Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79846 |
| ensemblid | ENSG00000105792.19 |
| hgncid | 26107 |
| symbol | CFAP69 |
| name | cilia and flagella associated protein 69 |
| refseq_nuc | NM_001039706.3 |
| refseq_prot | NP_001034795.2 |
| ensembl_nuc | ENST00000389297.8 |
| ensembl_prot | ENSP00000373948.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 90245174 |
| end | 90311063 |
| strand | + |
| ver | v1.2 |
| region | chr7:90245174-90311063 |
| region5000 | chr7:90240174-90316063 |
| regionname0 | CFAP69_chr7_90245174_90311063 |
| regionname5000 | CFAP69_chr7_90240174_90316063 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 941 | 181 | 44 | 22 | 94 | 3 | 18 | 74 | CFAP69_chr7_90240174_90316063 | CFAP69 | MWTEE others(936): Show |
chr7 | 90240174 | 90316063 |
| a0002 | 0/1 | 941 | 118 | 21 | 22 | 51 | 5 | 18 | 35 | CFAP69_chr7_90240174_90316063 | CFAP69 | MWTEE others(936): Show |
chr7 | 90240174 | 90316063 |
| a0003 | 1/0 | 941 | 17 | 3 | 9 | 0 | 3 | 1 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | MWTEE others(936): Show |
chr7 | 90240174 | 90316063 |
| a0004 | 0/0 | 941 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | MWTEE others(936): Show |
chr7 | 90240174 | 90316063 |
| a0005 | 0/0 | 941 | 4 | 0 | 2 | 0 | 1 | 1 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | MWTEE others(936): Show |
chr7 | 90240174 | 90316063 |
| a0006 | 0/0 | 941 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | MWTEE others(936): Show |
chr7 | 90240174 | 90316063 |
| a0007 | 0/0 | 941 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | MWTEE others(936): Show |
chr7 | 90240174 | 90316063 |
| a0008 | 0/0 | 941 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | MWTEE others(936): Show |
chr7 | 90240174 | 90316063 |
| a0009 | 0/0 | 941 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | MWTEE others(936): Show |
chr7 | 90240174 | 90316063 |
| a0010 | 0/0 | 941 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | MWTEE others(936): Show |
chr7 | 90240174 | 90316063 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 2823 | 97 | 16 | 15 | 49 | 3 | 14 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0001c0003 | 0/0 | 2823 | 35 | 2 | 3 | 27 | 0 | 3 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0001c0004 | 0/0 | 2823 | 31 | 11 | 3 | 16 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0001c0006 | 0/0 | 2823 | 7 | 7 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0001c0011 | 0/0 | 2823 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0001c0012 | 0/0 | 2823 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0001c0013 | 0/0 | 2823 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0001c0014 | 0/0 | 2823 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0001c0016 | 0/0 | 2823 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0001c0019 | 0/0 | 2823 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0002c0001 | 0/1 | 2823 | 118 | 21 | 22 | 51 | 5 | 18 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0003c0005 | 1/0 | 2823 | 17 | 3 | 9 | 0 | 3 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0004c0007 | 0/0 | 2823 | 6 | 5 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0005c0009 | 0/0 | 2823 | 4 | 0 | 2 | 0 | 1 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0006c0008 | 0/0 | 2823 | 4 | 3 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0007c0010 | 0/0 | 2823 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0008c0015 | 0/0 | 2823 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0009c0018 | 0/0 | 2823 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 | ||
| a0010c0017 | 0/0 | 2823 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | ATGTG others(2818): Show |
chr7 | 90240174 | 90316063 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002 | 0/0 | 3902 | 93 | 14 | 14 | 49 | 2 | 14 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0001c0002t0004 | 0/0 | 3902 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0001c0002t0005 | 0/0 | 3902 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0001c0002t0006 | 0/0 | 3902 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0001c0003t0001 | 0/0 | 3902 | 35 | 2 | 3 | 27 | 0 | 3 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0001c0004t0002 | 0/0 | 3902 | 31 | 11 | 3 | 16 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0001c0006t0001 | 0/0 | 3902 | 7 | 7 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0001c0011t0003 | 0/0 | 3902 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0001c0012t0002 | 0/0 | 3902 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0001c0013t0002 | 0/0 | 3902 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0001c0014t0002 | 0/0 | 3902 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0001c0016t0001 | 0/0 | 3902 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0001c0019t0002 | 0/0 | 3902 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0002c0001t0001 | 0/1 | 3902 | 117 | 21 | 22 | 51 | 5 | 17 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0002c0001t0007 | 0/0 | 3902 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0003c0005t0002 | 1/0 | 3902 | 17 | 3 | 9 | 0 | 3 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0004c0007t0001 | 0/0 | 3902 | 6 | 5 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0005c0009t0002 | 0/0 | 3902 | 4 | 0 | 2 | 0 | 1 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0006c0008t0002 | 0/0 | 3902 | 4 | 3 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0007c0010t0002 | 0/0 | 3902 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0008c0015t0002 | 0/0 | 3902 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0009c0018t0002 | 0/0 | 3902 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| a0010c0017t0001 | 0/0 | 3902 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | AGCAA others(3897): Show |
chr7 | 90240174 | 90316063 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0005g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0002t0006g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0004t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0006t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0006t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0006t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0006t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0006t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0006t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0006t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0011t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0011t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0011t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0012t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0012t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0013t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0013t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0014t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0014t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0016t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0001c0019t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0002c0001t0007g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0256 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0003c0005t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0004c0007t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0004c0007t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0004c0007t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0004c0007t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0004c0007t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0004c0007t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0005c0009t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0005c0009t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0005c0009t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0005c0009t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0006c0008t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0006c0008t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0006c0008t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0007c0010t0002g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0007c0010t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0008c0015t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0008c0015t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0009c0018t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| a0010c0017t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0001 | g0065 | EUR | GBR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00099 | hp2 | a0002 | c0001 | t0001 | g0271 | EUR | GBR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00140 | hp1 | a0002 | c0001 | t0001 | g0064 | EUR | GBR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00140 | hp2 | a0005 | c0009 | t0002 | g0282 | EUR | GBR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0133 | EUR | FIN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00323 | hp2 | a0002 | c0001 | t0001 | g0004 | EUR | FIN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0122 | EAS | CHS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0296 | EAS | CHS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | CHS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00423 | hp2 | a0001 | c0004 | t0002 | g0217 | EAS | CHS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0089 | EAS | CHS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0295 | EAS | CHS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0109 | EAS | CHS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00558 | hp2 | a0002 | c0001 | t0001 | g0153 | EAS | CHS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | CHS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | CHS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00639 | hp1 | a0001 | c0014 | t0002 | g0212 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00639 | hp2 | a0004 | c0007 | t0001 | g0267 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0290 | EAS | CHS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | CHS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00735 | hp1 | a0002 | c0001 | t0001 | g0058 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00735 | hp2 | a0005 | c0009 | t0002 | g0281 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00738 | hp1 | a0009 | c0018 | t0002 | g0173 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00738 | hp2 | a0006 | c0008 | t0002 | g0243 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG00741 | hp2 | a0003 | c0005 | t0002 | g0254 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01069 | hp1 | a0002 | c0001 | t0001 | g0072 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01069 | hp2 | a0003 | c0005 | t0002 | g0249 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0128 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01070 | hp2 | a0003 | c0005 | t0002 | g0250 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0147 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01074 | hp2 | a0003 | c0005 | t0002 | g0257 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01081 | hp2 | a0001 | c0004 | t0002 | g0220 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01106 | hp1 | a0002 | c0001 | t0001 | g0081 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01106 | hp2 | a0001 | c0002 | t0006 | g0103 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01167 | hp1 | a0003 | c0005 | t0002 | g0285 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01167 | hp2 | a0002 | c0001 | t0001 | g0055 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01169 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01169 | hp2 | a0003 | c0005 | t0002 | g0284 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01175 | hp1 | a0002 | c0001 | t0001 | g0085 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0136 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0140 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01192 | hp2 | a0002 | c0001 | t0001 | g0059 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01243 | hp1 | a0002 | c0001 | t0001 | g0272 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01243 | hp2 | a0002 | c0001 | t0001 | g0052 | AMR | PUR | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01255 | hp1 | a0003 | c0005 | t0002 | g0255 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0134 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01256 | hp1 | a0002 | c0001 | t0001 | g0057 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01256 | hp2 | a0002 | c0001 | t0001 | g0019 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01261 | hp1 | a0002 | c0001 | t0001 | g0053 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0186 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01358 | hp1 | a0002 | c0001 | t0001 | g0063 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0019 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01361 | hp1 | a0003 | c0005 | t0002 | g0251 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0135 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0139 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01433 | hp2 | a0003 | c0005 | t0002 | g0258 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01496 | hp1 | a0002 | c0001 | t0001 | g0068 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0170 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01515 | hp1 | a0003 | c0005 | t0002 | g0018 | EUR | IBS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0150 | EUR | IBS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01517 | hp1 | a0001 | c0002 | t0005 | g0145 | EUR | IBS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01517 | hp2 | a0003 | c0005 | t0002 | g0018 | EUR | IBS | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01884 | hp1 | a0002 | c0001 | t0001 | g0083 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01884 | hp2 | a0001 | c0004 | t0002 | g0221 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01891 | hp1 | a0007 | c0010 | t0002 | g0225 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01891 | hp2 | a0001 | c0019 | t0002 | g0164 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01934 | hp1 | a0002 | c0001 | t0001 | g0095 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01934 | hp2 | a0001 | c0004 | t0002 | g0205 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0111 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01975 | hp2 | a0001 | c0004 | t0002 | g0233 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0302 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0172 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0179 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0304 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0301 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01993 | hp2 | a0002 | c0001 | t0001 | g0076 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0171 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0110 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02027 | hp1 | a0001 | c0003 | t0001 | g0307 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02027 | hp2 | a0002 | c0001 | t0001 | g0051 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02040 | hp1 | a0001 | c0004 | t0002 | g0214 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0112 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0152 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0287 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0043 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02071 | hp2 | a0002 | c0001 | t0001 | g0090 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02074 | hp1 | a0001 | c0004 | t0002 | g0208 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02074 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02083 | hp1 | a0002 | c0001 | t0001 | g0042 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02083 | hp2 | a0002 | c0001 | t0001 | g0278 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02132 | hp1 | a0002 | c0001 | t0001 | g0039 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0291 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | KHV | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02145 | hp1 | a0004 | c0007 | t0001 | g0268 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02145 | hp2 | a0001 | c0004 | t0002 | g0229 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02155 | hp1 | a0001 | c0004 | t0002 | g0163 | EAS | CDX | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0098 | EAS | CDX | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02165 | hp1 | a0001 | c0004 | t0002 | g0206 | EAS | CDX | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02165 | hp2 | a0002 | c0001 | t0001 | g0113 | EAS | CDX | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02257 | hp1 | a0007 | c0010 | t0002 | g0002 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02257 | hp2 | a0002 | c0001 | t0001 | g0070 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02280 | hp1 | a0001 | c0004 | t0002 | g0227 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0102 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02300 | hp1 | a0002 | c0001 | t0001 | g0276 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0096 | AMR | PEL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02451 | hp1 | a0001 | c0014 | t0002 | g0211 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02451 | hp2 | a0004 | c0007 | t0001 | g0263 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0169 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0022 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02615 | hp2 | a0003 | c0005 | t0002 | g0246 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02622 | hp1 | a0001 | c0004 | t0002 | g0224 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02622 | hp2 | a0002 | c0001 | t0001 | g0269 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0142 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02698 | hp2 | a0002 | c0001 | t0001 | g0005 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02723 | hp1 | a0001 | c0004 | t0002 | g0222 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02723 | hp2 | a0002 | c0001 | t0001 | g0030 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0062 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02735 | hp2 | a0002 | c0001 | t0001 | g0087 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0313 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02738 | hp2 | a0003 | c0005 | t0002 | g0253 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0132 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0155 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02818 | hp1 | a0001 | c0011 | t0003 | g0159 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02818 | hp2 | a0001 | c0006 | t0001 | g0262 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0146 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02886 | hp2 | a0002 | c0001 | t0001 | g0084 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02895 | hp1 | a0002 | c0001 | t0001 | g0033 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02895 | hp2 | a0002 | c0001 | t0001 | g0045 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02896 | hp2 | a0006 | c0008 | t0002 | g0017 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02897 | hp1 | a0002 | c0001 | t0001 | g0032 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02897 | hp2 | a0006 | c0008 | t0002 | g0017 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02922 | hp1 | a0008 | c0015 | t0002 | g0245 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02922 | hp2 | a0002 | c0001 | t0001 | g0151 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0130 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02965 | hp2 | a0002 | c0001 | t0001 | g0036 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02970 | hp1 | a0004 | c0007 | t0001 | g0264 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02976 | hp2 | a0002 | c0001 | t0001 | g0041 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0101 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0031 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0160 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0125 | AFR | GWD | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03098 | hp1 | a0001 | c0004 | t0002 | g0230 | AFR | MSL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03098 | hp2 | a0001 | c0011 | t0003 | g0157 | AFR | MSL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03130 | hp1 | a0001 | c0004 | t0002 | g0226 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0161 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03139 | hp1 | a0001 | c0006 | t0001 | g0259 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03139 | hp2 | a0002 | c0001 | t0001 | g0061 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0310 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0144 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03225 | hp1 | a0002 | c0001 | t0001 | g0044 | AFR | MSL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03225 | hp2 | a0001 | c0004 | t0002 | g0223 | AFR | MSL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03453 | hp1 | a0001 | c0006 | t0001 | g0237 | AFR | MSL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03453 | hp2 | a0006 | c0008 | t0002 | g0242 | AFR | MSL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03486 | hp1 | a0001 | c0006 | t0001 | g0261 | AFR | MSL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03486 | hp2 | a0002 | c0001 | t0001 | g0073 | AFR | MSL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0277 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0014 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0014 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03492 | hp2 | a0002 | c0001 | t0007 | g0028 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03516 | hp1 | a0008 | c0015 | t0002 | g0244 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03516 | hp2 | a0002 | c0001 | t0001 | g0069 | AFR | ESN | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0118 | AFR | MSL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03579 | hp2 | a0001 | c0013 | t0002 | g0241 | AFR | MSL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03654 | hp1 | a0005 | c0009 | t0002 | g0283 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03654 | hp2 | a0002 | c0001 | t0001 | g0274 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0129 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03669 | hp2 | a0002 | c0001 | t0001 | g0165 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03704 | hp1 | a0002 | c0001 | t0001 | g0074 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0038 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0005 