a0001c0002t0001g0058 a0001c0008t0001g0051 a0001c0008t0001g0057 others(1): Show |
4 | HG00642.hp1 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210-3896A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547568 | |||||||
| chr6:17547571 | G | C | 2 | a0001c0002t0001g0058 a0001c0008t0001g0057 |
2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1210-3893G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547571 | |||||||
| chr6:17547584 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1210-3880G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547584 | |||||||
| chr6:17547596 | T | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0154 a0001c0001t0001g0178 others(2): Show |
5 | HG01192.hp2 NA18612.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210-3868T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547596 | |||||||
| chr6:17547601 | G | A | 1 | a0001c0002t0001g0173 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1210-3863G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547601 | |||||||
| chr6:17547608 | A | G | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1210-3856A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547608 | |||||||
| chr6:17547630 | C | A | 3 | a0001c0001t0001g0185 a0001c0001t0002g0043 a0001c0002t0001g0193 |
3 | HG00642.hp2 HG03017.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1210-3834C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547630 | |||||||
| chr6:17547637 | T | C | 6 | a0001c0001t0001g0185 a0001c0001t0002g0043 a0001c0001t0007g0201 others(3): Show |
6 | HG00642.hp2 HG01891.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210-3827T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547637 | |||||||
| chr6:17547644 | A | G | 51 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0021 others(48): Show |
51 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1210-3820A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547644 | |||||||
| chr6:17547648 | T | C | 2 | a0001c0001t0002g0003 a0001c0002t0001g0197 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1210-3816T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547648 | |||||||
| chr6:17547652 | T | C | 2 | a0001c0002t0001g0006 a0001c0009t0001g0015 |
2 | HG03491.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1210-3812T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547652 | |||||||
| chr6:17547658 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1210-3806A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547658 | |||||||
| chr6:17547668 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.1210-3796T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547668 | |||||||
| chr6:17547701 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1210-3763C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547701 | |||||||
| chr6:17547723 | C | G | 1 | a0001c0002t0001g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1210-3741C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547723 | |||||||
| chr6:17547809 | T | C | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1210-3655T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17547809 | |||||||
| chr6:17547840 | C | CA | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(75): Show |
78 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1210-3608dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17547840 | ||||||
| chr6:17548061 | A | G | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0009t0001g0013 |
3 | HG02145.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1210-3403A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548061 | |||||||
| chr6:17548105 | T | C | 3 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0002t0001g0198 |
3 | HG02630.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1210-3359T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548105 | |||||||
| chr6:17548282 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1210-3182G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548282 | |||||||
| chr6:17548306 | G | A | 44 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0024 others(41): Show |
44 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1210-3158G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548306 | |||||||
| chr6:17548344 | C | T | 1 | a0002c0004t0001g0073 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1210-3120C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548344 | |||||||
| chr6:17548361 | G | C | 4 | a0001c0001t0002g0126 a0001c0001t0002g0158 a0001c0001t0002g0175 others(1): Show |
4 | HG01981.hp1 NA18747.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210-3103G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548361 | |||||||
| chr6:17548511 | G | C | 1 | a0002c0005t0004g0025 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1210-2953G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548511 | |||||||
| chr6:17548553 | A | T | 1 | a0001c0001t0001g0049 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1210-2911A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548553 | |||||||
| chr6:17548699 | G | T | 12 | a0001c0001t0001g0049 a0001c0001t0001g0154 a0001c0001t0001g0178 others(9): Show |
12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1210-2765G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548699 | |||||||
| chr6:17548783 | G | A | 3 | a0001c0003t0002g0060 a0001c0003t0002g0064 a0001c0003t0002g0071 |
3 | HG02109.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1210-2681G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17548783 | |||||||
| chr6:17549191 | C | T | 118 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(115): Show |
118 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1210-2273C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17549191 | |||||||
| chr6:17549201 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0178 |
2 | NA18612.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1210-2263C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17549201 | |||||||
| chr6:17549409 | G | A | 2 | a0001c0001t0002g0003 a0004c0010t0002g0061 |
2 | HG01255.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1210-2055G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17549409 | |||||||
| chr6:17549723 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1210-1741C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17549723 | |||||||
| chr6:17549725 | A | G | 2 | a0001c0002t0001g0058 a0001c0008t0001g0057 |
2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1210-1739A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17549725 | |||||||
| chr6:17549927 | C | T | 76 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
76 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1210-1537C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17549927 | |||||||
| chr6:17550202 | C | T | 81 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
81 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1210-1262C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550202 | |||||||
| chr6:17550207 | T | C | 1 | a0001c0002t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1210-1257T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550207 | |||||||
