Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 200373 |
| ensemblid | ENSG00000163075.13 |
| hgncid | 33720 |
| symbol | CFAP221 |
| name | cilia and flagella associated protein 221 |
| refseq_nuc | NM_001271049.2 |
| refseq_prot | NP_001257978.2 |
| ensembl_nuc | ENST00000413369.8 |
| ensembl_prot | ENSP00000393222.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 119544449 |
| end | 119656661 |
| strand | + |
| ver | v1.2 |
| region | chr2:119544449-119656661 |
| region5000 | chr2:119539449-119661661 |
| regionname0 | CFAP221_chr2_119544449_119656661 |
| regionname5000 | CFAP221_chr2_119539449_119661661 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 840 | 110 | 31 | 18 | 50 | 1 | 10 | 39 | CFAP221_chr2_119539449_119661661 | CFAP221 | MAVVK others(835): Show |
chr2 | 119539449 | 119661661 |
| a0002 | 0/1 | 840 | 47 | 18 | 14 | 10 | 1 | 3 | 6 | CFAP221_chr2_119539449_119661661 | CFAP221 | MAVVK others(835): Show |
chr2 | 119539449 | 119661661 |
| a0003 | 0/0 | 840 | 38 | 6 | 7 | 19 | 0 | 6 | 14 | CFAP221_chr2_119539449_119661661 | CFAP221 | MAVVK others(835): Show |
chr2 | 119539449 | 119661661 |
| a0004 | 0/0 | 840 | 11 | 9 | 0 | 2 | 0 | 0 | 2 | CFAP221_chr2_119539449_119661661 | CFAP221 | MAVVK others(835): Show |
chr2 | 119539449 | 119661661 |
| a0005 | 0/0 | 840 | 10 | 7 | 1 | 1 | 0 | 1 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | MAVVK others(835): Show |
chr2 | 119539449 | 119661661 |
| a0006 | 0/0 | 840 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | MAVVK others(835): Show |
chr2 | 119539449 | 119661661 |
| a0007 | 1/0 | 840 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | MAVVK others(835): Show |
chr2 | 119539449 | 119661661 |
| a0008 | 0/0 | 840 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | MAVVK others(835): Show |
chr2 | 119539449 | 119661661 |
| a0009 | 0/0 | 840 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | MAVVK others(835): Show |
chr2 | 119539449 | 119661661 |
| a0010 | 0/0 | 840 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | MAVVK others(835): Show |
chr2 | 119539449 | 119661661 |
| a0011 | 0/0 | 840 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | MAVVK others(835): Show |
chr2 | 119539449 | 119661661 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2520 | 102 | 23 | 18 | 50 | 1 | 10 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0001c0006 | 0/0 | 2520 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0001c0007 | 0/0 | 2520 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0002c0002 | 0/0 | 2520 | 44 | 18 | 13 | 9 | 1 | 3 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0002c0008 | 0/1 | 2520 | 3 | 0 | 1 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0003c0003 | 0/0 | 2520 | 38 | 6 | 7 | 19 | 0 | 6 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0004c0005 | 0/0 | 2520 | 8 | 6 | 0 | 2 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0004c0010 | 0/0 | 2520 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0005c0004 | 0/0 | 2520 | 10 | 7 | 1 | 1 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0006c0009 | 0/0 | 2520 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0007c0011 | 1/0 | 2520 | 2 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0008c0012 | 0/0 | 2520 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0009c0014 | 0/0 | 2520 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0010c0015 | 0/0 | 2520 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 | ||
| a0011c0013 | 0/0 | 2520 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | ATGGC others(2515): Show |
chr2 | 119539449 | 119661661 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2823 | 63 | 12 | 10 | 31 | 0 | 10 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0001c0001t0002 | 0/0 | 2823 | 37 | 10 | 8 | 18 | 1 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0001c0001t0004 | 0/0 | 2823 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0001c0001t0005 | 0/0 | 2807 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2802): Show |
chr2 | 119539449 | 119661661 |
| a0001c0006t0001 | 0/0 | 2823 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0001c0007t0001 | 0/0 | 2823 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0002c0002t0001 | 0/0 | 2823 | 30 | 9 | 10 | 7 | 1 | 3 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0002c0002t0002 | 0/0 | 2823 | 12 | 7 | 3 | 2 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0002c0002t0003 | 0/0 | 2823 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0002c0008t0001 | 0/1 | 2823 | 2 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0002c0008t0002 | 0/0 | 2823 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0003c0003t0001 | 0/0 | 2823 | 8 | 0 | 1 | 7 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0003c0003t0002 | 0/0 | 2823 | 30 | 6 | 6 | 12 | 0 | 6 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0004c0005t0001 | 0/0 | 2823 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0004c0005t0002 | 0/0 | 2823 | 4 | 2 | 0 | 2 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0004c0010t0001 | 0/0 | 2823 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0005c0004t0001 | 0/0 | 2823 | 3 | 2 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0005c0004t0002 | 0/0 | 2823 | 7 | 5 | 1 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0006c0009t0002 | 0/0 | 2823 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0007c0011t0002 | 1/0 | 2823 | 2 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0008c0012t0001 | 0/0 | 2823 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0009c0014t0002 | 0/0 | 2823 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0010c0015t0001 | 0/0 | 2823 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| a0011c0013t0001 | 0/0 | 2823 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | GACGC others(2818): Show |
chr2 | 119539449 | 119661661 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0006t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0006t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0007t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0007t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0001c0007t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0002t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0008t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0008t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0002c0008t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0003c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0004c0005t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0004c0005t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0004c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0004c0005t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0004c0005t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0004c0005t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0004c0005t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0004c0010t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0004c0010t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0004c0010t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0005c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0005c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0005c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0005c0004t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0005c0004t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0005c0004t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0005c0004t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0005c0004t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0005c0004t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0005c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0006c0009t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0006c0009t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0006c0009t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0007c0011t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0007c0011t0002g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0008c0012t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0008c0012t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0009c0014t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0010c0015t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| a0011c0013t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | CHS | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00544 | hp1 | a0003 | c0003 | t0001 | g0042 | EAS | CHS | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00597 | hp2 | a0003 | c0003 | t0002 | g0075 | EAS | CHS | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0090 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00639 | hp2 | a0005 | c0004 | t0002 | g0128 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00733 | hp2 | a0003 | c0003 | t0002 | g0059 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0157 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0099 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01074 | hp1 | a0008 | c0012 | t0001 | g0197 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01074 | hp2 | a0003 | c0003 | t0002 | g0068 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01106 | hp1 | a0003 | c0003 | t0002 | g0060 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01168 | hp1 | a0002 | c0008 | t0001 | g0109 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01243 | hp2 | a0003 | c0003 | t0002 | g0106 | AMR | PUR | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0092 | AMR | CLM | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0220 | AMR | CLM | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01346 | hp2 | a0003 | c0003 | t0002 | g0079 | AMR | CLM | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0091 | AMR | CLM | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | CLM | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0081 | EUR | IBS | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0165 | EUR | IBS | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0041 | AMR | PEL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG01978 | hp2 | a0009 | c0014 | t0002 | g0148 | AMR | PEL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02027 | hp1 | a0002 | c0008 | t0002 | g0111 | EAS | KHV | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02027 | hp2 | a0003 | c0003 | t0002 | g0077 | EAS | KHV | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | KHV | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | KHV | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02074 | hp1 | a0003 | c0003 | t0002 | g0088 | EAS | KHV | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | KHV | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02132 | hp1 | a0003 | c0003 | t0002 | g0089 | EAS | KHV | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | ACB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02258 | hp1 | a0006 | c0009 | t0002 | g0102 | AFR | ACB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02258 | hp2 | a0008 | c0012 | t0001 | g0199 | AFR | ACB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02280 | hp1 | a0001 | c0006 | t0001 | g0034 | AFR | ACB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02280 | hp2 | a0006 | c0009 | t0002 | g0103 | AFR | ACB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02451 | hp1 | a0001 | c0007 | t0001 | g0161 | AFR | ACB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02451 | hp2 | a0002 | c0002 | t0003 | g0155 | AFR | ACB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02572 | hp1 | a0003 | c0003 | t0002 | g0048 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0218 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0054 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0105 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02622 | hp2 | a0004 | c0005 | t0002 | g0124 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02630 | hp2 | a0004 | c0005 | t0001 | g0125 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02647 | hp1 | a0004 | c0005 | t0001 | g0001 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0100 | SAS | PJL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02809 | hp2 | a0003 | c0003 | t0002 | g0049 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02895 | hp2 | a0003 | c0003 | t0002 | g0044 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02896 | hp1 | a0001 | c0006 | t0001 | g0028 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02896 | hp2 | a0005 | c0004 | t0001 | g0127 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0047 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02965 | hp1 | a0005 | c0004 | t0002 | g0131 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02976 | hp1 | a0004 | c0005 | t0001 | g0016 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03017 | hp2 | a0003 | c0003 | t0002 | g0085 | SAS | PJL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0036 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0069 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03098 | hp2 | a0001 | c0006 | t0001 | g0030 | AFR | MSL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03130 | hp1 | a0005 | c0004 | t0002 | g0129 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0053 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03139 | hp1 | a0005 | c0004 | t0002 | g0133 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03139 | hp2 | a0001 | c0007 | t0001 | g0003 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03195 | hp1 | a0001 | c0007 | t0001 | g0160 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03209 | hp1 | a0004 | c0005 | t0002 | g0123 | AFR | MSL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03209 | hp2 | a0004 | c0010 | t0001 | g0007 | AFR | MSL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0156 | AFR | MSL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03225 | hp2 | a0001 | c0006 | t0001 | g0029 | AFR | MSL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03453 | hp1 | a0004 | c0005 | t0001 | g0001 | AFR | MSL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | MSL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03486 | hp2 | a0004 | c0010 | t0001 | g0005 | AFR | MSL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03516 | hp2 | a0003 | c0003 | t0002 | g0062 | AFR | ESN | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03540 | hp1 | a0001 | c0007 | t0001 | g0003 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03540 | hp2 | a0007 | c0011 | t0002 | g0046 | AFR | GWD | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03654 | hp2 | a0003 | c0003 | t0002 | g0080 | SAS | PJL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03688 | hp2 | a0003 | c0003 | t0002 | g0108 | SAS | STU | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03704 | hp1 | a0003 | c0003 | t0002 | g0067 | SAS | PJL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0098 | SAS | BEB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03834 | hp2 | a0005 | c0004 | t0001 | g0204 | SAS | BEB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03927 | hp1 | a0003 | c0003 | t0002 | g0050 | SAS | BEB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG04115 | hp2 | a0003 | c0003 | t0002 | g0104 | SAS | STU | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | YRI | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18946 | hp1 | a0003 | c0003 | t0002 | g0107 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18957 | hp1 | a0010 | c0015 | t0001 | g0205 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18957 | hp2 | a0003 | c0003 | t0001 | g0072 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18961 | hp1 | a0003 | c0003 | t0002 | g0082 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18963 | hp2 | a0003 | c0003 | t0001 | g0074 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18965 | hp1 | a0003 | c0003 | t0002 | g0058 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18975 | hp1 | a0004 | c0005 | t0002 | g0037 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18980 | hp2 | a0004 | c0005 | t0002 | g0038 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18991 | hp2 | a0003 | c0003 | t0002 | g0063 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18994 | hp1 | a0003 | c0003 | t0002 | g0064 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18998 | hp1 | a0005 | c0004 | t0002 | g0171 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19001 | hp1 | a0003 | c0003 | t0001 | g0061 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19005 | hp2 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19030 | hp1 | a0004 | c0010 | t0001 | g0006 | AFR | LWK | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19030 | hp2 | a0005 | c0004 | t0002 | g0134 | AFR | LWK | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0158 | AFR | LWK | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | LWK | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19057 | hp2 | a0011 | c0013 | t0001 | g0052 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19066 | hp2 | a0003 | c0003 | t0002 | g0078 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19068 | hp1 | a0003 | c0003 | t0002 | g0076 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19084 | hp1 | a0003 | c0003 | t0002 | g0065 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19085 | hp2 | a0003 | c0003 | t0001 | g0114 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19090 | hp2 | a0003 | c0003 | t0001 | g0066 | EAS | JPT | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19240 | hp1 | a0005 | c0004 | t0001 | g0132 | AFR | YRI | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA19240 | hp2 | a0003 | c0003 | t0002 | g0045 | AFR | YRI | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ASW | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ASW | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | GIH | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0113 | SAS | GIH | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02109 | hp1 | a0002 | c0002 | t0003 | g0159 | AFR | ACB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02109 | hp2 | a0003 | c0003 | t0002 | g0043 | AFR | ACB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | MSL | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA20300 | hp1 | a0006 | c0009 | t0002 | g0094 | AFR | USA | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| NA20300 | hp2 | a0005 | c0004 | t0002 | g0130 | AFR | USA | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| homoSapiens | chm13v2 | a0002 | c0008 | t0001 | g0112 | REF | REF | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| homoSapiens | grch38p0 | a0007 | c0011 | t0002 | g0110 | REF | REF | CFAP221_chr2_119539449_119661661 | CFAP221 | chr2 | 119539449 | 119661661 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:119546244 | A | T | 6 | a0001 a0004 a0005 others(3): Show |
135 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(132): Show |
missense_variant | MODERATE | c.113A>T | p.Glu38Val | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/24 | 222/2823 | 113/2523 | 38/840 | chr2 | 119546244 | |||
| chr2:119587124 | C | T | 1 | a0011 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.533C>T | p.Thr178Ile | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/24 | 642/2823 | 533/2523 | 178/840 | chr2 | 119587124 | |||
| chr2:119601259 | T | C | 1 | a0009 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.673T>C | p.Phe225Leu | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/24 | 782/2823 | 673/2523 | 225/840 | chr2 | 119601259 | |||
| chr2:119601334 | G | A | 1 | a0006 | 3 | HG02258.hp1 HG02280.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.748G>A | p.Glu250Lys | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/24 | 857/2823 | 748/2523 | 250/840 | chr2 | 119601334 | |||
| chr2:119629939 | C | A | 1 | a0010 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.1715C>A | p.Ser572Tyr | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 17/24 | 1824/2823 | 1715/2523 | 572/840 | chr2 | 119629939 | |||
| chr2:119630836 | G | A | 9 | a0001 a0002 a0003 others(6): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
missense_variant | MODERATE | c.1909G>A | p.Val637Ile | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/24 | 2018/2823 | 1909/2523 | 637/840 | chr2 | 119630836 | |||
| chr2:119652040 | G | T | 2 | a0003 a0005 |
48 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(45): Show |
missense_variant | MODERATE | c.2385G>T | p.Met795Ile | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/24 | 2494/2823 | 2385/2523 | 795/840 | chr2 | 119652040 | |||
| chr2:119656408 | C | G | 1 | a0008 | 2 | HG01074.hp1 HG02258.hp2 |
missense_variant | MODERATE | c.2461C>G | p.Leu821Val | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 24/24 | 2570/2823 | 2461/2523 | 821/840 | chr2 | 119656408 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:119601228 | G | A | 1 | a0002c0008 | 2 | HG01168.hp1 HG02027.hp1 |
synonymous_variant | LOW | c.642G>A | p.Pro214Pro | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/24 | 751/2823 | 642/2523 | 214/840 | chr2 | 119601228 | |||
| chr2:119604917 | G | A | 1 | a0001c0006 | 4 | HG02280.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
synonymous_variant | LOW | c.954G>A | p.Ser318Ser | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 10/24 | 1063/2823 | 954/2523 | 318/840 | chr2 | 119604917 | |||
| chr2:119611724 | T | C | 13 | a0001c0001 a0001c0006 a0001c0007 others(10): Show |
215 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(212): Show |
synonymous_variant | LOW | c.1293T>C | p.Val431Val | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/24 | 1402/2823 | 1293/2523 | 431/840 | chr2 | 119611724 | |||
| chr2:119630578 | A | G | 1 | a0001c0007 | 4 | HG02451.hp1 HG03139.hp2 HG03195.hp1 others(1): Show |
synonymous_variant | LOW | c.1740A>G | p.Gln580Gln | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 18/24 | 1849/2823 | 1740/2523 | 580/840 | chr2 | 119630578 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:119544464 | CGCCGGCG others(9): Show |
C | 1 | a0001c0001t0005 | 1 | HG03471.hp2 | 5_prime_UTR_variant | MODIFIER | c.-89_-74delGCGCTGGC others(8): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 1/24 | 1648 | INFO_REALIGN_3_PRIME | chr2 | 119544464 | |||||
| chr2:119544469 | G | T | 1 | a0001c0006t0001 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-89G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 1/24 | 1663 | chr2 | 119544469 | ||||||
| chr2:119544483 | C | T | 1 | a0001c0001t0005 | 1 | HG03471.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-75C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 1/24 | chr2 | 119544483 | |||||||
| chr2:119544484 | G | C | 1 | a0001c0001t0005 | 1 | HG03471.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 1/24 | 1648 | chr2 | 119544484 | ||||||
| chr2:119656507 | C | T | 13 | a0001c0001t0001 a0001c0001t0005 a0001c0006t0001 others(10): Show |