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0138 | SAS | PJL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0194 | SAS | BEB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0279 | SAS | BEB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03834 | hp1 | a0002 | c0001 | t0001 | g0071 | SAS | BEB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03834 | hp2 | a0001 | c0004 | t0002 | g0215 | SAS | BEB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0176 | SAS | BEB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03927 | hp2 | a0002 | c0001 | t0001 | g0066 | SAS | BEB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03942 | hp1 | a0002 | c0001 | t0001 | g0273 | SAS | BEB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0185 | SAS | BEB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0168 | SAS | BEB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0149 | SAS | BEB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG04204 | hp1 | a0002 | c0001 | t0001 | g0037 | SAS | STU | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG04204 | hp2 | a0002 | c0001 | t0001 | g0275 | SAS | STU | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0040 | SAS | STU | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0148 | SAS | STU | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18522 | hp1 | a0007 | c0010 | t0002 | g0002 | AFR | YRI | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18522 | hp2 | a0001 | c0013 | t0002 | g0240 | AFR | YRI | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18612 | hp1 | a0001 | c0004 | t0002 | g0219 | EAS | CHB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18612 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | CHB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | CHB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18747 | hp2 | a0001 | c0004 | t0002 | g0213 | EAS | CHB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18906 | hp1 | a0001 | c0004 | t0002 | g0228 | AFR | YRI | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18906 | hp2 | a0003 | c0005 | t0002 | g0248 | AFR | YRI | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18942 | hp2 | a0002 | c0001 | t0001 | g0114 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18943 | hp1 | a0002 | c0001 | t0001 | g0100 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0299 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18944 | hp2 | a0001 | c0004 | t0002 | g0016 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18946 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18947 | hp2 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18948 | hp1 | a0001 | c0004 | t0002 | g0218 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18948 | hp2 | a0002 | c0001 | t0001 | g0092 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18949 | hp1 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18949 | hp2 | a0001 | c0004 | t0002 | g0015 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18957 | hp1 | a0002 | c0001 | t0001 | g0054 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18957 | hp2 | a0001 | c0004 | t0002 | g0015 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0306 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18959 | hp2 | a0002 | c0001 | t0001 | g0094 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0048 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18961 | hp2 | a0010 | c0017 | t0001 | g0060 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0050 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0298 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18965 | hp1 | a0002 | c0001 | t0001 | g0088 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18965 | hp2 | a0001 | c0003 | t0001 | g0288 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18968 | hp1 | a0002 | c0001 | t0001 | g0105 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0082 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18971 | hp2 | a0002 | c0001 | t0001 | g0107 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0292 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0047 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0308 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18983 | hp1 | a0001 | c0004 | t0002 | g0167 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18984 | hp1 | a0002 | c0001 | t0001 | g0046 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18985 | hp1 | a0002 | c0001 | t0001 | g0078 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18985 | hp2 | a0001 | c0004 | t0002 | g0216 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18986 | hp2 | a0002 | c0001 | t0001 | g0093 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18991 | hp2 | a0002 | c0001 | t0001 | g0108 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18992 | hp1 | a0001 | c0003 | t0001 | g0305 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18993 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18994 | hp1 | a0002 | c0001 | t0001 | g0097 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0312 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18999 | hp1 | a0001 | c0012 | t0002 | g0198 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0303 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19000 | hp2 | a0002 | c0001 | t0001 | g0106 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19001 | hp1 | a0002 | c0001 | t0001 | g0238 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19003 | hp1 | a0001 | c0003 | t0001 | g0309 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19004 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19006 | hp2 | a0002 | c0001 | t0001 | g0077 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0049 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0294 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19010 | hp1 | a0001 | c0004 | t0002 | g0016 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19012 | hp1 | a0001 | c0003 | t0001 | g0297 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0124 | AFR | LWK | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19030 | hp2 | a0001 | c0016 | t0001 | g0236 | AFR | LWK | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19043 | hp1 | a0001 | c0006 | t0001 | g0239 | AFR | LWK | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19043 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | LWK | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19054 | hp2 | a0002 | c0001 | t0001 | g0079 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0293 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0314 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19060 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19063 | hp2 | a0002 | c0001 | t0001 | g0117 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19064 | hp1 | a0002 | c0001 | t0001 | g0091 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19064 | hp2 | a0001 | c0012 | t0002 | g0235 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0099 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0300 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19076 | hp1 | a0001 | c0004 | t0002 | g0207 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19077 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19078 | hp2 | a0002 | c0001 | t0001 | g0067 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0289 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19082 | hp1 | a0001 | c0004 | t0002 | g0210 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19082 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0286 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19091 | hp1 | a0002 | c0001 | t0001 | g0116 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA20129 | hp1 | a0007 | c0010 | t0002 | g0002 | AFR | ASW | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA20129 | hp2 | a0001 | c0011 | t0003 | g0158 | AFR | ASW | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA20752 | hp1 | a0002 | c0001 | t0001 | g0004 | EUR | TSI | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA20752 | hp2 | a0003 | c0005 | t0002 | g0252 | EUR | TSI | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0009 | SAS | GIH | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0022 | SAS | GIH | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01123 | hp1 | a0005 | c0009 | t0002 | g0280 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG01123 | hp2 | a0002 | c0001 | t0001 | g0080 | AMR | CLM | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02109 | hp1 | a0001 | c0004 | t0002 | g0234 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02109 | hp2 | a0002 | c0001 | t0001 | g0270 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02486 | hp1 | a0002 | c0001 | t0001 | g0086 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0311 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02559 | hp1 | a0003 | c0005 | t0002 | g0247 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG02559 | hp2 | a0004 | c0007 | t0001 | g0265 | AFR | ACB | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03471 | hp1 | a0002 | c0001 | t0001 | g0035 | AFR | MSL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG03471 | hp2 | a0004 | c0007 | t0001 | g0266 | AFR | MSL | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG06807 | hp1 | a0001 | c0006 | t0001 | g0260 | AFR | USA | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0056 | AFR | USA | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18955 | hp1 | a0002 | c0001 | t0001 | g0115 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA20300 | hp1 | a0002 | c0001 | t0001 | g0034 | AFR | USA | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | USA | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA21309 | hp1 | a0001 | c0004 | t0002 | g0209 | AFR | LWK | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| NA21309 | hp2 | a0001 | c0006 | t0001 | g0162 | AFR | LWK | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0075 | REF | REF | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| homoSapiens | grch38p0 | a0003 | c0005 | t0002 | g0256 | REF | REF | CFAP69_chr7_90240174_90316063 | CFAP69 | chr7 | 90240174 | 90316063 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:90262017 | G | A | 1 | a0006 | 4 | HG00738.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
missense_variant | MODERATE | c.317G>A | p.Arg106His | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/23 | 568/3902 | 317/2826 | 106/941 | chr7 | 90262017 | |||
| chr7:90274042 | C | T | 1 | a0008 | 2 | HG02922.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.916C>T | p.Arg306Cys | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/23 | 1167/3902 | 916/2826 | 306/941 | chr7 | 90274042 | |||
| chr7:90282895 | C | T | 1 | a0004 | 6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
missense_variant | MODERATE | c.1376C>T | p.Pro459Leu | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/23 | 1627/3902 | 1376/2826 | 459/941 | chr7 | 90282895 | |||
| chr7:90282987 | G | A | 7 | a0001 a0002 a0004 others(4): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
missense_variant | MODERATE | c.1468G>A | p.Val490Met | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/23 | 1719/3902 | 1468/2826 | 490/941 | chr7 | 90282987 | |||
| chr7:90307043 | T | C | 1 | a0009 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.2408T>C | p.Ile803Thr | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 20/23 | 2659/3902 | 2408/2826 | 803/941 | chr7 | 90307043 | |||
| chr7:90307057 | G | A | 1 | a0010 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.2422G>A | p.Ala808Thr | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 20/23 | 2673/3902 | 2422/2826 | 808/941 | chr7 | 90307057 | |||
| chr7:90307778 | C | T | 1 | a0007 | 4 | HG01891.hp1 HG02257.hp1 NA18522.hp1 others(1): Show |
missense_variant | MODERATE | c.2474C>T | p.Thr825Met | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/23 | 2725/3902 | 2474/2826 | 825/941 | chr7 | 90307778 | |||
| chr7:90309274 | C | G | 8 | a0001 a0002 a0004 others(5): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
missense_variant | MODERATE | c.2562C>G | p.Ser854Arg | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 22/23 | 2813/3902 | 2562/2826 | 854/941 | chr7 | 90309274 | |||
| chr7:90309366 | C | T | 2 | a0002 a0010 |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
missense_variant&splice_region_variant | MODERATE | c.2654C>T | p.Thr885Met | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 22/23 | 2905/3902 | 2654/2826 | 885/941 | chr7 | 90309366 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:90245448 | G | T | 1 | a0001c0011 | 3 | HG02818.hp1 HG03098.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.24G>T | p.Ala8Ala | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/23 | 275/3902 | 24/2826 | 8/941 | chr7 | 90245448 | |||
| chr7:90245460 | C | T | 1 | a0008c0015 | 2 | HG02922.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.36C>T | p.Ala12Ala | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/23 | 287/3902 | 36/2826 | 12/941 | chr7 | 90245460 | |||
| chr7:90271539 | G | A | 1 | a0001c0011 | 3 | HG02818.hp1 HG03098.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.546G>A | p.Ala182Ala | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 7/23 | 797/3902 | 546/2826 | 182/941 | chr7 | 90271539 | |||
| chr7:90277232 | G | A | 1 | a0001c0012 | 2 | NA18999.hp1 NA19064.hp2 |
synonymous_variant | LOW | c.1053G>A | p.Leu351Leu | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/23 | 1304/3902 | 1053/2826 | 351/941 | chr7 | 90277232 | |||
| chr7:90277286 | A | G | 1 | a0001c0019 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1107A>G | p.Leu369Leu | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/23 | 1358/3902 | 1107/2826 | 369/941 | chr7 | 90277286 | |||
| chr7:90277295 | C | T | 7 | a0001c0002 a0001c0004 a0001c0011 others(4): Show |
140 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
synonymous_variant | LOW | c.1116C>T | p.Asn372Asn | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/23 | 1367/3902 | 1116/2826 | 372/941 | chr7 | 90277295 | |||
| chr7:90286381 | G | A | 1 | a0001c0016 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1638G>A | p.Glu546Glu | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/23 | 1889/3902 | 1638/2826 | 546/941 | chr7 | 90286381 | |||
| chr7:90288263 | C | T | 1 | a0006c0008 | 4 | HG00738.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.1686C>T | p.Ile562Ile | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/23 | 1937/3902 | 1686/2826 | 562/941 | chr7 | 90288263 | |||
| chr7:90304048 | G | A | 4 | a0001c0004 a0001c0013 a0001c0014 others(1): Show |
39 | HG00423.hp2 HG00639.hp1 HG01081.hp2 others(36): Show |
synonymous_variant | LOW | c.2130G>A | p.Ala710Ala | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 18/23 | 2381/3902 | 2130/2826 | 710/941 | chr7 | 90304048 | |||
| chr7:90306927 | T | C | 1 | a0001c0014 | 2 | HG00639.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.2292T>C | p.Tyr764Tyr | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 20/23 | 2543/3902 | 2292/2826 | 764/941 | chr7 | 90306927 | |||
| chr7:90307854 | G | A | 1 | a0001c0003 | 35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
splice_region_variant&synonymous_variant | LOW | c.2550G>A | p.Lys850Lys | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/23 | 2801/3902 | 2550/2826 | 850/941 | chr7 | 90307854 | |||
| chr7:90310113 | T | C | 1 | a0001c0003 | 35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
synonymous_variant | LOW | c.2701T>C | p.Leu901Leu | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 23/23 | 2952/3902 | 2701/2826 | 901/941 | chr7 | 90310113 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:90245252 | C | A | 1 | a0001c0002t0005 | 1 | HG01517.hp1 | 5_prime_UTR_variant | MODIFIER | c.-173C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/23 | 173 | chr7 | 90245252 | ||||||
| chr7:90310514 | G | A | 1 | a0001c0002t0006 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*276G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 23/23 | 276 | chr7 | 90310514 | ||||||
| chr7:90310627 | A | G | 2 | a0001c0002t0004 a0001c0011t0003 |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*389A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 23/23 | 389 | chr7 | 90310627 | ||||||
| chr7:90310852 | G | C | 1 | a0002c0001t0007 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*614G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 23/23 | 614 | chr7 | 90310852 | ||||||
| chr7:90310992 | C | T | 1 | a0001c0002t0004 | 2 | HG03041.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*754C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 23/23 | 754 | chr7 | 90310992 | ||||||
| chr7:90311017 | G | A | 7 | a0001c0003t0001 a0001c0006t0001 a0001c0016t0001 others(4): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*779G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 23/23 | 779 | chr7 | 90311017 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:90245716 | G | A | 1 | a0001c0002t0002g0023 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.120+172G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90245716 | |||||||
| chr7:90245730 | G | A | 140 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(137): Show |
149 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.120+186G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90245730 | |||||||
| chr7:90245960 | G | C | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+416G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90245960 | |||||||
| chr7:90246299 | G | C | 1 | a0001c0006t0001g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.120+755G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90246299 | |||||||
| chr7:90246315 | C | T | 1 | a0001c0003t0001g0314 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.120+771C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90246315 | |||||||
| chr7:90246508 | T | C | 1 | a0001c0004t0002g0163 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.120+964T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90246508 | |||||||
| chr7:90246694 | C | T | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.120+1150C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90246694 | |||||||
| chr7:90246816 | A | AT | 9 | a0001c0003t0001g0312 a0001c0003t0001g0313 a0002c0001t0001g0156 others(6): Show |
9 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.120+1287dupT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90246816 | ||||||
| chr7:90246816 | AT | A | 89 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(86): Show |
98 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.120+1287delT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90246816 | ||||||
| chr7:90247013 | A | G | 86 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(83): Show |
95 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.120+1469A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90247013 | |||||||
| chr7:90247051 | A | G | 142 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(139): Show |
155 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.120+1507A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90247051 | |||||||
| chr7:90247097 | C | T | 1 | a0001c0002t0002g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.120+1553C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90247097 | |||||||
| chr7:90247290 | G | A | 3 | a0001c0011t0003g0157 a0001c0011t0003g0158 a0001c0011t0003g0159 |
3 | HG02818.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.120+1746G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90247290 | |||||||
| chr7:90247349 | C | T | 1 | a0001c0006t0001g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.120+1805C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90247349 | |||||||
| chr7:90247401 | T | C | 2 | a0001c0003t0001g0286 a0001c0003t0001g0314 |
2 | NA19060.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.120+1857T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90247401 | |||||||
| chr7:90247450 | C | G | 1 | a0001c0002t0002g0154 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.120+1906C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90247450 | |||||||
| chr7:90247624 | G | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.120+2080G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90247624 | |||||||
| chr7:90247714 | T | C | 144 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(141): Show |
157 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.120+2170T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90247714 | |||||||
| chr7:90247718 | C | T | 11 | a0002c0001t0001g0019 a0002c0001t0001g0165 a0002c0001t0001g0271 others(8): Show |
12 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.120+2174C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90247718 | |||||||
| chr7:90247757 | A | G | 2 | a0002c0001t0001g0152 a0002c0001t0001g0153 |
2 | HG00558.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.120+2213A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90247757 | |||||||
| chr7:90247997 | C | T | 13 | a0002c0001t0001g0019 a0002c0001t0001g0165 a0002c0001t0001g0269 others(10): Show |
14 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.120+2453C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90247997 | |||||||
| chr7:90248501 | T | A | 2 | a0001c0011t0003g0157 a0001c0011t0003g0158 |
2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.120+2957T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90248501 | |||||||
| chr7:90249265 | T | C | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.120+3721T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90249265 | |||||||
| chr7:90249308 | C | T | 1 | a0002c0001t0001g0151 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.120+3764C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90249308 | |||||||
| chr7:90249485 | A | T | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.120+3941A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90249485 | |||||||
| chr7:90249504 | A | T | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.120+3960A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90249504 | |||||||
| chr7:90249525 | G | A | 1 | a0001c0002t0002g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.120+3981G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90249525 | |||||||
| chr7:90249681 | C | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.120+4137C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90249681 | |||||||
| chr7:90249725 | G | A | 1 | a0002c0001t0007g0028 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.120+4181G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90249725 | |||||||
