Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79886 |
| ensemblid | ENSG00000120159.13 |
| hgncid | 25834 |
| symbol | CAAP1 |
| name | caspase activity and apoptosis inhibitor 1 |
| refseq_nuc | NM_024828.4 |
| refseq_prot | NP_079104.3 |
| ensembl_nuc | ENST00000333916.8 |
| ensembl_prot | ENSP00000369431.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 26840685 |
| end | 26892802 |
| strand | - |
| ver | v1.2 |
| region | chr9:26840685-26892802 |
| region5000 | chr9:26835685-26897802 |
| regionname0 | CAAP1_chr9_26840685_26892802 |
| regionname5000 | CAAP1_chr9_26835685_26897802 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 361 | 344 | 64 | 68 | 155 | 18 | 37 | 116 | CAAP1_chr9_26835685_26897802 | CAAP1 | MTGKK others(356): Show |
chr9 | 26835685 | 26897802 |
| a0002 | 0/0 | 361 | 20 | 18 | 2 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | MTGKK others(356): Show |
chr9 | 26835685 | 26897802 |
| a0003 | 0/0 | 361 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | MTGKK others(356): Show |
chr9 | 26835685 | 26897802 |
| a0004 | 0/0 | 361 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | MTGKK others(356): Show |
chr9 | 26835685 | 26897802 |
| a0005 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | MTGKK others(356): Show |
chr9 | 26835685 | 26897802 |
| a0006 | 0/0 | 361 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | MTGKK others(356): Show |
chr9 | 26835685 | 26897802 |
| a0007 | 0/0 | 312 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | MTGKK others(307): Show |
chr9 | 26835685 | 26897802 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1083 | 234 | 55 | 52 | 77 | 18 | 30 | CAAP1_chr9_26835685_26897802 | CAAP1 | ATGAC others(1078): Show |
chr9 | 26835685 | 26897802 | ||
| a0001c0002 | 0/0 | 1083 | 110 | 9 | 16 | 78 | 0 | 7 | CAAP1_chr9_26835685_26897802 | CAAP1 | ATGAC others(1078): Show |
chr9 | 26835685 | 26897802 | ||
| a0002c0003 | 0/0 | 1083 | 19 | 17 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | ATGAC others(1078): Show |
chr9 | 26835685 | 26897802 | ||
| a0002c0007 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | ATGAC others(1078): Show |
chr9 | 26835685 | 26897802 | ||
| a0003c0004 | 0/0 | 1083 | 3 | 3 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | ATGAC others(1078): Show |
chr9 | 26835685 | 26897802 | ||
| a0004c0008 | 0/0 | 1083 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | ATGAC others(1078): Show |
chr9 | 26835685 | 26897802 | ||
| a0004c0010 | 0/0 | 1083 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | ATGAC others(1078): Show |
chr9 | 26835685 | 26897802 | ||
| a0005c0005 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | ATGAC others(1078): Show |
chr9 | 26835685 | 26897802 | ||
| a0006c0006 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | ATGAC others(1078): Show |
chr9 | 26835685 | 26897802 | ||
| a0007c0009 | 0/0 | 1083 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | ATGAC others(1078): Show |
chr9 | 26835685 | 26897802 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2789 | 183 | 42 | 29 | 73 | 14 | 23 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0001c0001t0002 | 0/0 | 2789 | 36 | 8 | 20 | 0 | 4 | 4 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0001c0001t0003 | 0/0 | 2789 | 3 | 0 | 3 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0001c0001t0004 | 0/0 | 2789 | 2 | 2 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0001c0001t0005 | 0/0 | 2789 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0001c0001t0006 | 0/0 | 2789 | 2 | 2 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0001c0001t0007 | 0/0 | 2789 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0001c0001t0008 | 0/0 | 2789 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0001c0001t0010 | 0/0 | 2789 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0001c0001t0013 | 0/0 | 2789 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0001c0001t0014 | 0/0 | 2789 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0001c0001t0016 | 0/0 | 2789 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0001c0002t0001 | 0/0 | 2789 | 109 | 9 | 16 | 77 | 0 | 7 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0001c0002t0012 | 0/0 | 2789 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0002c0003t0001 | 0/0 | 2789 | 19 | 17 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0002c0007t0011 | 0/0 | 2789 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0003c0004t0001 | 0/0 | 2789 | 3 | 3 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0004c0008t0001 | 0/0 | 2789 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0004c0010t0015 | 0/0 | 2789 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0005c0005t0009 | 0/0 | 2789 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0006c0006t0001 | 0/0 | 2789 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| a0007c0009t0001 | 0/0 | 2789 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | AGTGC others(2784): Show |
chr9 | 26835685 | 26897802 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0003 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0006g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0006g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0007g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0008g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0010g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0013g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0014g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0001t0016g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0001c0002t0012g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0002c0007t0011g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0003c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0003c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0003c0004t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0004c0008t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0004c0010t0015g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0005c0005t0009g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0006c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| a0007c0009t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | GBR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0225 | EUR | GBR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0231 | EUR | FIN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0229 | EUR | FIN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0132 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00558 | hp2 | a0005 | c0005 | t0009 | g0020 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0319 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0332 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0286 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0338 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0339 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0248 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0323 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01496 | hp2 | a0002 | c0003 | t0001 | g0030 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | IBS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01884 | hp1 | a0003 | c0004 | t0001 | g0100 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0037 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0341 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0322 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0335 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0277 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0336 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0327 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0344 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0146 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | CDX | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0039 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0268 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0001 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0351 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02451 | hp1 | a0003 | c0004 | t0001 | g0253 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02451 | hp2 | a0002 | c0003 | t0001 | g0026 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0024 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02683 | hp1 | a0004 | c0010 | t0015 | g0328 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02683 | hp2 | a0001 | c0001 | t0013 | g0087 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0308 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0353 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0342 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0345 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0027 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0340 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0121 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0025 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0022 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0346 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0295 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0034 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03098 | hp2 | a0002 | c0003 | t0001 | g0023 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0334 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0031 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0343 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0305 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0036 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03209 | hp2 | a0002 | c0003 | t0001 | g0035 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0038 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03540 | hp2 | a0006 | c0006 | t0001 | g0028 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0297 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0263 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0349 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0276 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG04184 | hp2 | a0001 | c0001 | t0016 | g0184 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG04199 | hp2 | a0007 | c0009 | t0001 | g0140 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG04228 | hp1 | a0004 | c0008 | t0001 | g0092 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0152 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | CHB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18906 | hp1 | a0002 | c0003 | t0001 | g0032 | AFR | YRI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0350 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18975 | hp1 | a0001 | c0001 | t0008 | g0207 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19030 | hp1 | a0002 | c0007 | t0011 | g0029 | AFR | LWK | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19030 | hp2 | a0003 | c0004 | t0001 | g0254 | AFR | LWK | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19058 | hp2 | a0001 | c0002 | t0012 | g0316 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19080 | hp1 | a0001 | c0001 | t0014 | g0187 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0347 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0348 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | YRI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0333 | AFR | ASW | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ASW | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | TSI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0232 | EUR | TSI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | GIH | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0352 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0021 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | USA | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | USA | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | USA | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | USA | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| NA21309 | hp2 | a0002 | c0003 | t0001 | g0033 | AFR | LWK | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0151 | REF | REF | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0066 | REF | REF | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:26842378 | C | A | 1 | a0007 | 1 | HG04199.hp2 | stop_gained | HIGH | c.1009G>T | p.Glu337* | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1096/2789 | 1009/1086 | 337/361 | chr9 | 26842378 | |||
| chr9:26842384 | G | A | 1 | a0007 | 1 | HG04199.hp2 | stop_gained | HIGH | c.1003C>T | p.Gln335* | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1090/2789 | 1003/1086 | 335/361 | chr9 | 26842384 | |||
| chr9:26842387 | G | C | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1000C>G | p.Gln334Glu | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1087/2789 | 1000/1086 | 334/361 | chr9 | 26842387 | |||
| chr9:26842392 | G | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.995C>A | p.Ser332Tyr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1082/2789 | 995/1086 | 332/361 | chr9 | 26842392 | |||
| chr9:26842393 | A | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.994T>A | p.Ser332Thr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1081/2789 | 994/1086 | 332/361 | chr9 | 26842393 | |||
| chr9:26842395 | G | C | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.992C>G | p.Pro331Arg | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1079/2789 | 992/1086 | 331/361 | chr9 | 26842395 | |||
| chr9:26842396 | G | A | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.991C>T | p.Pro331Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1078/2789 | 991/1086 | 331/361 | chr9 | 26842396 | |||
| chr9:26842398 | T | G | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.989A>C | p.Gln330Pro | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1076/2789 | 989/1086 | 330/361 | chr9 | 26842398 | |||
| chr9:26842399 | G | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.988C>A | p.Gln330Lys | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1075/2789 | 988/1086 | 330/361 | chr9 | 26842399 | |||
| chr9:26842405 | C | A | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.982G>T | p.Asp328Tyr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1069/2789 | 982/1086 | 328/361 | chr9 | 26842405 | |||
| chr9:26842408 | C | G | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.979G>C | p.Glu327Gln | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1066/2789 | 979/1086 | 327/361 | chr9 | 26842408 | |||
| chr9:26842413 | G | C | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.974C>G | p.Pro325Arg | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1061/2789 | 974/1086 | 325/361 | chr9 | 26842413 | |||
| chr9:26842414 | G | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.973C>A | p.Pro325Thr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1060/2789 | 973/1086 | 325/361 | chr9 | 26842414 | |||
| chr9:26842416 | G | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.971C>A | p.Pro324His | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1058/2789 | 971/1086 | 324/361 | chr9 | 26842416 | |||
| chr9:26842417 | G | A | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.970C>T | p.Pro324Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1057/2789 | 970/1086 | 324/361 | chr9 | 26842417 | |||
| chr9:26842420 | C | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.967G>A | p.Val323Ile | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1054/2789 | 967/1086 | 323/361 | chr9 | 26842420 | |||
| chr9:26842422 | G | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.965C>A | p.Ala322Asp | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1052/2789 | 965/1086 | 322/361 | chr9 | 26842422 | |||
| chr9:26842423 | C | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.964G>A | p.Ala322Thr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1051/2789 | 964/1086 | 322/361 | chr9 | 26842423 | |||
| chr9:26842428 | G | C | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.959C>G | p.Thr320Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1046/2789 | 959/1086 | 320/361 | chr9 | 26842428 | |||
| chr9:26842435 | C | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.952G>A | p.Ala318Thr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1039/2789 | 952/1086 | 318/361 | chr9 | 26842435 | |||
| chr9:26842441 | G | A | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.946C>T | p.Pro316Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1033/2789 | 946/1086 | 316/361 | chr9 | 26842441 | |||
| chr9:26842444 | C | G | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.943G>C | p.Glu315Gln | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1030/2789 | 943/1086 | 315/361 | chr9 | 26842444 | |||
| chr9:26842444 | C | T | 1 | a0004 | 2 | HG02683.hp1 HG04228.hp1 |
missense_variant | MODERATE | c.943G>A | p.Glu315Lys | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1030/2789 | 943/1086 | 315/361 | chr9 | 26842444 | |||
| chr9:26842445 | G | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.942C>A | p.Asn314Lys | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1029/2789 | 942/1086 | 314/361 | chr9 | 26842445 | |||
| chr9:26842449 | G | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.938C>A | p.Pro313Gln | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1025/2789 | 938/1086 | 313/361 | chr9 | 26842449 | |||
| chr9:26842450 | G | A | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.937C>T | p.Pro313Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1024/2789 | 937/1086 | 313/361 | chr9 | 26842450 | |||
| chr9:26842452 | C | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.935G>A | p.Ser312Asn | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1022/2789 | 935/1086 | 312/361 | chr9 | 26842452 | |||
| chr9:26842456 | A | C | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.931T>G | p.Ser311Ala | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1018/2789 | 931/1086 | 311/361 | chr9 | 26842456 | |||
| chr9:26842457 | C | A | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.930G>T | p.Glu310Asp | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1017/2789 | 930/1086 | 310/361 | chr9 | 26842457 | |||
| chr9:26842459 | C | A | 1 | a0007 | 1 | HG04199.hp2 | stop_gained | HIGH | c.928G>T | p.Glu310* | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1015/2789 | 928/1086 | 310/361 | chr9 | 26842459 | |||
| chr9:26842465 | G | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.922C>A | p.Leu308Met | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1009/2789 | 922/1086 | 308/361 | chr9 | 26842465 | |||
| chr9:26842467 | C | A | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.920G>T | p.Gly307Val | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1007/2789 | 920/1086 | 307/361 | chr9 | 26842467 | |||
| chr9:26842468 | C | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.919G>A | p.Gly307Arg | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1006/2789 | 919/1086 | 307/361 | chr9 | 26842468 | |||
| chr9:26842472 | A | C | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.915T>G | p.Ile305Met | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1002/2789 | 915/1086 | 305/361 | chr9 | 26842472 | |||
| chr9:26842478 | A | C | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.909T>G | p.Asn303Lys | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 996/2789 | 909/1086 | 303/361 | chr9 | 26842478 | |||
| chr9:26842479 | T | C | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.908A>G | p.Asn303Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 995/2789 | 908/1086 | 303/361 | chr9 | 26842479 | |||
| chr9:26842542 | T | C | 1 | a0003 | 3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.845A>G | p.Asn282Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 932/2789 | 845/1086 | 282/361 | chr9 | 26842542 | |||
| chr9:26861108 | C | T | 2 | a0002 a0006 |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
missense_variant | MODERATE | c.697G>A | p.Val233Met | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/6 | 784/2789 | 697/1086 | 233/361 | chr9 | 26861108 | |||
| chr9:26886139 | A | C | 1 | a0006 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.554T>G | p.Leu185Arg | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/6 | 641/2789 | 554/1086 | 185/361 | chr9 | 26886139 | |||
| chr9:26892525 | A | G | 1 | a0005 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.191T>C | p.Val64Ala | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/6 | 278/2789 | 191/1086 | 64/361 | chr9 | 26892525 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:26842394 | A | T | 1 | a0007c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.993T>A | p.Pro331Pro | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1080/2789 | 993/1086 | 331/361 | chr9 | 26842394 | |||
| chr9:26842415 | A | C | 1 | a0007c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.972T>G | p.Pro324Pro | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1059/2789 | 972/1086 | 324/361 | chr9 | 26842415 | |||
| chr9:26842418 | A | G | 1 | a0007c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.969T>C | p.Val323Val | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1056/2789 | 969/1086 | 323/361 | chr9 | 26842418 | |||
| chr9:26842426 | G | A | 1 | a0007c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.961C>T | p.Leu321Leu | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1048/2789 | 961/1086 | 321/361 | chr9 | 26842426 | |||
| chr9:26842427 | G | A | 1 | a0007c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.960C>T | p.Thr320Thr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1047/2789 | 960/1086 | 320/361 | chr9 | 26842427 | |||
| chr9:26842436 | T | C | 1 | a0007c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.951A>G | p.Lys317Lys | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1038/2789 | 951/1086 | 317/361 | chr9 | 26842436 | |||
| chr9:26842460 | T | A | 1 | a0007c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.927A>T | p.Ala309Ala | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1014/2789 | 927/1086 | 309/361 | chr9 | 26842460 | |||
| chr9:26842508 | G | A | 2 | a0002c0003 a0006c0006 |
20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
synonymous_variant | LOW | c.879C>T | p.Asp293Asp | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 966/2789 | 879/1086 | 293/361 | chr9 | 26842508 | |||
| chr9:26892656 | G | A | 2 | a0001c0002 a0004c0010 |
111 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