125 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*37C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 24/24 | 37 | chr2 | 119656507 | ||||||
| chr2:119656530 | G | A | 1 | a0001c0001t0004 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 24/24 | 60 | chr2 | 119656530 | ||||||
| chr2:119656593 | G | A | 1 | a0002c0002t0003 | 2 | HG02109.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*123G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 24/24 | 123 | chr2 | 119656593 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:119544804 | A | C | 1 | a0001c0001t0001g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-48+294A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 1/23 | chr2 | 119544804 | |||||||
| chr2:119544923 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-48+413C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 1/23 | chr2 | 119544923 | |||||||
| chr2:119545051 | A | AGAGGG | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG00738.hp2 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-48+555_-48+559dup others(5): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 119545051 | ||||||
| chr2:119545268 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-48+758C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 1/23 | chr2 | 119545268 | |||||||
| chr2:119545666 | A | G | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG00738.hp2 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-47-419A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 1/23 | chr2 | 119545666 | |||||||
| chr2:119545767 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-47-318A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 1/23 | chr2 | 119545767 | |||||||
| chr2:119545797 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-47-288C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 1/23 | chr2 | 119545797 | |||||||
| chr2:119546346 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.139+76G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119546346 | |||||||
| chr2:119546461 | G | A | 3 | a0004c0010t0001g0005 a0004c0010t0001g0006 a0004c0010t0001g0007 |
3 | HG03209.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.139+191G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119546461 | |||||||
| chr2:119546566 | C | T | 56 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0167 others(53): Show |
56 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.139+296C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119546566 | |||||||
| chr2:119546609 | G | A | 2 | a0002c0002t0002g0008 a0002c0002t0002g0009 |
2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.139+339G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119546609 | |||||||
| chr2:119546621 | A | C | 3 | a0001c0007t0001g0003 a0001c0007t0001g0160 a0001c0007t0001g0161 |
4 | HG02451.hp1 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.139+351A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119546621 | |||||||
| chr2:119546788 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.139+518G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119546788 | |||||||
| chr2:119546831 | T | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(29): Show |
34 | HG01168.hp2 HG01175.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.139+561T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119546831 | |||||||
| chr2:119547223 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.139+953A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119547223 | |||||||
| chr2:119547384 | A | AC | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.139+1118dupC | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr2 | 119547384 | ||||||
| chr2:119547503 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0002g0163 |
2 | NA19056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.139+1233G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119547503 | |||||||
| chr2:119548070 | C | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(1): Show |
4 | NA18941.hp1 NA18974.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-1015C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119548070 | |||||||
| chr2:119548241 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.140-844T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119548241 | |||||||
| chr2:119548329 | T | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
8 | HG01243.hp1 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.140-756T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119548329 | |||||||
| chr2:119548516 | G | A | 1 | a0002c0002t0001g0036 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.140-569G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119548516 | |||||||
| chr2:119548834 | T | C | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG00738.hp2 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.140-251T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119548834 | |||||||
| chr2:119549036 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.140-49A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 2/23 | chr2 | 119549036 | |||||||
| chr2:119549238 | G | T | 1 | a0001c0001t0001g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.240+53G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119549238 | |||||||
| chr2:119549286 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.240+101G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119549286 | |||||||
| chr2:119549787 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.240+602A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119549787 | |||||||
| chr2:119549884 | C | T | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG00738.hp2 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.240+699C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119549884 | |||||||
| chr2:119550133 | C | T | 2 | a0001c0001t0001g0035 a0002c0002t0002g0154 |
2 | HG03516.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.240+948C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119550133 | |||||||
| chr2:119550218 | A | G | 18 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0143 others(15): Show |
18 | HG00438.hp1 HG00738.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.240+1033A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119550218 | |||||||
| chr2:119550500 | A | C | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.240+1315A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119550500 | |||||||
| chr2:119550733 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG01243.hp1 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+1548C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119550733 | |||||||
| chr2:119550738 | T | C | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.240+1553T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119550738 | |||||||
| chr2:119551008 | A | G | 1 | a0004c0010t0001g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.240+1823A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119551008 | |||||||
| chr2:119551547 | G | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0118 a0001c0001t0001g0119 others(96): Show |
99 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.240+2362G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119551547 | |||||||
| chr2:119551625 | C | T | 1 | a0002c0002t0002g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240+2440C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119551625 | |||||||
| chr2:119551760 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.240+2575G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119551760 | |||||||
| chr2:119551851 | T | C | 2 | a0004c0010t0001g0005 a0004c0010t0001g0007 |
2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.240+2666T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119551851 | |||||||
| chr2:119551875 | T | A | 2 | a0002c0002t0001g0039 a0002c0002t0001g0040 |
2 | NA18971.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.240+2690T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119551875 | |||||||
| chr2:119552287 | T | TAATAAAT others(25): Show |
2 | a0002c0002t0001g0115 a0003c0003t0001g0114 |
2 | HG02976.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.240+3540_240+3571d others(34): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552287 | ||||||
| chr2:119552287 | T | TAATAAAT others(57): Show |
1 | a0002c0002t0002g0116 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.240+3508_240+3571d others(66): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552287 | ||||||
| chr2:119552287 | TAATAAAT others(25): Show |
T | 24 | a0002c0002t0001g0039 a0002c0002t0001g0040 a0002c0002t0001g0086 others(21): Show |
24 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.240+3540_240+3571d others(34): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552287 | ||||||
| chr2:119552287 | TAATAAAT others(57): Show |
T | 30 | a0002c0002t0001g0036 a0002c0002t0001g0069 a0002c0002t0001g0070 others(27): Show |
30 | HG00597.hp2 HG00733.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.240+3508_240+3571d others(66): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552287 | ||||||
| chr2:119552287 | TAATAAAT others(89): Show |
T | 15 | a0002c0002t0001g0047 a0002c0002t0001g0051 a0002c0002t0001g0055 others(12): Show |
15 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.240+3476_240+3571d others(98): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552287 | ||||||
| chr2:119552287 | TAATAAAT others(153): Show |
T | 2 | a0002c0002t0002g0008 a0003c0003t0001g0042 |
2 | HG00544.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.240+3412_240+3571d others(2): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552287 | ||||||
| chr2:119552333 | ATTTC | A | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG00738.hp2 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.240+3156_240+3159d others(6): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552333 | ||||||
| chr2:119552365 | A | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0118 a0001c0001t0001g0119 others(96): Show |
99 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.240+3180A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119552365 | |||||||
| chr2:119552397 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0215 |
2 | NA18948.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.240+3212A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119552397 | |||||||
| chr2:119552397 | ATTTCTTT others(93): Show |
A | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+3220_240+3319d others(102): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552397 | ||||||
| chr2:119552443 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.240+3258T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119552443 | |||||||
| chr2:119552518 | T | C | 1 | a0003c0003t0002g0041 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.240+3333T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119552518 | |||||||
| chr2:119552614 | TAGAAATA others(209): Show |
T | 11 | a0001c0001t0001g0118 a0001c0001t0001g0162 a0001c0001t0001g0167 others(8): Show |
11 | HG01496.hp2 HG02630.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.240+3463_240+3678d others(2): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552614 | ||||||
| chr2:119552646 | TAGAAATA others(177): Show |
T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(85): Show |
88 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.240+3495_240+3678d others(2): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552646 | ||||||
| chr2:119552651 | ATATTTCT others(181): Show |
A | 1 | a0001c0001t0002g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.240+3468_240+3655d others(2): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552651 | ||||||
| chr2:119552653 | ATTTCTTT others(29): Show |
A | 1 | a0003c0003t0002g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.240+3476_240+3511d others(38): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552653 | ||||||
| chr2:119552678 | T | G | 2 | a0002c0002t0001g0219 a0002c0002t0001g0221 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.240+3493T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119552678 | |||||||
| chr2:119552678 | TAGAAATA others(145): Show |
T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0138 others(13): Show |
17 | HG02258.hp2 HG02572.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.240+3527_240+3678d others(2): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552678 | ||||||
| chr2:119552689 | CTTTCTTT others(53): Show |
C | 1 | a0003c0003t0002g0108 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.240+3585_240+3644d others(62): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552689 | ||||||
| chr2:119552710 | T | G | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG00738.hp2 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.240+3525T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119552710 | |||||||
| chr2:119552710 | TAGAAATA others(113): Show |
T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(9): Show |
13 | HG01243.hp1 HG01496.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.240+3559_240+3678d others(2): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552710 | ||||||
| chr2:119552721 | CTTTCTTT others(81): Show |
C | 2 | a0002c0002t0001g0219 a0002c0002t0001g0221 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.240+3557_240+3644d others(90): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552721 | ||||||
| chr2:119552742 | T | G | 1 | a0002c0002t0001g0220 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.240+3557T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119552742 | |||||||
| chr2:119552742 | TAGAAATA others(81): Show |
T | 1 | a0001c0001t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.240+3572_240+3659d others(90): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552742 | ||||||
| chr2:119552749 | A | ATTTCTTT others(29): Show |
2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.240+3571_240+3572i others(38): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552749 | ||||||
| chr2:119552753 | CTTTAATA others(49): Show |
C | 3 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0002c0002t0001g0220 |
3 | HG01346.hp1 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.240+3572_240+3627d others(58): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552753 | ||||||
| chr2:119552809 | A | ATTTC | 3 | a0002c0002t0002g0218 a0004c0005t0002g0037 a0004c0005t0002g0038 |
3 | HG02615.hp1 NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.240+3628_240+3631d others(6): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119552809 | ||||||
| chr2:119552830 | G | T | 5 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0002c0002t0002g0218 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+3645G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119552830 | |||||||
| chr2:119552914 | C | G | 2 | a0004c0010t0001g0005 a0004c0010t0001g0007 |
2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.240+3729C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119552914 | |||||||
| chr2:119553000 | A | T | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.240+3815A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119553000 | |||||||
| chr2:119553037 | A | G | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.240+3852A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119553037 | |||||||
| chr2:119553252 | G | A | 1 | a0002c0002t0001g0086 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.240+4067G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119553252 | |||||||
| chr2:119553290 | C | T | 2 | a0004c0005t0001g0001 a0004c0005t0001g0016 |
3 | HG02647.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.240+4105C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119553290 | |||||||
| chr2:119553903 | A | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(134): Show |
139 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.240+4718A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119553903 | |||||||
| chr2:119553994 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.240+4809A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119553994 | |||||||
| chr2:119554102 | G | A | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+4917G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119554102 | |||||||
| chr2:119554618 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.241-5071C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119554618 | |||||||
| chr2:119554835 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.241-4854G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119554835 | |||||||
| chr2:119554903 | A | C | 1 | a0002c0002t0001g0057 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.241-4786A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119554903 | |||||||
| chr2:119555047 | C | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
9 | HG01168.hp2 HG02129.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.241-4642C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119555047 | |||||||
| chr2:119555164 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.241-4525T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119555164 | |||||||
| chr2:119555190 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.241-4499G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119555190 | |||||||
| chr2:119555279 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(140): Show |
145 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.241-4410A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119555279 | |||||||
| chr2:119555436 | C | T | 1 | a0003c0003t0002g0085 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.241-4253C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119555436 | |||||||
| chr2:119555614 | G | A | 1 | a0003c0003t0002g0058 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.241-4075G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119555614 | |||||||
| chr2:119555819 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG01243.hp1 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-3870C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119555819 | |||||||
| chr2:119556403 | A | T | 1 | a0001c0001t0001g0209 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.241-3286A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119556403 | |||||||
| chr2:119556546 | A | T | 2 | a0002c0002t0001g0083 a0002c0002t0001g0084 |
2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.241-3143A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119556546 | |||||||
| chr2:119556556 | C | CT | 6 | a0001c0001t0001g0015 a0002c0002t0002g0156 a0002c0002t0002g0157 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-3119dupT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119556556 | ||||||
| chr2:119556693 | C | T | 2 | a0002c0002t0001g0083 a0002c0002t0001g0084 |
2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.241-2996C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119556693 | |||||||
| chr2:119556879 | G | A | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG00738.hp2 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.241-2810G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119556879 | |||||||
| chr2:119556998 | T | C | 2 | a0003c0003t0002g0059 a0003c0003t0002g0060 |
2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.241-2691T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119556998 | |||||||
| chr2:119557017 | G | A | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG00738.hp2 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.241-2672G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119557017 | |||||||
| chr2:119557017 | G | T | 8 | a0005c0004t0001g0127 a0005c0004t0001g0132 a0005c0004t0002g0128 others(5): Show |
8 | HG00639.hp2 HG02896.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.241-2672G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119557017 | |||||||
| chr2:119557049 | C | T | 1 | a0003c0003t0002g0085 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.241-2640C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119557049 | |||||||
| chr2:119557275 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.241-2414C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119557275 | |||||||
| chr2:119557958 | C | CA | 12 | a0002c0002t0001g0047 a0002c0002t0001g0083 a0003c0003t0001g0061 others(9): Show |
12 | HG01175.hp2 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.241-1712dupA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119557958 | ||||||
| chr2:119557958 | CA | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(120): Show |
125 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.241-1712delA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 119557958 | ||||||
| chr2:119558064 | G | A | 7 | a0003c0003t0001g0042 a0003c0003t0001g0061 a0003c0003t0001g0114 others(4): Show |
7 | HG00544.hp1 NA18946.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-1625G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119558064 | |||||||
| chr2:119558123 | T | TA | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG00738.hp2 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.241-1566_241-1565i others(3): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119558123 | |||||||
| chr2:119558124 | T | C | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG00738.hp2 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.241-1565T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119558124 | |||||||
| chr2:119558161 | G | C | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
9 | HG01168.hp2 HG02129.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.241-1528G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119558161 | |||||||
| chr2:119558172 | A | G | 1 | a0002c0002t0001g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.241-1517A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119558172 | |||||||
| chr2:119558236 | C | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.241-1453C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119558236 | |||||||
| chr2:119558745 | G | A | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG00738.hp2 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.241-944G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119558745 | |||||||
| chr2:119559156 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.241-533C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119559156 | |||||||
| chr2:119559180 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG01243.hp1 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-509C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119559180 | |||||||
| chr2:119559348 | A | G | 1 | a0004c0010t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.241-341A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119559348 | |||||||