| chr6:17550246 | A | AAAAT | 22 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0042 others(19): Show |
22 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1210-1197_1210-119 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550246 | ||||||
| chr6:17550390 | C | T | 4 | a0001c0001t0001g0165 a0001c0002t0001g0098 a0001c0002t0001g0161 others(1): Show |
4 | HG00609.hp1 NA18939.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210-1074C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550390 | |||||||
| chr6:17550394 | C | CT | 38 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0032 others(35): Show |
38 | HG00597.hp2 HG00735.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1210-1043dupT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550394 | ||||||
| chr6:17550394 | C | CTT | 17 | a0001c0001t0001g0049 a0001c0001t0001g0069 a0001c0001t0001g0178 others(14): Show |
17 | HG00597.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1210-1044_1210-104 others(6): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550394 | ||||||
| chr6:17550394 | C | CTTT | 9 | a0001c0001t0001g0154 a0001c0001t0001g0196 a0001c0001t0002g0027 others(6): Show |
9 | HG02135.hp2 HG03017.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1210-1045_1210-104 others(7): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550394 | ||||||
| chr6:17550394 | CT | C | 21 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0045 others(18): Show |
21 | HG00099.hp1 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.1210-1043delT | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550394 | ||||||
| chr6:17550394 | CTTTT | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1210-1046_1210-104 others(8): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550394 | ||||||
| chr6:17550394 | CTTTTT | C | 70 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0019 others(67): Show |
70 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1210-1047_1210-104 others(9): Show |
CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 17550394 | ||||||
| chr6:17550434 | A | G | 7 | a0001c0001t0001g0069 a0001c0003t0001g0065 a0001c0003t0001g0072 others(4): Show |
7 | HG01496.hp2 HG02055.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1210-1030A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550434 | |||||||
| chr6:17550567 | C | T | 5 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
5 | HG01167.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210-897C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550567 | |||||||
| chr6:17550582 | C | T | 4 | a0001c0003t0001g0065 a0001c0003t0001g0072 a0001c0003t0001g0075 others(1): Show |
4 | HG01496.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210-882C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550582 | |||||||
| chr6:17550805 | A | G | 1 | a0001c0013t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1210-659A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550805 | |||||||
| chr6:17550961 | G | A | 8 | a0001c0001t0001g0052 a0001c0002t0001g0058 a0001c0002t0001g0074 others(5): Show |
8 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1210-503G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550961 | |||||||
| chr6:17550985 | A | G | 1 | a0001c0009t0001g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1210-479A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17550985 | |||||||
| chr6:17551146 | A | G | 57 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0022 others(54): Show |
57 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.1210-318A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17551146 | |||||||
| chr6:17551424 | G | A | 1 | a0001c0001t0002g0172 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1210-40G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 11/12 | chr6 | 17551424 | |||||||
| chr6:17551765 | C | T | 81 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
81 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1350+161C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17551765 | |||||||
| chr6:17551999 | T | G | 1 | a0001c0006t0001g0034 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1350+395T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17551999 | |||||||
| chr6:17552101 | G | A | 1 | a0002c0004t0002g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1350+497G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552101 | |||||||
| chr6:17552150 | C | G | 1 | a0001c0001t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1350+546C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552150 | |||||||
| chr6:17552269 | T | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0154 a0001c0001t0001g0178 others(2): Show |
5 | HG01109.hp1 NA18612.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1350+665T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552269 | |||||||
| chr6:17552447 | G | T | 1 | a0001c0006t0001g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1350+843G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552447 | |||||||
| chr6:17552449 | G | A | 1 | a0001c0006t0001g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1350+845G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552449 | |||||||
| chr6:17552466 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1350+862C>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552466 | |||||||
| chr6:17552569 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1350+965T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552569 | |||||||
| chr6:17552814 | T | A | 1 | a0002c0004t0002g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1350+1210T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552814 | |||||||
| chr6:17552823 | A | G | 1 | a0001c0001t0001g0026 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1350+1219A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552823 | |||||||
| chr6:17552900 | A | T | 1 | a0004c0010t0001g0063 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1350+1296A>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17552900 | |||||||
| chr6:17553127 | A | G | 2 | a0001c0002t0001g0058 a0001c0008t0001g0057 |
2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1350+1523A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553127 | |||||||
| chr6:17553188 | A | C | 8 | a0001c0001t0001g0052 a0001c0002t0001g0058 a0001c0002t0001g0074 others(5): Show |
8 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1350+1584A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553188 | |||||||
| chr6:17553201 | G | A | 2 | a0001c0002t0001g0062 a0001c0009t0001g0015 |
2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1350+1597G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553201 | |||||||
| chr6:17553275 | C | T | 5 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
5 | HG01167.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1350+1671C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553275 | |||||||
| chr6:17553357 | G | A | 5 | a0001c0001t0001g0049 a0001c0001t0001g0154 a0001c0001t0001g0178 others(2): Show |
5 | HG01109.hp1 NA18612.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1350+1753G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553357 | |||||||