synonymous_variant | LOW | c.60C>T | p.Ala20Ala | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/6 | 147/2789 | 60/1086 | 20/361 | chr9 | 26892656 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:26841055 | A | G | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1246T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1246 | chr9 | 26841055 | ||||||
| chr9:26841143 | G | A | 1 | a0002c0007t0011 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1158C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1158 | chr9 | 26841143 | ||||||
| chr9:26841230 | A | G | 1 | a0005c0005t0009 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1071T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1071 | chr9 | 26841230 | ||||||
| chr9:26841431 | T | C | 1 | a0001c0002t0012 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*870A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 870 | chr9 | 26841431 | ||||||
| chr9:26841550 | G | C | 1 | a0001c0001t0013 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*751C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 751 | chr9 | 26841550 | ||||||
| chr9:26841704 | G | A | 1 | a0001c0001t0004 | 2 | HG03041.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*597C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 597 | chr9 | 26841704 | ||||||
| chr9:26841720 | A | G | 1 | a0001c0001t0008 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*581T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 581 | chr9 | 26841720 | ||||||
| chr9:26841784 | G | C | 1 | a0001c0001t0003 | 3 | HG01167.hp1 HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*517C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 517 | chr9 | 26841784 | ||||||
| chr9:26841798 | G | A | 2 | a0001c0001t0002 a0001c0001t0003 |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*503C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 503 | chr9 | 26841798 | ||||||
| chr9:26841809 | G | A | 1 | a0001c0001t0005 | 2 | HG00423.hp2 HG02080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*492C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 492 | chr9 | 26841809 | ||||||
| chr9:26841931 | A | T | 1 | a0001c0001t0007 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*370T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 370 | chr9 | 26841931 | ||||||
| chr9:26841970 | G | A | 1 | a0001c0001t0014 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*331C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 331 | chr9 | 26841970 | ||||||
| chr9:26842046 | T | C | 1 | a0004c0010t0015 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*255A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 255 | chr9 | 26842046 | ||||||
| chr9:26842151 | G | C | 1 | a0001c0001t0016 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 150 | chr9 | 26842151 | ||||||
| chr9:26892789 | G | A | 1 | a0001c0001t0006 | 2 | HG02559.hp2 HG02717.hp2 |
5_prime_UTR_variant | MODIFIER | c.-74C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/6 | 74 | chr9 | 26892789 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:26842672 | C | A | 19 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(16): Show |
20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.740-25G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26842672 | |||||||
| chr9:26842794 | T | C | 7 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(4): Show |
7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.740-147A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26842794 | |||||||
| chr9:26843195 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.740-548C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843195 | |||||||
| chr9:26843204 | C | T | 1 | a0001c0002t0001g0266 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.740-557G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843204 | |||||||
| chr9:26843234 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.740-587G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843234 | |||||||
| chr9:26843285 | T | C | 1 | a0003c0004t0001g0100 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.740-638A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843285 | |||||||
| chr9:26843290 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.740-643A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843290 | |||||||
| chr9:26843344 | G | A | 14 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(11): Show |
14 | HG01256.hp2 HG02056.hp2 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.740-697C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843344 | |||||||
| chr9:26843431 | T | C | 3 | a0002c0003t0001g0032 a0002c0003t0001g0033 a0002c0003t0001g0034 |
3 | HG03041.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.740-784A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843431 | |||||||
| chr9:26843457 | G | T | 2 | a0002c0003t0001g0025 a0002c0003t0001g0035 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.740-810C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843457 | |||||||
| chr9:26843486 | C | A | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.740-839G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843486 | |||||||
| chr9:26843594 | GT | G | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.740-948delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843594 | |||||||
| chr9:26843598 | T | TC | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-952_740-951ins others(1): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843598 | |||||||
| chr9:26843730 | G | C | 2 | a0002c0003t0001g0025 a0002c0003t0001g0035 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.740-1083C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843730 | |||||||
| chr9:26843837 | C | A | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(119): Show |
132 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.740-1190G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843837 | |||||||
| chr9:26843910 | A | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG02615.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.740-1263T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843910 | |||||||
| chr9:26844078 | C | A | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-1431G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844078 | |||||||
| chr9:26844133 | A | G | 19 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(16): Show |
20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.740-1486T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844133 | |||||||
| chr9:26844175 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0157 a0001c0001t0001g0175 |
4 | HG01243.hp2 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-1528A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844175 | |||||||
| chr9:26844187 | A | G | 1 | a0001c0002t0001g0271 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.740-1540T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844187 | |||||||
| chr9:26844289 | G | A | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.740-1642C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844289 | |||||||
| chr9:26844318 | T | C | 1 | a0002c0007t0011g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.740-1671A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844318 | |||||||
| chr9:26844325 | C | A | 4 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-1678G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844325 | |||||||
| chr9:26844353 | G | A | 3 | a0002c0003t0001g0032 a0002c0003t0001g0033 a0002c0003t0001g0034 |
3 | HG03041.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.740-1706C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844353 | |||||||
| chr9:26844357 | C | CA | 11 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0056 others(8): Show |
12 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.740-1711dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844357 | |||||||
| chr9:26844642 | T | A | 1 | a0001c0002t0001g0300 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.740-1995A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844642 | |||||||
| chr9:26844793 | T | C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG00733.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-2146A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844793 | |||||||
| chr9:26844844 | A | C | 1 | a0002c0003t0001g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.740-2197T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844844 | |||||||
| chr9:26844845 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
187 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.740-2198G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844845 | |||||||
| chr9:26845128 | A | T | 18 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(15): Show |
18 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.740-2481T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845128 | |||||||
| chr9:26845206 | GT | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 |
3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.740-2560delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845206 | |||||||
| chr9:26845229 | G | A | 1 | a0001c0002t0001g0298 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.740-2582C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845229 | |||||||
| chr9:26845282 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.740-2635C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845282 | |||||||
| chr9:26845305 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(117): Show |
130 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.740-2658G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845305 | |||||||
| chr9:26845470 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.740-2823C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845470 | |||||||
| chr9:26845485 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.740-2838G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845485 | |||||||
| chr9:26845601 | C | T | 7 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(4): Show |
7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.740-2954G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845601 | |||||||
| chr9:26845602 | C | G | 19 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(16): Show |
20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.740-2955G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845602 | |||||||
| chr9:26845618 | C | T | 1 | a0002c0007t0011g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.740-2971G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845618 | |||||||
| chr9:26845734 | G | T | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-3087C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845734 | |||||||
| chr9:26845841 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG00140.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.740-3194G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845841 | |||||||
| chr9:26845849 | G | A | 3 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0035 |
3 | HG02451.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.740-3202C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845849 | |||||||
| chr9:26845980 | G | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-3333C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845980 | |||||||
| chr9:26845980 | G | GT | 23 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(20): Show |
23 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.740-3334dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845980 | |||||||
| chr9:26846074 | T | C | 19 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(16): Show |
20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.740-3427A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846074 | |||||||
| chr9:26846107 | T | A | 1 | a0005c0005t0009g0020 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.740-3460A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846107 | |||||||
| chr9:26846113 | A | AC | 19 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(16): Show |
20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.740-3467dupG | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846113 | |||||||
| chr9:26846116 | C | G | 1 | a0005c0005t0009g0020 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.740-3469G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846116 | |||||||
| chr9:26846184 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.740-3537G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846184 | |||||||
| chr9:26846185 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
189 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.740-3538T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846185 | |||||||
| chr9:26846247 | C | T | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-3600G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846247 | |||||||
| chr9:26846355 | G | T | 1 | a0006c0006t0001g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.740-3708C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846355 | |||||||
| chr9:26846403 | G | A | 1 | a0002c0007t0011g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.740-3756C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846403 | |||||||
| chr9:26846415 | C | CA | 23 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(20): Show |
23 | HG00642.hp2 HG00735.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.740-3769dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | |||||||
| chr9:26846415 | C | CAA | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0069 others(66): Show |
75 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.740-3770_740-3769d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | |||||||
| chr9:26846415 | C | CAAA | 39 | a0001c0001t0001g0040 a0001c0001t0001g0075 a0001c0001t0001g0085 others(36): Show |
43 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.740-3771_740-3769d others(5): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | |||||||
| chr9:26846415 | C | CAAAA | 6 | a0001c0002t0001g0258 a0001c0002t0001g0279 a0001c0002t0001g0280 others(3): Show |
6 | HG00621.hp2 HG02027.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.740-3772_740-3769d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | |||||||
| chr9:26846415 | CA | C | 30 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(27): Show |
35 | HG00609.hp2 HG00733.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.740-3769delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | |||||||
| chr9:26846415 | CAAAAAAA others(4): Show |
C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(18): Show |
22 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(19): Show |
intron_variant | MODIFIER | c.740-3779_740-3769d others(13): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | |||||||
| chr9:26846415 | CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0001g0305 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.740-3781_740-3769d others(15): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | |||||||
| chr9:26846437 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | NA18747.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.740-3790T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846437 | |||||||
| chr9:26846438 | A | AG | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01496.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.740-3792_740-3791i others(3): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846438 | |||||||
| chr9:26846438 | A | G | 2 | a0002c0003t0001g0023 a0002c0003t0001g0024 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.740-3791T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846438 | |||||||
| chr9:26846439 | AG | A | 13 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0110 others(10): Show |
13 | HG01256.hp2 HG02056.hp2 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.740-3793delC | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846439 | |||||||
| chr9:26846440 | G | A | 13 | a0001c0001t0001g0109 a0001c0001t0001g0117 a0001c0001t0001g0118 others(10): Show |
13 | HG00733.hp1 HG01891.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.740-3793C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846440 | |||||||
| chr9:26846441 | A | AG | 3 | a0002c0003t0001g0027 a0002c0003t0001g0036 a0002c0003t0001g0039 |
3 | HG02257.hp2 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.740-3795_740-3794i others(3): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846441 | |||||||
| chr9:26846441 | A | G | 3 | a0002c0003t0001g0037 a0002c0003t0001g0038 a0002c0007t0011g0029 |
3 | HG01891.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.740-3794T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846441 | |||||||
| chr9:26846442 | AG | A | 11 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(8): Show |
12 | HG01192.hp2 HG01496.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.740-3796delC | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846442 | |||||||
| chr9:26846443 | G | A | 3 | a0002c0003t0001g0027 a0002c0003t0001g0036 a0002c0003t0001g0039 |
3 | HG02257.hp2 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.740-3796C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846443 | |||||||
| chr9:26846443 | G | GAA | 3 | a0002c0003t0001g0037 a0002c0003t0001g0038 a0002c0007t0011g0029 |
3 | HG01891.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.740-3798_740-3797d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846443 | |||||||
| chr9:26846448 | A | G | 3 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0035 |
3 | HG02451.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.740-3801T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846448 | |||||||
| chr9:26846453 | A | G | 3 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0035 |
3 | HG02451.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.740-3806T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846453 | |||||||
| chr9:26846751 | G | A | 3 | a0001c0002t0001g0348 a0003c0004t0001g0253 a0003c0004t0001g0254 |
3 | HG02451.hp1 NA19030.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.740-4104C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846751 | |||||||
| chr9:26846782 | G | A | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-4135C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846782 | |||||||
| chr9:26846810 | C | G | 5 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG02615.hp2 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.740-4163G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846810 | |||||||
| chr9:26846862 | T | C | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-4215A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846862 | |||||||
| chr9:26846928 | C | G | 7 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(4): Show |
7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.740-4281G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846928 | |||||||
| chr9:26847021 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.740-4374C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847021 | |||||||
| chr9:26847117 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.740-4470A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847117 | |||||||
| chr9:26847135 | A | G | 2 | a0001c0001t0002g0125 a0001c0001t0002g0126 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.740-4488T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847135 | |||||||
| chr9:26847198 | A | AT | 13 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): Show |
13 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.740-4552dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | ATTT | 18 | a0001c0001t0001g0042 a0001c0001t0001g0096 a0001c0001t0001g0154 others(15): Show |
18 | HG00140.hp1 HG00738.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.740-4554_740-4552d others(5): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | ATTTT | 29 | a0001c0001t0001g0137 a0001c0001t0001g0157 a0001c0001t0001g0158 others(26): Show |
29 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.740-4555_740-4552d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | ATTTTT | 21 | a0001c0001t0001g0005 a0001c0001t0001g0135 a0001c0001t0001g0148 others(18): Show |
23 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.740-4556_740-4552d others(7): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | ATTTTTT | 11 | a0001c0001t0001g0010 a0001c0001t0001g0134 a0001c0001t0001g0139 others(8): Show |
12 | HG01123.hp2 HG01515.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.740-4557_740-4552d others(8): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0099 a0001c0001t0001g0179 |
2 | HG00735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.740-4561_740-4552d others(12): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | ATTTTTTT others(4): Show |
4 | a0001c0001t0001g0082 a0001c0001t0001g0147 a0001c0001t0001g0178 others(1): Show |
4 | HG01258.hp1 HG03130.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-4562_740-4552d others(13): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0194 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.740-4563_740-4552d others(14): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0193 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.740-4564_740-4552d others(15): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0080 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.740-4565_740-4552d others(16): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0095 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.740-4566_740-4552d others(17): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0177 a0001c0001t0001g0222 |
2 | HG01975.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.740-4567_740-4552d others(18): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | ATTTTTTT others(12): Show |
2 | a0001c0001t0001g0094 a0001c0001t0001g0097 |
2 | HG00408.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.740-4570_740-4552d others(21): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0098 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.740-4573_740-4552d others(24): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | A | T | 1 | a0001c0001t0002g0205 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.740-4551T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | ATTT | A | 11 | a0001c0001t0001g0108 a0001c0001t0001g0111 a0001c0001t0001g0113 others(8): Show |
11 | HG00609.hp1 HG01099.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.740-4554_740-4552d others(5): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | ATTTT | A | 44 | a0001c0001t0001g0074 a0001c0001t0001g0085 a0001c0001t0001g0089 others(41): Show |