| chr7:90249790 | C | T | 2 | a0001c0003t0001g0310 a0001c0003t0001g0311 |
2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.120+4246C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90249790 | |||||||
| chr7:90249887 | G | A | 5 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(2): Show |
5 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+4343G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90249887 | |||||||
| chr7:90249944 | T | A | 1 | a0001c0002t0002g0166 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.120+4400T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90249944 | |||||||
| chr7:90250175 | T | C | 297 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(294): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.120+4631T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90250175 | |||||||
| chr7:90250187 | G | GGA | 6 | a0001c0003t0001g0304 a0001c0003t0001g0305 a0001c0003t0001g0306 others(3): Show |
6 | HG01074.hp2 HG01433.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.120+4690_120+4691d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | G | GGAGA | 6 | a0001c0002t0002g0118 a0001c0002t0002g0119 a0001c0002t0002g0120 others(3): Show |
6 | HG02027.hp1 HG03579.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.120+4688_120+4691d others(6): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | G | GGAGAGA | 5 | a0001c0002t0002g0027 a0001c0002t0002g0121 a0001c0002t0002g0122 others(2): Show |
5 | HG00408.hp1 HG02976.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+4686_120+4691d others(8): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | G | GGAGAGAG others(1): Show |
7 | a0001c0002t0002g0125 a0001c0002t0002g0126 a0001c0002t0002g0127 others(4): Show |
7 | HG00597.hp1 HG01070.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+4684_120+4691d others(10): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | G | GGAGAGAG others(3): Show |
6 | a0001c0002t0002g0008 a0001c0002t0002g0130 a0004c0007t0001g0263 others(3): Show |
7 | HG00140.hp2 HG00735.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+4682_120+4691d others(12): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | G | GGAGAGAG others(5): Show |
5 | a0001c0002t0002g0009 a0001c0002t0002g0131 a0001c0002t0002g0132 others(2): Show |
6 | HG00741.hp1 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+4680_120+4691d others(14): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | G | GGAGAGAG others(7): Show |
6 | a0001c0002t0002g0133 a0001c0002t0002g0134 a0001c0002t0002g0135 others(3): Show |
6 | HG00323.hp1 HG01175.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.120+4678_120+4691d others(16): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | G | GGAGAGAG others(9): Show |
6 | a0001c0002t0002g0024 a0001c0002t0002g0138 a0001c0002t0002g0139 others(3): Show |
6 | HG01081.hp1 HG01192.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+4676_120+4691d others(18): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | G | GGAGAGAG others(11): Show |
9 | a0001c0002t0002g0142 a0001c0002t0002g0143 a0001c0002t0002g0144 others(6): Show |
9 | HG01517.hp1 HG01891.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.120+4674_120+4691d others(20): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | G | GGAGAGAG others(13): Show |
2 | a0001c0002t0002g0147 a0001c0002t0002g0148 |
2 | HG01074.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.120+4672_120+4691d others(22): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | G | GGAGAGAG others(15): Show |
3 | a0001c0002t0002g0149 a0004c0007t0001g0267 a0004c0007t0001g0268 |
3 | HG00639.hp2 HG02145.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.120+4670_120+4691d others(24): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | G | GGAGAGAG others(19): Show |
1 | a0001c0002t0002g0150 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.120+4666_120+4691d others(28): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | G | GGAGAGAG others(21): Show |
1 | a0001c0002t0004g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.120+4664_120+4691d others(30): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | GGA | G | 21 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(18): Show |
25 | HG00438.hp2 HG00673.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.120+4690_120+4691d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | GGAGA | G | 7 | a0001c0003t0001g0288 a0001c0003t0001g0289 a0001c0011t0003g0157 others(4): Show |
7 | HG00738.hp2 HG02818.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+4688_120+4691d others(6): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | GGAGAGA | G | 5 | a0003c0005t0002g0246 a0003c0005t0002g0247 a0003c0005t0002g0248 others(2): Show |
6 | HG02559.hp1 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.120+4686_120+4691d others(8): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | GGAGAGAG others(1): Show |
G | 19 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0006g0103 others(16): Show |
20 | HG00558.hp1 HG00558.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.120+4684_120+4691d others(10): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | GGAGAGAG others(3): Show |
G | 37 | a0001c0006t0001g0237 a0002c0001t0001g0006 a0002c0001t0001g0067 others(34): Show |
38 | HG00438.hp1 HG01069.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.120+4682_120+4691d others(12): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | GGAGAGAG others(5): Show |
G | 12 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(9): Show |
12 | HG00099.hp1 HG00140.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.120+4680_120+4691d others(14): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | GGAGAGAG others(7): Show |
G | 43 | a0001c0002t0002g0232 a0001c0004t0002g0233 a0001c0004t0002g0234 others(40): Show |
48 | HG00323.hp2 HG00735.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.120+4678_120+4691d others(16): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250187 | GGAGAGAG others(9): Show |
G | 92 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(89): Show |
102 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.120+4676_120+4691d others(18): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90250187 | ||||||
| chr7:90250236 | C | A | 9 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(6): Show |
9 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.120+4692C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90250236 | |||||||
| chr7:90250249 | C | T | 2 | a0008c0015t0002g0244 a0008c0015t0002g0245 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.120+4705C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90250249 | |||||||
| chr7:90250279 | C | A | 1 | a0001c0004t0002g0167 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.120+4735C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90250279 | |||||||
| chr7:90250362 | A | T | 1 | a0001c0003t0001g0306 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.120+4818A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90250362 | |||||||
| chr7:90250363 | G | A | 1 | a0001c0003t0001g0306 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.120+4819G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90250363 | |||||||
| chr7:90250397 | A | G | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.120+4853A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90250397 | |||||||
| chr7:90250548 | G | A | 2 | a0002c0001t0001g0029 a0002c0001t0001g0030 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.121-4875G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90250548 | |||||||
| chr7:90250583 | G | T | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.121-4840G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90250583 | |||||||
| chr7:90250655 | A | T | 1 | a0002c0001t0001g0066 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.121-4768A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90250655 | |||||||
| chr7:90250681 | T | C | 1 | a0003c0005t0002g0246 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.121-4742T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90250681 | |||||||
| chr7:90250778 | C | G | 1 | a0002c0001t0001g0061 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.121-4645C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90250778 | |||||||
| chr7:90250984 | T | C | 5 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(2): Show |
5 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-4439T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90250984 | |||||||
| chr7:90251027 | A | T | 85 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(82): Show |
94 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.121-4396A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90251027 | |||||||
| chr7:90251040 | C | G | 99 | a0001c0013t0002g0240 a0001c0013t0002g0241 a0002c0001t0001g0001 others(96): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.121-4383C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90251040 | |||||||
| chr7:90251077 | C | T | 1 | a0001c0003t0001g0303 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.121-4346C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90251077 | |||||||
| chr7:90251228 | A | G | 1 | a0010c0017t0001g0060 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.121-4195A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90251228 | |||||||
| chr7:90251234 | C | T | 99 | a0001c0013t0002g0240 a0001c0013t0002g0241 a0002c0001t0001g0001 others(96): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.121-4189C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90251234 | |||||||
| chr7:90251270 | G | A | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-4153G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90251270 | |||||||
| chr7:90251399 | G | A | 1 | a0002c0001t0001g0067 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.121-4024G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90251399 | |||||||
| chr7:90251509 | T | G | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.121-3914T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90251509 | |||||||
| chr7:90251635 | A | G | 145 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(142): Show |
155 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.121-3788A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90251635 | |||||||
| chr7:90251643 | T | C | 1 | a0001c0002t0002g0168 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.121-3780T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90251643 | |||||||
| chr7:90251666 | G | A | 48 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(45): Show |
53 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.121-3757G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90251666 | |||||||
| chr7:90251670 | C | CA | 46 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(43): Show |
49 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.121-3745dupA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90251670 | ||||||
| chr7:90251919 | A | T | 143 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(140): Show |
156 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.121-3504A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90251919 | |||||||
| chr7:90251925 | G | C | 143 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(140): Show |
156 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.121-3498G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90251925 | |||||||
| chr7:90252018 | T | TA | 130 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(127): Show |
142 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.121-3394dupA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252018 | ||||||
| chr7:90252110 | C | CTG | 20 | a0001c0002t0002g0010 a0001c0002t0002g0166 a0001c0002t0002g0168 others(17): Show |
21 | HG01192.hp2 HG01981.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.121-3278_121-3277d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252110 | ||||||
| chr7:90252110 | C | CTGTG | 8 | a0001c0002t0002g0011 a0001c0002t0002g0182 a0001c0002t0002g0183 others(5): Show |
10 | HG00639.hp1 HG00673.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.121-3280_121-3277d others(6): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252110 | ||||||
| chr7:90252110 | C | CTGTGTG | 33 | a0001c0002t0002g0012 a0001c0002t0002g0013 a0001c0002t0002g0014 others(30): Show |
39 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.121-3282_121-3277d others(8): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252110 | ||||||
| chr7:90252110 | C | CTGTGTGT others(1): Show |
12 | a0001c0002t0002g0025 a0001c0002t0002g0026 a0001c0002t0002g0197 others(9): Show |
12 | HG01975.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.121-3284_121-3277d others(10): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252110 | ||||||
| chr7:90252110 | C | CTGTGTGT others(3): Show |
8 | a0001c0002t0002g0200 a0001c0002t0002g0201 a0001c0002t0002g0202 others(5): Show |
9 | HG03098.hp1 HG03453.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-3286_121-3277d others(12): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252110 | ||||||
| chr7:90252110 | C | CTGTGTGT others(5): Show |
2 | a0001c0002t0002g0204 a0001c0002t0002g0232 |
2 | NA18955.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.121-3288_121-3277d others(14): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252110 | ||||||
| chr7:90252110 | CTG | C | 55 | a0001c0002t0002g0170 a0001c0002t0002g0171 a0001c0002t0002g0172 others(52): Show |
58 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.121-3278_121-3277d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252110 | ||||||
| chr7:90252110 | CTGTG | C | 19 | a0001c0003t0001g0302 a0001c0006t0001g0239 a0002c0001t0001g0007 others(16): Show |
20 | HG00140.hp1 HG01358.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.121-3280_121-3277d others(6): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252110 | ||||||
| chr7:90252110 | CTGTGTG | C | 31 | a0001c0002t0002g0027 a0001c0003t0001g0022 a0001c0003t0001g0286 others(28): Show |
32 | HG00408.hp2 HG00438.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.121-3282_121-3277d others(8): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252110 | ||||||
| chr7:90252110 | CTGTGTGT others(1): Show |
C | 57 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(54): Show |
62 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.121-3284_121-3277d others(10): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252110 | ||||||
| chr7:90252110 | CTGTGTGT others(3): Show |
C | 1 | a0001c0003t0001g0304 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.121-3286_121-3277d others(12): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252110 | ||||||
| chr7:90252110 | CTGTGTGT others(5): Show |
C | 18 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(15): Show |
19 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.121-3288_121-3277d others(14): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252110 | ||||||
| chr7:90252110 | CTGTGTGT others(7): Show |
C | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-3290_121-3277d others(16): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 90252110 | ||||||
| chr7:90252146 | GCA | G | 3 | a0002c0001t0001g0114 a0002c0001t0001g0115 a0002c0001t0001g0116 |
3 | NA18942.hp2 NA18955.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.121-3276_121-3275d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90252146 | |||||||
| chr7:90252148 | A | G | 143 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(140): Show |
156 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.121-3275A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90252148 | |||||||
| chr7:90252171 | G | A | 1 | a0001c0002t0002g0175 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.121-3252G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90252171 | |||||||
| chr7:90252222 | A | G | 46 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0067 others(43): Show |
48 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.121-3201A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90252222 | |||||||
| chr7:90252460 | G | A | 1 | a0001c0002t0002g0200 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.121-2963G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90252460 | |||||||
| chr7:90252524 | A | G | 1 | a0004c0007t0001g0266 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.121-2899A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90252524 | |||||||
| chr7:90252561 | T | C | 42 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(39): Show |
44 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.121-2862T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90252561 | |||||||
| chr7:90252678 | A | G | 1 | a0001c0006t0001g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.121-2745A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90252678 | |||||||
| chr7:90252832 | A | G | 84 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(81): Show |
93 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.121-2591A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90252832 | |||||||
| chr7:90252919 | A | T | 2 | a0007c0010t0002g0002 a0007c0010t0002g0225 |
4 | HG01891.hp1 HG02257.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-2504A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90252919 | |||||||
| chr7:90252930 | G | A | 1 | a0001c0003t0001g0296 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.121-2493G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90252930 | |||||||
| chr7:90253075 | C | T | 2 | a0001c0002t0002g0196 a0001c0019t0002g0164 |
2 | HG00597.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.121-2348C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90253075 | |||||||
| chr7:90253183 | T | G | 1 | a0002c0001t0001g0087 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.121-2240T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90253183 | |||||||
| chr7:90253243 | A | G | 2 | a0001c0013t0002g0240 a0001c0013t0002g0241 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.121-2180A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90253243 | |||||||
| chr7:90253421 | C | T | 2 | a0008c0015t0002g0244 a0008c0015t0002g0245 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.121-2002C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90253421 | |||||||
| chr7:90253447 | G | C | 2 | a0001c0002t0002g0118 a0001c0002t0002g0125 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.121-1976G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90253447 | |||||||
| chr7:90253451 | T | C | 56 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(53): Show |
60 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.121-1972T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90253451 | |||||||
| chr7:90253516 | G | A | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-1907G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90253516 | |||||||
| chr7:90253559 | G | T | 299 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(296): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.121-1864G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90253559 | |||||||
| chr7:90253638 | C | T | 1 | a0002c0001t0001g0042 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.121-1785C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90253638 | |||||||
| chr7:90253655 | C | T | 1 | a0001c0004t0002g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.121-1768C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90253655 | |||||||
| chr7:90253761 | A | C | 7 | a0001c0013t0002g0240 a0001c0013t0002g0241 a0002c0001t0001g0029 others(4): Show |
7 | HG02723.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.121-1662A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90253761 | |||||||
| chr7:90253815 | C | T | 84 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(81): Show |
93 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.121-1608C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90253815 | |||||||
| chr7:90254320 | G | A | 2 | a0001c0006t0001g0259 a0001c0006t0001g0260 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.121-1103G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90254320 | |||||||
| chr7:90254423 | C | A | 143 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(140): Show |
156 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.121-1000C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90254423 | |||||||
| chr7:90254554 | T | A | 1 | a0002c0001t0001g0034 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.121-869T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90254554 | |||||||
| chr7:90254558 | A | G | 1 | a0002c0001t0001g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.121-865A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90254558 | |||||||
| chr7:90254663 | G | A | 1 | a0002c0001t0001g0271 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.121-760G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90254663 | |||||||
| chr7:90254718 | G | A | 1 | a0002c0001t0001g0088 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.121-705G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90254718 | |||||||
| chr7:90254853 | G | A | 9 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(6): Show |
9 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-570G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90254853 | |||||||
| chr7:90254854 | A | G | 3 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 |
3 | HG00140.hp2 HG00735.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.121-569A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90254854 | |||||||
| chr7:90255080 | T | C | 1 | a0001c0002t0002g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.121-343T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90255080 | |||||||
| chr7:90255171 | G | A | 34 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(31): Show |
36 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.121-252G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90255171 | |||||||
| chr7:90255283 | G | T | 56 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(53): Show |
60 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.121-140G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90255283 | |||||||
| chr7:90255353 | A | G | 9 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(6): Show |
9 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-70A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90255353 | |||||||
| chr7:90255361 | G | C | 1 | a0001c0002t0002g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.121-62G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90255361 | |||||||
| chr7:90255387 | G | C | 9 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(6): Show |