| chr2:119559532 | T | A | 1 | a0001c0001t0002g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.241-157T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 3/23 | chr2 | 119559532 | |||||||
| chr2:119559849 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.327+74G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 4/23 | chr2 | 119559849 | |||||||
| chr2:119559872 | T | A | 4 | a0001c0001t0002g0027 a0001c0007t0001g0003 a0001c0007t0001g0160 others(1): Show |
5 | HG01175.hp1 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-56T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 4/23 | chr2 | 119559872 | |||||||
| chr2:119560045 | C | CT | 111 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0021 others(108): Show |
113 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.426+39dupT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 119560045 | ||||||
| chr2:119560045 | C | CTT | 17 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(14): Show |
17 | HG01168.hp2 HG02129.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.426+38_426+39dupTT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr2 | 119560045 | ||||||
| chr2:119560150 | G | T | 6 | a0002c0002t0001g0036 a0002c0002t0001g0055 a0002c0002t0001g0057 others(3): Show |
6 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.426+124G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 5/23 | chr2 | 119560150 | |||||||
| chr2:119560319 | G | A | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.426+293G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 5/23 | chr2 | 119560319 | |||||||
| chr2:119560472 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.426+446G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 5/23 | chr2 | 119560472 | |||||||
| chr2:119560860 | G | A | 1 | a0001c0001t0002g0137 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.426+834G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 5/23 | chr2 | 119560860 | |||||||
| chr2:119560961 | T | C | 1 | a0002c0002t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.426+935T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 5/23 | chr2 | 119560961 | |||||||
| chr2:119561015 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.426+989G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 5/23 | chr2 | 119561015 | |||||||
| chr2:119561222 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0002g0020 |
2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.427-792G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 5/23 | chr2 | 119561222 | |||||||
| chr2:119561327 | T | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(132): Show |
137 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.427-687T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 5/23 | chr2 | 119561327 | |||||||
| chr2:119561887 | G | A | 1 | a0002c0002t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.427-127G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 5/23 | chr2 | 119561887 | |||||||
| chr2:119562214 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.527+100C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119562214 | |||||||
| chr2:119562253 | C | CAAAA | 58 | a0001c0001t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0047 others(55): Show |
58 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.527+149_527+152dup others(4): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119562253 | ||||||
| chr2:119562253 | C | CAAAAA | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(124): Show |
129 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.527+148_527+152dup others(5): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119562253 | ||||||
| chr2:119562253 | C | CAAAAAA | 8 | a0001c0001t0001g0138 a0001c0001t0001g0178 a0001c0001t0001g0215 others(5): Show |
8 | HG02615.hp1 HG03098.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.527+147_527+152dup others(6): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119562253 | ||||||
| chr2:119562290 | G | A | 1 | a0004c0010t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.527+176G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119562290 | |||||||
| chr2:119562350 | C | T | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG00738.hp2 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.527+236C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119562350 | |||||||
| chr2:119562551 | G | C | 3 | a0002c0002t0001g0219 a0002c0002t0001g0220 a0002c0002t0001g0221 |
3 | HG00738.hp2 HG00741.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.527+437G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119562551 | |||||||
| chr2:119562740 | G | C | 1 | a0001c0001t0001g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.527+626G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119562740 | |||||||
| chr2:119563024 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.527+910T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119563024 | |||||||
| chr2:119563052 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.527+938G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119563052 | |||||||
| chr2:119563354 | C | G | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.527+1240C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119563354 | |||||||
| chr2:119563408 | C | G | 2 | a0001c0001t0001g0206 a0001c0001t0002g0207 |
2 | NA18994.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.527+1294C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119563408 | |||||||
| chr2:119563761 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.527+1647T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119563761 | |||||||
| chr2:119563879 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.527+1765G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119563879 | |||||||
| chr2:119564241 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(146): Show |
151 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.527+2127A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119564241 | |||||||
| chr2:119564680 | G | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
8 | HG01243.hp1 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.527+2566G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119564680 | |||||||
| chr2:119564737 | T | G | 1 | a0001c0001t0001g0217 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.527+2623T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119564737 | |||||||
| chr2:119565095 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.527+2981C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119565095 | |||||||
| chr2:119565406 | T | C | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.527+3292T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119565406 | |||||||
| chr2:119565431 | C | T | 1 | a0003c0003t0001g0061 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.527+3317C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119565431 | |||||||
| chr2:119565656 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.527+3542T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119565656 | |||||||
| chr2:119565685 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
147 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.527+3571T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119565685 | |||||||
| chr2:119565732 | A | C | 1 | a0005c0004t0002g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.527+3618A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119565732 | |||||||
| chr2:119565915 | C | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
9 | HG01168.hp2 HG02129.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.527+3801C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119565915 | |||||||
| chr2:119565987 | T | G | 5 | a0004c0010t0001g0005 a0004c0010t0001g0006 a0004c0010t0001g0007 others(2): Show |
5 | HG00639.hp2 HG02896.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.527+3873T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119565987 | |||||||
| chr2:119566378 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.527+4264C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119566378 | |||||||
| chr2:119566516 | T | G | 2 | a0001c0001t0001g0217 a0002c0002t0002g0091 |
2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.527+4402T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119566516 | |||||||
| chr2:119566555 | AC | A | 10 | a0002c0002t0001g0047 a0003c0003t0002g0043 a0003c0003t0002g0044 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.527+4448delC | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119566555 | ||||||
| chr2:119566582 | A | G | 1 | a0004c0010t0001g0005 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.527+4468A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119566582 | |||||||
| chr2:119566633 | A | T | 2 | a0004c0005t0001g0001 a0004c0005t0001g0016 |
3 | HG02647.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.527+4519A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119566633 | |||||||
| chr2:119567094 | C | T | 2 | a0002c0002t0001g0219 a0002c0002t0001g0221 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.527+4980C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119567094 | |||||||
| chr2:119567218 | A | G | 37 | a0002c0002t0001g0047 a0002c0002t0003g0159 a0003c0003t0001g0061 others(34): Show |
37 | HG00597.hp2 HG00639.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.527+5104A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119567218 | |||||||
| chr2:119567249 | T | C | 77 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
78 | HG00438.hp2 HG00597.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.527+5135T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119567249 | |||||||
| chr2:119567284 | A | G | 2 | a0006c0009t0002g0102 a0006c0009t0002g0103 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.527+5170A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119567284 | |||||||
| chr2:119567583 | C | A | 6 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0002g0022 others(3): Show |
6 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.527+5469C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119567583 | |||||||
| chr2:119567655 | TTGTA | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
8 | HG01243.hp1 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.527+5544_527+5547d others(6): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119567655 | ||||||
| chr2:119567841 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.527+5727C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119567841 | |||||||
| chr2:119567891 | A | G | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.527+5777A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119567891 | |||||||
| chr2:119568044 | A | G | 4 | a0001c0001t0001g0126 a0004c0005t0001g0125 a0004c0005t0002g0123 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.527+5930A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119568044 | |||||||
| chr2:119568489 | G | A | 2 | a0004c0010t0001g0005 a0004c0010t0001g0007 |
2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.527+6375G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119568489 | |||||||
| chr2:119568497 | C | G | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.527+6383C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119568497 | |||||||
| chr2:119568505 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.527+6391G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119568505 | |||||||
| chr2:119568710 | C | T | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.527+6596C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119568710 | |||||||
| chr2:119568772 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG02717.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.527+6658G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119568772 | |||||||
| chr2:119568958 | A | G | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.527+6844A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119568958 | |||||||
| chr2:119568963 | C | A | 13 | a0003c0003t0001g0066 a0003c0003t0001g0072 a0003c0003t0001g0073 others(10): Show |
13 | HG00597.hp2 HG01978.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.527+6849C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119568963 | |||||||
| chr2:119568984 | T | A | 15 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(12): Show |
15 | HG02129.hp2 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.527+6870T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119568984 | |||||||
| chr2:119569099 | A | AT | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.527+6994dupT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119569099 | ||||||
| chr2:119569270 | C | G | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.527+7156C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119569270 | |||||||
| chr2:119569408 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.527+7294G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119569408 | |||||||
| chr2:119569410 | A | AC | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.527+7298dupC | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119569410 | ||||||
| chr2:119569951 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.527+7837A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119569951 | |||||||
| chr2:119570496 | C | A | 55 | a0001c0007t0001g0003 a0001c0007t0001g0160 a0001c0007t0001g0161 others(52): Show |
56 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.527+8382C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119570496 | |||||||
| chr2:119570510 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.527+8396C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119570510 | |||||||
| chr2:119570795 | G | A | 1 | a0002c0002t0001g0220 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.527+8681G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119570795 | |||||||
| chr2:119570943 | T | C | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.527+8829T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119570943 | |||||||
| chr2:119571073 | C | CA | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.527+8965dupA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119571073 | ||||||
| chr2:119571133 | C | CT | 64 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0026 others(61): Show |
65 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.527+9043dupT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119571133 | ||||||
| chr2:119571133 | C | CTT | 21 | a0001c0001t0001g0203 a0002c0002t0001g0055 a0002c0002t0001g0057 others(18): Show |
21 | HG00544.hp1 HG00741.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.527+9042_527+9043d others(4): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119571133 | ||||||
| chr2:119571134 | T | C | 13 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0023 others(10): Show |
13 | HG01175.hp1 HG02129.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.527+9020T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119571134 | |||||||
| chr2:119571135 | T | C | 1 | a0001c0001t0001g0014 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.527+9021T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119571135 | |||||||
| chr2:119571225 | C | T | 41 | a0002c0002t0001g0047 a0003c0003t0001g0042 a0003c0003t0001g0061 others(38): Show |
41 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.527+9111C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119571225 | |||||||
| chr2:119571232 | C | T | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.527+9118C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119571232 | |||||||
| chr2:119571288 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.527+9174C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119571288 | |||||||
| chr2:119571392 | C | T | 2 | a0004c0005t0001g0001 a0004c0005t0001g0016 |
3 | HG02647.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.527+9278C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119571392 | |||||||
| chr2:119571432 | G | A | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.527+9318G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119571432 | |||||||
| chr2:119571475 | G | A | 4 | a0001c0006t0001g0028 a0001c0006t0001g0029 a0001c0006t0001g0030 others(1): Show |
4 | HG02280.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.527+9361G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119571475 | |||||||
| chr2:119571733 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.527+9619C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119571733 | |||||||
| chr2:119571738 | G | A | 1 | a0002c0002t0001g0087 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.527+9624G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119571738 | |||||||
| chr2:119571834 | C | G | 49 | a0001c0007t0001g0003 a0001c0007t0001g0160 a0001c0007t0001g0161 others(46): Show |
50 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.527+9720C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119571834 | |||||||
| chr2:119571878 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.527+9764G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119571878 | |||||||
| chr2:119571955 | TTGCCCCT others(11): Show |
T | 60 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(57): Show |
61 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.527+9863_527+9880d others(20): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119571955 | ||||||
| chr2:119572199 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.527+10085T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119572199 | |||||||
| chr2:119572291 | G | A | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.527+10177G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119572291 | |||||||
| chr2:119572333 | T | G | 2 | a0003c0003t0002g0049 a0003c0003t0002g0106 |
2 | HG01243.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.527+10219T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119572333 | |||||||
| chr2:119572366 | G | C | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.527+10252G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119572366 | |||||||
| chr2:119572605 | A | G | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.527+10491A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119572605 | |||||||
| chr2:119572685 | G | T | 6 | a0002c0002t0001g0036 a0002c0002t0001g0055 a0002c0002t0001g0057 others(3): Show |
6 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.527+10571G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119572685 | |||||||
| chr2:119572931 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.527+10817T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119572931 | |||||||
| chr2:119572935 | T | A | 1 | a0001c0001t0002g0179 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.527+10821T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119572935 | |||||||
| chr2:119572995 | T | A | 30 | a0003c0003t0001g0042 a0003c0003t0001g0061 a0003c0003t0001g0066 others(27): Show |
30 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.527+10881T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119572995 | |||||||
| chr2:119573295 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.527+11181C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119573295 | |||||||
| chr2:119573719 | C | T | 1 | a0003c0003t0001g0090 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.527+11605C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119573719 | |||||||
| chr2:119573915 | A | G | 1 | a0002c0002t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.527+11801A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119573915 | |||||||
| chr2:119573930 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.527+11816A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119573930 | |||||||
| chr2:119573965 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.527+11851C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119573965 | |||||||
| chr2:119574031 | C | G | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.527+11917C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119574031 | |||||||
| chr2:119574064 | A | G | 2 | a0003c0003t0002g0050 a0003c0003t0002g0108 |
2 | HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.527+11950A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119574064 | |||||||
| chr2:119574246 | CA | C | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.527+12133delA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119574246 | |||||||
| chr2:119574400 | A | C | 4 | a0001c0001t0001g0149 a0002c0002t0001g0081 a0002c0002t0001g0098 others(1): Show |
4 | HG01071.hp2 HG01516.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.527+12286A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119574400 | |||||||
| chr2:119574891 | A | C | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.528-12228A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119574891 | |||||||
| chr2:119575510 | T | C | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.528-11609T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119575510 | |||||||
| chr2:119575637 | G | T | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.528-11482G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119575637 | |||||||
| chr2:119575807 | T | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG01243.hp1 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.528-11312T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119575807 | |||||||
| chr2:119576112 | C | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG02717.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.528-11007C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119576112 | |||||||
| chr2:119576300 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.528-10819C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119576300 | |||||||
| chr2:119576351 | C | A | 5 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0139 others(2): Show |
5 | NA18970.hp1 NA18971.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.528-10768C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119576351 | |||||||
| chr2:119576394 | C | G | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.528-10725C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119576394 | |||||||
| chr2:119576629 | A | G | 1 | a0005c0004t0001g0204 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.528-10490A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119576629 | |||||||
| chr2:119576941 | C | A | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.528-10178C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119576941 | |||||||
| chr2:119577179 | TG | T | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.528-9936delG | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119577179 | ||||||