46 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.740-4555_740-4552d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | ATTTTT | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(80): Show |
91 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.740-4556_740-4552d others(7): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | ATTTTTT | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0081 a0001c0001t0001g0103 others(11): Show |
15 | HG00323.hp1 HG01109.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.740-4557_740-4552d others(8): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | ATTTTTTT | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0159 a0001c0001t0001g0165 others(5): Show |
9 | HG00733.hp2 HG01981.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-4558_740-4552d others(9): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | ATTTTTTT others(1): Show |
A | 33 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(30): Show |
37 | HG00423.hp1 HG00609.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.740-4559_740-4552d others(10): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0133 a0002c0007t0011g0029 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.740-4561_740-4552d others(12): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0002g0226 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.740-4562_740-4552d others(13): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0153 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.740-4563_740-4552d others(14): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0093 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.740-4565_740-4552d others(16): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | ATTTTTTT others(9): Show |
A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0076 |
2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.740-4567_740-4552d others(18): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847198 | ATTTTTTT others(13): Show |
A | 1 | a0001c0002t0001g0337 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.740-4571_740-4552d others(22): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | |||||||
| chr9:26847235 | C | G | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-4588G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847235 | |||||||
| chr9:26847238 | G | A | 3 | a0003c0004t0001g0100 a0003c0004t0001g0253 a0003c0004t0001g0254 |
3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.740-4591C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847238 | |||||||
| chr9:26847304 | T | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0069 others(10): Show |
14 | HG00438.hp1 HG00673.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.740-4657A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847304 | |||||||
| chr9:26847444 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.740-4797C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847444 | |||||||
| chr9:26847461 | G | A | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-4814C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847461 | |||||||
| chr9:26847503 | C | T | 3 | a0003c0004t0001g0100 a0003c0004t0001g0253 a0003c0004t0001g0254 |
3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.740-4856G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847503 | |||||||
| chr9:26847509 | C | T | 10 | a0001c0001t0002g0247 a0002c0003t0001g0001 a0002c0003t0001g0021 others(7): Show |
11 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.740-4862G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847509 | |||||||
| chr9:26847512 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0008g0207 |
2 | NA18975.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.740-4865G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847512 | |||||||
| chr9:26847530 | T | A | 5 | a0001c0001t0002g0236 a0001c0001t0002g0240 a0001c0001t0002g0246 others(2): Show |
5 | HG00642.hp1 HG01069.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.740-4883A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847530 | |||||||
| chr9:26847545 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.740-4898A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847545 | |||||||
| chr9:26847649 | G | A | 2 | a0004c0008t0001g0092 a0004c0010t0015g0328 |
2 | HG02683.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.740-5002C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847649 | |||||||
| chr9:26847717 | T | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(28): Show |
33 | HG00408.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.740-5070A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847717 | |||||||
| chr9:26847729 | T | C | 1 | a0001c0001t0002g0245 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.740-5082A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847729 | |||||||
| chr9:26847757 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.740-5110G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847757 | |||||||
| chr9:26847979 | T | C | 23 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(20): Show |
23 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.740-5332A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847979 | |||||||
| chr9:26848007 | T | C | 1 | a0006c0006t0001g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.740-5360A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848007 | |||||||
| chr9:26848071 | A | C | 1 | a0001c0001t0001g0172 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.740-5424T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848071 | |||||||
| chr9:26848108 | T | C | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-5461A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848108 | |||||||
| chr9:26848115 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-5468A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848115 | |||||||
| chr9:26848357 | A | C | 1 | a0001c0001t0001g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-5710T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848357 | |||||||
| chr9:26848358 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-5711G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848358 | |||||||
| chr9:26848409 | A | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
185 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.740-5762T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848409 | |||||||
| chr9:26848440 | C | T | 1 | a0001c0002t0001g0297 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.740-5793G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848440 | |||||||
| chr9:26848446 | G | C | 1 | a0001c0001t0001g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-5799C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848446 | |||||||
| chr9:26848470 | T | G | 1 | a0001c0002t0001g0277 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.740-5823A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848470 | |||||||
| chr9:26848515 | C | CA | 10 | a0001c0001t0001g0109 a0001c0002t0001g0269 a0001c0002t0001g0270 others(7): Show |
11 | HG01192.hp2 HG02027.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.740-5869dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848515 | |||||||
| chr9:26848523 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
188 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.740-5876C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848523 | |||||||
| chr9:26848568 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-5921T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848568 | |||||||
| chr9:26848569 | T | A | 1 | a0001c0001t0001g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-5922A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848569 | |||||||
| chr9:26848632 | A | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-5985T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848632 | |||||||
| chr9:26848647 | C | T | 1 | a0001c0002t0001g0321 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.740-6000G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848647 | |||||||
| chr9:26848652 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-6005A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848652 | |||||||
| chr9:26848711 | T | C | 3 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 |
4 | HG01192.hp2 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-6064A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848711 | |||||||
| chr9:26848838 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-6191T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848838 | |||||||
| chr9:26848839 | T | A | 1 | a0001c0001t0001g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-6192A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848839 | |||||||
| chr9:26848907 | T | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(111): Show |
124 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.740-6260A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848907 | |||||||
| chr9:26848928 | A | C | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0215 |
3 | HG00741.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.740-6281T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848928 | |||||||
| chr9:26848944 | T | C | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-6297A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848944 | |||||||
| chr9:26849116 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.740-6469A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849116 | |||||||
| chr9:26849372 | C | T | 1 | a0001c0002t0001g0261 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.740-6725G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849372 | |||||||
| chr9:26849415 | T | C | 1 | a0001c0001t0002g0244 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.740-6768A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849415 | |||||||
| chr9:26849442 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-6795T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849442 | |||||||
| chr9:26849446 | T | C | 4 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-6799A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849446 | |||||||
| chr9:26849498 | T | G | 5 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG02615.hp2 HG02683.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.740-6851A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849498 | |||||||
| chr9:26849572 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.740-6925A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849572 | |||||||
| chr9:26849597 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-6950G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849597 | |||||||
| chr9:26849608 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.740-6961T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849608 | |||||||
| chr9:26849619 | T | A | 1 | a0001c0001t0001g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-6972A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849619 | |||||||
| chr9:26849684 | CCTTTTTT others(1): Show |
C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-7045_740-7038d others(10): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849684 | |||||||
| chr9:26849744 | G | A | 10 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(7): Show |
10 | HG00597.hp2 HG02135.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.740-7097C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849744 | |||||||
| chr9:26849812 | G | C | 19 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(16): Show |
20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.740-7165C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849812 | |||||||
| chr9:26849841 | A | AT | 6 | a0001c0001t0001g0155 a0001c0001t0004g0083 a0001c0001t0004g0084 others(3): Show |
6 | HG01978.hp1 HG03041.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.740-7195dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849841 | |||||||
| chr9:26849841 | AT | A | 9 | a0001c0001t0001g0157 a0001c0002t0001g0259 a0001c0002t0001g0289 others(6): Show |
9 | HG00438.hp1 HG00673.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.740-7195delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849841 | |||||||
| chr9:26849950 | T | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-7303A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849950 | |||||||
| chr9:26849963 | C | T | 2 | a0001c0001t0001g0139 a0001c0002t0001g0319 |
2 | HG00597.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.740-7316G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849963 | |||||||
| chr9:26850039 | C | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG02615.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.740-7392G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850039 | |||||||
| chr9:26850058 | TTGATCTG others(8): Show |
T | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-7426_740-7412d others(17): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850058 | |||||||
| chr9:26850144 | A | C | 1 | a0002c0007t0011g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.740-7497T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850144 | |||||||
| chr9:26850196 | G | T | 4 | a0002c0003t0001g0036 a0002c0003t0001g0037 a0002c0003t0001g0038 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-7549C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850196 | |||||||
| chr9:26850208 | C | T | 2 | a0002c0003t0001g0030 a0002c0003t0001g0031 |
2 | HG01496.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.740-7561G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850208 | |||||||
| chr9:26850316 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.740-7669G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850316 | |||||||
| chr9:26850495 | G | A | 14 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(11): Show |
14 | HG01256.hp2 HG02056.hp2 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.740-7848C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850495 | |||||||
| chr9:26850595 | C | T | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.740-7948G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850595 | |||||||
| chr9:26850611 | C | T | 45 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(42): Show |
46 | HG00733.hp1 HG01192.hp2 HG01256.hp2 others(43): Show |
intron_variant | MODIFIER | c.740-7964G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850611 | |||||||
| chr9:26850719 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
7 | HG01515.hp2 HG01517.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.740-8072A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850719 | |||||||
| chr9:26850768 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.740-8121T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850768 | |||||||
| chr9:26850994 | G | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0258 |
3 | HG02015.hp2 NA18945.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.740-8347C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850994 | |||||||
| chr9:26851098 | T | TAGAAGTA others(343): Show |
1 | a0001c0001t0001g0165 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.740-8452_740-8451i others(352): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851098 | |||||||
| chr9:26851197 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(113): Show |
126 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.740-8550G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851197 | |||||||
| chr9:26851223 | A | C | 6 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(3): Show |
6 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.740-8576T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851223 | |||||||
| chr9:26851265 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-8618T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851265 | |||||||
| chr9:26851342 | T | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(121): Show |
134 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.740-8695A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851342 | |||||||
| chr9:26851343 | G | A | 2 | a0001c0002t0001g0338 a0001c0002t0001g0339 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.740-8696C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851343 | |||||||
| chr9:26851347 | G | A | 1 | a0002c0007t0011g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.740-8700C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851347 | |||||||
| chr9:26851403 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.740-8756C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851403 | |||||||
| chr9:26851411 | C | T | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-8764G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851411 | |||||||
| chr9:26851482 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(113): Show |
126 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.740-8835G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851482 | |||||||
| chr9:26851483 | C | T | 9 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0018 others(6): Show |
12 | HG00639.hp1 HG01081.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.740-8836G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851483 | |||||||
| chr9:26851516 | T | C | 2 | a0001c0002t0001g0344 a0001c0002t0001g0345 |
2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.740-8869A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851516 | |||||||
| chr9:26851931 | A | G | 1 | a0001c0002t0001g0277 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.739+9135T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851931 | |||||||
| chr9:26851937 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.739+9129A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851937 | |||||||
| chr9:26851943 | A | G | 1 | a0001c0002t0001g0280 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.739+9123T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851943 | |||||||
| chr9:26851951 | T | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0069 others(81): Show |
92 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.739+9115A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851951 | |||||||
| chr9:26852028 | A | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(117): Show |
130 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.739+9038T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852028 | |||||||
| chr9:26852062 | A | T | 14 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(11): Show |
14 | HG01256.hp2 HG02056.hp2 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.739+9004T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852062 | |||||||
| chr9:26852282 | C | T | 1 | a0002c0003t0001g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.739+8784G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852282 | |||||||
| chr9:26852327 | C | T | 2 | a0004c0008t0001g0092 a0004c0010t0015g0328 |
2 | HG02683.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.739+8739G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852327 | |||||||
| chr9:26852386 | C | T | 2 | a0002c0003t0001g0025 a0002c0003t0001g0035 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.739+8680G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852386 | |||||||
| chr9:26852387 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.739+8679C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852387 | |||||||
| chr9:26852470 | A | C | 1 | a0004c0008t0001g0092 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.739+8596T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852470 | |||||||
| chr9:26852534 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.739+8532A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852534 | |||||||
| chr9:26852543 | G | C | 1 | a0001c0002t0001g0320 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.739+8523C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852543 | |||||||
| chr9:26852605 | T | C | 1 | a0004c0010t0015g0328 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.739+8461A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852605 | |||||||
| chr9:26852631 | C | G | 1 | a0001c0002t0001g0257 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.739+8435G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852631 | |||||||
| chr9:26852772 | G | C | 8 | a0001c0001t0002g0127 a0001c0001t0002g0224 a0001c0001t0002g0226 others(5): Show |
8 | HG01123.hp1 HG01928.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.739+8294C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852772 | |||||||
| chr9:26853203 | T | C | 6 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(3): Show |
6 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.739+7863A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853203 | |||||||
| chr9:26853285 | T | C | 1 | a0001c0002t0001g0257 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.739+7781A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853285 | |||||||
| chr9:26853286 | G | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+7780C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853286 | |||||||
| chr9:26853421 | T | A | 2 | a0002c0007t0011g0029 a0006c0006t0001g0028 |
2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.739+7645A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853421 | |||||||
| chr9:26853487 | A | G | 1 | a0002c0003t0001g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.739+7579T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853487 | |||||||
| chr9:26853781 | A | T | 1 | a0001c0001t0002g0242 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.739+7285T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853781 | |||||||
| chr9:26853824 | C | G | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+7242G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853824 | |||||||
| chr9:26853847 | T | G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0107 |
3 | NA18960.hp1 NA18973.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.739+7219A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853847 | |||||||
| chr9:26853895 | A | G | 3 | a0003c0004t0001g0100 a0003c0004t0001g0253 a0003c0004t0001g0254 |
3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.739+7171T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853895 | |||||||
| chr9:26854073 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.739+6993A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854073 | |||||||