9 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-36G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 1/22 | chr7 | 90255387 | |||||||
| chr7:90255511 | C | T | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.180+29C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90255511 | |||||||
| chr7:90255606 | A | C | 1 | a0002c0001t0001g0041 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.180+124A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90255606 | |||||||
| chr7:90255627 | G | T | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.180+145G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90255627 | |||||||
| chr7:90255658 | T | G | 1 | a0002c0001t0001g0089 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.180+176T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90255658 | |||||||
| chr7:90255666 | G | T | 2 | a0001c0004t0002g0222 a0001c0004t0002g0223 |
2 | HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.180+184G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90255666 | |||||||
| chr7:90255882 | T | G | 4 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0266 others(1): Show |
4 | HG00639.hp2 HG02451.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+400T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90255882 | |||||||
| chr7:90256135 | C | T | 87 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(84): Show |
96 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.180+653C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90256135 | |||||||
| chr7:90256164 | C | T | 1 | a0001c0002t0002g0120 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.180+682C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90256164 | |||||||
| chr7:90256426 | T | G | 1 | a0001c0003t0001g0290 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.180+944T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90256426 | |||||||
| chr7:90256523 | T | TA | 34 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0003t0001g0020 others(31): Show |
37 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.180+1057dupA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 90256523 | ||||||
| chr7:90256523 | TA | T | 8 | a0001c0013t0002g0241 a0003c0005t0002g0250 a0004c0007t0001g0263 others(5): Show |
8 | HG00639.hp2 HG01070.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+1057delA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 90256523 | ||||||
| chr7:90256539 | A | T | 1 | a0002c0001t0001g0082 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.180+1057A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90256539 | |||||||
| chr7:90256742 | T | G | 2 | a0008c0015t0002g0244 a0008c0015t0002g0245 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.180+1260T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90256742 | |||||||
| chr7:90256923 | T | G | 1 | a0001c0002t0002g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.181-1175T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90256923 | |||||||
| chr7:90256984 | A | T | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.181-1114A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90256984 | |||||||
| chr7:90257056 | C | T | 1 | a0001c0002t0002g0175 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.181-1042C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90257056 | |||||||
| chr7:90257114 | G | A | 1 | a0001c0006t0001g0261 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.181-984G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90257114 | |||||||
| chr7:90257494 | T | C | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.181-604T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90257494 | |||||||
| chr7:90257704 | C | T | 1 | a0002c0001t0001g0081 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.181-394C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90257704 | |||||||
| chr7:90257966 | C | T | 1 | a0005c0009t0002g0282 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.181-132C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90257966 | |||||||
| chr7:90258043 | A | T | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.181-55A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90258043 | |||||||
| chr7:90258050 | C | T | 8 | a0001c0004t0002g0221 a0001c0004t0002g0227 a0001c0004t0002g0228 others(5): Show |
10 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.181-48C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 2/22 | chr7 | 90258050 | |||||||
| chr7:90258210 | G | A | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.246+47G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90258210 | |||||||
| chr7:90258269 | A | C | 1 | a0001c0014t0002g0212 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.246+106A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90258269 | |||||||
| chr7:90258273 | G | T | 97 | a0002c0001t0001g0001 a0002c0001t0001g0003 a0002c0001t0001g0004 others(94): Show |
104 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.246+110G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90258273 | |||||||
| chr7:90258316 | G | A | 2 | a0008c0015t0002g0244 a0008c0015t0002g0245 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.246+153G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90258316 | |||||||
| chr7:90258341 | G | A | 56 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(53): Show |
60 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.246+178G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90258341 | |||||||
| chr7:90258407 | T | C | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+244T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90258407 | |||||||
| chr7:90258563 | C | T | 85 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(82): Show |
94 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.246+400C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90258563 | |||||||
| chr7:90258670 | G | A | 2 | a0001c0011t0003g0157 a0001c0011t0003g0158 |
2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.246+507G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90258670 | |||||||
| chr7:90258717 | T | C | 1 | a0002c0001t0001g0272 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.246+554T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90258717 | |||||||
| chr7:90258874 | C | T | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.246+711C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90258874 | |||||||
| chr7:90259366 | G | A | 13 | a0002c0001t0001g0019 a0002c0001t0001g0165 a0002c0001t0001g0269 others(10): Show |
14 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.246+1203G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90259366 | |||||||
| chr7:90259470 | G | GTGTT | 4 | a0002c0001t0001g0068 a0002c0001t0001g0072 a0002c0001t0001g0073 others(1): Show |
4 | HG01069.hp1 HG01496.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1333_246+1336d others(6): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | 90259470 | ||||||
| chr7:90259470 | G | GTTTT | 91 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(88): Show |
100 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.246+1308_246+1309i others(6): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | 90259470 | ||||||
| chr7:90259470 | GTGTT | G | 87 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(84): Show |
95 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.246+1333_246+1336d others(6): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | 90259470 | ||||||
| chr7:90259472 | G | T | 13 | a0002c0001t0001g0019 a0002c0001t0001g0165 a0002c0001t0001g0269 others(10): Show |
14 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.246+1309G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90259472 | |||||||
| chr7:90259476 | G | T | 45 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(42): Show |
48 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.246+1313G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90259476 | |||||||
| chr7:90259480 | G | T | 1 | a0001c0002t0002g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.246+1317G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90259480 | |||||||
| chr7:90259596 | T | A | 1 | a0001c0004t0002g0230 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246+1433T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90259596 | |||||||
| chr7:90259618 | G | T | 2 | a0002c0001t0001g0005 a0002c0001t0001g0059 |
3 | HG01192.hp2 HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.246+1455G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90259618 | |||||||
| chr7:90259667 | T | C | 1 | a0001c0002t0002g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.246+1504T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90259667 | |||||||
| chr7:90259733 | G | A | 1 | a0005c0009t0002g0283 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.246+1570G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90259733 | |||||||
| chr7:90259885 | A | G | 296 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(293): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.246+1722A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90259885 | |||||||
| chr7:90259890 | A | C | 250 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(247): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.246+1727A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90259890 | |||||||
| chr7:90260026 | C | G | 1 | a0001c0004t0002g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.246+1863C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90260026 | |||||||
| chr7:90260271 | A | G | 101 | a0002c0001t0001g0001 a0002c0001t0001g0003 a0002c0001t0001g0004 others(98): Show |
108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.247-1676A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90260271 | |||||||
| chr7:90260312 | G | A | 1 | a0002c0001t0001g0059 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.247-1635G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90260312 | |||||||
| chr7:90260317 | G | A | 1 | a0002c0001t0001g0087 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.247-1630G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90260317 | |||||||
| chr7:90260441 | G | A | 2 | a0001c0003t0001g0303 a0001c0003t0001g0307 |
2 | HG02027.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.247-1506G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90260441 | |||||||
| chr7:90260592 | C | T | 1 | a0001c0002t0002g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.247-1355C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90260592 | |||||||
| chr7:90260684 | A | C | 1 | a0001c0019t0002g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.247-1263A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90260684 | |||||||
| chr7:90260735 | T | C | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.247-1212T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90260735 | |||||||
| chr7:90260809 | C | T | 1 | a0001c0006t0001g0237 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.247-1138C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90260809 | |||||||
| chr7:90260909 | A | G | 1 | a0001c0004t0002g0220 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.247-1038A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90260909 | |||||||
| chr7:90261054 | C | A | 97 | a0002c0001t0001g0001 a0002c0001t0001g0003 a0002c0001t0001g0004 others(94): Show |
104 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.247-893C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90261054 | |||||||
| chr7:90261082 | A | AT | 50 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(47): Show |
52 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.247-850dupT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | 90261082 | ||||||
| chr7:90261082 | A | ATT | 82 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(79): Show |
91 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.247-851_247-850dup others(2): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | 90261082 | ||||||
| chr7:90261082 | AT | A | 9 | a0001c0019t0002g0164 a0003c0005t0002g0249 a0003c0005t0002g0255 others(6): Show |
9 | HG00639.hp2 HG01069.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-850delT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | 90261082 | ||||||
| chr7:90261211 | C | G | 3 | a0006c0008t0002g0017 a0006c0008t0002g0242 a0006c0008t0002g0243 |
4 | HG00738.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-736C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90261211 | |||||||
| chr7:90261227 | C | T | 1 | a0001c0019t0002g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.247-720C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90261227 | |||||||
| chr7:90261233 | G | A | 87 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(84): Show |
96 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.247-714G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90261233 | |||||||
| chr7:90261293 | T | A | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.247-654T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90261293 | |||||||
| chr7:90261308 | C | T | 87 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(84): Show |
96 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.247-639C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90261308 | |||||||
| chr7:90261360 | A | C | 42 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(39): Show |
44 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.247-587A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90261360 | |||||||
| chr7:90261384 | TA | T | 87 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(84): Show |
96 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.247-559delA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | 90261384 | ||||||
| chr7:90261599 | T | C | 1 | a0002c0001t0001g0046 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.247-348T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90261599 | |||||||
| chr7:90261655 | A | G | 2 | a0002c0001t0001g0044 a0002c0001t0001g0045 |
2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.247-292A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90261655 | |||||||
| chr7:90261662 | T | C | 4 | a0001c0019t0002g0164 a0006c0008t0002g0017 a0006c0008t0002g0242 others(1): Show |
5 | HG00738.hp2 HG01891.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-285T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90261662 | |||||||
| chr7:90261726 | T | C | 99 | a0001c0013t0002g0240 a0001c0013t0002g0241 a0002c0001t0001g0001 others(96): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.247-221T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90261726 | |||||||
| chr7:90261745 | G | A | 1 | a0001c0002t0002g0025 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.247-202G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90261745 | |||||||
| chr7:90261853 | G | A | 4 | a0001c0019t0002g0164 a0006c0008t0002g0017 a0006c0008t0002g0242 others(1): Show |
5 | HG00738.hp2 HG01891.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-94G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 3/22 | chr7 | 90261853 | |||||||
| chr7:90262204 | C | T | 295 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(292): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.356+148C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90262204 | |||||||
| chr7:90262231 | C | T | 1 | a0001c0019t0002g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.356+175C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90262231 | |||||||
| chr7:90262298 | C | G | 1 | a0001c0002t0002g0195 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.356+242C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90262298 | |||||||
| chr7:90262446 | T | C | 47 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(44): Show |
49 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.356+390T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90262446 | |||||||
| chr7:90262863 | G | C | 42 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(39): Show |
44 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.356+807G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90262863 | |||||||
| chr7:90262876 | T | G | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.356+820T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90262876 | |||||||
| chr7:90262921 | C | A | 1 | a0001c0002t0002g0177 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.356+865C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90262921 | |||||||
| chr7:90262972 | T | G | 240 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(237): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.356+916T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90262972 | |||||||
| chr7:90263121 | C | T | 2 | a0008c0015t0002g0244 a0008c0015t0002g0245 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.356+1065C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263121 | |||||||
| chr7:90263162 | A | G | 2 | a0008c0015t0002g0244 a0008c0015t0002g0245 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.356+1106A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263162 | |||||||
| chr7:90263435 | A | G | 1 | a0002c0001t0001g0095 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.356+1379A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263435 | |||||||
| chr7:90263467 | G | C | 1 | a0006c0008t0002g0243 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.356+1411G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263467 | |||||||
| chr7:90263495 | T | C | 1 | a0001c0002t0002g0023 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.356+1439T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263495 | |||||||
| chr7:90263501 | T | C | 1 | a0001c0014t0002g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.356+1445T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263501 | |||||||
| chr7:90263623 | A | T | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.356+1567A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263623 | |||||||
| chr7:90263739 | C | T | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.357-1562C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263739 | |||||||
| chr7:90263745 | CAT | C | 3 | a0001c0011t0003g0157 a0001c0011t0003g0158 a0001c0011t0003g0159 |
3 | HG02818.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.357-1555_357-1554d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263745 | |||||||
| chr7:90263857 | G | A | 1 | a0008c0015t0002g0245 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.357-1444G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263857 | |||||||
| chr7:90263884 | A | G | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.357-1417A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263884 | |||||||
| chr7:90263901 | T | A | 3 | a0001c0002t0002g0200 a0001c0002t0002g0204 a0001c0002t0002g0231 |
3 | NA18955.hp2 NA18968.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.357-1400T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263901 | |||||||
| chr7:90263947 | T | G | 1 | a0002c0001t0001g0069 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.357-1354T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263947 | |||||||
| chr7:90263948 | G | A | 85 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(82): Show |
94 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.357-1353G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90263948 | |||||||
| chr7:90264035 | G | A | 1 | a0003c0005t0002g0258 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.357-1266G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264035 | |||||||
| chr7:90264091 | G | GAA | 21 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0286 others(18): Show |
23 | HG00408.hp2 HG00673.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.357-1197_357-1196d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264091 | ||||||
| chr7:90264091 | G | GAAA | 7 | a0001c0003t0001g0020 a0001c0003t0001g0291 a0001c0003t0001g0297 others(4): Show |
8 | HG01981.hp2 HG02135.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.357-1198_357-1196d others(5): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264091 | ||||||
| chr7:90264091 | G | GAAAA | 6 | a0001c0002t0002g0231 a0001c0002t0002g0232 a0001c0003t0001g0293 others(3): Show |
6 | NA18522.hp2 NA18747.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.357-1199_357-1196d others(6): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264091 | ||||||
| chr7:90264100 | AAAAAATA others(9): Show |
A | 1 | a0008c0015t0002g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.357-1199_357-1184d others(18): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264100 | ||||||
| chr7:90264100 | AAAAAATA others(19): Show |
A | 1 | a0001c0019t0002g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.357-1199_357-1174d others(28): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264100 | ||||||
| chr7:90264102 | AAAATATA others(15): Show |
A | 1 | a0001c0002t0004g0160 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.357-1197_357-1176d others(24): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264102 | ||||||
| chr7:90264103 | AAATATAT others(6): Show |
A | 1 | a0001c0002t0002g0137 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.357-1196_357-1184d others(15): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264103 | ||||||
| chr7:90264104 | A | AAAAAAAA others(6): Show |
1 | a0001c0004t0002g0209 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.357-1196_357-1195i others(15): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264104 | ||||||
| chr7:90264104 | A | AAAAATAT others(6): Show |
1 | a0001c0002t0002g0123 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.357-1196_357-1195i others(15): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264104 | ||||||
| chr7:90264104 | A | T | 1 | a0003c0005t0002g0258 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.357-1197A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264104 | |||||||
| chr7:90264104 | AAT | A | 6 | a0001c0002t0002g0121 a0001c0002t0002g0176 a0001c0004t0002g0207 others(3): Show |
6 | HG01074.hp2 HG01884.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.357-1152_357-1151d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264104 | ||||||
| chr7:90264104 | AATAT | A | 8 | a0001c0002t0002g0202 a0001c0004t0002g0015 a0001c0004t0002g0205 others(5): Show |
10 | HG01169.hp2 HG01255.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.357-1154_357-1151d others(6): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264104 | ||||||
| chr7:90264104 | AATATAT | A | 13 | a0001c0002t0002g0010 a0001c0002t0002g0128 a0001c0002t0002g0138 others(10): Show |
14 | HG01070.hp1 HG01891.hp1 HG03710.hp2 others(11): Show |