| chr2:119577280 | T | A | 1 | a0001c0001t0001g0012 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.528-9839T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577280 | |||||||
| chr2:119577299 | T | C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.528-9820T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577299 | |||||||
| chr2:119577319 | A | G | 1 | a0003c0003t0002g0080 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.528-9800A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577319 | |||||||
| chr2:119577350 | C | T | 1 | a0003c0003t0002g0085 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.528-9769C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577350 | |||||||
| chr2:119577357 | G | C | 2 | a0002c0002t0001g0092 a0002c0002t0001g0101 |
2 | HG01261.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.528-9762G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577357 | |||||||
| chr2:119577378 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.528-9741A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577378 | |||||||
| chr2:119577487 | G | A | 2 | a0004c0010t0001g0005 a0004c0010t0001g0007 |
2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.528-9632G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577487 | |||||||
| chr2:119577511 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.528-9608T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577511 | |||||||
| chr2:119577583 | T | C | 2 | a0002c0002t0001g0219 a0002c0002t0001g0221 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.528-9536T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577583 | |||||||
| chr2:119577612 | C | T | 3 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0009c0014t0002g0148 |
3 | HG01496.hp1 HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.528-9507C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577612 | |||||||
| chr2:119577704 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.528-9415T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577704 | |||||||
| chr2:119577791 | G | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
8 | HG01243.hp1 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.528-9328G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577791 | |||||||
| chr2:119577806 | C | T | 1 | a0001c0001t0002g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.528-9313C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577806 | |||||||
| chr2:119577807 | G | A | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.528-9312G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577807 | |||||||
| chr2:119577874 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.528-9245C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577874 | |||||||
| chr2:119577908 | A | C | 88 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(85): Show |
90 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.528-9211A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577908 | |||||||
| chr2:119577980 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.528-9139G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119577980 | |||||||
| chr2:119578151 | C | G | 1 | a0003c0003t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.528-8968C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119578151 | |||||||
| chr2:119578191 | C | A | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.528-8928C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119578191 | |||||||
| chr2:119578432 | C | T | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.528-8687C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119578432 | |||||||
| chr2:119578720 | C | T | 1 | a0002c0002t0001g0040 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.528-8399C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119578720 | |||||||
| chr2:119578753 | T | C | 18 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(15): Show |
18 | HG01175.hp1 HG02129.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.528-8366T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119578753 | |||||||
| chr2:119578900 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.528-8219A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119578900 | |||||||
| chr2:119578968 | G | A | 62 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(59): Show |
63 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.528-8151G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119578968 | |||||||
| chr2:119578973 | C | T | 1 | a0002c0002t0001g0086 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.528-8146C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119578973 | |||||||
| chr2:119579080 | G | T | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.528-8039G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119579080 | |||||||
| chr2:119579210 | AATAT | A | 4 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(1): Show |
4 | HG00735.hp1 HG02109.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.528-7908_528-7905d others(6): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119579210 | |||||||
| chr2:119579215 | T | A | 1 | a0002c0002t0003g0155 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.528-7904T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119579215 | |||||||
| chr2:119579292 | G | A | 1 | a0001c0001t0005g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.528-7827G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119579292 | |||||||
| chr2:119579294 | G | T | 2 | a0004c0005t0001g0001 a0004c0005t0001g0016 |
3 | HG02647.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.528-7825G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119579294 | |||||||
| chr2:119579518 | A | G | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.528-7601A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119579518 | |||||||
| chr2:119579740 | A | G | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.528-7379A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119579740 | |||||||
| chr2:119580091 | A | C | 1 | a0001c0001t0001g0201 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.528-7028A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119580091 | |||||||
| chr2:119580118 | T | G | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.528-7001T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119580118 | |||||||
| chr2:119580771 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG02717.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.528-6348C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119580771 | |||||||
| chr2:119581045 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.528-6074C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119581045 | |||||||
| chr2:119581387 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
8 | HG01243.hp1 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.528-5732C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119581387 | |||||||
| chr2:119581423 | C | T | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.528-5696C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119581423 | |||||||
| chr2:119581543 | T | C | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.528-5576T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119581543 | |||||||
| chr2:119581635 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.528-5484G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119581635 | |||||||
| chr2:119581906 | A | G | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.528-5213A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119581906 | |||||||
| chr2:119581911 | A | G | 2 | a0003c0003t0001g0090 a0003c0003t0002g0079 |
2 | HG00639.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.528-5208A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119581911 | |||||||
| chr2:119582044 | G | A | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.528-5075G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119582044 | |||||||
| chr2:119582164 | A | C | 88 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(85): Show |
90 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.528-4955A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119582164 | |||||||
| chr2:119582430 | T | A | 1 | a0005c0004t0002g0129 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.528-4689T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119582430 | |||||||
| chr2:119582442 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.528-4677A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119582442 | |||||||
| chr2:119582457 | C | CT | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(7): Show |
11 | HG01243.hp1 HG01978.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.528-4645dupT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119582457 | ||||||
| chr2:119582716 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.528-4403A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119582716 | |||||||
| chr2:119582767 | A | G | 1 | a0003c0003t0002g0085 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.528-4352A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119582767 | |||||||
| chr2:119582828 | GTCATAGG others(27): Show |
G | 3 | a0002c0002t0002g0156 a0002c0002t0003g0155 a0002c0002t0003g0159 |
3 | HG02109.hp1 HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.528-4287_528-4254d others(36): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119582828 | ||||||
| chr2:119582907 | T | C | 1 | a0004c0010t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.528-4212T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119582907 | |||||||
| chr2:119583163 | A | G | 3 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0009c0014t0002g0148 |
3 | HG01496.hp1 HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.528-3956A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119583163 | |||||||
| chr2:119583395 | C | CT | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(198): Show |
202 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.528-3704dupT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119583395 | ||||||
| chr2:119583395 | C | CTT | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(6): Show |
10 | HG01243.hp1 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.528-3705_528-3704d others(4): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119583395 | ||||||
| chr2:119583448 | C | A | 4 | a0001c0001t0001g0176 a0001c0001t0002g0177 a0001c0001t0002g0187 others(1): Show |
4 | HG00438.hp2 NA18612.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.528-3671C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119583448 | |||||||
| chr2:119583483 | T | C | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.528-3636T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119583483 | |||||||
| chr2:119583553 | G | A | 1 | a0011c0013t0001g0052 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.528-3566G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119583553 | |||||||
| chr2:119583666 | T | G | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.528-3453T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119583666 | |||||||
| chr2:119583681 | C | T | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.528-3438C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119583681 | |||||||
| chr2:119583761 | G | A | 6 | a0002c0002t0001g0036 a0002c0002t0001g0055 a0002c0002t0001g0057 others(3): Show |
6 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.528-3358G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119583761 | |||||||
| chr2:119584145 | A | G | 1 | a0002c0002t0001g0097 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.528-2974A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119584145 | |||||||
| chr2:119584248 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.528-2871G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119584248 | |||||||
| chr2:119584345 | T | G | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.528-2774T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119584345 | |||||||
| chr2:119584384 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.528-2735C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119584384 | |||||||
| chr2:119584493 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.528-2626G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119584493 | |||||||
| chr2:119584586 | C | CA | 18 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(15): Show |
18 | HG01175.hp1 HG02129.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.528-2521dupA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 119584586 | ||||||
| chr2:119584946 | T | A | 1 | a0001c0001t0002g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.528-2173T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119584946 | |||||||
| chr2:119584991 | C | T | 1 | a0002c0002t0001g0087 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.528-2128C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119584991 | |||||||
| chr2:119585013 | T | G | 41 | a0002c0002t0001g0047 a0003c0003t0001g0042 a0003c0003t0001g0061 others(38): Show |
41 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.528-2106T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119585013 | |||||||
| chr2:119585101 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.528-2018C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119585101 | |||||||
| chr2:119585121 | G | C | 88 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(85): Show |
90 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.528-1998G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119585121 | |||||||
| chr2:119585370 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.528-1749T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119585370 | |||||||
| chr2:119585595 | T | C | 3 | a0006c0009t0002g0094 a0006c0009t0002g0102 a0006c0009t0002g0103 |
3 | HG02258.hp1 HG02280.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.528-1524T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119585595 | |||||||
| chr2:119585680 | C | T | 2 | a0002c0002t0001g0219 a0002c0002t0001g0221 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.528-1439C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119585680 | |||||||
| chr2:119585983 | G | C | 49 | a0001c0007t0001g0003 a0001c0007t0001g0160 a0001c0007t0001g0161 others(46): Show |
50 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.528-1136G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119585983 | |||||||
| chr2:119585999 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.528-1120T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119585999 | |||||||
| chr2:119586256 | G | A | 88 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(85): Show |
90 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.528-863G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119586256 | |||||||
| chr2:119586334 | A | C | 1 | a0001c0001t0001g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.528-785A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 6/23 | chr2 | 119586334 | |||||||
| chr2:119587297 | T | A | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.631+75T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119587297 | |||||||
| chr2:119587547 | G | T | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.631+325G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119587547 | |||||||
| chr2:119587615 | G | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.631+393G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119587615 | |||||||
| chr2:119587781 | A | G | 2 | a0002c0002t0001g0219 a0002c0002t0001g0221 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.631+559A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119587781 | |||||||
| chr2:119588341 | T | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(15): Show |
18 | HG01175.hp1 HG02129.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.631+1119T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119588341 | |||||||
| chr2:119588612 | C | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(215): Show |
220 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.631+1390C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119588612 | |||||||
| chr2:119588931 | T | C | 88 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(85): Show |
90 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.631+1709T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119588931 | |||||||
| chr2:119588937 | G | A | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.631+1715G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119588937 | |||||||
| chr2:119589016 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.631+1794A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119589016 | |||||||
| chr2:119589182 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.631+1960C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119589182 | |||||||
| chr2:119589187 | C | T | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.631+1965C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119589187 | |||||||
| chr2:119589189 | CCACCAGT others(8): Show |
C | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+1969_631+1983d others(17): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 119589189 | ||||||
| chr2:119589271 | T | A | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.631+2049T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119589271 | |||||||
| chr2:119589377 | T | C | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.631+2155T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119589377 | |||||||
| chr2:119589383 | T | C | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.631+2161T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119589383 | |||||||
| chr2:119589395 | A | G | 55 | a0001c0007t0001g0003 a0001c0007t0001g0160 a0001c0007t0001g0161 others(52): Show |
56 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.631+2173A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119589395 | |||||||
| chr2:119589526 | A | G | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.631+2304A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119589526 | |||||||
| chr2:119589556 | A | G | 1 | a0002c0002t0001g0040 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.631+2334A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119589556 | |||||||
| chr2:119589650 | G | C | 88 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(85): Show |
90 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.631+2428G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119589650 | |||||||
| chr2:119589681 | C | G | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.631+2459C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119589681 | |||||||
| chr2:119589766 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(1): Show |
4 | NA18941.hp1 NA18974.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+2544C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119589766 | |||||||
| chr2:119589944 | AT | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG01243.hp1 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.631+2731delT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 119589944 | ||||||
| chr2:119590719 | G | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(15): Show |
18 | HG01175.hp1 HG02129.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.631+3497G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119590719 | |||||||
| chr2:119590882 | C | A | 55 | a0001c0007t0001g0003 a0001c0007t0001g0160 a0001c0007t0001g0161 others(52): Show |
56 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.631+3660C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119590882 | |||||||
| chr2:119591100 | G | A | 79 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(76): Show |
80 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.631+3878G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119591100 | |||||||
| chr2:119591157 | G | A | 2 | a0004c0005t0001g0001 a0004c0005t0001g0016 |
3 | HG02647.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.631+3935G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119591157 | |||||||
| chr2:119591190 | C | G | 59 | a0001c0001t0002g0022 a0001c0007t0001g0003 a0001c0007t0001g0160 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.631+3968C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119591190 | |||||||
| chr2:119591392 | TTGGTAGC others(2): Show |
T | 41 | a0001c0001t0001g0162 a0001c0001t0001g0172 a0001c0001t0001g0173 others(38): Show |
41 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.631+4175_631+4183d others(11): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 119591392 | ||||||
| chr2:119591408 | GT | G | 3 | a0001c0001t0001g0164 a0001c0001t0002g0181 a0002c0002t0001g0086 |
3 | NA18949.hp1 NA18949.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.631+4190delT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 119591408 | ||||||
| chr2:119591923 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.631+4701G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119591923 | |||||||
| chr2:119592084 | A | G | 1 | a0004c0005t0001g0125 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.631+4862A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119592084 | |||||||
| chr2:119592464 | C | T | 3 | a0003c0003t0001g0074 a0003c0003t0002g0063 a0003c0003t0002g0075 |
3 | HG00597.hp2 NA18963.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.631+5242C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119592464 | |||||||
| chr2:119592690 | A | G | 60 | a0001c0001t0002g0022 a0001c0001t0002g0135 a0001c0007t0001g0003 others(57): Show |
61 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.631+5468A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119592690 | |||||||
| chr2:119592815 | C | T | 55 | a0001c0007t0001g0003 a0001c0007t0001g0160 a0001c0007t0001g0161 others(52): Show |
56 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.631+5593C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119592815 | |||||||
| chr2:119593370 | T | A | 79 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(76): Show |
80 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.631+6148T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119593370 | |||||||
| chr2:119593837 | C | CA | 8 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0139 others(5): Show |
8 | NA18971.hp1 NA18971.hp2 NA18986.hp1 others(5): Show |
intron_variant | MODIFIER | c.631+6625dupA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 119593837 | ||||||
| chr2:119593855 | AAAC | A | 3 | a0001c0001t0002g0163 a0001c0001t0002g0166 a0001c0001t0004g0194 |
3 | NA18965.hp2 NA19056.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.631+6645_631+6647d others(5): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 119593855 | ||||||
| chr2:119594161 | C | T | 1 | a0002c0002t0002g0158 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.631+6939C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119594161 | |||||||