| chr9:26854132 | G | GA | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+6933dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854132 | |||||||
| chr9:26854194 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.739+6872G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854194 | |||||||
| chr9:26854449 | A | G | 1 | a0001c0002t0001g0263 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.739+6617T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854449 | |||||||
| chr9:26854482 | G | GCTGAATG others(3): Show |
20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+6574_739+6583d others(12): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854482 | |||||||
| chr9:26854535 | C | T | 2 | a0001c0001t0002g0251 a0001c0001t0002g0252 |
2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.739+6531G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854535 | |||||||
| chr9:26854740 | G | T | 8 | a0001c0001t0002g0127 a0001c0001t0002g0224 a0001c0001t0002g0226 others(5): Show |
8 | HG01123.hp1 HG01928.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.739+6326C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854740 | |||||||
| chr9:26854802 | A | G | 4 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+6264T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854802 | |||||||
| chr9:26854825 | G | A | 7 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(4): Show |
7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.739+6241C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854825 | |||||||
| chr9:26854990 | A | C | 8 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(5): Show |
8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.739+6076T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854990 | |||||||
| chr9:26855058 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.739+6008A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855058 | |||||||
| chr9:26855078 | T | G | 1 | a0001c0001t0001g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.739+5988A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855078 | |||||||
| chr9:26855103 | G | C | 4 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+5963C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855103 | |||||||
| chr9:26855128 | T | C | 1 | a0001c0001t0002g0225 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.739+5938A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855128 | |||||||
| chr9:26855316 | G | A | 1 | a0003c0004t0001g0100 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.739+5750C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855316 | |||||||
| chr9:26855322 | G | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG00733.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.739+5744C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855322 | |||||||
| chr9:26855323 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.739+5743C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855323 | |||||||
| chr9:26855635 | C | T | 1 | a0001c0002t0001g0312 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.739+5431G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855635 | |||||||
| chr9:26856013 | T | G | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.739+5053A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856013 | |||||||
| chr9:26856128 | A | AG | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
147 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.739+4937dupC | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856128 | |||||||
| chr9:26856131 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.739+4935C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856131 | |||||||
| chr9:26856131 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.739+4935C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856131 | |||||||
| chr9:26856133 | G | GA | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+4932_739+4933i others(3): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856133 | |||||||
| chr9:26856218 | C | T | 2 | a0001c0001t0004g0083 a0001c0001t0004g0084 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.739+4848G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856218 | |||||||
| chr9:26856279 | T | G | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+4787A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856279 | |||||||
| chr9:26856421 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG00140.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.739+4645T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856421 | |||||||
| chr9:26856441 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.739+4625C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856441 | |||||||
| chr9:26856707 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.739+4359A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856707 | |||||||
| chr9:26856754 | A | C | 23 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(20): Show |
23 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.739+4312T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856754 | |||||||
| chr9:26856866 | A | G | 1 | a0001c0002t0001g0346 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.739+4200T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856866 | |||||||
| chr9:26856986 | T | C | 8 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(5): Show |
8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.739+4080A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856986 | |||||||
| chr9:26856990 | G | A | 1 | a0001c0001t0010g0121 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.739+4076C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856990 | |||||||
| chr9:26857047 | G | C | 1 | a0001c0001t0001g0006 | 2 | HG02015.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.739+4019C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857047 | |||||||
| chr9:26857089 | GT | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+3976delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857089 | |||||||
| chr9:26857232 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0218 a0001c0001t0014g0187 |
3 | NA18944.hp2 NA18970.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.739+3834G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857232 | |||||||
| chr9:26857246 | C | T | 309 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(306): Show |
327 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.739+3820G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857246 | |||||||
| chr9:26857316 | C | G | 23 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(20): Show |
23 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.739+3750G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857316 | |||||||
| chr9:26857351 | G | A | 9 | a0001c0002t0001g0280 a0001c0002t0001g0281 a0001c0002t0001g0282 others(6): Show |
9 | HG00621.hp2 NA18959.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+3715C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857351 | |||||||
| chr9:26857359 | T | C | 60 | a0001c0001t0001g0137 a0001c0001t0001g0241 a0001c0001t0002g0011 others(57): Show |
62 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.739+3707A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857359 | |||||||
| chr9:26857543 | A | C | 1 | a0001c0002t0001g0270 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.739+3523T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857543 | |||||||
| chr9:26857564 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+3502C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857564 | |||||||
| chr9:26857582 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.739+3484T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857582 | |||||||
| chr9:26857877 | C | CA | 128 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(125): Show |
138 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.739+3188dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857877 | |||||||
| chr9:26857899 | T | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+3167A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857899 | |||||||
| chr9:26857960 | A | G | 14 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(11): Show |
14 | HG01256.hp2 HG02056.hp2 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.739+3106T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857960 | |||||||
| chr9:26858226 | AGAGATAT others(8): Show |
A | 21 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(18): Show |
21 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.739+2825_739+2839d others(17): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858226 | |||||||
| chr9:26858243 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.739+2823G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858243 | |||||||
| chr9:26858353 | T | C | 1 | a0001c0002t0001g0288 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.739+2713A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858353 | |||||||
| chr9:26858447 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+2619G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858447 | |||||||
| chr9:26858524 | A | T | 1 | a0002c0003t0001g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.739+2542T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858524 | |||||||
| chr9:26858531 | G | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+2535C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858531 | |||||||
| chr9:26858557 | T | C | 9 | a0001c0002t0001g0280 a0001c0002t0001g0281 a0001c0002t0001g0282 others(6): Show |
9 | HG00621.hp2 NA18959.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+2509A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858557 | |||||||
| chr9:26858561 | G | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+2505C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858561 | |||||||
| chr9:26858608 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.739+2458C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858608 | |||||||
| chr9:26858632 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0085 others(168): Show |
182 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.739+2434A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858632 | |||||||
| chr9:26858679 | C | T | 1 | a0006c0006t0001g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.739+2387G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858679 | |||||||
| chr9:26858738 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0150 |
3 | HG00099.hp2 HG00280.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.739+2328C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858738 | |||||||
| chr9:26858813 | G | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0085 others(168): Show |
182 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.739+2253C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858813 | |||||||
| chr9:26858822 | C | CAA | 20 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(17): Show |
20 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.739+2242_739+2243d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858822 | |||||||
| chr9:26858822 | CA | C | 15 | a0001c0001t0001g0137 a0001c0001t0001g0216 a0001c0001t0002g0204 others(12): Show |
16 | HG01192.hp2 HG01255.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.739+2243delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858822 | |||||||
| chr9:26858833 | A | G | 2 | a0003c0004t0001g0253 a0003c0004t0001g0254 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.739+2233T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858833 | |||||||
| chr9:26858954 | C | T | 73 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0014 others(70): Show |
80 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.739+2112G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858954 | |||||||
| chr9:26858978 | T | C | 8 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(5): Show |
8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.739+2088A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858978 | |||||||
| chr9:26858984 | G | C | 4 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+2082C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858984 | |||||||
| chr9:26858996 | C | CA | 150 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0054 others(147): Show |
161 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.739+2069dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858996 | |||||||
| chr9:26858996 | C | CAA | 6 | a0001c0001t0001g0056 a0001c0001t0001g0110 a0001c0002t0001g0266 others(3): Show |
6 | HG00621.hp1 HG03098.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.739+2068_739+2069d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858996 | |||||||
| chr9:26858996 | CA | C | 10 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0097 others(7): Show |
10 | HG00408.hp2 HG01070.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.739+2069delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858996 | |||||||
| chr9:26859142 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.739+1924C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859142 | |||||||
| chr9:26859145 | C | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG02615.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.739+1921G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859145 | |||||||
| chr9:26859352 | CTGAG | C | 8 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0147 others(5): Show |
8 | HG01123.hp2 HG01192.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.739+1710_739+1713d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859352 | |||||||
| chr9:26859373 | C | A | 2 | a0002c0003t0001g0025 a0002c0003t0001g0035 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.739+1693G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859373 | |||||||
| chr9:26859476 | C | T | 1 | a0001c0002t0001g0334 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.739+1590G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859476 | |||||||
| chr9:26859503 | G | C | 1 | a0001c0002t0001g0325 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.739+1563C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859503 | |||||||
| chr9:26859509 | G | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+1557C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859509 | |||||||
| chr9:26859642 | T | C | 3 | a0002c0003t0001g0032 a0002c0003t0001g0033 a0002c0003t0001g0034 |
3 | HG03041.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.739+1424A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859642 | |||||||
| chr9:26859664 | T | C | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.739+1402A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859664 | |||||||
| chr9:26859722 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.739+1344T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859722 | |||||||
| chr9:26860123 | A | G | 1 | a0005c0005t0009g0020 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.739+943T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860123 | |||||||
| chr9:26860125 | A | C | 1 | a0005c0005t0009g0020 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.739+941T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860125 | |||||||
| chr9:26860230 | A | G | 3 | a0003c0004t0001g0100 a0003c0004t0001g0253 a0003c0004t0001g0254 |
3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.739+836T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860230 | |||||||
| chr9:26860357 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.739+709A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860357 | |||||||
| chr9:26860360 | T | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0085 others(167): Show |
181 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.739+706A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860360 | |||||||
| chr9:26860361 | G | A | 4 | a0001c0002t0001g0289 a0001c0002t0001g0290 a0001c0002t0001g0293 others(1): Show |
4 | HG00438.hp1 HG00673.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.739+705C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860361 | |||||||
| chr9:26860558 | C | T | 1 | a0001c0002t0001g0302 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.739+508G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860558 | |||||||
| chr9:26860568 | G | A | 4 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+498C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860568 | |||||||
| chr9:26860578 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.739+488C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860578 | |||||||
| chr9:26860611 | T | C | 1 | a0001c0002t0001g0318 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.739+455A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860611 | |||||||
| chr9:26860652 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.739+414G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860652 | |||||||
| chr9:26860706 | G | A | 2 | a0001c0002t0001g0273 a0001c0002t0001g0291 |
2 | NA18981.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.739+360C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860706 | |||||||
| chr9:26860713 | A | AC | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+352dupG | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860713 | |||||||
| chr9:26860715 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0195 a0001c0001t0001g0199 |
3 | NA18612.hp1 NA18982.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.739+351G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860715 | |||||||
| chr9:26860723 | T | G | 47 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(44): Show |
48 | HG00733.hp1 HG01192.hp2 HG01256.hp2 others(45): Show |
intron_variant | MODIFIER | c.739+343A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860723 | |||||||
| chr9:26860733 | G | C | 2 | a0002c0003t0001g0001 a0002c0003t0001g0022 |
3 | HG01192.hp2 HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.739+333C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860733 | |||||||
| chr9:26860740 | A | G | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+326T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860740 | |||||||
| chr9:26860748 | G | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+318C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860748 | |||||||
| chr9:26860780 | G | C | 1 | a0004c0008t0001g0092 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.739+286C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860780 | |||||||
| chr9:26860891 | A | G | 1 | a0001c0002t0001g0320 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.739+175T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860891 | |||||||
| chr9:26861032 | A | C | 4 | a0002c0003t0001g0036 a0002c0003t0001g0037 a0002c0003t0001g0038 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.739+34T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26861032 | |||||||
| chr9:26861154 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.666-15A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26861154 | |||||||
| chr9:26861300 | A | G | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.666-161T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26861300 | |||||||
| chr9:26861435 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-296A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26861435 | |||||||
| chr9:26861605 | G | A | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG00733.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-466C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26861605 | |||||||
| chr9:26861675 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.666-536C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26861675 | |||||||
| chr9:26861757 | T | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA19077.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.666-618A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26861757 | |||||||
| chr9:26862002 | G | GTT | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-864_666-863ins others(2): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862002 | |||||||
| chr9:26862021 | C | T | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-882G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862021 | |||||||
| chr9:26862170 | C | T | 19 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(16): Show |
20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.666-1031G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862170 | |||||||
| chr9:26862350 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.666-1211G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862350 | |||||||
| chr9:26862379 | T | C | 23 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(20): Show |
23 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.666-1240A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862379 | |||||||
| chr9:26862415 | C | CA | 27 | a0001c0001t0001g0064 a0001c0001t0001g0217 a0001c0001t0001g0220 others(24): Show |
28 | HG00408.hp1 HG01192.hp2 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.666-1277dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862415 | |||||||
| chr9:26862518 | T | C | 2 | a0002c0003t0001g0030 a0002c0003t0001g0031 |
2 | HG01496.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.666-1379A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862518 | |||||||
| chr9:26862704 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0157 a0001c0001t0001g0175 others(3): Show |
7 | HG01243.hp2 HG02280.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.666-1565C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862704 | |||||||
| chr9:26862806 | C | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-1667G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862806 | |||||||
| chr9:26862961 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG01516.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.666-1822C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862961 | |||||||
| chr9:26863119 | C | T | 2 | a0001c0001t0004g0083 a0001c0001t0004g0084 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.666-1980G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863119 | |||||||
| chr9:26863181 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.666-2042A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863181 | |||||||
| chr9:26863245 | C | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(109): Show |
121 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.666-2106G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863245 | |||||||