intron_variant | MODIFIER | c.357-1156_357-1151d others(8): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264104 | ||||||
| chr7:90264104 | AATATATA others(1): Show |
A | 25 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0002t0002g0013 others(22): Show |
28 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.357-1158_357-1151d others(10): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264104 | ||||||
| chr7:90264104 | AATATATA others(3): Show |
A | 3 | a0001c0002t0002g0171 a0005c0009t0002g0283 a0009c0018t0002g0173 |
3 | HG00738.hp1 HG02004.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.357-1160_357-1151d others(12): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264104 | ||||||
| chr7:90264104 | AATATATA others(9): Show |
A | 16 | a0002c0001t0001g0006 a0002c0001t0001g0043 a0002c0001t0001g0076 others(13): Show |
17 | HG00438.hp1 HG01934.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.357-1166_357-1151d others(18): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264104 | ||||||
| chr7:90264104 | AATATATA others(11): Show |
A | 46 | a0002c0001t0001g0001 a0002c0001t0001g0003 a0002c0001t0001g0005 others(43): Show |
51 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.357-1168_357-1151d others(20): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264104 | ||||||
| chr7:90264104 | AATATATA others(13): Show |
A | 1 | a0002c0001t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.357-1170_357-1151d others(22): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264104 | ||||||
| chr7:90264104 | AATATATA others(15): Show |
A | 4 | a0001c0002t0004g0161 a0001c0011t0003g0157 a0001c0011t0003g0158 others(1): Show |
4 | HG02818.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.357-1172_357-1151d others(24): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264104 | ||||||
| chr7:90264104 | AATATATA others(25): Show |
A | 11 | a0002c0001t0001g0019 a0002c0001t0001g0165 a0002c0001t0001g0271 others(8): Show |
12 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.357-1182_357-1151d others(34): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 90264104 | ||||||
| chr7:90264105 | AT | A | 5 | a0001c0002t0002g0008 a0001c0002t0002g0122 a0001c0002t0002g0131 others(2): Show |
5 | HG00323.hp1 HG00408.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.357-1195delT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264105 | |||||||
| chr7:90264105 | ATAT | A | 15 | a0001c0002t0002g0009 a0001c0002t0002g0024 a0001c0002t0002g0101 others(12): Show |
16 | HG00423.hp2 HG01081.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.357-1195_357-1193d others(5): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264105 | |||||||
| chr7:90264105 | ATATAT | A | 13 | a0001c0002t0002g0008 a0001c0002t0002g0139 a0001c0002t0002g0141 others(10): Show |
15 | HG00639.hp1 HG01167.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.357-1195_357-1191d others(7): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264105 | |||||||
| chr7:90264105 | ATATATAT | A | 12 | a0001c0002t0002g0027 a0001c0002t0002g0120 a0001c0002t0002g0126 others(9): Show |
12 | HG00597.hp1 HG02615.hp1 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.357-1195_357-1189d others(9): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264105 | |||||||
| chr7:90264105 | ATATATAT others(2): Show |
A | 12 | a0001c0002t0002g0011 a0001c0002t0002g0142 a0001c0002t0002g0144 others(9): Show |
12 | HG00639.hp2 HG01496.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.357-1195_357-1187d others(11): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264105 | |||||||
| chr7:90264105 | ATATATAT others(4): Show |
A | 4 | a0001c0002t0002g0119 a0001c0004t0002g0220 a0003c0005t0002g0246 others(1): Show |
4 | HG01081.hp2 HG02451.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.357-1195_357-1185d others(13): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264105 | |||||||
| chr7:90264105 | ATATATAT others(6): Show |
A | 9 | a0001c0002t0002g0118 a0001c0002t0002g0124 a0001c0002t0002g0125 others(6): Show |
9 | HG01361.hp2 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.357-1195_357-1183d others(15): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264105 | |||||||
| chr7:90264105 | ATATATAT others(8): Show |
A | 6 | a0002c0001t0001g0088 a0002c0001t0001g0117 a0004c0007t0001g0265 others(3): Show |
6 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.357-1195_357-1181d others(17): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264105 | |||||||
| chr7:90264105 | ATATATAT others(10): Show |
A | 12 | a0002c0001t0001g0034 a0002c0001t0001g0035 a0002c0001t0001g0036 others(9): Show |
12 | HG02004.hp2 HG02056.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.357-1195_357-1179d others(19): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264105 | |||||||
| chr7:90264105 | ATATATAT others(12): Show |
A | 23 | a0002c0001t0001g0004 a0002c0001t0001g0031 a0002c0001t0001g0038 others(20): Show |
24 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.357-1195_357-1177d others(21): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264105 | |||||||
| chr7:90264105 | ATATATAT others(14): Show |
A | 2 | a0006c0008t0002g0017 a0006c0008t0002g0242 |
3 | HG02896.hp2 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.357-1195_357-1175d others(23): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264105 | |||||||
| chr7:90264105 | ATATATAT others(16): Show |
A | 1 | a0006c0008t0002g0243 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.357-1195_357-1173d others(25): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264105 | |||||||
| chr7:90264106 | T | A | 46 | a0001c0002t0002g0199 a0001c0002t0002g0200 a0001c0002t0002g0203 others(43): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.357-1195T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264106 | |||||||
| chr7:90264108 | T | A | 54 | a0001c0002t0002g0008 a0001c0002t0002g0121 a0001c0002t0002g0122 others(51): Show |
57 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.357-1193T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264108 | |||||||
| chr7:90264110 | T | A | 62 | a0001c0002t0002g0024 a0001c0002t0002g0101 a0001c0002t0002g0176 others(59): Show |
67 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.357-1191T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264110 | |||||||
| chr7:90264112 | T | A | 78 | a0001c0002t0002g0008 a0001c0002t0002g0010 a0001c0002t0002g0128 others(75): Show |
86 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.357-1189T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264112 | |||||||
| chr7:90264114 | T | A | 109 | a0001c0002t0002g0008 a0001c0002t0002g0010 a0001c0002t0002g0011 others(106): Show |
120 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.357-1187T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264114 | |||||||
| chr7:90264116 | T | A | 108 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(105): Show |
120 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.357-1185T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264116 | |||||||
| chr7:90264118 | T | A | 94 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(91): Show |
103 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.357-1183T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264118 | |||||||
| chr7:90264120 | T | A | 68 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(65): Show |
77 | HG00423.hp1 HG00597.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.357-1181T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264120 | |||||||
| chr7:90264122 | T | A | 56 | a0001c0002t0002g0012 a0001c0002t0002g0013 a0001c0002t0002g0014 others(53): Show |
60 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.357-1179T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264122 | |||||||
| chr7:90264124 | T | A | 79 | a0001c0002t0002g0023 a0001c0002t0002g0187 a0001c0002t0002g0188 others(76): Show |
85 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.357-1177T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264124 | |||||||
| chr7:90264126 | T | A | 95 | a0001c0006t0001g0237 a0002c0001t0001g0001 a0002c0001t0001g0003 others(92): Show |
102 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.357-1175T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264126 | |||||||
| chr7:90264128 | T | A | 91 | a0002c0001t0001g0001 a0002c0001t0001g0003 a0002c0001t0001g0004 others(88): Show |
99 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.357-1173T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264128 | |||||||
| chr7:90264130 | T | A | 67 | a0002c0001t0001g0001 a0002c0001t0001g0003 a0002c0001t0001g0004 others(64): Show |
73 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.357-1171T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264130 | |||||||
| chr7:90264132 | T | A | 5 | a0002c0001t0001g0047 a0002c0001t0001g0080 a0002c0001t0001g0106 others(2): Show |
5 | HG01123.hp2 HG02056.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.357-1169T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264132 | |||||||
| chr7:90264138 | T | A | 6 | a0002c0001t0001g0019 a0002c0001t0001g0272 a0002c0001t0001g0273 others(3): Show |
7 | HG01243.hp1 HG01256.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.357-1163T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264138 | |||||||
| chr7:90264139 | A | G | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.357-1162A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264139 | |||||||
| chr7:90264149 | A | G | 1 | a0002c0001t0001g0041 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.357-1152A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264149 | |||||||
| chr7:90264198 | C | A | 1 | a0002c0001t0001g0088 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.357-1103C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264198 | |||||||
| chr7:90264460 | T | C | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.357-841T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264460 | |||||||
| chr7:90264501 | G | T | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.357-800G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264501 | |||||||
| chr7:90264631 | A | G | 240 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(237): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.357-670A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264631 | |||||||
| chr7:90264694 | T | C | 99 | a0001c0013t0002g0240 a0001c0013t0002g0241 a0002c0001t0001g0001 others(96): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.357-607T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264694 | |||||||
| chr7:90264764 | C | G | 1 | a0002c0001t0001g0276 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.357-537C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264764 | |||||||
| chr7:90264834 | G | A | 1 | a0001c0003t0001g0293 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.357-467G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264834 | |||||||
| chr7:90264855 | G | A | 3 | a0001c0002t0002g0119 a0001c0002t0002g0121 a0001c0002t0002g0141 |
3 | NA18944.hp1 NA18998.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.357-446G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264855 | |||||||
| chr7:90264874 | A | G | 87 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(84): Show |
96 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.357-427A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90264874 | |||||||
| chr7:90265056 | C | T | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.357-245C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90265056 | |||||||
| chr7:90265086 | C | A | 1 | a0002c0001t0001g0031 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.357-215C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90265086 | |||||||
| chr7:90265110 | G | A | 2 | a0002c0001t0001g0152 a0002c0001t0001g0153 |
2 | HG00558.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.357-191G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90265110 | |||||||
| chr7:90265188 | G | C | 3 | a0001c0011t0003g0157 a0001c0011t0003g0158 a0001c0011t0003g0159 |
3 | HG02818.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.357-113G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 4/22 | chr7 | 90265188 | |||||||
| chr7:90265523 | G | T | 10 | a0002c0001t0001g0006 a0002c0001t0001g0088 a0002c0001t0001g0089 others(7): Show |
11 | HG00438.hp1 HG02135.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.433+146G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90265523 | |||||||
| chr7:90265524 | C | T | 10 | a0002c0001t0001g0006 a0002c0001t0001g0088 a0002c0001t0001g0089 others(7): Show |
11 | HG00438.hp1 HG02135.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.433+147C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90265524 | |||||||
| chr7:90265786 | C | G | 1 | a0001c0006t0001g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.433+409C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90265786 | |||||||
| chr7:90265831 | A | G | 6 | a0002c0001t0001g0067 a0002c0001t0001g0077 a0002c0001t0001g0078 others(3): Show |
6 | NA18943.hp1 NA18969.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.433+454A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90265831 | |||||||
| chr7:90265902 | G | C | 1 | a0002c0001t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.433+525G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90265902 | |||||||
| chr7:90265948 | C | T | 249 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(246): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.433+571C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90265948 | |||||||
| chr7:90266336 | G | A | 2 | a0003c0005t0002g0247 a0003c0005t0002g0248 |
2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.433+959G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90266336 | |||||||
| chr7:90266400 | T | A | 16 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(13): Show |
17 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.433+1023T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90266400 | |||||||
| chr7:90266440 | A | G | 1 | a0001c0016t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433+1063A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90266440 | |||||||
| chr7:90266467 | C | A | 1 | a0001c0002t0002g0142 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.433+1090C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90266467 | |||||||
| chr7:90266678 | C | T | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.433+1301C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90266678 | |||||||
| chr7:90267008 | A | G | 1 | a0001c0002t0002g0169 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.434-1278A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90267008 | |||||||
| chr7:90267056 | C | A | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.434-1230C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90267056 | |||||||
| chr7:90267294 | C | A | 3 | a0001c0002t0002g0189 a0001c0002t0002g0190 a0001c0002t0002g0196 |
3 | HG00597.hp2 NA18991.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.434-992C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90267294 | |||||||
| chr7:90267294 | C | T | 1 | a0001c0002t0002g0129 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.434-992C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90267294 | |||||||
| chr7:90267399 | C | T | 1 | a0001c0002t0002g0119 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.434-887C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90267399 | |||||||
| chr7:90267946 | A | G | 295 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(292): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.434-340A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90267946 | |||||||
| chr7:90268083 | T | A | 1 | a0002c0001t0001g0097 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.434-203T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90268083 | |||||||
| chr7:90268148 | A | T | 2 | a0002c0001t0001g0274 a0002c0001t0001g0275 |
2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.434-138A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90268148 | |||||||
| chr7:90268221 | G | A | 1 | a0001c0002t0002g0023 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.434-65G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 5/22 | chr7 | 90268221 | |||||||
| chr7:90268389 | A | C | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.532+5A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90268389 | |||||||
| chr7:90268437 | C | T | 2 | a0008c0015t0002g0244 a0008c0015t0002g0245 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.532+53C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90268437 | |||||||
| chr7:90268496 | A | G | 1 | a0002c0001t0001g0273 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.532+112A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90268496 | |||||||
| chr7:90268515 | T | C | 129 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(126): Show |
140 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.532+131T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90268515 | |||||||
| chr7:90268572 | T | C | 1 | a0002c0001t0001g0059 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.532+188T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90268572 | |||||||
| chr7:90268721 | G | T | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.532+337G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90268721 | |||||||
| chr7:90268856 | C | A | 2 | a0001c0002t0002g0130 a0001c0002t0002g0146 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.532+472C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90268856 | |||||||
| chr7:90269087 | T | A | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+703T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90269087 | |||||||
| chr7:90269087 | T | TA | 100 | a0001c0013t0002g0240 a0001c0013t0002g0241 a0002c0001t0001g0001 others(97): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.532+715dupA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr7 | 90269087 | ||||||
| chr7:90269088 | A | T | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.532+704A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90269088 | |||||||
| chr7:90269470 | T | C | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.532+1086T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90269470 | |||||||
| chr7:90269505 | A | G | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.532+1121A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90269505 | |||||||
| chr7:90269515 | A | G | 1 | a0003c0005t0002g0246 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.532+1131A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90269515 | |||||||
| chr7:90269533 | TC | T | 3 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 |
3 | HG00140.hp2 HG00735.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.532+1150delC | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90269533 | |||||||
| chr7:90269660 | T | C | 1 | a0002c0001t0001g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.532+1276T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90269660 | |||||||
| chr7:90269934 | T | C | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.532+1550T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90269934 | |||||||
| chr7:90269974 | C | T | 2 | a0008c0015t0002g0244 a0008c0015t0002g0245 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.533-1552C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90269974 | |||||||
| chr7:90269993 | A | G | 3 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 |
3 | HG00140.hp2 HG00735.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.533-1533A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90269993 | |||||||
| chr7:90270040 | C | T | 1 | a0001c0002t0002g0014 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.533-1486C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90270040 | |||||||
| chr7:90270091 | A | G | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.533-1435A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90270091 | |||||||
| chr7:90270174 | G | T | 97 | a0002c0001t0001g0001 a0002c0001t0001g0003 a0002c0001t0001g0004 others(94): Show |
104 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.533-1352G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90270174 | |||||||
| chr7:90270661 | G | A | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.533-865G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90270661 | |||||||
| chr7:90270802 | A | G | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.533-724A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90270802 | |||||||
| chr7:90270808 | A | G | 59 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(56): Show |
63 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.533-718A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90270808 | |||||||
| chr7:90270893 | A | C | 99 | a0001c0013t0002g0240 a0001c0013t0002g0241 a0002c0001t0001g0001 others(96): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.533-633A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90270893 | |||||||
| chr7:90270965 | T | C | 13 | a0002c0001t0001g0019 a0002c0001t0001g0165 a0002c0001t0001g0269 others(10): Show |
14 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.533-561T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90270965 | |||||||
| chr7:90270982 | C | T | 2 | a0001c0002t0002g0124 a0001c0002t0002g0132 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.533-544C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90270982 | |||||||
| chr7:90271010 | AGTAAT | A | 4 | a0001c0002t0002g0118 a0001c0002t0002g0125 a0001c0002t0002g0137 others(1): Show |
4 | HG02809.hp2 HG02896.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.533-514_533-510del others(5): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr7 | 90271010 | ||||||
| chr7:90271069 | T | C | 158 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(155): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.533-457T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90271069 | |||||||
| chr7:90271096 | TA | T | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.533-429delA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90271096 | |||||||
| chr7:90271176 | C | T | 5 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(2): Show |
5 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.533-350C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90271176 | |||||||
| chr7:90271317 | G | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.533-209G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90271317 | |||||||