| chr2:119594172 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 |
3 | NA18974.hp1 NA18990.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.631+6950C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119594172 | |||||||
| chr2:119594233 | T | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(215): Show |
220 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.632-6985T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119594233 | |||||||
| chr2:119594392 | C | T | 1 | a0002c0002t0002g0157 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.632-6826C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119594392 | |||||||
| chr2:119594402 | AT | A | 5 | a0001c0001t0002g0022 a0001c0001t0002g0135 a0002c0002t0001g0219 others(2): Show |
5 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.632-6807delT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 119594402 | ||||||
| chr2:119594524 | G | A | 1 | a0001c0001t0002g0184 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.632-6694G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119594524 | |||||||
| chr2:119594741 | C | G | 9 | a0002c0002t0001g0047 a0003c0003t0002g0043 a0003c0003t0002g0044 others(6): Show |
9 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.632-6477C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119594741 | |||||||
| chr2:119594902 | G | A | 2 | a0003c0003t0002g0085 a0003c0003t0002g0104 |
2 | HG03017.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.632-6316G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119594902 | |||||||
| chr2:119595740 | C | T | 32 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(29): Show |
33 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.632-5478C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119595740 | |||||||
| chr2:119596166 | G | A | 2 | a0001c0001t0002g0032 a0001c0001t0002g0033 |
2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.632-5052G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119596166 | |||||||
| chr2:119596304 | C | T | 1 | a0003c0003t0001g0061 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.632-4914C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119596304 | |||||||
| chr2:119596425 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.632-4793C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119596425 | |||||||
| chr2:119596433 | A | G | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.632-4785A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119596433 | |||||||
| chr2:119596464 | G | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(186): Show |
190 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(187): Show |
intron_variant | MODIFIER | c.632-4754G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119596464 | |||||||
| chr2:119596638 | G | A | 7 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0195 others(4): Show |
7 | HG00544.hp2 HG02071.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.632-4580G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119596638 | |||||||
| chr2:119596711 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.632-4507G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119596711 | |||||||
| chr2:119597080 | A | G | 1 | a0002c0002t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.632-4138A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119597080 | |||||||
| chr2:119597113 | A | G | 3 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0009c0014t0002g0148 |
3 | HG01496.hp1 HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.632-4105A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119597113 | |||||||
| chr2:119597113 | A | T | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.632-4105A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119597113 | |||||||
| chr2:119597431 | G | A | 61 | a0001c0001t0002g0135 a0001c0007t0001g0003 a0001c0007t0001g0160 others(58): Show |
62 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.632-3787G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119597431 | |||||||
| chr2:119597671 | C | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(205): Show |
209 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(206): Show |
intron_variant | MODIFIER | c.632-3547C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119597671 | |||||||
| chr2:119597917 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(183): Show |
187 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(184): Show |
intron_variant | MODIFIER | c.632-3301T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119597917 | |||||||
| chr2:119598102 | A | T | 1 | a0002c0002t0001g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.632-3116A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119598102 | |||||||
| chr2:119598298 | C | G | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.632-2920C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119598298 | |||||||
| chr2:119598419 | G | A | 4 | a0001c0001t0002g0135 a0001c0007t0001g0003 a0001c0007t0001g0160 others(1): Show |
5 | HG02257.hp1 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.632-2799G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119598419 | |||||||
| chr2:119598480 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(206): Show |
210 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.632-2738T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119598480 | |||||||
| chr2:119598564 | T | G | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.632-2654T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119598564 | |||||||
| chr2:119599082 | A | G | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.632-2136A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119599082 | |||||||
| chr2:119599162 | T | G | 1 | a0003c0003t0002g0079 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.632-2056T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119599162 | |||||||
| chr2:119599310 | C | T | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.632-1908C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119599310 | |||||||
| chr2:119599395 | AAGTTTGG others(12): Show |
A | 1 | a0001c0001t0001g0024 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.632-1821_632-1803d others(21): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | 119599395 | ||||||
| chr2:119599513 | A | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0118 a0001c0001t0001g0138 others(23): Show |
26 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.632-1705A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119599513 | |||||||
| chr2:119600020 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(187): Show |
191 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.632-1198G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119600020 | |||||||
| chr2:119600198 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(183): Show |
187 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(184): Show |
intron_variant | MODIFIER | c.632-1020T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119600198 | |||||||
| chr2:119600329 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.632-889A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119600329 | |||||||
| chr2:119600939 | A | G | 1 | a0001c0001t0002g0177 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.632-279A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119600939 | |||||||
| chr2:119601012 | A | G | 1 | a0003c0003t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.632-206A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119601012 | |||||||
| chr2:119601098 | G | T | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.632-120G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119601098 | |||||||
| chr2:119601187 | G | T | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.632-31G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 7/23 | chr2 | 119601187 | |||||||
| chr2:119601562 | G | A | 1 | a0003c0003t0002g0088 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.791+185G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119601562 | |||||||
| chr2:119601737 | A | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(16): Show |
19 | HG01175.hp1 HG02129.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.791+360A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119601737 | |||||||
| chr2:119601811 | A | G | 1 | a0002c0002t0001g0083 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.791+434A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119601811 | |||||||
| chr2:119602150 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0167 |
2 | NA18612.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.791+773C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119602150 | |||||||
| chr2:119602197 | G | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(187): Show |
191 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.791+820G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119602197 | |||||||
| chr2:119602289 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.791+912C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119602289 | |||||||
| chr2:119602646 | G | A | 2 | a0002c0002t0002g0157 a0002c0002t0002g0158 |
2 | HG00735.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.791+1269G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119602646 | |||||||
| chr2:119603157 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0189 |
2 | NA18973.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.792-1515G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119603157 | |||||||
| chr2:119603243 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(187): Show |
191 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.792-1429C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119603243 | |||||||
| chr2:119603393 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.792-1279C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119603393 | |||||||
| chr2:119603829 | G | A | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.792-843G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119603829 | |||||||
| chr2:119604119 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.792-553G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119604119 | |||||||
| chr2:119604190 | C | G | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.792-482C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119604190 | |||||||
| chr2:119604207 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(187): Show |
191 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.792-465T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119604207 | |||||||
| chr2:119604389 | A | T | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.792-283A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | chr2 | 119604389 | |||||||
| chr2:119604452 | C | CA | 6 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0003c0003t0001g0061 others(3): Show |
6 | HG00597.hp2 HG02074.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.792-211dupA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | 119604452 | ||||||
| chr2:119604831 | C | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(182): Show |
186 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.912+39C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 9/23 | chr2 | 119604831 | |||||||
| chr2:119605321 | T | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(207): Show |
211 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.1133+32T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119605321 | |||||||
| chr2:119605423 | A | G | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1133+134A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119605423 | |||||||
| chr2:119606115 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1133+826C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119606115 | |||||||
| chr2:119606167 | CA | C | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133+881delA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | 119606167 | ||||||
| chr2:119606170 | A | AT | 16 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(13): Show |
16 | HG02280.hp1 HG02559.hp1 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.1133+895dupT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | 119606170 | ||||||
| chr2:119606170 | A | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(188): Show |
192 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.1133+881A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119606170 | |||||||
| chr2:119606194 | G | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(192): Show |
196 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(193): Show |
intron_variant | MODIFIER | c.1133+905G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119606194 | |||||||
| chr2:119606225 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1133+936C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119606225 | |||||||
| chr2:119606431 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1133+1142C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119606431 | |||||||
| chr2:119606466 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(126): Show |
129 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1133+1177T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119606466 | |||||||
| chr2:119606475 | G | T | 1 | a0002c0002t0001g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1133+1186G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119606475 | |||||||
| chr2:119606528 | C | T | 3 | a0001c0007t0001g0003 a0001c0007t0001g0160 a0001c0007t0001g0161 |
4 | HG02451.hp1 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1133+1239C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119606528 | |||||||
| chr2:119606571 | C | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(16): Show |
19 | HG02129.hp2 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1133+1282C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119606571 | |||||||
| chr2:119606661 | G | A | 1 | a0002c0002t0001g0220 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1133+1372G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119606661 | |||||||
| chr2:119606734 | G | A | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(16): Show |
19 | HG02129.hp2 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1133+1445G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119606734 | |||||||
| chr2:119606847 | G | C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1133+1558G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119606847 | |||||||
| chr2:119607090 | T | C | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134-1412T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119607090 | |||||||
| chr2:119607395 | A | G | 1 | a0004c0010t0001g0005 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1134-1107A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119607395 | |||||||
| chr2:119607440 | AATC | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(118): Show |
121 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.1134-1059_1134-105 others(7): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | 119607440 | ||||||
| chr2:119607817 | C | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1134-685C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119607817 | |||||||
| chr2:119607948 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(206): Show |
210 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.1134-554T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119607948 | |||||||
| chr2:119608028 | C | A | 214 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(211): Show |
215 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.1134-474C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119608028 | |||||||
| chr2:119608044 | C | T | 1 | a0001c0001t0002g0179 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1134-458C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119608044 | |||||||
| chr2:119608288 | T | A | 2 | a0001c0001t0001g0002 a0001c0001t0002g0002 |
2 | HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1134-214T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119608288 | |||||||
| chr2:119608380 | T | C | 1 | a0001c0001t0001g0014 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1134-122T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | chr2 | 119608380 | |||||||
| chr2:119608481 | G | GT | 213 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(210): Show |
214 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(211): Show |
splice_region_variant&intron_variant | LOW | c.1134-9dupT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | 119608481 | ||||||
| chr2:119608719 | T | C | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1221+130T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119608719 | |||||||
| chr2:119608853 | T | C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1221+264T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119608853 | |||||||
| chr2:119608907 | G | A | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1221+318G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119608907 | |||||||
| chr2:119609244 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1221+655A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119609244 | |||||||
| chr2:119609345 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1221+756C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119609345 | |||||||
| chr2:119609504 | T | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(211): Show |
215 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.1221+915T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119609504 | |||||||
| chr2:119609505 | G | A | 1 | a0004c0010t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1221+916G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119609505 | |||||||
| chr2:119610074 | G | A | 3 | a0003c0003t0001g0066 a0003c0003t0001g0072 a0003c0003t0001g0073 |
3 | NA18957.hp2 NA19005.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1221+1485G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119610074 | |||||||
| chr2:119610485 | A | G | 45 | a0001c0001t0001g0150 a0001c0001t0001g0162 a0001c0001t0001g0172 others(42): Show |
45 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.1222-1168A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119610485 | |||||||
| chr2:119610734 | T | A | 1 | a0002c0002t0002g0116 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1222-919T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119610734 | |||||||
| chr2:119610783 | A | G | 34 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0145 others(31): Show |
34 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1222-870A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119610783 | |||||||
| chr2:119610888 | C | T | 1 | a0001c0007t0001g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1222-765C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119610888 | |||||||
| chr2:119611176 | G | A | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222-477G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119611176 | |||||||
| chr2:119611416 | A | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(215): Show |
220 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.1222-237A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119611416 | |||||||
| chr2:119611420 | C | CA | 21 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(18): Show |
22 | HG01168.hp1 HG01243.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1222-213dupA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 119611420 | ||||||
| chr2:119611420 | C | CAA | 115 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(112): Show |
115 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.1222-214_1222-213d others(4): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 119611420 | ||||||
| chr2:119611529 | A | G | 44 | a0002c0002t0001g0097 a0003c0003t0001g0042 a0003c0003t0001g0061 others(41): Show |
44 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1222-124A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119611529 | |||||||
| chr2:119611564 | A | G | 1 | a0001c0001t0001g0025 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1222-89A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 12/23 | chr2 | 119611564 | |||||||
| chr2:119611942 | C | T | 1 | a0002c0002t0002g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1311+200C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119611942 | |||||||
| chr2:119611955 | T | C | 2 | a0004c0005t0001g0001 a0004c0005t0001g0016 |
3 | HG02647.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1311+213T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119611955 | |||||||
| chr2:119612361 | G | T | 214 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(211): Show |
215 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.1311+619G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119612361 | |||||||
| chr2:119612372 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(207): Show |
211 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.1311+630G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119612372 | |||||||
| chr2:119612441 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1311+699G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119612441 | |||||||
| chr2:119612589 | A | T | 2 | a0002c0002t0002g0053 a0002c0002t0002g0054 |
2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1311+847A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119612589 | |||||||
| chr2:119612761 | T | G | 1 | a0001c0001t0002g0147 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1311+1019T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119612761 | |||||||
| chr2:119613002 | G | T | 2 | a0001c0001t0001g0217 a0002c0002t0001g0101 |
2 | HG01361.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1311+1260G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119613002 | |||||||
| chr2:119613118 | C | T | 2 | a0002c0002t0002g0008 a0002c0002t0002g0009 |
2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1311+1376C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119613118 | |||||||
| chr2:119613235 | G | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(211): Show |
215 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.1311+1493G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119613235 | |||||||
| chr2:119613344 | G | T | 1 | a0002c0002t0002g0158 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1311+1602G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119613344 | |||||||
| chr2:119613452 | T | C | 1 | a0003c0003t0002g0108 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1311+1710T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119613452 | |||||||
| chr2:119613489 | A | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(215): Show |