| chr9:26863249 | A | G | 1 | a0001c0002t0001g0279 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.666-2110T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863249 | |||||||
| chr9:26863356 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.666-2217C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863356 | |||||||
| chr9:26863532 | C | T | 1 | a0002c0007t0011g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666-2393G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863532 | |||||||
| chr9:26863671 | C | A | 2 | a0001c0002t0001g0340 a0001c0002t0001g0343 |
2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.666-2532G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863671 | |||||||
| chr9:26863772 | T | TA | 14 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0079 others(11): Show |
14 | HG00558.hp2 HG00741.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.666-2634dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863772 | |||||||
| chr9:26863772 | TA | T | 146 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.666-2634delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863772 | |||||||
| chr9:26863772 | TAA | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(22): Show |
27 | HG00323.hp1 HG01069.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.666-2635_666-2634d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863772 | |||||||
| chr9:26863773 | A | T | 2 | a0002c0003t0001g0023 a0002c0003t0001g0026 |
2 | HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.666-2634T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863773 | |||||||
| chr9:26863774 | A | T | 5 | a0002c0003t0001g0021 a0002c0003t0001g0024 a0002c0003t0001g0025 others(2): Show |
5 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-2635T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863774 | |||||||
| chr9:26863775 | A | T | 11 | a0002c0003t0001g0001 a0002c0003t0001g0022 a0002c0003t0001g0027 others(8): Show |
12 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.666-2636T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863775 | |||||||
| chr9:26863896 | A | G | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-2757T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863896 | |||||||
| chr9:26863978 | T | C | 7 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(4): Show |
7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.666-2839A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863978 | |||||||
| chr9:26863997 | A | C | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.666-2858T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863997 | |||||||
| chr9:26864041 | G | C | 9 | a0001c0002t0001g0280 a0001c0002t0001g0281 a0001c0002t0001g0282 others(6): Show |
9 | HG00621.hp2 NA18959.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-2902C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864041 | |||||||
| chr9:26864121 | A | C | 1 | a0002c0007t0011g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666-2982T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864121 | |||||||
| chr9:26864251 | T | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-3112A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864251 | |||||||
| chr9:26864490 | A | AC | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-3352dupG | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864490 | |||||||
| chr9:26864530 | C | T | 3 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0035 |
3 | HG02451.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.666-3391G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864530 | |||||||
| chr9:26864565 | T | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-3426A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864565 | |||||||
| chr9:26864566 | G | A | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.666-3427C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864566 | |||||||
| chr9:26864604 | C | A | 3 | a0002c0003t0001g0032 a0002c0003t0001g0033 a0002c0003t0001g0034 |
3 | HG03041.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.666-3465G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864604 | |||||||
| chr9:26864614 | C | T | 1 | a0004c0008t0001g0092 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.666-3475G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864614 | |||||||
| chr9:26864681 | G | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(119): Show |
132 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.666-3542C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864681 | |||||||
| chr9:26864709 | T | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-3570A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864709 | |||||||
| chr9:26864726 | A | G | 2 | a0001c0001t0004g0083 a0001c0001t0004g0084 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.666-3587T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864726 | |||||||
| chr9:26864731 | A | G | 4 | a0001c0001t0001g0167 a0001c0001t0001g0196 a0001c0001t0001g0198 others(1): Show |
4 | HG02129.hp2 HG02132.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-3592T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864731 | |||||||
| chr9:26864780 | G | T | 35 | a0001c0001t0002g0011 a0001c0001t0002g0127 a0001c0001t0002g0205 others(32): Show |
36 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.666-3641C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864780 | |||||||
| chr9:26864835 | C | G | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-3696G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864835 | |||||||
| chr9:26864856 | C | T | 1 | a0001c0002t0001g0296 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.666-3717G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864856 | |||||||
| chr9:26864930 | G | T | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.666-3791C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864930 | |||||||
| chr9:26865003 | C | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-3864G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865003 | |||||||
| chr9:26865040 | T | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-3901A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865040 | |||||||
| chr9:26865049 | T | A | 1 | a0001c0002t0001g0300 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.666-3910A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865049 | |||||||
| chr9:26865449 | G | A | 21 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(18): Show |
21 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.666-4310C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865449 | |||||||
| chr9:26865460 | GT | G | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4322delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865460 | |||||||
| chr9:26865481 | G | T | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4342C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865481 | |||||||
| chr9:26865501 | G | T | 1 | a0001c0001t0002g0252 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.666-4362C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865501 | |||||||
| chr9:26865516 | CTA | C | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4379_666-4378d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865516 | |||||||
| chr9:26865524 | C | CA | 14 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0102 others(11): Show |
15 | HG00323.hp1 HG01074.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.666-4386dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865524 | |||||||
| chr9:26865524 | CA | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(115): Show |
127 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.666-4386delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865524 | |||||||
| chr9:26865538 | A | T | 8 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(5): Show |
8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.666-4399T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865538 | |||||||
| chr9:26865579 | AG | A | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4441delC | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865579 | |||||||
| chr9:26865698 | A | G | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4559T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865698 | |||||||
| chr9:26865820 | G | C | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4681C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865820 | |||||||
| chr9:26865891 | A | T | 38 | a0001c0001t0002g0011 a0001c0001t0002g0125 a0001c0001t0002g0126 others(35): Show |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.666-4752T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865891 | |||||||
| chr9:26865897 | A | G | 1 | a0003c0004t0001g0100 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.666-4758T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865897 | |||||||
| chr9:26865904 | T | C | 5 | a0001c0001t0004g0083 a0001c0001t0004g0084 a0003c0004t0001g0100 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-4765A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865904 | |||||||
| chr9:26865990 | A | G | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4851T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865990 | |||||||
| chr9:26866001 | T | C | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4862A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866001 | |||||||
| chr9:26866003 | T | C | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4864A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866003 | |||||||
| chr9:26866008 | G | A | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4869C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866008 | |||||||
| chr9:26866018 | T | C | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4879A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866018 | |||||||
| chr9:26866135 | CCA | C | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4998_666-4997d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866135 | |||||||
| chr9:26866168 | A | G | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-5029T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866168 | |||||||
| chr9:26866171 | C | T | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-5032G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866171 | |||||||
| chr9:26866222 | C | T | 1 | a0001c0002t0001g0270 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.666-5083G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866222 | |||||||
| chr9:26866232 | T | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0085 others(168): Show |
182 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.666-5093A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866232 | |||||||
| chr9:26866264 | T | C | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-5125A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866264 | |||||||
| chr9:26866331 | T | C | 1 | a0001c0002t0001g0293 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.666-5192A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866331 | |||||||
| chr9:26866486 | T | G | 1 | a0002c0003t0001g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.666-5347A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866486 | |||||||
| chr9:26866644 | T | C | 25 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(22): Show |
25 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.666-5505A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866644 | |||||||
| chr9:26866648 | A | G | 1 | a0001c0001t0002g0204 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.666-5509T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866648 | |||||||
| chr9:26866736 | A | T | 1 | a0001c0001t0001g0007 | 2 | HG01081.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.666-5597T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866736 | |||||||
| chr9:26866778 | T | C | 1 | a0001c0002t0001g0267 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.666-5639A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866778 | |||||||
| chr9:26866912 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.666-5773G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866912 | |||||||
| chr9:26866913 | G | T | 5 | a0001c0001t0001g0101 a0001c0001t0001g0109 a0001c0001t0001g0115 others(2): Show |
5 | HG01256.hp2 HG02735.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-5774C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866913 | |||||||
| chr9:26866925 | G | T | 10 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(7): Show |
10 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.666-5786C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866925 | |||||||
| chr9:26867088 | T | C | 3 | a0003c0004t0001g0100 a0003c0004t0001g0253 a0003c0004t0001g0254 |
3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.666-5949A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867088 | |||||||
| chr9:26867123 | G | A | 1 | a0004c0008t0001g0092 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.666-5984C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867123 | |||||||
| chr9:26867129 | G | C | 1 | a0001c0002t0001g0284 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.666-5990C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867129 | |||||||
| chr9:26867211 | C | G | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-6072G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867211 | |||||||
| chr9:26867213 | T | C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG00733.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-6074A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867213 | |||||||
| chr9:26867335 | C | T | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-6196G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867335 | |||||||
| chr9:26867496 | C | G | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-6357G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867496 | |||||||
| chr9:26867565 | A | C | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-6426T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867565 | |||||||
| chr9:26867682 | A | G | 1 | a0001c0002t0001g0346 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.666-6543T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867682 | |||||||
| chr9:26867708 | T | C | 11 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0027 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-6569A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867708 | |||||||
| chr9:26867740 | G | C | 1 | a0002c0007t0011g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666-6601C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867740 | |||||||
| chr9:26867768 | T | C | 1 | a0001c0002t0001g0300 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.666-6629A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867768 | |||||||
| chr9:26867773 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | NA18964.hp1 NA18967.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-6634A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867773 | |||||||
| chr9:26867839 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.666-6700A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867839 | |||||||
| chr9:26868024 | TA | T | 7 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(4): Show |
7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.666-6886delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868024 | |||||||
| chr9:26868087 | T | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-6948A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868087 | |||||||
| chr9:26868211 | C | T | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0085 others(167): Show |
181 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.666-7072G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868211 | |||||||
| chr9:26868222 | TTTGTGA | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.666-7089_666-7084d others(8): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868222 | |||||||
| chr9:26868284 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.666-7145T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868284 | |||||||
| chr9:26868371 | T | C | 10 | a0001c0001t0001g0131 a0001c0001t0001g0181 a0001c0001t0001g0188 others(7): Show |
10 | HG00423.hp2 HG02165.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.666-7232A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868371 | |||||||
| chr9:26868402 | C | A | 2 | a0002c0003t0001g0025 a0002c0003t0001g0035 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.666-7263G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868402 | |||||||
| chr9:26868697 | A | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-7558T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868697 | |||||||
| chr9:26868701 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.666-7562G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868701 | |||||||
| chr9:26868791 | CAA | C | 7 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(4): Show |
7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.666-7654_666-7653d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868791 | |||||||
| chr9:26869203 | T | A | 27 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(24): Show |
27 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.666-8064A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869203 | |||||||
| chr9:26869374 | T | C | 1 | a0005c0005t0009g0020 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.666-8235A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869374 | |||||||
| chr9:26869513 | G | GA | 5 | a0001c0001t0001g0142 a0001c0001t0002g0204 a0001c0002t0001g0258 others(2): Show |
5 | HG01255.hp1 HG03942.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-8375dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869513 | |||||||
| chr9:26869534 | T | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(120): Show |
133 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.666-8395A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869534 | |||||||
| chr9:26869599 | G | A | 19 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(16): Show |
20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.666-8460C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869599 | |||||||
| chr9:26869602 | C | T | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-8463G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869602 | |||||||
| chr9:26869621 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.666-8482T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869621 | |||||||
| chr9:26869657 | G | A | 1 | a0002c0003t0001g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.666-8518C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869657 | |||||||
| chr9:26869753 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-8614T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869753 | |||||||
| chr9:26869827 | T | C | 5 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0002g0229 others(2): Show |
5 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-8688A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869827 | |||||||
| chr9:26870039 | C | CT | 16 | a0001c0001t0001g0081 a0001c0001t0001g0101 a0001c0001t0001g0122 others(13): Show |
16 | HG00099.hp2 HG00735.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.666-8901dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870039 | |||||||
| chr9:26870039 | C | CTT | 26 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(23): Show |
26 | HG00733.hp1 HG02055.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.666-8902_666-8901d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870039 | |||||||
| chr9:26870039 | CT | C | 29 | a0001c0001t0001g0004 a0001c0001t0001g0057 a0001c0001t0001g0058 others(26): Show |
30 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.666-8901delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870039 | |||||||
| chr9:26870039 | CTT | C | 17 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(14): Show |
18 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.666-8902_666-8901d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870039 | |||||||
| chr9:26870059 | T | A | 1 | a0001c0002t0001g0338 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.666-8920A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870059 | |||||||
| chr9:26870169 | C | G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0107 |
3 | NA18960.hp1 NA18973.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.666-9030G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870169 | |||||||
| chr9:26870218 | T | C | 3 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 |
4 | HG01192.hp2 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-9079A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870218 | |||||||
| chr9:26870227 | G | A | 4 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-9088C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870227 | |||||||
| chr9:26870257 | G | C | 3 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 |
4 | HG01192.hp2 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-9118C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870257 | |||||||
| chr9:26870273 | T | C | 1 | a0002c0003t0001g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.666-9134A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870273 | |||||||
| chr9:26870481 | C | A | 1 | a0006c0006t0001g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.666-9342G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870481 | |||||||
| chr9:26870488 | A | G | 1 | a0001c0001t0005g0146 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.666-9349T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870488 | |||||||
| chr9:26870523 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(134): Show |
146 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.666-9384G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870523 | |||||||
| chr9:26870547 | T | TAC | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(123): Show |
136 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.666-9410_666-9409d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870547 | |||||||
| chr9:26870566 | G | A | 2 | a0001c0001t0004g0083 a0001c0001t0004g0084 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.666-9427C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870566 | |||||||
| chr9:26870587 | C | CGT | 21 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0046 others(18): Show |