| chr7:90271395 | C | T | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.533-131C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90271395 | |||||||
| chr7:90271486 | G | A | 1 | a0001c0019t0002g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.533-40G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 6/22 | chr7 | 90271486 | |||||||
| chr7:90271725 | A | C | 299 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(296): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.682+50A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 7/22 | chr7 | 90271725 | |||||||
| chr7:90272320 | T | C | 1 | a0002c0001t0001g0271 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.860+362T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90272320 | |||||||
| chr7:90272429 | G | A | 1 | a0002c0001t0001g0080 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.860+471G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90272429 | |||||||
| chr7:90272432 | G | A | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.860+474G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90272432 | |||||||
| chr7:90272439 | C | T | 34 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 others(31): Show |
36 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.860+481C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90272439 | |||||||
| chr7:90272544 | T | A | 1 | a0002c0001t0001g0069 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.860+586T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90272544 | |||||||
| chr7:90272692 | G | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.860+734G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90272692 | |||||||
| chr7:90272861 | C | A | 1 | a0002c0001t0001g0078 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.860+903C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90272861 | |||||||
| chr7:90272930 | T | G | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.860+972T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90272930 | |||||||
| chr7:90272940 | G | A | 128 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(125): Show |
140 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.860+982G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90272940 | |||||||
| chr7:90272960 | C | T | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.860+1002C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90272960 | |||||||
| chr7:90273038 | G | A | 2 | a0001c0006t0001g0237 a0001c0016t0001g0236 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.861-949G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273038 | |||||||
| chr7:90273050 | C | T | 1 | a0001c0019t0002g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.861-937C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273050 | |||||||
| chr7:90273219 | A | G | 99 | a0001c0013t0002g0240 a0001c0013t0002g0241 a0002c0001t0001g0001 others(96): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.861-768A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273219 | |||||||
| chr7:90273291 | T | C | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.861-696T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273291 | |||||||
| chr7:90273442 | T | G | 4 | a0001c0003t0001g0287 a0001c0003t0001g0293 a0001c0003t0001g0294 others(1): Show |
4 | HG00438.hp2 HG02056.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.861-545T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273442 | |||||||
| chr7:90273643 | C | T | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-344C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273643 | |||||||
| chr7:90273660 | A | G | 7 | a0001c0013t0002g0240 a0001c0013t0002g0241 a0002c0001t0001g0029 others(4): Show |
7 | HG02723.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.861-327A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273660 | |||||||
| chr7:90273729 | G | A | 1 | a0003c0005t0002g0255 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.861-258G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273729 | |||||||
| chr7:90273759 | A | G | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.861-228A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273759 | |||||||
| chr7:90273768 | A | G | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.861-219A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273768 | |||||||
| chr7:90273865 | C | T | 1 | a0002c0001t0001g0270 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.861-122C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273865 | |||||||
| chr7:90273905 | G | A | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.861-82G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273905 | |||||||
| chr7:90273916 | A | T | 30 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(27): Show |
33 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.861-71A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273916 | |||||||
| chr7:90273936 | A | G | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.861-51A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 8/22 | chr7 | 90273936 | |||||||
| chr7:90274177 | A | G | 1 | a0002c0001t0001g0112 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.984+67A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90274177 | |||||||
| chr7:90274430 | G | A | 1 | a0001c0003t0001g0304 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.984+320G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90274430 | |||||||
| chr7:90274654 | AC | A | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.984+547delC | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 90274654 | ||||||
| chr7:90274733 | T | C | 1 | a0001c0002t0002g0203 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.984+623T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90274733 | |||||||
| chr7:90274857 | T | C | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.984+747T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90274857 | |||||||
| chr7:90275037 | G | T | 1 | a0001c0004t0002g0233 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.984+927G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275037 | |||||||
| chr7:90275060 | T | C | 1 | a0002c0001t0001g0091 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.984+950T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275060 | |||||||
| chr7:90275234 | T | C | 24 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(21): Show |
25 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.984+1124T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275234 | |||||||
| chr7:90275286 | A | G | 27 | a0001c0006t0001g0162 a0001c0006t0001g0237 a0001c0006t0001g0239 others(24): Show |
28 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.984+1176A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275286 | |||||||
| chr7:90275370 | G | C | 1 | a0002c0001t0001g0063 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.984+1260G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275370 | |||||||
| chr7:90275397 | T | G | 1 | a0002c0001t0001g0038 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.984+1287T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275397 | |||||||
| chr7:90275445 | T | C | 1 | a0001c0002t0002g0023 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.984+1335T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275445 | |||||||
| chr7:90275515 | C | G | 2 | a0005c0009t0002g0280 a0005c0009t0002g0281 |
2 | HG00735.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.984+1405C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275515 | |||||||
| chr7:90275526 | G | C | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.984+1416G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275526 | |||||||
| chr7:90275590 | C | CT | 131 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(128): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.985-1454dupT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 90275590 | ||||||
| chr7:90275590 | C | CTT | 68 | a0001c0002t0002g0009 a0001c0002t0002g0023 a0001c0002t0002g0024 others(65): Show |
69 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.985-1455_985-1454d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 90275590 | ||||||
| chr7:90275590 | C | CTTT | 15 | a0001c0002t0002g0135 a0001c0002t0002g0136 a0001c0002t0002g0172 others(12): Show |
16 | HG00738.hp1 HG01175.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.985-1456_985-1454d others(5): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 90275590 | ||||||
| chr7:90275590 | C | G | 1 | a0008c0015t0002g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.984+1480C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275590 | |||||||
| chr7:90275590 | CTTT | C | 15 | a0001c0006t0001g0162 a0001c0006t0001g0237 a0001c0006t0001g0239 others(12): Show |
16 | HG00639.hp2 HG01256.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.985-1456_985-1454d others(5): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 90275590 | ||||||
| chr7:90275590 | CTTTT | C | 9 | a0002c0001t0001g0165 a0002c0001t0001g0269 a0002c0001t0001g0270 others(6): Show |
9 | HG00099.hp2 HG01243.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.985-1457_985-1454d others(6): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 90275590 | ||||||
| chr7:90275590 | CTTTTTTT others(2): Show |
C | 31 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(28): Show |
34 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.985-1462_985-1454d others(11): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 90275590 | ||||||
| chr7:90275590 | CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0002g0187 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.985-1463_985-1454d others(12): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 90275590 | ||||||
| chr7:90275590 | CTTTTTTT others(6): Show |
C | 3 | a0001c0002t0002g0008 a0001c0002t0002g0127 a0001c0002t0002g0131 |
4 | HG00597.hp1 NA18969.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.985-1466_985-1454d others(15): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 90275590 | ||||||
| chr7:90275595 | T | G | 1 | a0001c0006t0001g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.985-1478T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275595 | |||||||
| chr7:90275706 | A | G | 1 | a0002c0001t0001g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.985-1367A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275706 | |||||||
| chr7:90275787 | A | G | 1 | a0001c0002t0002g0121 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.985-1286A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275787 | |||||||
| chr7:90275797 | T | A | 2 | a0003c0005t0002g0247 a0003c0005t0002g0248 |
2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.985-1276T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275797 | |||||||
| chr7:90275805 | T | C | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.985-1268T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275805 | |||||||
| chr7:90275827 | C | T | 1 | a0002c0001t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.985-1246C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275827 | |||||||
| chr7:90275891 | C | T | 1 | a0001c0003t0001g0306 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.985-1182C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275891 | |||||||
| chr7:90275997 | G | A | 1 | a0003c0005t0002g0251 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.985-1076G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90275997 | |||||||
| chr7:90276152 | C | T | 1 | a0001c0003t0001g0308 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.985-921C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90276152 | |||||||
| chr7:90276160 | C | A | 1 | a0003c0005t0002g0253 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.985-913C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90276160 | |||||||
| chr7:90276189 | C | A | 295 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(292): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.985-884C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90276189 | |||||||
| chr7:90276266 | T | G | 1 | a0001c0006t0001g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.985-807T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90276266 | |||||||
| chr7:90276502 | C | T | 1 | a0006c0008t0002g0017 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.985-571C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90276502 | |||||||
| chr7:90276515 | A | G | 295 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(292): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.985-558A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90276515 | |||||||
| chr7:90276842 | GA | G | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.985-229delA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 90276842 | ||||||
| chr7:90277009 | C | T | 2 | a0001c0002t0004g0160 a0001c0002t0004g0161 |
2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.985-64C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90277009 | |||||||
| chr7:90277029 | T | A | 1 | a0001c0002t0002g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.985-44T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 9/22 | chr7 | 90277029 | |||||||
| chr7:90277369 | A | G | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1155+35A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90277369 | |||||||
| chr7:90277423 | C | A | 1 | a0001c0002t0002g0175 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1155+89C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90277423 | |||||||
| chr7:90277424 | G | A | 1 | a0002c0001t0001g0035 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1155+90G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90277424 | |||||||
| chr7:90277440 | A | G | 5 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(2): Show |
5 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1155+106A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90277440 | |||||||
| chr7:90278024 | T | C | 2 | a0002c0001t0001g0031 a0002c0001t0001g0042 |
2 | HG02083.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1155+690T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90278024 | |||||||
| chr7:90278068 | A | G | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1155+734A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90278068 | |||||||
| chr7:90278398 | G | A | 1 | a0002c0001t0001g0037 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1155+1064G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90278398 | |||||||
| chr7:90278434 | A | C | 2 | a0002c0001t0001g0004 a0002c0001t0001g0055 |
3 | HG00323.hp2 HG01167.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1155+1100A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90278434 | |||||||
| chr7:90278508 | A | T | 2 | a0001c0002t0002g0025 a0001c0002t0002g0026 |
2 | NA18942.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1156-1169A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90278508 | |||||||
| chr7:90278570 | ATAATAAA others(8): Show |
A | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1156-1104_1156-109 others(19): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr7 | 90278570 | ||||||
| chr7:90278582 | A | G | 1 | a0001c0006t0001g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1156-1095A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90278582 | |||||||
| chr7:90278688 | C | T | 2 | a0001c0002t0004g0160 a0001c0002t0004g0161 |
2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1156-989C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90278688 | |||||||
| chr7:90278731 | A | G | 2 | a0001c0002t0004g0160 a0001c0002t0004g0161 |
2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1156-946A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90278731 | |||||||
| chr7:90278943 | G | A | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-734G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90278943 | |||||||
| chr7:90278971 | A | T | 4 | a0001c0004t0002g0209 a0001c0004t0002g0222 a0001c0004t0002g0223 others(1): Show |
4 | HG02109.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1156-706A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90278971 | |||||||
| chr7:90279034 | C | A | 1 | a0002c0001t0001g0271 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1156-643C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90279034 | |||||||
| chr7:90279054 | C | T | 1 | a0001c0016t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1156-623C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90279054 | |||||||
| chr7:90279518 | T | TG | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1156-158dupG | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr7 | 90279518 | ||||||
| chr7:90279519 | G | T | 126 | a0001c0006t0001g0162 a0001c0006t0001g0237 a0001c0006t0001g0239 others(123): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1156-158G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90279519 | |||||||
| chr7:90279537 | A | G | 123 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(120): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.1156-140A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90279537 | |||||||
| chr7:90279541 | T | C | 1 | a0001c0016t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1156-136T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 11/22 | chr7 | 90279541 | |||||||
| chr7:90280128 | G | A | 126 | a0001c0006t0001g0162 a0001c0006t0001g0237 a0001c0006t0001g0239 others(123): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1372+235G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90280128 | |||||||
| chr7:90280201 | CTTTG | C | 49 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(46): Show |
51 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.1372+319_1372+322d others(6): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr7 | 90280201 | ||||||
| chr7:90280300 | C | T | 1 | a0005c0009t0002g0282 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1372+407C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90280300 | |||||||
| chr7:90280343 | T | G | 295 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(292): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1372+450T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90280343 | |||||||
| chr7:90280395 | C | T | 49 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0012 others(46): Show |
54 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.1372+502C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90280395 | |||||||
| chr7:90280405 | C | A | 288 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(285): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1372+512C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90280405 | |||||||
| chr7:90280466 | G | A | 1 | a0001c0004t0002g0229 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1372+573G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90280466 | |||||||
| chr7:90280643 | T | A | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1372+750T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90280643 | |||||||
| chr7:90280668 | G | A | 123 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(120): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.1372+775G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90280668 | |||||||
| chr7:90280772 | A | G | 1 | a0002c0001t0001g0279 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1372+879A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90280772 | |||||||
| chr7:90280885 | G | C | 1 | a0002c0001t0001g0151 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1372+992G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90280885 | |||||||
| chr7:90280895 | C | T | 1 | a0002c0001t0001g0081 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1372+1002C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90280895 | |||||||
| chr7:90281527 | G | A | 9 | a0001c0003t0001g0296 a0001c0003t0001g0297 a0001c0003t0001g0298 others(6): Show |
9 | HG00408.hp2 HG01978.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1373-1365G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90281527 | |||||||
| chr7:90281647 | G | A | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1373-1245G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90281647 | |||||||
| chr7:90281696 | A | G | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1373-1196A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90281696 | |||||||
| chr7:90281775 | G | A | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1373-1117G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90281775 | |||||||
| chr7:90281861 | G | A | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1373-1031G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90281861 | |||||||
| chr7:90281874 | G | T | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1373-1018G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90281874 | |||||||
| chr7:90281923 | G | A | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1373-969G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90281923 | |||||||
| chr7:90282188 | T | TA | 295 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(292): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1373-693dupA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr7 | 90282188 | ||||||
| chr7:90282848 | T | C | 2 | a0001c0002t0004g0160 a0001c0002t0004g0161 |
2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1373-44T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 12/22 | chr7 | 90282848 | |||||||
| chr7:90283159 | A | T | 3 | a0001c0002t0002g0011 a0001c0002t0002g0177 a0001c0002t0002g0183 |
4 | NA18946.hp2 NA18962.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1537+103A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90283159 | |||||||
| chr7:90283192 | C | T | 1 | a0001c0002t0002g0124 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1537+136C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90283192 | |||||||
| chr7:90283199 | C | T | 128 | a0001c0006t0001g0162 a0001c0006t0001g0237 a0001c0006t0001g0239 others(125): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1537+143C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90283199 | |||||||
| chr7:90283415 | A | G | 3 | a0002c0001t0001g0034 a0002c0001t0001g0035 a0002c0001t0001g0036 |
3 | HG02965.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1537+359A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90283415 | |||||||
| chr7:90283779 | T | A | 1 | a0004c0007t0001g0268 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1537+723T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90283779 | |||||||
| chr7:90283799 | A | G | 1 | a0002c0001t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1537+743A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90283799 | |||||||