220 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.1311+1747A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119613489 | |||||||
| chr2:119613935 | G | A | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1312-1676G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119613935 | |||||||
| chr2:119614293 | T | A | 1 | a0001c0001t0002g0032 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1312-1318T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119614293 | |||||||
| chr2:119614615 | C | T | 2 | a0002c0002t0001g0051 a0011c0013t0001g0052 |
2 | NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1312-996C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119614615 | |||||||
| chr2:119614797 | A | G | 1 | a0002c0002t0002g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1312-814A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119614797 | |||||||
| chr2:119614957 | G | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(215): Show |
220 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.1312-654G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119614957 | |||||||
| chr2:119615409 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(215): Show |
220 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.1312-202C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119615409 | |||||||
| chr2:119615441 | C | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(16): Show |
19 | HG02129.hp2 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1312-170C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119615441 | |||||||
| chr2:119615450 | G | C | 1 | a0001c0001t0002g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1312-161G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119615450 | |||||||
| chr2:119615461 | T | TA | 4 | a0002c0002t0001g0036 a0002c0002t0001g0055 a0002c0002t0002g0053 others(1): Show |
4 | HG02257.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-146dupA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr2 | 119615461 | ||||||
| chr2:119615579 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1312-32A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 13/23 | chr2 | 119615579 | |||||||
| chr2:119615790 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1410+81C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119615790 | |||||||
| chr2:119615932 | G | A | 1 | a0004c0010t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1410+223G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119615932 | |||||||
| chr2:119616393 | G | A | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1410+684G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119616393 | |||||||
| chr2:119616460 | C | T | 2 | a0004c0005t0001g0001 a0004c0005t0001g0016 |
3 | HG02647.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1410+751C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119616460 | |||||||
| chr2:119616492 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(210): Show |
214 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(211): Show |
intron_variant | MODIFIER | c.1410+783G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119616492 | |||||||
| chr2:119617194 | G | A | 5 | a0002c0002t0001g0039 a0002c0002t0001g0040 a0002c0002t0001g0087 others(2): Show |
5 | HG02056.hp2 HG02071.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1410+1485G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119617194 | |||||||
| chr2:119617352 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1410+1643C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119617352 | |||||||
| chr2:119617579 | C | T | 1 | a0001c0006t0001g0034 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1410+1870C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119617579 | |||||||
| chr2:119617653 | C | A | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1410+1944C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119617653 | |||||||
| chr2:119617895 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0167 |
2 | NA18612.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1410+2186C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119617895 | |||||||
| chr2:119618358 | G | A | 2 | a0004c0005t0001g0001 a0004c0005t0001g0016 |
3 | HG02647.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1410+2649G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119618358 | |||||||
| chr2:119618527 | T | C | 6 | a0002c0002t0001g0036 a0002c0002t0001g0055 a0002c0002t0001g0057 others(3): Show |
6 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1410+2818T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119618527 | |||||||
| chr2:119618756 | A | G | 1 | a0002c0002t0001g0081 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1410+3047A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119618756 | |||||||
| chr2:119618792 | G | T | 1 | a0003c0003t0001g0114 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1410+3083G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119618792 | |||||||
| chr2:119618897 | G | C | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1410+3188G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119618897 | |||||||
| chr2:119618995 | C | G | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1410+3286C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119618995 | |||||||
| chr2:119619014 | C | T | 1 | a0002c0002t0001g0084 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1410+3305C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119619014 | |||||||
| chr2:119619087 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1410+3378T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119619087 | |||||||
| chr2:119619219 | A | G | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(7): Show |
11 | HG01243.hp1 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1410+3510A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119619219 | |||||||
| chr2:119619329 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1410+3620C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119619329 | |||||||
| chr2:119620007 | T | C | 52 | a0002c0002t0001g0097 a0003c0003t0001g0042 a0003c0003t0001g0061 others(49): Show |
52 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1410+4298T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119620007 | |||||||
| chr2:119620010 | A | G | 51 | a0002c0002t0001g0097 a0003c0003t0001g0042 a0003c0003t0001g0061 others(48): Show |
51 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1410+4301A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119620010 | |||||||
| chr2:119620075 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1410+4366G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119620075 | |||||||
| chr2:119620145 | G | A | 1 | a0001c0006t0001g0034 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1410+4436G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119620145 | |||||||
| chr2:119620165 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1410+4456C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119620165 | |||||||
| chr2:119620421 | A | T | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1410+4712A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119620421 | |||||||
| chr2:119621015 | G | A | 1 | a0002c0002t0001g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1411-4568G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119621015 | |||||||
| chr2:119621017 | G | A | 1 | a0003c0003t0001g0042 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1411-4566G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119621017 | |||||||
| chr2:119621118 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(209): Show |
213 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(210): Show |
intron_variant | MODIFIER | c.1411-4465A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119621118 | |||||||
| chr2:119621191 | C | T | 1 | a0005c0004t0002g0129 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1411-4392C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119621191 | |||||||
| chr2:119621223 | C | CA | 13 | a0001c0001t0002g0022 a0002c0002t0001g0036 a0002c0002t0001g0055 others(10): Show |
13 | HG00738.hp2 HG00741.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1411-4345dupA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 119621223 | ||||||
| chr2:119621223 | CA | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0175 a0003c0003t0002g0049 others(2): Show |
5 | HG02630.hp2 HG02809.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411-4345delA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 119621223 | ||||||
| chr2:119621438 | T | C | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1411-4145T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119621438 | |||||||
| chr2:119621539 | G | A | 2 | a0002c0002t0001g0083 a0002c0002t0001g0084 |
2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1411-4044G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119621539 | |||||||
| chr2:119621801 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1411-3782G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119621801 | |||||||
| chr2:119621847 | A | G | 2 | a0004c0005t0001g0001 a0004c0005t0001g0016 |
3 | HG02647.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1411-3736A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119621847 | |||||||
| chr2:119622117 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(209): Show |
213 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(210): Show |
intron_variant | MODIFIER | c.1411-3466C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119622117 | |||||||
| chr2:119622121 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1411-3462C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119622121 | |||||||
| chr2:119623007 | G | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(209): Show |
213 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(210): Show |
intron_variant | MODIFIER | c.1411-2576G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119623007 | |||||||
| chr2:119623033 | A | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG02129.hp2 NA18941.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1411-2550A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119623033 | |||||||
| chr2:119623376 | C | G | 2 | a0003c0003t0002g0049 a0003c0003t0002g0106 |
2 | HG01243.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1411-2207C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119623376 | |||||||
| chr2:119623629 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1411-1954T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119623629 | |||||||
| chr2:119623697 | C | T | 1 | a0002c0002t0002g0056 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1411-1886C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119623697 | |||||||
| chr2:119623939 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1411-1644C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119623939 | |||||||
| chr2:119624052 | C | A | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1411-1531C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119624052 | |||||||
| chr2:119624533 | A | T | 3 | a0005c0004t0002g0129 a0005c0004t0002g0133 a0005c0004t0002g0134 |
3 | HG03130.hp1 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1411-1050A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119624533 | |||||||
| chr2:119624787 | G | A | 1 | a0001c0001t0005g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1411-796G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119624787 | |||||||
| chr2:119624829 | A | G | 1 | a0002c0002t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1411-754A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119624829 | |||||||
| chr2:119625021 | TA | T | 7 | a0004c0005t0001g0001 a0004c0005t0001g0016 a0004c0005t0002g0037 others(4): Show |
8 | HG02647.hp1 HG02976.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.1411-550delA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 119625021 | ||||||
| chr2:119625108 | C | G | 1 | a0001c0001t0001g0023 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1411-475C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119625108 | |||||||
| chr2:119625206 | C | T | 3 | a0001c0007t0001g0003 a0001c0007t0001g0160 a0001c0007t0001g0161 |
4 | HG02451.hp1 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411-377C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119625206 | |||||||
| chr2:119625353 | G | A | 6 | a0002c0002t0001g0036 a0002c0002t0001g0055 a0002c0002t0001g0057 others(3): Show |
6 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411-230G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119625353 | |||||||
| chr2:119625459 | G | A | 1 | a0003c0003t0001g0090 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1411-124G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119625459 | |||||||
| chr2:119625500 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1411-83G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | chr2 | 119625500 | |||||||
| chr2:119625562 | CATT | C | 47 | a0001c0001t0001g0150 a0001c0001t0001g0162 a0001c0001t0001g0172 others(44): Show |
47 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1411-18_1411-16del others(3): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 119625562 | ||||||
| chr2:119625720 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0164 a0001c0001t0001g0191 others(1): Show |
4 | NA18946.hp2 NA18949.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1516+32G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119625720 | |||||||
| chr2:119626027 | G | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.1516+339G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119626027 | |||||||
| chr2:119626038 | G | A | 3 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0009c0014t0002g0148 |
3 | HG01496.hp1 HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1516+350G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119626038 | |||||||
| chr2:119626071 | G | A | 3 | a0001c0001t0002g0147 a0003c0003t0002g0064 a0009c0014t0002g0148 |
3 | HG01978.hp2 HG02273.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1516+383G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119626071 | |||||||
| chr2:119626324 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1516+636G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119626324 | |||||||
| chr2:119626383 | C | T | 3 | a0004c0005t0001g0001 a0004c0005t0001g0016 a0004c0010t0001g0006 |
4 | HG02647.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1516+695C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119626383 | |||||||
| chr2:119626538 | A | G | 59 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(56): Show |
60 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1516+850A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119626538 | |||||||
| chr2:119626614 | G | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.1516+926G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119626614 | |||||||
| chr2:119626931 | G | GA | 36 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0149 others(33): Show |
37 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1517-709dupA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr2 | 119626931 | ||||||
| chr2:119627051 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1517-602C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119627051 | |||||||
| chr2:119627151 | A | C | 4 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0001t0002g0165 others(1): Show |
4 | HG00735.hp2 HG00741.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.1517-502A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119627151 | |||||||
| chr2:119627324 | A | G | 1 | a0002c0002t0001g0081 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1517-329A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119627324 | |||||||
| chr2:119627354 | A | T | 1 | a0005c0004t0002g0129 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1517-299A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119627354 | |||||||
| chr2:119627518 | GATAT | G | 29 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(26): Show |
29 | HG00639.hp2 HG01074.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.1517-111_1517-108d others(6): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr2 | 119627518 | ||||||
| chr2:119627518 | GATATAT | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(178): Show |
182 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.1517-113_1517-108d others(8): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr2 | 119627518 | ||||||
| chr2:119627544 | T | C | 1 | a0003c0003t0001g0061 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1517-109T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119627544 | |||||||
| chr2:119627581 | C | G | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1517-72C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119627581 | |||||||
| chr2:119627649 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG01175.hp1 | splice_region_variant&intron_variant | LOW | c.1517-4A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 15/23 | chr2 | 119627649 | |||||||
| chr2:119627912 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1650+126G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119627912 | |||||||
| chr2:119627914 | A | C | 1 | a0001c0001t0002g0022 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1650+128A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119627914 | |||||||
| chr2:119627973 | A | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(203): Show |
207 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.1650+187A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119627973 | |||||||
| chr2:119628066 | C | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(119): Show |
122 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1650+280C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628066 | |||||||
| chr2:119628069 | C | A | 1 | a0001c0001t0001g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1650+283C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628069 | |||||||
| chr2:119628120 | G | A | 2 | a0002c0002t0001g0097 a0005c0004t0002g0171 |
2 | NA18998.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1650+334G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628120 | |||||||
| chr2:119628141 | T | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.1650+355T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628141 | |||||||
| chr2:119628270 | T | TTC | 2 | a0002c0002t0002g0156 a0002c0002t0003g0159 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1650+502_1650+503d others(4): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 119628270 | ||||||
| chr2:119628289 | T | TCTCTG | 3 | a0001c0001t0001g0196 a0001c0001t0001g0206 a0001c0001t0002g0165 |
3 | HG00597.hp1 HG01516.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1650+503_1650+504i others(7): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628289 | |||||||
| chr2:119628289 | T | TCTCTGTG others(10): Show |
1 | a0001c0001t0001g0162 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1650+503_1650+504i others(19): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628289 | |||||||
| chr2:119628289 | T | TCTG | 32 | a0001c0001t0001g0021 a0002c0002t0001g0097 a0003c0003t0001g0042 others(29): Show |
32 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1650+503_1650+504i others(5): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628289 | |||||||
| chr2:119628289 | T | TCTGG | 20 | a0001c0001t0001g0026 a0001c0001t0001g0118 a0001c0001t0001g0126 others(17): Show |
21 | HG01109.hp2 HG01243.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.1650+503_1650+504i others(6): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628289 | |||||||
| chr2:119628289 | T | TCTGGG | 3 | a0003c0003t0001g0074 a0003c0003t0002g0065 a0003c0003t0002g0107 |
3 | NA18946.hp1 NA18963.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1650+503_1650+504i others(7): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628289 | |||||||
| chr2:119628289 | T | TCTGTGTG others(10): Show |
1 | a0001c0001t0002g0207 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1650+503_1650+504i others(19): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628289 | |||||||
| chr2:119628290 | G | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(141): Show |
144 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.1650+504G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628290 | |||||||
| chr2:119628290 | G | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0162 a0001c0001t0002g0207 others(1): Show |
4 | HG02630.hp1 NA19043.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1650+504G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628290 | |||||||
| chr2:119628291 | G | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(141): Show |
144 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.1650+505G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628291 | |||||||
| chr2:119628292 | G | GTGTGTGT others(2): Show |
2 | a0001c0001t0002g0165 a0002c0002t0001g0221 |
2 | HG00738.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1650+506_1650+507i others(11): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628292 | |||||||
| chr2:119628292 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0001g0206 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1650+506_1650+507i others(13): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628292 | |||||||
| chr2:119628292 | G | GTGTGTGT others(6): Show |
1 | a0001c0001t0001g0196 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1650+506_1650+507i others(15): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628292 | |||||||
| chr2:119628292 | G | T | 17 | a0001c0001t0001g0026 a0001c0001t0001g0118 a0001c0001t0001g0126 others(14): Show |
18 | HG01109.hp2 HG01358.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.1650+506G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628292 | |||||||
| chr2:119628294 | G | GGTGTGT | 21 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0145 others(18): Show |
21 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1650+543_1650+548d others(8): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 119628294 | ||||||
| chr2:119628294 | G | GGTGTGTG others(1): Show |
19 | a0001c0001t0001g0004 a0001c0001t0001g0119 a0001c0001t0001g0138 others(16): Show |
19 | HG01175.hp1 HG01261.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.1650+541_1650+548d others(10): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 119628294 | ||||||
| chr2:119628294 | G | GGTGTGTG others(3): Show |
18 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0144 others(15): Show |
18 | HG00733.hp1 HG00738.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1650+539_1650+548d others(12): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 119628294 | ||||||