21 | HG00639.hp2 HG01074.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-9450_666-9449d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870587 | |||||||
| chr9:26870587 | C | CGTGT | 5 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(2): Show |
6 | HG01192.hp2 HG01496.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.666-9452_666-9449d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870587 | |||||||
| chr9:26870587 | CGT | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(12): Show |
16 | HG00323.hp1 HG01258.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.666-9450_666-9449d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870587 | |||||||
| chr9:26870587 | CGTGT | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(144): Show |
157 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.666-9452_666-9449d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870587 | |||||||
| chr9:26870677 | C | T | 103 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0014 others(100): Show |
111 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.666-9538G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870677 | |||||||
| chr9:26870749 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.666-9610G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870749 | |||||||
| chr9:26870766 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.666-9627C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870766 | |||||||
| chr9:26870855 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.666-9716C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870855 | |||||||
| chr9:26871270 | G | GT | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-10132dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871270 | |||||||
| chr9:26871326 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | NA19009.hp2 NA19055.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-10187G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871326 | |||||||
| chr9:26871480 | G | C | 6 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(3): Show |
6 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.666-10341C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871480 | |||||||
| chr9:26871500 | G | C | 28 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(25): Show |
30 | HG00323.hp1 HG01192.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.666-10361C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871500 | |||||||
| chr9:26871501 | T | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-10362A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871501 | |||||||
| chr9:26871560 | C | T | 104 | a0001c0001t0002g0127 a0001c0002t0001g0012 a0001c0002t0001g0013 others(101): Show |
112 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.666-10421G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871560 | |||||||
| chr9:26871577 | T | TAA | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-10440_666-1043 others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871577 | |||||||
| chr9:26871577 | TA | T | 7 | a0001c0001t0001g0090 a0001c0001t0002g0204 a0001c0001t0002g0227 others(4): Show |
7 | HG01070.hp2 HG01255.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.666-10439delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871577 | |||||||
| chr9:26871661 | C | T | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.666-10522G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871661 | |||||||
| chr9:26871662 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG02015.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.666-10523C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871662 | |||||||
| chr9:26871788 | C | T | 1 | a0001c0002t0001g0266 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.666-10649G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871788 | |||||||
| chr9:26871837 | T | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
192 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.666-10698A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871837 | |||||||
| chr9:26871901 | C | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-10762G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871901 | |||||||
| chr9:26871914 | A | AAAAT | 5 | a0001c0001t0001g0006 a0001c0001t0001g0105 a0001c0002t0001g0344 others(2): Show |
6 | HG01496.hp1 HG02015.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.666-10779_666-1077 others(8): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871914 | |||||||
| chr9:26871914 | A | AAAATAAA others(5): Show |
5 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0032 others(2): Show |
5 | HG01496.hp2 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-10787_666-1077 others(16): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871914 | |||||||
| chr9:26871914 | A | AAAATAAA others(9): Show |
6 | a0002c0003t0001g0001 a0002c0003t0001g0022 a0002c0003t0001g0036 others(3): Show |
7 | HG01192.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.666-10791_666-1077 others(20): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871914 | |||||||
| chr9:26871914 | A | AAAATAAA others(13): Show |
5 | a0002c0003t0001g0023 a0002c0003t0001g0024 a0002c0003t0001g0026 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-10795_666-1077 others(24): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871914 | |||||||
| chr9:26871914 | A | AAAATAAA others(17): Show |
1 | a0002c0003t0001g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.666-10799_666-1077 others(28): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871914 | |||||||
| chr9:26871942 | T | TAAATAAA others(9): Show |
1 | a0002c0003t0001g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.666-10804_666-1080 others(20): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871942 | |||||||
| chr9:26871992 | T | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
194 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.666-10853A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871992 | |||||||
| chr9:26872053 | G | A | 19 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(16): Show |
20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.666-10914C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872053 | |||||||
| chr9:26872472 | C | T | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-11333G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872472 | |||||||
| chr9:26872540 | T | C | 1 | a0002c0007t0011g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666-11401A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872540 | |||||||
| chr9:26872553 | A | AAT | 24 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(21): Show |
25 | HG01069.hp2 HG01070.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.666-11416_666-1141 others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | |||||||
| chr9:26872553 | A | AATAT | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-11418_666-1141 others(8): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | |||||||
| chr9:26872553 | A | AATATATA others(9): Show |
1 | a0002c0003t0001g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.666-11430_666-1141 others(20): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | |||||||
| chr9:26872553 | A | AATATATA others(13): Show |
3 | a0002c0003t0001g0021 a0002c0003t0001g0032 a0002c0003t0001g0034 |
3 | HG03041.hp2 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.666-11434_666-1141 others(24): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | |||||||
| chr9:26872553 | A | AATATATA others(15): Show |
1 | a0002c0003t0001g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.666-11415_666-1141 others(26): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | |||||||
| chr9:26872553 | A | AATATATA others(19): Show |
3 | a0002c0003t0001g0001 a0002c0003t0001g0022 a0002c0003t0001g0030 |
4 | HG01192.hp2 HG01496.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-11415_666-1141 others(30): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | |||||||
| chr9:26872553 | A | AATATATA others(23): Show |
1 | a0006c0006t0001g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.666-11415_666-1141 others(34): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | |||||||
| chr9:26872553 | A | AATATATA others(25): Show |
1 | a0002c0003t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-11415_666-1141 others(36): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | |||||||
| chr9:26872553 | A | AATATATA others(29): Show |
2 | a0002c0003t0001g0023 a0002c0003t0001g0037 |
2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.666-11415_666-1141 others(40): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | |||||||
| chr9:26872553 | A | AATATATA others(35): Show |
1 | a0002c0003t0001g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.666-11415_666-1141 others(46): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | |||||||
| chr9:26872553 | A | AATATATA others(39): Show |
1 | a0002c0003t0001g0036 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.666-11415_666-1141 others(50): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | |||||||
| chr9:26872553 | A | ATATATAT others(18): Show |
1 | a0002c0007t0011g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666-11415_666-1141 others(29): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | |||||||
| chr9:26872553 | AATAT | A | 3 | a0002c0003t0001g0025 a0002c0003t0001g0026 a0002c0003t0001g0035 |
3 | HG02451.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.666-11418_666-1141 others(8): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | |||||||
| chr9:26872573 | T | TATATATA others(10): Show |
1 | a0002c0003t0001g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.666-11435_666-1143 others(21): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872573 | |||||||
| chr9:26872573 | T | TATATATA others(36): Show |
1 | a0002c0003t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.666-11435_666-1143 others(47): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872573 | |||||||
| chr9:26872759 | T | C | 13 | a0001c0001t0002g0223 a0001c0001t0002g0227 a0001c0001t0002g0228 others(10): Show |
13 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.666-11620A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872759 | |||||||
| chr9:26872767 | A | G | 27 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(24): Show |
27 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.666-11628T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872767 | |||||||
| chr9:26872856 | CTTT | C | 19 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(16): Show |
20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.666-11720_666-1171 others(7): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872856 | |||||||
| chr9:26872915 | C | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-11776G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872915 | |||||||
| chr9:26872946 | A | G | 1 | a0001c0002t0001g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.666-11807T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872946 | |||||||
| chr9:26872978 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.665+11832A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872978 | |||||||
| chr9:26873012 | G | C | 1 | a0001c0001t0010g0121 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.665+11798C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873012 | |||||||
| chr9:26873027 | G | A | 1 | a0005c0005t0009g0020 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.665+11783C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873027 | |||||||
| chr9:26873109 | T | G | 17 | a0001c0002t0001g0012 a0001c0002t0001g0017 a0001c0002t0001g0258 others(14): Show |
19 | HG00621.hp2 HG02015.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.665+11701A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873109 | |||||||
| chr9:26873152 | C | G | 1 | a0001c0002t0001g0296 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.665+11658G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873152 | |||||||
| chr9:26873195 | T | C | 1 | a0004c0008t0001g0092 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.665+11615A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873195 | |||||||
| chr9:26873379 | G | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+11431C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873379 | |||||||
| chr9:26873410 | C | A | 1 | a0001c0002t0001g0345 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.665+11400G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873410 | |||||||
| chr9:26873472 | T | C | 2 | a0001c0002t0001g0344 a0001c0002t0001g0345 |
2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.665+11338A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873472 | |||||||
| chr9:26873502 | A | C | 3 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 |
4 | HG01192.hp2 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+11308T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873502 | |||||||
| chr9:26873663 | G | A | 3 | a0002c0003t0001g0032 a0002c0003t0001g0033 a0002c0003t0001g0034 |
3 | HG03041.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.665+11147C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873663 | |||||||
| chr9:26873739 | A | G | 19 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(16): Show |
20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.665+11071T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873739 | |||||||
| chr9:26873809 | T | C | 1 | a0001c0002t0001g0308 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.665+11001A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873809 | |||||||
| chr9:26873858 | C | T | 13 | a0001c0001t0002g0223 a0001c0001t0002g0227 a0001c0001t0002g0228 others(10): Show |
13 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.665+10952G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873858 | |||||||
| chr9:26873946 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+10864C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873946 | |||||||
| chr9:26873979 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.665+10831C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873979 | |||||||
| chr9:26874076 | A | G | 1 | a0002c0003t0001g0032 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.665+10734T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874076 | |||||||
| chr9:26874100 | G | A | 3 | a0003c0004t0001g0100 a0003c0004t0001g0253 a0003c0004t0001g0254 |
3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.665+10710C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874100 | |||||||
| chr9:26874137 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.665+10673C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874137 | |||||||
| chr9:26874206 | C | CA | 58 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(55): Show |
58 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.665+10603dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874206 | |||||||
| chr9:26874206 | C | CAA | 9 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
9 | HG00423.hp2 HG02886.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+10602_665+1060 others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874206 | |||||||
| chr9:26874206 | CA | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0051 others(43): Show |
49 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.665+10603delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874206 | |||||||
| chr9:26874206 | CAA | C | 83 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0102 others(80): Show |
90 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.665+10602_665+1060 others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874206 | |||||||
| chr9:26874206 | CAAA | C | 8 | a0001c0001t0010g0121 a0001c0002t0001g0264 a0001c0002t0001g0268 others(5): Show |
8 | HG01167.hp2 HG02273.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.665+10601_665+1060 others(7): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874206 | |||||||
| chr9:26874233 | A | T | 1 | a0001c0002t0001g0267 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.665+10577T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874233 | |||||||
| chr9:26874234 | T | A | 1 | a0001c0001t0002g0245 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.665+10576A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874234 | |||||||
| chr9:26874273 | A | G | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+10537T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874273 | |||||||
| chr9:26874336 | T | C | 1 | a0002c0003t0001g0030 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.665+10474A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874336 | |||||||
| chr9:26874345 | T | C | 28 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(25): Show |
30 | HG00323.hp1 HG01192.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.665+10465A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874345 | |||||||
| chr9:26874434 | A | G | 10 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(7): Show |
10 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+10376T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874434 | |||||||
| chr9:26874484 | C | T | 101 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(98): Show |
108 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.665+10326G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874484 | |||||||
| chr9:26874559 | C | A | 11 | a0001c0002t0001g0338 a0001c0002t0001g0339 a0002c0003t0001g0001 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.665+10251G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874559 | |||||||
| chr9:26874636 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0106 |
2 | HG01361.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.665+10174A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874636 | |||||||
| chr9:26874761 | AAAGGAGC others(6): Show |
A | 2 | a0001c0002t0001g0301 a0001c0002t0001g0329 |
2 | NA18951.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.665+10036_665+1004 others(17): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874761 | |||||||
| chr9:26874812 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.665+9998C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874812 | |||||||
| chr9:26875042 | A | G | 8 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(5): Show |
8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+9768T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875042 | |||||||
| chr9:26875126 | A | G | 2 | a0001c0002t0001g0344 a0001c0002t0001g0345 |
2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.665+9684T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875126 | |||||||
| chr9:26875161 | G | T | 1 | a0001c0002t0001g0321 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.665+9649C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875161 | |||||||
| chr9:26875382 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.665+9428A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875382 | |||||||
| chr9:26875557 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.665+9253C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875557 | |||||||
| chr9:26875646 | CAG | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+9162_665+9163d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875646 | |||||||
| chr9:26875665 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.665+9145G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875665 | |||||||
| chr9:26875674 | T | C | 1 | a0001c0002t0001g0312 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.665+9136A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875674 | |||||||
| chr9:26875676 | T | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(20): Show |
27 | HG00609.hp2 HG00733.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.665+9134A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875676 | |||||||
| chr9:26875788 | G | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(20): Show |
27 | HG00609.hp2 HG00733.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.665+9022C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875788 | |||||||
| chr9:26875789 | A | T | 13 | a0001c0001t0001g0070 a0001c0002t0001g0311 a0001c0002t0001g0312 others(10): Show |
13 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.665+9021T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875789 | |||||||
| chr9:26875834 | C | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+8976G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875834 | |||||||
| chr9:26876250 | C | T | 1 | a0001c0002t0001g0346 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.665+8560G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876250 | |||||||
| chr9:26876253 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0076 |
2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.665+8557G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876253 | |||||||
| chr9:26876314 | G | A | 2 | a0001c0002t0001g0338 a0001c0002t0001g0339 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.665+8496C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876314 | |||||||
| chr9:26876422 | G | C | 19 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(16): Show |
20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.665+8388C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876422 | |||||||
| chr9:26876470 | A | AG | 32 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(29): Show |
33 | HG01069.hp2 HG01256.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.665+8339dupC | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876470 | |||||||
| chr9:26876472 | G | GGT | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0040 others(115): Show |
128 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.665+8337_665+8338i others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876472 | |||||||
| chr9:26876472 | G | GGTT | 3 | a0001c0002t0001g0312 a0001c0002t0001g0331 a0001c0002t0001g0344 |
3 | HG00438.hp2 HG02055.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.665+8337_665+8338i others(5): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876472 | |||||||
| chr9:26876472 | G | GT | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0063 others(8): Show |
11 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.665+8337dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876472 | |||||||
| chr9:26876472 | GTTT | G | 7 | a0002c0003t0001g0021 a0002c0003t0001g0025 a0002c0003t0001g0035 others(4): Show |
7 | HG01891.hp1 HG02257.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+8335_665+8337d others(5): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876472 | |||||||