| chr7:90283955 | C | T | 121 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(118): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1537+899C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90283955 | |||||||
| chr7:90283956 | A | G | 5 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(2): Show |
5 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1537+900A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90283956 | |||||||
| chr7:90284226 | A | G | 5 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(2): Show |
5 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1537+1170A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90284226 | |||||||
| chr7:90284228 | G | A | 1 | a0005c0009t0002g0283 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1537+1172G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90284228 | |||||||
| chr7:90284254 | G | A | 2 | a0002c0001t0001g0271 a0002c0001t0001g0272 |
2 | HG00099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1537+1198G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90284254 | |||||||
| chr7:90284255 | G | T | 2 | a0002c0001t0001g0271 a0002c0001t0001g0272 |
2 | HG00099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1537+1199G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90284255 | |||||||
| chr7:90284256 | C | A | 2 | a0002c0001t0001g0271 a0002c0001t0001g0272 |
2 | HG00099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1537+1200C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90284256 | |||||||
| chr7:90284257 | T | A | 2 | a0002c0001t0001g0271 a0002c0001t0001g0272 |
2 | HG00099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1537+1201T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90284257 | |||||||
| chr7:90284388 | A | G | 121 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(118): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1537+1332A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90284388 | |||||||
| chr7:90284632 | G | A | 1 | a0001c0006t0001g0237 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1537+1576G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90284632 | |||||||
| chr7:90284632 | G | C | 121 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(118): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1537+1576G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90284632 | |||||||
| chr7:90285074 | G | T | 121 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(118): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1538-1207G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90285074 | |||||||
| chr7:90285875 | G | C | 1 | a0001c0016t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1538-406G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90285875 | |||||||
| chr7:90285949 | T | G | 5 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(2): Show |
5 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1538-332T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90285949 | |||||||
| chr7:90286000 | C | T | 5 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(2): Show |
5 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1538-281C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90286000 | |||||||
| chr7:90286024 | G | A | 121 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(118): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1538-257G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90286024 | |||||||
| chr7:90286232 | T | G | 1 | a0001c0002t0002g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1538-49T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 13/22 | chr7 | 90286232 | |||||||
| chr7:90286701 | G | A | 1 | a0001c0004t0002g0016 | 2 | NA18944.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1656+302G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90286701 | |||||||
| chr7:90286852 | C | T | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1656+453C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90286852 | |||||||
| chr7:90286885 | T | C | 299 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(296): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1656+486T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90286885 | |||||||
| chr7:90286946 | G | A | 1 | a0001c0013t0002g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1656+547G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90286946 | |||||||
| chr7:90286959 | GCGC | G | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1656+562_1656+564d others(5): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | 90286959 | ||||||
| chr7:90286963 | C | G | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1656+564C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90286963 | |||||||
| chr7:90287014 | G | A | 1 | a0002c0001t0001g0091 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1656+615G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90287014 | |||||||
| chr7:90287047 | C | T | 1 | a0001c0002t0002g0014 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1656+648C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90287047 | |||||||
| chr7:90287068 | G | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1656+669G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90287068 | |||||||
| chr7:90287085 | GA | G | 62 | a0001c0002t0002g0154 a0001c0003t0001g0299 a0001c0003t0001g0300 others(59): Show |
67 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1656+705delA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | 90287085 | ||||||
| chr7:90287085 | GAA | G | 44 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0057 others(41): Show |
46 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1656+704_1656+705d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | 90287085 | ||||||
| chr7:90287145 | A | T | 13 | a0002c0001t0001g0019 a0002c0001t0001g0165 a0002c0001t0001g0269 others(10): Show |
14 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1656+746A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90287145 | |||||||
| chr7:90287345 | T | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1657-889T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90287345 | |||||||
| chr7:90287368 | A | G | 3 | a0001c0002t0002g0009 a0001c0002t0002g0134 a0001c0002t0002g0136 |
4 | HG00741.hp1 HG01175.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1657-866A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90287368 | |||||||
| chr7:90287397 | C | G | 1 | a0002c0001t0001g0067 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1657-837C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90287397 | |||||||
| chr7:90287521 | T | A | 1 | a0001c0002t0002g0147 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1657-713T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90287521 | |||||||
| chr7:90288013 | A | G | 2 | a0008c0015t0002g0244 a0008c0015t0002g0245 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1657-221A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90288013 | |||||||
| chr7:90288061 | A | G | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1657-173A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 14/22 | chr7 | 90288061 | |||||||
| chr7:90288448 | A | G | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1775+96A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90288448 | |||||||
| chr7:90288641 | A | G | 2 | a0002c0001t0001g0044 a0002c0001t0001g0045 |
2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1775+289A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90288641 | |||||||
| chr7:90288665 | TA | T | 5 | a0001c0011t0003g0157 a0001c0011t0003g0158 a0001c0011t0003g0159 others(2): Show |
6 | HG01256.hp2 HG01358.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1775+322delA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90288665 | ||||||
| chr7:90288678 | T | TTTTTTTT others(230): Show |
1 | a0002c0001t0001g0034 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1775+327_1775+328i others(239): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90288678 | ||||||
| chr7:90288883 | A | AT | 127 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(124): Show |
139 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1775+541dupT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90288883 | ||||||
| chr7:90288961 | A | G | 3 | a0002c0001t0001g0034 a0002c0001t0001g0035 a0002c0001t0001g0036 |
3 | HG02965.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1775+609A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90288961 | |||||||
| chr7:90288964 | T | C | 156 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(153): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1775+612T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90288964 | |||||||
| chr7:90289018 | G | T | 1 | a0001c0003t0001g0291 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1775+666G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90289018 | |||||||
| chr7:90289206 | G | A | 2 | a0001c0006t0001g0237 a0001c0016t0001g0236 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1775+854G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90289206 | |||||||
| chr7:90289240 | T | A | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1775+888T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90289240 | |||||||
| chr7:90289361 | C | T | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1775+1009C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90289361 | |||||||
| chr7:90289430 | C | CT | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1775+1085dupT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90289430 | ||||||
| chr7:90289501 | G | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1775+1149G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90289501 | |||||||
| chr7:90289698 | C | G | 1 | a0001c0004t0002g0219 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1775+1346C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90289698 | |||||||
| chr7:90289720 | G | T | 1 | a0001c0002t0002g0150 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1775+1368G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90289720 | |||||||
| chr7:90289774 | A | G | 1 | a0001c0002t0002g0195 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1775+1422A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90289774 | |||||||
| chr7:90289873 | C | A | 2 | a0001c0002t0004g0160 a0001c0002t0004g0161 |
2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1775+1521C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90289873 | |||||||
| chr7:90289931 | G | A | 1 | a0001c0002t0002g0012 | 2 | NA18960.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1775+1579G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90289931 | |||||||
| chr7:90290134 | C | T | 1 | a0001c0004t0002g0207 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1775+1782C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90290134 | |||||||
| chr7:90290162 | A | T | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1775+1810A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90290162 | |||||||
| chr7:90290166 | G | A | 2 | a0008c0015t0002g0244 a0008c0015t0002g0245 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1775+1814G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90290166 | |||||||
| chr7:90290181 | C | T | 1 | a0001c0006t0001g0237 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1775+1829C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90290181 | |||||||
| chr7:90290182 | A | G | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1775+1830A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90290182 | |||||||
| chr7:90290409 | A | T | 1 | a0002c0001t0001g0064 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1775+2057A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90290409 | |||||||
| chr7:90290502 | C | G | 2 | a0001c0002t0004g0160 a0001c0002t0004g0161 |
2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1775+2150C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90290502 | |||||||
| chr7:90290616 | A | G | 1 | a0001c0002t0002g0180 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1775+2264A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90290616 | |||||||
| chr7:90290743 | GTCTTT | G | 12 | a0001c0004t0002g0206 a0001c0004t0002g0210 a0001c0004t0002g0228 others(9): Show |
13 | HG00741.hp2 HG01074.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1775+2468_1775+247 others(9): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90290743 | ||||||
| chr7:90290743 | GTCTTTTC others(3): Show |
G | 59 | a0001c0002t0002g0012 a0001c0002t0002g0023 a0001c0002t0002g0024 others(56): Show |
65 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.1775+2463_1775+247 others(14): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90290743 | ||||||
| chr7:90290743 | GTCTTTTC others(8): Show |
G | 58 | a0001c0002t0002g0008 a0001c0002t0002g0013 a0001c0002t0002g0025 others(55): Show |
64 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.1775+2458_1775+247 others(19): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90290743 | ||||||
| chr7:90290743 | GTCTTTTC others(13): Show |
G | 63 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(60): Show |
68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1775+2453_1775+247 others(24): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90290743 | ||||||
| chr7:90290743 | GTCTTTTC others(18): Show |
G | 52 | a0001c0002t0002g0027 a0001c0002t0002g0101 a0001c0002t0002g0102 others(49): Show |
53 | HG00558.hp1 HG01069.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1775+2448_1775+247 others(29): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90290743 | ||||||
| chr7:90290743 | GTCTTTTC others(23): Show |
G | 13 | a0001c0006t0001g0237 a0002c0001t0001g0006 a0002c0001t0001g0052 others(10): Show |
14 | HG00438.hp1 HG01243.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1775+2443_1775+247 others(34): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90290743 | ||||||
| chr7:90290743 | GTCTTTTC others(28): Show |
G | 10 | a0002c0001t0001g0077 a0002c0001t0001g0078 a0002c0001t0001g0079 others(7): Show |
11 | HG00738.hp2 HG02896.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1775+2438_1775+247 others(39): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90290743 | ||||||
| chr7:90290743 | GTCTTTTC others(33): Show |
G | 6 | a0001c0019t0002g0164 a0002c0001t0001g0044 a0002c0001t0001g0045 others(3): Show |
6 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1775+2433_1775+247 others(44): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90290743 | ||||||
| chr7:90290743 | GTCTTTTC others(38): Show |
G | 2 | a0001c0002t0004g0160 a0001c0002t0004g0161 |
2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1775+2428_1775+247 others(49): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90290743 | ||||||
| chr7:90290743 | GTCTTTTC others(43): Show |
G | 31 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(28): Show |
34 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1775+2423_1775+247 others(54): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90290743 | ||||||
| chr7:90290743 | GTCTTTTC others(48): Show |
G | 3 | a0001c0011t0003g0157 a0001c0011t0003g0158 a0001c0011t0003g0159 |
3 | HG02818.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1775+2418_1775+247 others(59): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90290743 | ||||||
| chr7:90290743 | GTCTTTTC others(53): Show |
G | 1 | a0001c0003t0001g0314 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1775+2413_1775+247 others(64): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90290743 | ||||||
| chr7:90290774 | T | C | 1 | a0001c0004t0002g0215 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1775+2422T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90290774 | |||||||
| chr7:90290954 | C | T | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1775+2602C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90290954 | |||||||
| chr7:90291035 | T | C | 1 | a0002c0001t0001g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1775+2683T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90291035 | |||||||
| chr7:90291439 | C | A | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1775+3087C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90291439 | |||||||
| chr7:90291552 | C | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1775+3200C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90291552 | |||||||
| chr7:90291570 | T | C | 1 | a0001c0011t0003g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1775+3218T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90291570 | |||||||
| chr7:90291654 | T | C | 1 | a0002c0001t0001g0114 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1775+3302T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90291654 | |||||||
| chr7:90291725 | G | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1775+3373G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90291725 | |||||||
| chr7:90291758 | C | T | 156 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(153): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1775+3406C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90291758 | |||||||
| chr7:90291798 | A | G | 2 | a0008c0015t0002g0244 a0008c0015t0002g0245 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1775+3446A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90291798 | |||||||
| chr7:90292197 | A | G | 121 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(118): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1775+3845A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90292197 | |||||||
| chr7:90292371 | A | T | 1 | a0001c0002t0002g0121 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1775+4019A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90292371 | |||||||
| chr7:90292809 | T | C | 1 | a0001c0004t0002g0167 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1775+4457T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90292809 | |||||||
| chr7:90292855 | A | C | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1775+4503A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90292855 | |||||||
| chr7:90293002 | A | T | 3 | a0001c0002t0002g0010 a0001c0002t0002g0166 a0001c0002t0002g0178 |
4 | NA18961.hp1 NA18984.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1775+4650A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90293002 | |||||||
| chr7:90293016 | A | G | 13 | a0002c0001t0001g0019 a0002c0001t0001g0165 a0002c0001t0001g0269 others(10): Show |
14 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1775+4664A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90293016 | |||||||
| chr7:90293103 | C | T | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1776-4646C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90293103 | |||||||
| chr7:90293104 | G | A | 3 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0006g0103 |
3 | HG01106.hp2 HG02280.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1776-4645G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90293104 | |||||||
| chr7:90293139 | A | G | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1776-4610A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90293139 | |||||||
| chr7:90293144 | T | C | 126 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(123): Show |
137 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1776-4605T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90293144 | |||||||
| chr7:90293238 | C | T | 1 | a0001c0002t0002g0169 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1776-4511C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90293238 | |||||||
| chr7:90293308 | G | A | 2 | a0003c0005t0002g0247 a0003c0005t0002g0248 |
2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1776-4441G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90293308 | |||||||
| chr7:90293792 | A | G | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1776-3957A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90293792 | |||||||
| chr7:90293903 | A | G | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1776-3846A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90293903 | |||||||
| chr7:90293971 | C | T | 3 | a0001c0011t0003g0157 a0001c0011t0003g0158 a0001c0011t0003g0159 |
3 | HG02818.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1776-3778C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90293971 | |||||||
| chr7:90293988 | G | A | 1 | a0002c0001t0001g0045 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1776-3761G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90293988 | |||||||
| chr7:90294278 | G | A | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1776-3471G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90294278 | |||||||
| chr7:90294408 | T | G | 1 | a0002c0001t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1776-3341T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90294408 | |||||||
| chr7:90294575 | A | G | 16 | a0002c0001t0001g0007 a0002c0001t0001g0094 a0002c0001t0001g0104 others(13): Show |
17 | HG00558.hp1 HG01975.hp1 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.1776-3174A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90294575 | |||||||
| chr7:90294623 | G | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1776-3126G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90294623 | |||||||
| chr7:90294653 | G | A | 1 | a0002c0001t0001g0238 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1776-3096G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90294653 | |||||||
| chr7:90294705 | G | C | 125 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(122): Show |
136 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1776-3044G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90294705 | |||||||
| chr7:90294790 | A | G | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1776-2959A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90294790 | |||||||
| chr7:90294918 | T | G | 121 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(118): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1776-2831T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90294918 | |||||||
| chr7:90294923 | T | G | 156 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(153): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1776-2826T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90294923 | |||||||
| chr7:90294972 | G | A | 1 | a0002c0001t0001g0067 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1776-2777G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90294972 | |||||||
| chr7:90295086 | C | A | 121 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(118): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1776-2663C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295086 | |||||||