| chr2:119628294 | G | GGTGTGTG others(5): Show |
28 | a0001c0001t0001g0017 a0001c0001t0001g0173 a0001c0001t0001g0175 others(25): Show |
28 | HG00438.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1650+537_1650+548d others(14): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 119628294 | ||||||
| chr2:119628294 | G | GGTGTGTG others(7): Show |
19 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0121 others(16): Show |
19 | HG01070.hp2 HG01175.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1650+535_1650+548d others(16): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 119628294 | ||||||
| chr2:119628294 | G | GGTGTGTG others(9): Show |
6 | a0001c0001t0001g0176 a0001c0001t0001g0215 a0001c0001t0002g0141 others(3): Show |
6 | HG01074.hp1 HG02622.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.1650+533_1650+548d others(18): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 119628294 | ||||||
| chr2:119628294 | G | GGTGTGTG others(11): Show |
3 | a0001c0001t0001g0190 a0001c0001t0001g0223 a0002c0002t0001g0040 |
3 | HG02559.hp2 HG03654.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1650+531_1650+548d others(20): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 119628294 | ||||||
| chr2:119628294 | G | GGTGTGTG others(13): Show |
3 | a0001c0001t0001g0150 a0001c0001t0001g0167 a0001c0001t0002g0170 |
3 | HG00438.hp1 HG01496.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1650+529_1650+548d others(22): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 119628294 | ||||||
| chr2:119628294 | G | GGTGTGTG others(17): Show |
1 | a0001c0001t0001g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1650+525_1650+548d others(26): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 119628294 | ||||||
| chr2:119628294 | G | GTGT | 6 | a0003c0003t0001g0074 a0003c0003t0002g0048 a0003c0003t0002g0062 others(3): Show |
6 | HG02572.hp1 HG03516.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.1650+508_1650+509i others(5): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628294 | |||||||
| chr2:119628294 | G | GTGTGT | 19 | a0002c0002t0001g0097 a0003c0003t0001g0042 a0003c0003t0001g0114 others(16): Show |
19 | HG00544.hp1 HG00597.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.1650+508_1650+509i others(7): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628294 | |||||||
| chr2:119628294 | G | GTGTGTGT | 5 | a0001c0001t0001g0021 a0001c0001t0001g0214 a0003c0003t0001g0061 others(2): Show |
5 | HG00639.hp1 HG00733.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650+508_1650+509i others(9): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628294 | |||||||
| chr2:119628294 | G | GTGTGTGT others(2): Show |
2 | a0003c0003t0002g0077 a0003c0003t0002g0078 |
2 | HG02027.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1650+508_1650+509i others(11): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628294 | |||||||
| chr2:119628294 | G | GTGTGTGT others(4): Show |
3 | a0003c0003t0001g0066 a0003c0003t0001g0072 a0003c0003t0002g0067 |
3 | HG03704.hp1 NA18957.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1650+508_1650+509i others(13): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628294 | |||||||
| chr2:119628294 | G | GTGTGTGT others(6): Show |
2 | a0003c0003t0001g0073 a0003c0003t0002g0068 |
2 | HG01074.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1650+508_1650+509i others(15): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628294 | |||||||
| chr2:119628294 | G | T | 32 | a0001c0001t0001g0026 a0001c0001t0001g0118 a0001c0001t0001g0126 others(29): Show |
33 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1650+508G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628294 | |||||||
| chr2:119628294 | GGT | G | 6 | a0001c0001t0002g0010 a0002c0002t0001g0047 a0004c0005t0001g0001 others(3): Show |
7 | HG02647.hp1 HG02922.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1650+547_1650+548d others(4): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 119628294 | ||||||
| chr2:119628294 | GGTGTGTG others(3): Show |
G | 1 | a0003c0003t0002g0076 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1650+539_1650+548d others(12): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 119628294 | ||||||
| chr2:119628306 | T | G | 1 | a0003c0003t0002g0076 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1650+520T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628306 | |||||||
| chr2:119628334 | T | TGTGTGTG others(6): Show |
1 | a0008c0012t0001g0199 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1650+548_1650+549i others(15): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628334 | |||||||
| chr2:119628495 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1650+709A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628495 | |||||||
| chr2:119628798 | T | C | 1 | a0002c0002t0001g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1650+1012T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628798 | |||||||
| chr2:119628956 | T | C | 1 | a0004c0010t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1651-919T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119628956 | |||||||
| chr2:119629376 | G | T | 3 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0009c0014t0002g0148 |
3 | HG01496.hp1 HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1651-499G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119629376 | |||||||
| chr2:119629546 | C | A | 1 | a0001c0001t0004g0194 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1651-329C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119629546 | |||||||
| chr2:119629586 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1651-289A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119629586 | |||||||
| chr2:119629587 | C | T | 6 | a0002c0002t0001g0036 a0002c0002t0001g0055 a0002c0002t0001g0057 others(3): Show |
6 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1651-288C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119629587 | |||||||
| chr2:119629693 | T | A | 1 | a0003c0003t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1651-182T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119629693 | |||||||
| chr2:119629701 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1651-174G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 16/23 | chr2 | 119629701 | |||||||
| chr2:119629976 | T | A | 1 | a0001c0001t0001g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1731+21T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 17/23 | chr2 | 119629976 | |||||||
| chr2:119630061 | G | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(215): Show |
220 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.1731+106G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 17/23 | chr2 | 119630061 | |||||||
| chr2:119630064 | T | C | 20 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0143 others(17): Show |
20 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1731+109T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 17/23 | chr2 | 119630064 | |||||||
| chr2:119630361 | A | C | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1732-209A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 17/23 | chr2 | 119630361 | |||||||
| chr2:119630552 | A | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(16): Show |
19 | HG02129.hp2 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1732-18A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 17/23 | chr2 | 119630552 | |||||||
| chr2:119630743 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1840-24C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 18/23 | chr2 | 119630743 | |||||||
| chr2:119630744 | G | A | 7 | a0003c0003t0002g0043 a0003c0003t0002g0044 a0003c0003t0002g0045 others(4): Show |
7 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1840-23G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 18/23 | chr2 | 119630744 | |||||||
| chr2:119631416 | G | A | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1974+515G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119631416 | |||||||
| chr2:119632269 | T | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.1974+1368T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119632269 | |||||||
| chr2:119632500 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1974+1599T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119632500 | |||||||
| chr2:119632701 | CA | C | 169 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(166): Show |
170 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.1974+1817delA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 119632701 | ||||||
| chr2:119633095 | G | A | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.1974+2194G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119633095 | |||||||
| chr2:119633348 | G | GA | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.1974+2456dupA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 119633348 | ||||||
| chr2:119633565 | C | A | 1 | a0001c0001t0001g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1974+2664C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119633565 | |||||||
| chr2:119633573 | A | G | 2 | a0003c0003t0002g0049 a0003c0003t0002g0106 |
2 | HG01243.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1974+2672A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119633573 | |||||||
| chr2:119633730 | AT | A | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.1974+2830delT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119633730 | |||||||
| chr2:119634247 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0118 a0001c0001t0001g0138 others(22): Show |
25 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1974+3346G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119634247 | |||||||
| chr2:119634385 | C | T | 2 | a0002c0002t0001g0036 a0002c0002t0001g0055 |
2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1974+3484C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119634385 | |||||||
| chr2:119634460 | G | A | 2 | a0002c0002t0001g0219 a0002c0002t0001g0221 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1974+3559G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119634460 | |||||||
| chr2:119634513 | G | A | 4 | a0004c0005t0002g0037 a0004c0005t0002g0038 a0004c0010t0001g0005 others(1): Show |
4 | HG03209.hp2 HG03486.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1974+3612G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119634513 | |||||||
| chr2:119634595 | TA | T | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1975-3657delA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 119634595 | ||||||
| chr2:119634762 | A | T | 1 | a0002c0002t0001g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1975-3497A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119634762 | |||||||
| chr2:119634982 | A | G | 3 | a0004c0005t0001g0001 a0004c0005t0001g0016 a0004c0010t0001g0006 |
4 | HG02647.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975-3277A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119634982 | |||||||
| chr2:119635019 | TAAG | T | 3 | a0004c0005t0001g0001 a0004c0005t0001g0016 a0004c0010t0001g0006 |
4 | HG02647.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975-3237_1975-323 others(7): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 119635019 | ||||||
| chr2:119635146 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1975-3113A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119635146 | |||||||
| chr2:119635154 | C | T | 2 | a0004c0005t0001g0016 a0011c0013t0001g0052 |
2 | HG02976.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1975-3105C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119635154 | |||||||
| chr2:119635421 | A | T | 1 | a0001c0001t0002g0117 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1975-2838A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119635421 | |||||||
| chr2:119636078 | A | G | 2 | a0003c0003t0002g0050 a0003c0003t0002g0108 |
2 | HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1975-2181A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119636078 | |||||||
| chr2:119636079 | C | G | 2 | a0003c0003t0002g0050 a0003c0003t0002g0108 |
2 | HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1975-2180C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119636079 | |||||||
| chr2:119636080 | TC | T | 2 | a0003c0003t0002g0050 a0003c0003t0002g0108 |
2 | HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1975-2178delC | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119636080 | |||||||
| chr2:119636082 | T | A | 2 | a0003c0003t0002g0050 a0003c0003t0002g0108 |
2 | HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1975-2177T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119636082 | |||||||
| chr2:119636156 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1975-2103G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119636156 | |||||||
| chr2:119636341 | A | G | 2 | a0001c0001t0002g0163 a0001c0001t0002g0207 |
2 | NA19056.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1975-1918A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119636341 | |||||||
| chr2:119636398 | A | ATACTC | 4 | a0004c0005t0002g0037 a0004c0005t0002g0038 a0004c0010t0001g0005 others(1): Show |
4 | HG03209.hp2 HG03486.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975-1860_1975-185 others(9): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 119636398 | ||||||
| chr2:119636533 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1975-1726G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119636533 | |||||||
| chr2:119636852 | A | C | 1 | a0001c0001t0002g0187 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1975-1407A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119636852 | |||||||
| chr2:119636912 | G | A | 33 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0149 others(30): Show |
33 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1975-1347G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119636912 | |||||||
| chr2:119637023 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1975-1236G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119637023 | |||||||
| chr2:119637132 | G | A | 1 | a0005c0004t0002g0129 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1975-1127G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119637132 | |||||||
| chr2:119637209 | G | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(212): Show |
216 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(213): Show |
intron_variant | MODIFIER | c.1975-1050G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119637209 | |||||||
| chr2:119637371 | C | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(203): Show |
207 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.1975-888C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119637371 | |||||||
| chr2:119637384 | G | A | 1 | a0003c0003t0002g0048 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1975-875G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119637384 | |||||||
| chr2:119637413 | G | A | 1 | a0006c0009t0002g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1975-846G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119637413 | |||||||
| chr2:119637629 | A | AAC | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1975-628_1975-627d others(4): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr2 | 119637629 | ||||||
| chr2:119637730 | A | G | 3 | a0001c0007t0001g0003 a0001c0007t0001g0160 a0001c0007t0001g0161 |
4 | HG02451.hp1 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975-529A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119637730 | |||||||
| chr2:119637762 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(215): Show |
220 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.1975-497C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119637762 | |||||||
| chr2:119637901 | A | T | 1 | a0001c0001t0002g0187 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1975-358A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119637901 | |||||||
| chr2:119638056 | A | C | 1 | a0001c0001t0002g0187 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1975-203A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119638056 | |||||||
| chr2:119638081 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.1975-178A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119638081 | |||||||
| chr2:119638197 | G | C | 7 | a0003c0003t0002g0043 a0003c0003t0002g0044 a0003c0003t0002g0045 others(4): Show |
7 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1975-62G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 19/23 | chr2 | 119638197 | |||||||
| chr2:119638461 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2133+44C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119638461 | |||||||
| chr2:119638576 | G | A | 2 | a0002c0002t0002g0157 a0002c0002t0002g0158 |
2 | HG00735.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2133+159G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119638576 | |||||||
| chr2:119638598 | C | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.2133+181C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119638598 | |||||||
| chr2:119638661 | A | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(204): Show |
208 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(205): Show |
intron_variant | MODIFIER | c.2133+244A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119638661 | |||||||
| chr2:119638721 | T | A | 1 | a0001c0001t0002g0187 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2133+304T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119638721 | |||||||
| chr2:119638722 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2133+305G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119638722 | |||||||
| chr2:119638834 | C | G | 1 | a0003c0003t0002g0080 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2133+417C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119638834 | |||||||
| chr2:119639074 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2133+657G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119639074 | |||||||
| chr2:119639082 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2133+665G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119639082 | |||||||
| chr2:119639214 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2134-567A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119639214 | |||||||
| chr2:119639242 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2134-539C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119639242 | |||||||
| chr2:119639311 | T | C | 1 | a0001c0001t0002g0187 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2134-470T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119639311 | |||||||
| chr2:119639312 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2134-469C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119639312 | |||||||
| chr2:119639313 | T | C | 1 | a0001c0001t0002g0187 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2134-468T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119639313 | |||||||
| chr2:119639364 | C | T | 2 | a0003c0003t0002g0050 a0003c0003t0002g0108 |
2 | HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2134-417C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119639364 | |||||||
| chr2:119639691 | A | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0208 |
2 | HG02071.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.2134-90A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 20/23 | chr2 | 119639691 | |||||||
| chr2:119640118 | A | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(217): Show |
222 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(219): Show |
intron_variant | MODIFIER | c.2225+246A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119640118 | |||||||
| chr2:119640138 | CTGAAATA others(5): Show |
C | 1 | a0001c0001t0002g0187 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2225+267_2225+278d others(14): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119640138 | |||||||
| chr2:119640179 | C | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2225+307C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119640179 | |||||||
| chr2:119640190 | A | G | 1 | a0003c0003t0002g0043 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2225+318A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119640190 | |||||||
| chr2:119640214 | C | CA | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(184): Show |
188 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(185): Show |
intron_variant | MODIFIER | c.2225+354dupA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr2 | 119640214 | ||||||
| chr2:119640214 | C | CAA | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(16): Show |
19 | HG02129.hp2 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.2225+353_2225+354d others(4): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr2 | 119640214 | ||||||
| chr2:119640355 | A | G | 1 | a0003c0003t0002g0079 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2225+483A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119640355 | |||||||
| chr2:119640481 | A | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(203): Show |
207 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.2225+609A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119640481 | |||||||
| chr2:119640665 | T | C | 6 | a0002c0002t0001g0036 a0002c0002t0001g0055 a0002c0002t0001g0057 others(3): Show |
6 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2225+793T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119640665 | |||||||
| chr2:119640666 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2225+794C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119640666 | |||||||
| chr2:119640719 | G | A | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2225+847G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119640719 | |||||||
| chr2:119640890 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2225+1018C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119640890 | |||||||
| chr2:119641109 | T | G | 44 | a0001c0001t0001g0150 a0001c0001t0001g0162 a0001c0001t0001g0172 others(41): Show |
44 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2225+1237T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119641109 | |||||||
| chr2:119641205 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(203): Show |
207 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.2225+1333G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119641205 | |||||||
| chr2:119641443 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2225+1571C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119641443 | |||||||
| chr2:119641448 | AC | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(7): Show |
11 | HG01243.hp1 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2225+1577delC | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119641448 | |||||||