| chr9:26876472 | GTTTT | G | 8 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(5): Show |
8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+8334_665+8337d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876472 | |||||||
| chr9:26876473 | T | G | 8 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0118 others(5): Show |
8 | HG00733.hp1 HG01070.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.665+8337A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876473 | |||||||
| chr9:26876475 | T | G | 4 | a0002c0003t0001g0001 a0002c0003t0001g0022 a0002c0003t0001g0023 others(1): Show |
5 | HG01192.hp2 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+8335A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876475 | |||||||
| chr9:26876476 | T | G | 7 | a0002c0003t0001g0021 a0002c0003t0001g0025 a0002c0003t0001g0035 others(4): Show |
7 | HG01891.hp1 HG02257.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+8334A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876476 | |||||||
| chr9:26876477 | T | G | 8 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(5): Show |
8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+8333A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876477 | |||||||
| chr9:26876481 | T | G | 3 | a0001c0002t0001g0302 a0001c0002t0001g0303 a0001c0002t0001g0304 |
3 | NA18974.hp2 NA19009.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.665+8329A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876481 | |||||||
| chr9:26876580 | A | C | 8 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(5): Show |
8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+8230T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876580 | |||||||
| chr9:26876592 | T | C | 6 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(3): Show |
6 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+8218A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876592 | |||||||
| chr9:26876658 | T | G | 6 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(3): Show |
6 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+8152A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876658 | |||||||
| chr9:26877008 | G | A | 2 | a0001c0002t0001g0344 a0001c0002t0001g0345 |
2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.665+7802C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877008 | |||||||
| chr9:26877022 | C | G | 2 | a0001c0001t0002g0255 a0001c0001t0002g0256 |
2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.665+7788G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877022 | |||||||
| chr9:26877184 | C | G | 2 | a0001c0001t0004g0083 a0001c0001t0004g0084 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.665+7626G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877184 | |||||||
| chr9:26877261 | T | C | 8 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(5): Show |
8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+7549A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877261 | |||||||
| chr9:26877403 | C | T | 1 | a0001c0002t0001g0266 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.665+7407G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877403 | |||||||
| chr9:26877750 | C | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG02615.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.665+7060G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877750 | |||||||
| chr9:26877885 | A | G | 1 | a0001c0001t0002g0223 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.665+6925T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877885 | |||||||
| chr9:26877888 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.665+6922A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877888 | |||||||
| chr9:26877894 | AATT | A | 21 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(18): Show |
21 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.665+6913_665+6915d others(5): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877894 | |||||||
| chr9:26877993 | G | A | 1 | a0001c0002t0001g0305 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.665+6817C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877993 | |||||||
| chr9:26878045 | A | C | 1 | a0001c0001t0002g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.665+6765T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878045 | |||||||
| chr9:26878103 | A | G | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+6707T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878103 | |||||||
| chr9:26878105 | T | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+6705A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878105 | |||||||
| chr9:26878147 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.665+6663T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878147 | |||||||
| chr9:26878297 | A | G | 23 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(20): Show |
27 | HG00609.hp2 HG00733.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.665+6513T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878297 | |||||||
| chr9:26878376 | G | C | 35 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(32): Show |
35 | HG00408.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.665+6434C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878376 | |||||||
| chr9:26878471 | T | C | 1 | a0001c0002t0001g0320 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.665+6339A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878471 | |||||||
| chr9:26878678 | T | A | 1 | a0006c0006t0001g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.665+6132A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878678 | |||||||
| chr9:26878813 | TA | T | 11 | a0001c0001t0001g0168 a0002c0003t0001g0025 a0002c0003t0001g0026 others(8): Show |
11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.665+5996delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878813 | |||||||
| chr9:26878813 | TAA | T | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+5995_665+5996d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878813 | |||||||
| chr9:26878979 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.665+5831G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878979 | |||||||
| chr9:26879208 | T | C | 1 | a0002c0007t0011g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.665+5602A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879208 | |||||||
| chr9:26879230 | T | G | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+5580A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879230 | |||||||
| chr9:26879375 | C | G | 6 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(3): Show |
6 | HG00423.hp1 HG02080.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+5435G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879375 | |||||||
| chr9:26879421 | T | C | 1 | a0002c0007t0011g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.665+5389A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879421 | |||||||
| chr9:26879536 | T | C | 1 | a0002c0003t0001g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.665+5274A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879536 | |||||||
| chr9:26879855 | C | T | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+4955G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879855 | |||||||
| chr9:26879860 | G | T | 1 | a0006c0006t0001g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.665+4950C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879860 | |||||||
| chr9:26879900 | T | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+4910A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879900 | |||||||
| chr9:26879938 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.665+4872C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879938 | |||||||
| chr9:26880074 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+4736G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880074 | |||||||
| chr9:26880092 | T | A | 1 | a0001c0002t0001g0265 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.665+4718A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880092 | |||||||
| chr9:26880093 | C | T | 1 | a0001c0002t0001g0265 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.665+4717G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880093 | |||||||
| chr9:26880093 | CCG | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0107 |
3 | NA18960.hp1 NA18973.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.665+4715_665+4716d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880093 | |||||||
| chr9:26880094 | CG | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0070 others(116): Show |
126 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.665+4715delC | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880094 | |||||||
| chr9:26880094 | CGG | C | 160 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(157): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.665+4714_665+4715d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880094 | |||||||
| chr9:26880095 | G | C | 1 | a0001c0002t0001g0265 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.665+4715C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880095 | |||||||
| chr9:26880095 | G | T | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.665+4715C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880095 | |||||||
| chr9:26880096 | G | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0107 |
3 | NA18960.hp1 NA18973.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.665+4714C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880096 | |||||||
| chr9:26880101 | G | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.665+4709C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880101 | |||||||
| chr9:26880107 | T | G | 8 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(5): Show |
8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+4703A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880107 | |||||||
| chr9:26880173 | G | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+4637C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880173 | |||||||
| chr9:26880224 | C | T | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+4586G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880224 | |||||||
| chr9:26880242 | A | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+4568T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880242 | |||||||
| chr9:26880337 | C | T | 1 | a0002c0003t0001g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.665+4473G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880337 | |||||||
| chr9:26880343 | G | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+4467C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880343 | |||||||
| chr9:26880419 | G | A | 1 | a0007c0009t0001g0140 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.665+4391C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880419 | |||||||
| chr9:26880459 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+4351C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880459 | |||||||
| chr9:26880554 | T | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0069 others(109): Show |
121 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.665+4256A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880554 | |||||||
| chr9:26880770 | G | T | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
3 | HG02630.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.665+4040C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880770 | |||||||
| chr9:26880886 | C | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
193 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.665+3924G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880886 | |||||||
| chr9:26880920 | A | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+3890T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880920 | |||||||
| chr9:26881101 | A | G | 170 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(167): Show |
181 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.665+3709T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881101 | |||||||
| chr9:26881188 | G | C | 8 | a0001c0001t0001g0082 a0001c0001t0001g0167 a0001c0001t0001g0195 others(5): Show |
8 | HG02129.hp2 HG02132.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.665+3622C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881188 | |||||||
| chr9:26881273 | C | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(7): Show |
11 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.665+3537G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881273 | |||||||
| chr9:26881301 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+3509T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881301 | |||||||
| chr9:26881362 | A | G | 2 | a0001c0001t0004g0083 a0001c0001t0004g0084 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.665+3448T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881362 | |||||||
| chr9:26881365 | T | G | 1 | a0001c0002t0001g0306 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.665+3445A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881365 | |||||||
| chr9:26881537 | C | T | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+3273G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881537 | |||||||
| chr9:26881595 | T | C | 1 | a0001c0002t0001g0307 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.665+3215A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881595 | |||||||
| chr9:26881729 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.665+3081G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881729 | |||||||
| chr9:26881838 | G | T | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+2972C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881838 | |||||||
| chr9:26881864 | T | A | 3 | a0003c0004t0001g0100 a0003c0004t0001g0253 a0003c0004t0001g0254 |
3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.665+2946A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881864 | |||||||
| chr9:26881901 | C | T | 343 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(340): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.665+2909G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881901 | |||||||
| chr9:26882245 | G | A | 1 | a0001c0002t0001g0012 | 2 | HG02015.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.665+2565C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882245 | |||||||
| chr9:26882438 | T | G | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+2372A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882438 | |||||||
| chr9:26882459 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.665+2351A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882459 | |||||||
| chr9:26882536 | T | C | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+2274A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882536 | |||||||
| chr9:26882541 | T | C | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.665+2269A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882541 | |||||||
| chr9:26882586 | G | A | 2 | a0002c0003t0001g0025 a0002c0003t0001g0035 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.665+2224C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882586 | |||||||
| chr9:26882600 | G | A | 1 | a0001c0001t0007g0152 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.665+2210C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882600 | |||||||
| chr9:26882614 | C | T | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.665+2196G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882614 | |||||||
| chr9:26882631 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.665+2179G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882631 | |||||||
| chr9:26882672 | C | T | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+2138G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882672 | |||||||
| chr9:26882814 | T | C | 1 | a0003c0004t0001g0100 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.665+1996A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882814 | |||||||
| chr9:26882994 | C | A | 1 | a0002c0003t0001g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.665+1816G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882994 | |||||||
| chr9:26883001 | A | G | 2 | a0001c0002t0001g0340 a0001c0002t0001g0343 |
2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.665+1809T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883001 | |||||||
| chr9:26883048 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0159 others(7): Show |
12 | HG00733.hp2 HG01081.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.665+1762G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883048 | |||||||
| chr9:26883049 | G | A | 2 | a0001c0001t0001g0202 a0001c0002t0001g0308 |
2 | HG02698.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.665+1761C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883049 | |||||||
| chr9:26883096 | T | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
167 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.665+1714A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883096 | |||||||
| chr9:26883151 | C | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(163): Show |
177 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.665+1659G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883151 | |||||||
| chr9:26883158 | C | T | 1 | a0002c0007t0011g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.665+1652G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883158 | |||||||
| chr9:26883204 | C | T | 3 | a0001c0001t0001g0048 a0001c0002t0001g0338 a0001c0002t0001g0339 |
3 | HG01167.hp2 HG01169.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.665+1606G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883204 | |||||||
| chr9:26883361 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.665+1449C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883361 | |||||||
| chr9:26883686 | A | T | 1 | a0001c0001t0001g0208 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.665+1124T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883686 | |||||||
| chr9:26883701 | C | T | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+1109G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883701 | |||||||
| chr9:26883704 | C | T | 1 | a0002c0003t0001g0030 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.665+1106G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883704 | |||||||
| chr9:26883846 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0201 |
3 | NA18998.hp1 NA19002.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.665+964A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883846 | |||||||
| chr9:26884047 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+763A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884047 | |||||||
| chr9:26884100 | C | A | 8 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(5): Show |
8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+710G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884100 | |||||||
| chr9:26884268 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.665+542A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884268 | |||||||
| chr9:26884307 | A | T | 2 | a0001c0002t0001g0262 a0001c0002t0001g0264 |
2 | NA18747.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.665+503T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884307 | |||||||
| chr9:26884364 | C | T | 2 | a0001c0002t0001g0262 a0001c0002t0001g0264 |
2 | NA18747.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.665+446G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884364 | |||||||
| chr9:26884410 | C | A | 1 | a0001c0001t0010g0121 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.665+400G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884410 | |||||||
| chr9:26884459 | T | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+351A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884459 | |||||||
| chr9:26884477 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+333G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884477 | |||||||
| chr9:26884506 | A | G | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+304T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884506 | |||||||
| chr9:26884543 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.665+267C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884543 | |||||||
| chr9:26884546 | G | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+264C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884546 | |||||||
| chr9:26884594 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.665+216C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884594 | |||||||
| chr9:26884706 | T | C | 2 | a0001c0001t0004g0083 a0001c0001t0004g0084 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.665+104A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884706 | |||||||
| chr9:26884739 | C | T | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+71G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884739 | |||||||
| chr9:26885013 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.590-128T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885013 | |||||||
| chr9:26885041 | T | C | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.590-156A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885041 | |||||||
| chr9:26885074 | C | CT | 19 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0062 others(16): Show |
20 | HG01243.hp2 HG01928.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.590-190dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885074 | |||||||
| chr9:26885074 | C | T | 1 | a0001c0001t0001g0006 | 2 | HG02015.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.590-189G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885074 | |||||||
| chr9:26885074 | CT | C | 23 | a0001c0001t0001g0107 a0001c0001t0001g0122 a0001c0001t0001g0154 others(20): Show |
24 | HG01192.hp2 HG01256.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.590-190delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885074 | |||||||
| chr9:26885075 | T | C | 1 | a0001c0001t0004g0083 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.590-190A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885075 | |||||||
| chr9:26885076 | T | C | 1 | a0001c0001t0004g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.590-191A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885076 | |||||||
| chr9:26885095 | T | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA19077.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.590-210A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885095 | |||||||