| chr6:17553376 | TA | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(180): Show |
183 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.1350+1775delA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 17553376 | ||||||
| chr6:17553514 | T | C | 3 | a0001c0001t0001g0052 a0001c0002t0001g0058 a0001c0008t0001g0057 |
3 | HG00642.hp1 HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1350+1910T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553514 | |||||||
| chr6:17553526 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(194): Show |
197 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.1350+1922A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553526 | |||||||
| chr6:17553544 | A | C | 1 | a0002c0005t0001g0203 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1350+1940A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553544 | |||||||
| chr6:17553632 | C | CA | 27 | a0001c0001t0001g0052 a0001c0001t0001g0069 a0001c0001t0001g0196 others(24): Show |
27 | HG00438.hp2 HG00597.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1350+2044dupA | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 17553632 | ||||||
| chr6:17553644 | A | C | 2 | a0001c0001t0002g0162 a0001c0001t0002g0181 |
2 | NA18939.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1350+2040A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553644 | |||||||
| chr6:17553780 | G | A | 1 | a0001c0003t0002g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1350+2176G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553780 | |||||||
| chr6:17553782 | C | T | 59 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0022 others(56): Show |
59 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1350+2178C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553782 | |||||||
| chr6:17553879 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350+2275C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553879 | |||||||
| chr6:17553888 | G | A | 1 | a0003c0007t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1350+2284G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553888 | |||||||
| chr6:17553889 | C | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0042 others(17): Show |
20 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1350+2285C>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553889 | |||||||
| chr6:17553979 | T | C | 1 | a0001c0006t0001g0018 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1350+2375T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17553979 | |||||||
| chr6:17554384 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1351-1975A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554384 | |||||||
| chr6:17554477 | C | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0005g0200 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1351-1882C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554477 | |||||||
| chr6:17554507 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1351-1852A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554507 | |||||||
| chr6:17554668 | G | A | 81 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
81 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1351-1691G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554668 | |||||||
| chr6:17554821 | T | G | 1 | a0001c0001t0001g0005 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1351-1538T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554821 | |||||||
| chr6:17554871 | G | C | 12 | a0001c0001t0001g0049 a0001c0001t0001g0154 a0001c0001t0001g0178 others(9): Show |
12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1351-1488G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554871 | |||||||
| chr6:17554911 | A | G | 1 | a0001c0014t0008g0016 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1351-1448A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554911 | |||||||
| chr6:17554936 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351-1423G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554936 | |||||||
| chr6:17554940 | G | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1351-1419G>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17554940 | |||||||
| chr6:17555025 | A | G | 1 | a0001c0014t0008g0016 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1351-1334A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555025 | |||||||
| chr6:17555259 | A | G | 1 | a0001c0003t0002g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1351-1100A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555259 | |||||||
| chr6:17555277 | C | T | 1 | a0001c0009t0001g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1351-1082C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555277 | |||||||
| chr6:17555338 | T | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1351-1021T>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555338 | |||||||
| chr6:17555350 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1351-1009A>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555350 | |||||||
| chr6:17555355 | C | T | 12 | a0001c0001t0001g0049 a0001c0001t0001g0154 a0001c0001t0001g0178 others(9): Show |
12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1351-1004C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555355 | |||||||
| chr6:17555582 | G | C | 1 | a0001c0006t0001g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1351-777G>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555582 | |||||||
| chr6:17555666 | C | T | 5 | a0001c0003t0001g0065 a0001c0003t0001g0072 a0001c0003t0001g0075 others(2): Show |
5 | HG01496.hp2 HG02055.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1351-693C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555666 | |||||||
| chr6:17555731 | T | C | 1 | a0001c0002t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1351-628T>C | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555731 | |||||||
| chr6:17555746 | T | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0042 others(9): Show |
12 | HG00099.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1351-613T>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555746 | |||||||
| chr6:17555930 | G | A | 2 | a0001c0006t0001g0121 a0001c0006t0001g0155 |
2 | HG02135.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1351-429G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555930 | |||||||
| chr6:17555970 | G | A | 1 | a0001c0001t0002g0150 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1351-389G>A | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17555970 | |||||||
| chr6:17556053 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351-306C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17556053 | |||||||
| chr6:17556279 | C | T | 12 | a0001c0001t0001g0049 a0001c0001t0001g0154 a0001c0001t0001g0178 others(9): Show |
12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1351-80C>T | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17556279 | |||||||
| chr6:17556296 | A | G | 5 | a0001c0001t0001g0049 a0001c0001t0001g0154 a0001c0001t0001g0178 others(2): Show |
5 | HG01109.hp1 NA18612.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1351-63A>G | CAP2 | ENSG00000112186.13 | transcript | ENST00000229922.7 | protein_coding | 12/12 | chr6 | 17556296 |