| chr2:119641539 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(207): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.2225+1667G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119641539 | |||||||
| chr2:119641679 | A | G | 1 | a0002c0002t0003g0155 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2225+1807A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119641679 | |||||||
| chr2:119641698 | T | C | 58 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(55): Show |
59 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.2225+1826T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119641698 | |||||||
| chr2:119641818 | A | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(16): Show |
19 | HG02129.hp2 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.2225+1946A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119641818 | |||||||
| chr2:119641930 | C | T | 1 | a0003c0003t0001g0061 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2225+2058C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119641930 | |||||||
| chr2:119641958 | A | G | 7 | a0004c0005t0001g0001 a0004c0005t0001g0016 a0004c0005t0002g0037 others(4): Show |
8 | HG02647.hp1 HG02976.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.2225+2086A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119641958 | |||||||
| chr2:119642306 | A | C | 18 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0143 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2225+2434A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119642306 | |||||||
| chr2:119642533 | CT | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0183 a0001c0001t0002g0027 others(8): Show |
12 | HG01109.hp2 HG01175.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2225+2687delT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr2 | 119642533 | ||||||
| chr2:119642533 | CTT | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(141): Show |
144 | HG00544.hp1 HG00597.hp2 HG00733.hp1 others(141): Show |
intron_variant | MODIFIER | c.2225+2686_2225+268 others(6): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr2 | 119642533 | ||||||
| chr2:119642533 | CTTT | C | 47 | a0001c0001t0001g0150 a0001c0001t0001g0162 a0001c0001t0001g0172 others(44): Show |
47 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.2225+2685_2225+268 others(7): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr2 | 119642533 | ||||||
| chr2:119642583 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2225+2711C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119642583 | |||||||
| chr2:119642779 | A | C | 1 | a0002c0002t0002g0116 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2225+2907A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119642779 | |||||||
| chr2:119642939 | T | C | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0193 |
3 | HG00738.hp1 HG01358.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.2225+3067T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119642939 | |||||||
| chr2:119642970 | A | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2225+3098A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119642970 | |||||||
| chr2:119642986 | T | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(16): Show |
19 | HG02129.hp2 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.2225+3114T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119642986 | |||||||
| chr2:119643122 | G | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.2225+3250G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119643122 | |||||||
| chr2:119643241 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2225+3369T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119643241 | |||||||
| chr2:119643362 | C | G | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2225+3490C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119643362 | |||||||
| chr2:119643557 | A | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.2226-3401A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119643557 | |||||||
| chr2:119643626 | C | G | 1 | a0001c0001t0002g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2226-3332C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119643626 | |||||||
| chr2:119643787 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(122): Show |
125 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.2226-3171C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119643787 | |||||||
| chr2:119643851 | T | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(121): Show |
124 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.2226-3107T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119643851 | |||||||
| chr2:119644069 | C | G | 1 | a0002c0008t0001g0109 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2226-2889C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119644069 | |||||||
| chr2:119644171 | A | C | 7 | a0001c0001t0001g0172 a0001c0001t0002g0163 a0001c0001t0002g0166 others(4): Show |
7 | NA18964.hp1 NA18965.hp2 NA19056.hp2 others(4): Show |
intron_variant | MODIFIER | c.2226-2787A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119644171 | |||||||
| chr2:119644385 | C | T | 4 | a0004c0005t0002g0037 a0004c0005t0002g0038 a0004c0010t0001g0005 others(1): Show |
4 | HG03209.hp2 HG03486.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2226-2573C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119644385 | |||||||
| chr2:119644606 | C | T | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2226-2352C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119644606 | |||||||
| chr2:119644873 | A | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(215): Show |
220 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.2226-2085A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119644873 | |||||||
| chr2:119644993 | C | CCCCG | 27 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0024 others(24): Show |
27 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.2226-1962_2226-196 others(8): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr2 | 119644993 | ||||||
| chr2:119644994 | C | CCCG | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(179): Show |
183 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.2226-1962_2226-196 others(7): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr2 | 119644994 | ||||||
| chr2:119645120 | G | A | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(16): Show |
19 | HG02129.hp2 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.2226-1838G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119645120 | |||||||
| chr2:119645130 | GTC | G | 6 | a0002c0002t0001g0069 a0002c0002t0001g0070 a0002c0002t0001g0071 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2226-1812_2226-181 others(6): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr2 | 119645130 | ||||||
| chr2:119645364 | C | G | 3 | a0004c0005t0001g0001 a0004c0005t0001g0016 a0004c0010t0001g0006 |
4 | HG02647.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2226-1594C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119645364 | |||||||
| chr2:119645392 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2226-1566G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119645392 | |||||||
| chr2:119645400 | C | A | 1 | a0001c0001t0001g0195 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2226-1558C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119645400 | |||||||
| chr2:119645401 | T | A | 1 | a0001c0001t0001g0195 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2226-1557T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119645401 | |||||||
| chr2:119645518 | A | G | 1 | a0003c0003t0002g0079 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2226-1440A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119645518 | |||||||
| chr2:119645526 | T | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0167 |
2 | NA18612.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.2226-1432T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119645526 | |||||||
| chr2:119645616 | A | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(215): Show |
220 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.2226-1342A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119645616 | |||||||
| chr2:119645799 | G | T | 33 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0149 others(30): Show |
33 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.2226-1159G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119645799 | |||||||
| chr2:119645803 | C | G | 57 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(54): Show |
58 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.2226-1155C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119645803 | |||||||
| chr2:119645894 | T | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(215): Show |
220 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.2226-1064T>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119645894 | |||||||
| chr2:119645977 | G | A | 1 | a0002c0002t0001g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2226-981G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119645977 | |||||||
| chr2:119645992 | T | C | 1 | a0002c0002t0001g0097 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2226-966T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119645992 | |||||||
| chr2:119646111 | C | G | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2226-847C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119646111 | |||||||
| chr2:119646432 | G | A | 48 | a0003c0003t0001g0042 a0003c0003t0001g0061 a0003c0003t0001g0066 others(45): Show |
48 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.2226-526G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119646432 | |||||||
| chr2:119646448 | G | C | 1 | a0002c0002t0002g0056 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2226-510G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119646448 | |||||||
| chr2:119646621 | G | A | 2 | a0004c0010t0001g0005 a0004c0010t0001g0007 |
2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2226-337G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119646621 | |||||||
| chr2:119646643 | A | G | 5 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0139 others(2): Show |
5 | NA18970.hp2 NA18971.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.2226-315A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119646643 | |||||||
| chr2:119646864 | A | G | 1 | a0003c0003t0002g0062 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2226-94A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 21/23 | chr2 | 119646864 | |||||||
| chr2:119647053 | AT | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(206): Show |
210 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.2318+17delT | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr2 | 119647053 | ||||||
| chr2:119647157 | A | G | 1 | a0007c0011t0002g0046 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2318+107A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119647157 | |||||||
| chr2:119647604 | T | C | 3 | a0001c0001t0002g0141 a0001c0001t0002g0184 a0001c0001t0002g0186 |
3 | NA18941.hp2 NA18970.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2318+554T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119647604 | |||||||
| chr2:119647958 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2318+908C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119647958 | |||||||
| chr2:119648027 | A | C | 2 | a0004c0005t0001g0001 a0004c0005t0001g0016 |
3 | HG02647.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2318+977A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119648027 | |||||||
| chr2:119648231 | C | G | 1 | a0004c0010t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2318+1181C>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119648231 | |||||||
| chr2:119648548 | T | C | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2318+1498T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119648548 | |||||||
| chr2:119648602 | C | A | 3 | a0004c0005t0001g0001 a0004c0005t0001g0016 a0004c0010t0001g0006 |
4 | HG02647.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2318+1552C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119648602 | |||||||
| chr2:119648620 | C | T | 6 | a0002c0002t0001g0036 a0002c0002t0001g0055 a0002c0002t0001g0057 others(3): Show |
6 | HG01109.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2318+1570C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119648620 | |||||||
| chr2:119648699 | G | A | 3 | a0004c0005t0001g0001 a0004c0005t0001g0016 a0004c0010t0001g0006 |
4 | HG02647.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2318+1649G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119648699 | |||||||
| chr2:119648864 | G | T | 1 | a0001c0001t0002g0222 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2318+1814G>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119648864 | |||||||
| chr2:119648933 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02572.hp2 HG02717.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2318+1883C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119648933 | |||||||
| chr2:119649090 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.2318+2040A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119649090 | |||||||
| chr2:119649140 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2318+2090G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119649140 | |||||||
| chr2:119649201 | G | C | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2318+2151G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119649201 | |||||||
| chr2:119649228 | T | C | 1 | a0002c0002t0001g0095 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2318+2178T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119649228 | |||||||
| chr2:119649423 | A | G | 1 | a0001c0001t0002g0147 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2318+2373A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119649423 | |||||||
| chr2:119649575 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2319-2399G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119649575 | |||||||
| chr2:119649791 | C | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(16): Show |
19 | HG02129.hp2 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.2319-2183C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119649791 | |||||||
| chr2:119649795 | C | T | 1 | a0011c0013t0001g0052 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2319-2179C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119649795 | |||||||
| chr2:119649802 | C | T | 2 | a0004c0005t0002g0037 a0004c0005t0002g0038 |
2 | NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2319-2172C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119649802 | |||||||
| chr2:119650096 | G | A | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2319-1878G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119650096 | |||||||
| chr2:119650423 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2319-1551C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119650423 | |||||||
| chr2:119650579 | T | A | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2319-1395T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119650579 | |||||||
| chr2:119650666 | A | G | 1 | a0002c0002t0001g0093 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2319-1308A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119650666 | |||||||
| chr2:119650824 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(156): Show |
160 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.2319-1150T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119650824 | |||||||
| chr2:119650974 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2319-1000T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119650974 | |||||||
| chr2:119651165 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2319-809C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119651165 | |||||||
| chr2:119651259 | G | A | 7 | a0004c0005t0001g0001 a0004c0005t0001g0016 a0004c0005t0002g0037 others(4): Show |
8 | HG02647.hp1 HG02976.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.2319-715G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119651259 | |||||||
| chr2:119651386 | A | C | 3 | a0001c0001t0001g0162 a0001c0001t0001g0196 a0001c0001t0001g0206 |
3 | HG00597.hp1 NA18994.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2319-588A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119651386 | |||||||
| chr2:119651487 | A | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2319-487A>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119651487 | |||||||
| chr2:119651493 | GA | G | 19 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(16): Show |
20 | HG01243.hp1 HG02056.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2319-466delA | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr2 | 119651493 | ||||||
| chr2:119651493 | GAA | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(193): Show |
196 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(193): Show |
intron_variant | MODIFIER | c.2319-467_2319-466d others(4): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr2 | 119651493 | ||||||
| chr2:119651504 | A | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0203 |
2 | HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2319-470A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119651504 | |||||||
| chr2:119651775 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(155): Show |
159 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.2319-199C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119651775 | |||||||
| chr2:119651854 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.2319-120A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119651854 | |||||||
| chr2:119651857 | G | A | 4 | a0004c0005t0002g0037 a0004c0005t0002g0038 a0004c0010t0001g0005 others(1): Show |
4 | HG03209.hp2 HG03486.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2319-117G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 22/23 | chr2 | 119651857 | |||||||
| chr2:119652331 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(215): Show |
220 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.2414+262C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119652331 | |||||||
| chr2:119652406 | G | A | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.2414+337G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119652406 | |||||||
| chr2:119652857 | A | G | 1 | a0002c0002t0002g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2414+788A>G | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119652857 | |||||||
| chr2:119652968 | T | A | 1 | a0002c0002t0001g0087 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2414+899T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119652968 | |||||||
| chr2:119653003 | A | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(16): Show |
19 | HG02129.hp2 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.2414+934A>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119653003 | |||||||
| chr2:119653133 | C | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.2414+1064C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119653133 | |||||||
| chr2:119653152 | G | A | 3 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0002c0002t0002g0154 |
3 | NA18964.hp1 NA19066.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2414+1083G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119653152 | |||||||
| chr2:119653349 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2414+1280C>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119653349 | |||||||
| chr2:119653562 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2414+1493T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119653562 | |||||||
| chr2:119653652 | T | A | 1 | a0004c0010t0001g0005 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2414+1583T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119653652 | |||||||
| chr2:119653671 | T | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(155): Show |
159 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.2414+1602T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119653671 | |||||||
| chr2:119654404 | CCTT | C | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2415-1957_2415-195 others(7): Show |
CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119654404 | |||||||
| chr2:119654432 | C | T | 1 | a0001c0001t0002g0179 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2415-1930C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119654432 | |||||||
| chr2:119654822 | G | A | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2415-1540G>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119654822 | |||||||
| chr2:119655256 | C | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(207): Show |
211 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.2415-1106C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119655256 | |||||||
| chr2:119655592 | C | T | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2415-770C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119655592 | |||||||
| chr2:119655652 | G | C | 2 | a0004c0005t0001g0001 a0004c0005t0001g0016 |
3 | HG02647.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2415-710G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119655652 | |||||||
| chr2:119655715 | C | T | 3 | a0004c0005t0001g0001 a0004c0005t0001g0016 a0004c0010t0001g0006 |
4 | HG02647.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2415-647C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119655715 | |||||||
| chr2:119655765 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2415-597C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119655765 | |||||||
| chr2:119655849 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2415-513C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119655849 | |||||||
| chr2:119655870 | G | C | 1 | a0001c0001t0002g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2415-492G>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119655870 | |||||||
| chr2:119655922 | C | T | 1 | a0002c0002t0001g0083 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2415-440C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119655922 | |||||||
| chr2:119656061 | T | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.2415-301T>C | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119656061 | |||||||
| chr2:119656141 | T | A | 4 | a0001c0001t0002g0022 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2415-221T>A | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119656141 | |||||||
| chr2:119656273 | C | T | 1 | a0004c0010t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2415-89C>T | CFAP221 | ENSG00000163075.13 | transcript | ENST00000413369.8 | protein_coding | 23/23 | chr2 | 119656273 |