| chr9:26885099 | C | G | 1 | a0006c0006t0001g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.590-214G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885099 | |||||||
| chr9:26885099 | C | T | 1 | a0002c0003t0001g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.590-214G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885099 | |||||||
| chr9:26885121 | G | A | 3 | a0003c0004t0001g0100 a0003c0004t0001g0253 a0003c0004t0001g0254 |
3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.590-236C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885121 | |||||||
| chr9:26885169 | C | T | 128 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0135 others(125): Show |
137 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.590-284G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885169 | |||||||
| chr9:26885203 | A | C | 1 | a0001c0001t0002g0223 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.590-318T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885203 | |||||||
| chr9:26885212 | G | A | 2 | a0002c0003t0001g0030 a0002c0003t0001g0031 |
2 | HG01496.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.590-327C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885212 | |||||||
| chr9:26885261 | G | C | 2 | a0002c0003t0001g0025 a0002c0003t0001g0035 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.590-376C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885261 | |||||||
| chr9:26885292 | G | C | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.590-407C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885292 | |||||||
| chr9:26885297 | G | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.590-412C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885297 | |||||||
| chr9:26885354 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0137 |
2 | HG01192.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.590-469G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885354 | |||||||
| chr9:26885370 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.590-485G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885370 | |||||||
| chr9:26885371 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.590-486C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885371 | |||||||
| chr9:26885406 | G | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(7): Show |
11 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.590-521C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885406 | |||||||
| chr9:26885661 | G | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.589+443C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885661 | |||||||
| chr9:26885681 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.589+423A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885681 | |||||||
| chr9:26885775 | C | T | 22 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(19): Show |
22 | HG00733.hp1 HG01256.hp2 HG02615.hp2 others(19): Show |
intron_variant | MODIFIER | c.589+329G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885775 | |||||||
| chr9:26885822 | T | C | 17 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(14): Show |
17 | HG00733.hp1 HG01256.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.589+282A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885822 | |||||||
| chr9:26885824 | A | AT | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.589+279dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885824 | |||||||
| chr9:26885935 | T | C | 1 | a0001c0002t0001g0257 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.589+169A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885935 | |||||||
| chr9:26885941 | T | C | 1 | a0003c0004t0001g0100 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.589+163A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885941 | |||||||
| chr9:26885992 | A | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(8): Show |
12 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.589+112T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885992 | |||||||
| chr9:26886230 | C | T | 1 | a0001c0002t0001g0311 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.505-42G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886230 | |||||||
| chr9:26886395 | C | T | 92 | a0001c0001t0002g0127 a0001c0002t0001g0012 a0001c0002t0001g0013 others(89): Show |
100 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.505-207G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886395 | |||||||
| chr9:26886546 | T | G | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.505-358A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886546 | |||||||
| chr9:26886551 | A | T | 343 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(340): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.505-363T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886551 | |||||||
| chr9:26886587 | A | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(7): Show |
11 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.505-399T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886587 | |||||||
| chr9:26886780 | C | T | 1 | a0001c0002t0001g0261 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.504+533G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886780 | |||||||
| chr9:26886793 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0069 others(103): Show |
115 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.504+520A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886793 | |||||||
| chr9:26886822 | A | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.504+491T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886822 | |||||||
| chr9:26886934 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.504+379G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886934 | |||||||
| chr9:26886939 | G | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.504+374C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886939 | |||||||
| chr9:26886997 | C | A | 1 | a0001c0001t0001g0010 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.504+316G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886997 | |||||||
| chr9:26887069 | G | A | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.504+244C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26887069 | |||||||
| chr9:26887113 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.504+200C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26887113 | |||||||
| chr9:26887300 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.504+13A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26887300 | |||||||
| chr9:26887537 | C | T | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.304-24G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26887537 | |||||||
| chr9:26887585 | A | G | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.304-72T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26887585 | |||||||
| chr9:26887738 | T | C | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.304-225A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26887738 | |||||||
| chr9:26887758 | A | C | 1 | a0002c0003t0001g0023 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.304-245T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26887758 | |||||||
| chr9:26887898 | G | C | 2 | a0001c0001t0002g0251 a0001c0001t0002g0252 |
2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.304-385C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26887898 | |||||||
| chr9:26887978 | T | C | 39 | a0001c0001t0001g0241 a0001c0001t0002g0011 a0001c0001t0002g0125 others(36): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.304-465A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26887978 | |||||||
| chr9:26888070 | C | T | 1 | a0002c0003t0001g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.304-557G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888070 | |||||||
| chr9:26888176 | CTGTTAGC others(4): Show |
C | 2 | a0001c0001t0004g0083 a0001c0001t0004g0084 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.304-674_304-664del others(11): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888176 | |||||||
| chr9:26888209 | G | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.304-696C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888209 | |||||||
| chr9:26888328 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.304-815G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888328 | |||||||
| chr9:26888434 | C | A | 1 | a0001c0002t0001g0351 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.304-921G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888434 | |||||||
| chr9:26888548 | T | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.304-1035A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888548 | |||||||
| chr9:26888741 | G | C | 1 | a0005c0005t0009g0020 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.304-1228C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888741 | |||||||
| chr9:26888747 | T | C | 1 | a0001c0001t0008g0207 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.304-1234A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888747 | |||||||
| chr9:26888789 | T | C | 3 | a0003c0004t0001g0100 a0003c0004t0001g0253 a0003c0004t0001g0254 |
3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.304-1276A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888789 | |||||||
| chr9:26888901 | T | C | 1 | a0001c0002t0001g0320 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.304-1388A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888901 | |||||||
| chr9:26888968 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.304-1455T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888968 | |||||||
| chr9:26889031 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.304-1518T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889031 | |||||||
| chr9:26889136 | G | A | 24 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0109 others(21): Show |
24 | HG00733.hp1 HG01256.hp2 HG02615.hp2 others(21): Show |
intron_variant | MODIFIER | c.304-1623C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889136 | |||||||
| chr9:26889246 | G | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.304-1733C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889246 | |||||||
| chr9:26889269 | T | C | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | NA18963.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.304-1756A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889269 | |||||||
| chr9:26889287 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-1774C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889287 | |||||||
| chr9:26889313 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.304-1800C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889313 | |||||||
| chr9:26889409 | A | G | 1 | a0002c0003t0001g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.304-1896T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889409 | |||||||
| chr9:26889420 | AAAAAACA others(5): Show |
A | 1 | a0002c0003t0001g0022 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.304-1919_304-1908d others(14): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889420 | |||||||
| chr9:26889565 | G | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.304-2052C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889565 | |||||||
| chr9:26889636 | G | T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
6 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-2123C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889636 | |||||||
| chr9:26889697 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.304-2184G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889697 | |||||||
| chr9:26889746 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.304-2233A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889746 | |||||||
| chr9:26889781 | T | C | 2 | a0001c0002t0001g0333 a0001c0002t0001g0334 |
2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.304-2268A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889781 | |||||||
| chr9:26889793 | A | G | 1 | a0001c0002t0001g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.304-2280T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889793 | |||||||
| chr9:26889807 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.304-2294C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889807 | |||||||
| chr9:26889831 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.304-2318C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889831 | |||||||
| chr9:26889855 | G | A | 1 | a0001c0001t0002g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.304-2342C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889855 | |||||||
| chr9:26889866 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-2353A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889866 | |||||||
| chr9:26889867 | C | CA | 66 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(63): Show |
67 | HG00621.hp1 HG00733.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.304-2355dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889867 | |||||||
| chr9:26889897 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.304-2384G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889897 | |||||||
| chr9:26889958 | T | C | 2 | a0001c0001t0002g0125 a0001c0001t0002g0126 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.304-2445A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889958 | |||||||
| chr9:26889981 | T | C | 3 | a0002c0003t0001g0032 a0002c0003t0001g0033 a0002c0003t0001g0034 |
3 | HG03041.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.303+2432A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889981 | |||||||
| chr9:26889995 | A | T | 1 | a0001c0001t0001g0040 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.303+2418T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889995 | |||||||
| chr9:26890090 | T | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.303+2323A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890090 | |||||||
| chr9:26890126 | T | A | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.303+2287A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890126 | |||||||
| chr9:26890127 | T | C | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG02895.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.303+2286A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890127 | |||||||
| chr9:26890328 | G | A | 3 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 |
4 | HG01192.hp2 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+2085C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890328 | |||||||
| chr9:26890360 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.303+2053C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890360 | |||||||
| chr9:26890378 | G | GA | 35 | a0001c0001t0001g0222 a0001c0001t0001g0241 a0001c0001t0002g0011 others(32): Show |
36 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.303+2034dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890378 | |||||||
| chr9:26890378 | GA | G | 21 | a0001c0002t0001g0259 a0002c0003t0001g0001 a0002c0003t0001g0021 others(18): Show |
22 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.303+2034delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890378 | |||||||
| chr9:26890570 | A | T | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.303+1843T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890570 | |||||||
| chr9:26890576 | C | T | 8 | a0002c0003t0001g0027 a0002c0003t0001g0030 a0002c0003t0001g0031 others(5): Show |
8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+1837G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890576 | |||||||
| chr9:26890805 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0005g0132 |
2 | HG00423.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.303+1608G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890805 | |||||||
| chr9:26890837 | C | T | 1 | a0002c0003t0001g0026 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.303+1576G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890837 | |||||||
| chr9:26890874 | G | A | 1 | a0001c0002t0001g0336 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.303+1539C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890874 | |||||||
| chr9:26890876 | C | T | 2 | a0001c0001t0004g0083 a0001c0001t0004g0084 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.303+1537G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890876 | |||||||
| chr9:26890921 | G | A | 1 | a0001c0002t0001g0337 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.303+1492C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890921 | |||||||
| chr9:26890953 | C | CA | 23 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(20): Show |
24 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.303+1459dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890953 | |||||||
| chr9:26891097 | C | T | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.303+1316G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891097 | |||||||
| chr9:26891237 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1176T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891237 | |||||||
| chr9:26891238 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1175T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891238 | |||||||
| chr9:26891241 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1172C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891241 | |||||||
| chr9:26891242 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1171G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891242 | |||||||
| chr9:26891243 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1170T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891243 | |||||||
| chr9:26891245 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0082 others(175): Show |
189 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.303+1168T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891245 | |||||||
| chr9:26891247 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1166T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891247 | |||||||
| chr9:26891248 | A | T | 1 | a0001c0001t0001g0082 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1165T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891248 | |||||||
| chr9:26891301 | C | CAA | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.303+1111_303+1112i others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891301 | |||||||
| chr9:26891335 | T | A | 1 | a0001c0001t0001g0250 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.303+1078A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891335 | |||||||
| chr9:26891566 | CACA | C | 95 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0014 others(92): Show |
103 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.303+844_303+846del others(3): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891566 | |||||||
| chr9:26891766 | G | C | 103 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0014 others(100): Show |
111 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.303+647C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891766 | |||||||
| chr9:26891789 | G | A | 2 | a0001c0001t0002g0251 a0001c0001t0002g0252 |
2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.303+624C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891789 | |||||||
| chr9:26891829 | T | C | 2 | a0003c0004t0001g0253 a0003c0004t0001g0254 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.303+584A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891829 | |||||||
| chr9:26891831 | G | C | 20 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(17): Show |
21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.303+582C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891831 | |||||||
| chr9:26891861 | T | C | 2 | a0002c0003t0001g0025 a0002c0003t0001g0035 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.303+552A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891861 | |||||||
| chr9:26891904 | T | G | 103 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0014 others(100): Show |
111 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.303+509A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891904 | |||||||
| chr9:26892015 | G | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0258 |
3 | HG02015.hp2 NA18945.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.303+398C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892015 | |||||||
| chr9:26892049 | C | G | 1 | a0002c0003t0001g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.303+364G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892049 | |||||||
| chr9:26892075 | G | A | 7 | a0001c0002t0001g0019 a0001c0002t0001g0346 a0001c0002t0001g0347 others(4): Show |
8 | HG02300.hp2 HG03017.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.303+338C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892075 | |||||||
| chr9:26892097 | G | C | 2 | a0002c0003t0001g0023 a0002c0003t0001g0024 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.303+316C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892097 | |||||||
| chr9:26892136 | A | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.303+277T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892136 | |||||||
| chr9:26892139 | G | C | 311 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(308): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.303+274C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892139 | |||||||
| chr9:26892185 | A | T | 9 | a0002c0003t0001g0001 a0002c0003t0001g0021 a0002c0003t0001g0022 others(6): Show |
10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.303+228T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892185 | |||||||
| chr9:26892221 | T | C | 4 | a0002c0003t0001g0036 a0002c0003t0001g0037 a0002c0003t0001g0038 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.303+192A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892221 | |||||||
| chr9:26892303 | A | G | 123 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0014 others(120): Show |
132 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.303+110T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892303 | |||||||
| chr9:26892325 | C | T | 1 | a0001c0002t0001g0257 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.303+88G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892325 | |||||||
| chr9:26892337 | C | A | 2 | a0001c0001t0002g0255 a0001c0001t0002g0256 |
2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.303+76G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892337 |