| chr7:90295136 | A | G | 2 | a0001c0002t0002g0182 a0001c0002t0002g0191 |
2 | HG00673.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1776-2613A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295136 | |||||||
| chr7:90295215 | A | G | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1776-2534A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295215 | |||||||
| chr7:90295219 | G | T | 1 | a0001c0004t0002g0214 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1776-2530G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295219 | |||||||
| chr7:90295365 | C | G | 1 | a0001c0004t0002g0220 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1776-2384C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295365 | |||||||
| chr7:90295453 | G | A | 122 | a0001c0002t0002g0120 a0001c0006t0001g0162 a0001c0006t0001g0259 others(119): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.1776-2296G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295453 | |||||||
| chr7:90295477 | G | A | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1776-2272G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295477 | |||||||
| chr7:90295563 | C | T | 1 | a0001c0019t0002g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1776-2186C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295563 | |||||||
| chr7:90295604 | G | A | 3 | a0001c0011t0003g0157 a0001c0011t0003g0158 a0001c0011t0003g0159 |
3 | HG02818.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1776-2145G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295604 | |||||||
| chr7:90295661 | C | A | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1776-2088C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295661 | |||||||
| chr7:90295753 | G | A | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1776-1996G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295753 | |||||||
| chr7:90295895 | C | T | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1776-1854C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295895 | |||||||
| chr7:90295914 | T | C | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1776-1835T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295914 | |||||||
| chr7:90295926 | T | C | 2 | a0001c0004t0002g0226 a0001c0004t0002g0230 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1776-1823T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295926 | |||||||
| chr7:90295930 | C | T | 1 | a0001c0002t0002g0187 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1776-1819C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295930 | |||||||
| chr7:90295976 | C | G | 299 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(296): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1776-1773C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90295976 | |||||||
| chr7:90296003 | G | A | 2 | a0008c0015t0002g0244 a0008c0015t0002g0245 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1776-1746G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90296003 | |||||||
| chr7:90296049 | G | A | 1 | a0001c0019t0002g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1776-1700G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90296049 | |||||||
| chr7:90296061 | C | T | 1 | a0003c0005t0002g0246 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1776-1688C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90296061 | |||||||
| chr7:90296153 | C | A | 2 | a0001c0002t0002g0124 a0001c0002t0002g0132 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1776-1596C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90296153 | |||||||
| chr7:90296222 | C | A | 1 | a0002c0001t0001g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1776-1527C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90296222 | |||||||
| chr7:90296247 | G | A | 139 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(136): Show |
151 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1776-1502G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90296247 | |||||||
| chr7:90296376 | G | A | 1 | a0001c0003t0001g0303 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1776-1373G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90296376 | |||||||
| chr7:90296579 | C | G | 1 | a0001c0019t0002g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1776-1170C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90296579 | |||||||
| chr7:90296693 | A | G | 1 | a0001c0004t0002g0210 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1776-1056A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90296693 | |||||||
| chr7:90296959 | AGGTGCC | A | 4 | a0002c0001t0001g0046 a0002c0001t0001g0047 a0002c0001t0001g0049 others(1): Show |
4 | NA18961.hp2 NA18975.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1776-787_1776-782d others(8): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr7 | 90296959 | ||||||
| chr7:90296994 | G | A | 2 | a0002c0001t0001g0065 a0002c0001t0001g0087 |
2 | HG00099.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1776-755G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90296994 | |||||||
| chr7:90297152 | G | T | 2 | a0008c0015t0002g0244 a0008c0015t0002g0245 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1776-597G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90297152 | |||||||
| chr7:90297226 | T | C | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1776-523T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90297226 | |||||||
| chr7:90297531 | A | T | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1776-218A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90297531 | |||||||
| chr7:90297577 | A | T | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1776-172A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90297577 | |||||||
| chr7:90297645 | T | G | 2 | a0007c0010t0002g0002 a0007c0010t0002g0225 |
4 | HG01891.hp1 HG02257.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1776-104T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 15/22 | chr7 | 90297645 | |||||||
| chr7:90297866 | A | T | 1 | a0001c0004t0002g0167 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1857+36A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90297866 | |||||||
| chr7:90297877 | T | A | 299 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(296): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1857+47T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90297877 | |||||||
| chr7:90297886 | G | A | 2 | a0002c0001t0001g0019 a0002c0001t0001g0276 |
3 | HG01256.hp2 HG01358.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1857+56G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90297886 | |||||||
| chr7:90298004 | A | C | 4 | a0002c0001t0001g0046 a0002c0001t0001g0047 a0002c0001t0001g0049 others(1): Show |
4 | NA18961.hp2 NA18975.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857+174A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90298004 | |||||||
| chr7:90298107 | A | G | 3 | a0001c0002t0002g0200 a0001c0002t0002g0204 a0001c0002t0002g0231 |
3 | NA18955.hp2 NA18968.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1857+277A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90298107 | |||||||
| chr7:90298141 | A | G | 1 | a0001c0002t0002g0128 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1857+311A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90298141 | |||||||
| chr7:90298302 | T | C | 127 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(124): Show |
138 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1857+472T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90298302 | |||||||
| chr7:90298358 | A | G | 13 | a0002c0001t0001g0019 a0002c0001t0001g0165 a0002c0001t0001g0269 others(10): Show |
14 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.1857+528A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90298358 | |||||||
| chr7:90298480 | G | C | 1 | a0002c0001t0001g0081 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1857+650G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90298480 | |||||||
| chr7:90298487 | A | G | 1 | a0002c0001t0001g0111 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1857+657A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90298487 | |||||||
| chr7:90298541 | A | C | 2 | a0001c0013t0002g0240 a0001c0013t0002g0241 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1857+711A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90298541 | |||||||
| chr7:90298729 | G | A | 3 | a0001c0003t0001g0293 a0001c0003t0001g0294 a0001c0003t0001g0295 |
3 | HG00438.hp2 NA19007.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1857+899G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90298729 | |||||||
| chr7:90298755 | G | A | 2 | a0002c0001t0001g0062 a0002c0001t0001g0095 |
2 | HG01934.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1857+925G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90298755 | |||||||
| chr7:90298893 | A | G | 1 | a0002c0001t0001g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1858-974A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90298893 | |||||||
| chr7:90298982 | A | G | 2 | a0003c0005t0002g0247 a0003c0005t0002g0248 |
2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1858-885A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90298982 | |||||||
| chr7:90299319 | A | G | 1 | a0005c0009t0002g0283 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1858-548A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90299319 | |||||||
| chr7:90299323 | G | A | 5 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(2): Show |
5 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1858-544G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90299323 | |||||||
| chr7:90299371 | A | G | 1 | a0001c0002t0002g0180 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1858-496A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90299371 | |||||||
| chr7:90299581 | T | C | 1 | a0001c0002t0002g0184 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1858-286T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90299581 | |||||||
| chr7:90299767 | A | C | 1 | a0001c0002t0002g0129 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1858-100A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90299767 | |||||||
| chr7:90299796 | C | CT | 154 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(151): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1858-61dupT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr7 | 90299796 | ||||||
| chr7:90299811 | A | G | 1 | a0010c0017t0001g0060 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1858-56A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 16/22 | chr7 | 90299811 | |||||||
| chr7:90300164 | G | GT | 294 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(291): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2050+121dupT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr7 | 90300164 | ||||||
| chr7:90300215 | T | C | 3 | a0002c0001t0001g0165 a0002c0001t0001g0277 a0002c0001t0001g0279 |
3 | HG03490.hp1 HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2050+156T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300215 | |||||||
| chr7:90300300 | TA | T | 295 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(292): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.2050+251delA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr7 | 90300300 | ||||||
| chr7:90300303 | A | T | 2 | a0002c0001t0001g0044 a0002c0001t0001g0045 |
2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2050+244A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300303 | |||||||
| chr7:90300486 | T | C | 1 | a0001c0002t0002g0120 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2050+427T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300486 | |||||||
| chr7:90300509 | G | A | 1 | a0001c0006t0001g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2050+450G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300509 | |||||||
| chr7:90300514 | T | C | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2050+455T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300514 | |||||||
| chr7:90300636 | ATTTTTTT others(4): Show |
A | 120 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(117): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.2050+596_2050+606d others(13): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr7 | 90300636 | ||||||
| chr7:90300645 | TTTTTTTT others(3): Show |
T | 1 | a0002c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2050+596_2050+605d others(12): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr7 | 90300645 | ||||||
| chr7:90300654 | T | TTC | 29 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(26): Show |
32 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.2050+595_2050+596i others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300654 | |||||||
| chr7:90300655 | C | T | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2050+596C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300655 | |||||||
| chr7:90300733 | C | T | 4 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0266 others(1): Show |
4 | HG00639.hp2 HG02451.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050+674C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300733 | |||||||
| chr7:90300760 | C | A | 5 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(2): Show |
5 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2050+701C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300760 | |||||||
| chr7:90300781 | G | A | 4 | a0002c0001t0001g0062 a0002c0001t0001g0076 a0002c0001t0001g0095 others(1): Show |
4 | HG01934.hp1 HG01993.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.2050+722G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300781 | |||||||
| chr7:90300828 | T | G | 1 | a0001c0003t0001g0304 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2050+769T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300828 | |||||||
| chr7:90300832 | G | T | 3 | a0001c0002t0002g0189 a0001c0002t0002g0190 a0001c0002t0002g0196 |
3 | HG00597.hp2 NA18991.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.2050+773G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300832 | |||||||
| chr7:90300851 | G | A | 295 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(292): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.2050+792G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300851 | |||||||
| chr7:90300866 | G | T | 121 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(118): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.2050+807G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300866 | |||||||
| chr7:90300889 | G | A | 1 | a0009c0018t0002g0173 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2050+830G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300889 | |||||||
| chr7:90300957 | A | G | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2050+898A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90300957 | |||||||
| chr7:90300975 | C | CT | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2050+926dupT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr7 | 90300975 | ||||||
| chr7:90301008 | G | A | 3 | a0006c0008t0002g0017 a0006c0008t0002g0242 a0006c0008t0002g0243 |
4 | HG00738.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2050+949G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301008 | |||||||
| chr7:90301055 | G | A | 2 | a0003c0005t0002g0247 a0003c0005t0002g0248 |
2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2050+996G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301055 | |||||||
| chr7:90301124 | A | G | 1 | a0002c0001t0001g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2050+1065A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301124 | |||||||
| chr7:90301141 | G | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2050+1082G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301141 | |||||||
| chr7:90301220 | A | C | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2050+1161A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301220 | |||||||
| chr7:90301294 | A | G | 1 | a0002c0001t0001g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2050+1235A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301294 | |||||||
| chr7:90301333 | A | T | 131 | a0001c0002t0002g0013 a0001c0002t0002g0027 a0001c0002t0002g0192 others(128): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.2050+1274A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301333 | |||||||
| chr7:90301427 | A | C | 1 | a0001c0003t0001g0300 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2050+1368A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301427 | |||||||
| chr7:90301443 | A | G | 2 | a0002c0001t0001g0044 a0002c0001t0001g0045 |
2 | HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2050+1384A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301443 | |||||||
| chr7:90301618 | A | C | 1 | a0001c0006t0001g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2050+1559A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301618 | |||||||
| chr7:90301652 | A | T | 4 | a0002c0001t0001g0046 a0002c0001t0001g0047 a0002c0001t0001g0049 others(1): Show |
4 | NA18961.hp2 NA18975.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050+1593A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301652 | |||||||
| chr7:90301854 | G | T | 3 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 |
3 | HG00140.hp2 HG00735.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.2050+1795G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301854 | |||||||
| chr7:90301861 | C | T | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2050+1802C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301861 | |||||||
| chr7:90301958 | C | T | 1 | a0001c0013t0002g0241 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2050+1899C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301958 | |||||||
| chr7:90301960 | C | T | 1 | a0001c0013t0002g0241 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2050+1901C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301960 | |||||||
| chr7:90301969 | C | T | 1 | a0001c0013t0002g0241 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2050+1910C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301969 | |||||||
| chr7:90301970 | A | G | 1 | a0001c0013t0002g0241 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2050+1911A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301970 | |||||||
| chr7:90301982 | G | T | 127 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(124): Show |
138 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.2050+1923G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301982 | |||||||
| chr7:90301996 | G | T | 1 | a0001c0002t0002g0119 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2050+1937G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90301996 | |||||||
| chr7:90302062 | T | G | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-1907T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90302062 | |||||||
| chr7:90302201 | A | G | 121 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(118): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.2051-1768A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90302201 | |||||||
| chr7:90302253 | T | C | 3 | a0002c0001t0001g0034 a0002c0001t0001g0035 a0002c0001t0001g0036 |
3 | HG02965.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2051-1716T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90302253 | |||||||
| chr7:90302506 | T | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2051-1463T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90302506 | |||||||
| chr7:90302513 | G | C | 1 | a0002c0001t0001g0279 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2051-1456G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90302513 | |||||||
| chr7:90302536 | A | T | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2051-1433A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90302536 | |||||||
| chr7:90302582 | ATTTCCCC others(8): Show |
A | 1 | a0003c0005t0002g0254 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2051-1382_2051-136 others(19): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr7 | 90302582 | ||||||
| chr7:90302678 | T | G | 5 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(2): Show |
5 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051-1291T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90302678 | |||||||
| chr7:90302718 | T | C | 2 | a0003c0005t0002g0249 a0003c0005t0002g0250 |
2 | HG01069.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.2051-1251T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90302718 | |||||||
| chr7:90302730 | G | A | 1 | a0002c0001t0001g0238 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2051-1239G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90302730 | |||||||
| chr7:90303011 | T | A | 1 | a0001c0002t0002g0129 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2051-958T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90303011 | |||||||
| chr7:90303055 | A | G | 1 | a0001c0002t0006g0103 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2051-914A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90303055 | |||||||
| chr7:90303514 | CT | C | 3 | a0001c0011t0003g0157 a0001c0011t0003g0158 a0001c0011t0003g0159 |
3 | HG02818.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2051-453delT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr7 | 90303514 | ||||||
| chr7:90303567 | T | C | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2051-402T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90303567 | |||||||
| chr7:90303665 | A | G | 1 | a0001c0019t0002g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2051-304A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 17/22 | chr7 | 90303665 | |||||||
| chr7:90304237 | A | AC | 7 | a0001c0002t0002g0192 a0001c0002t0002g0204 a0001c0004t0002g0217 others(4): Show |
7 | HG00423.hp2 HG02145.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2188+135dupC | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr7 | 90304237 | ||||||
| chr7:90304452 | C | G | 1 | a0002c0001t0001g0081 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2189-292C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 18/22 | chr7 | 90304452 | |||||||
| chr7:90304560 | C | G | 97 | a0002c0001t0001g0001 a0002c0001t0001g0003 a0002c0001t0001g0004 others(94): Show |
104 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2189-184C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 18/22 | chr7 | 90304560 | |||||||
| chr7:90304598 | A | C | 2 | a0001c0002t0002g0148 a0001c0002t0002g0149 |
2 | HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2189-146A>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 18/22 | chr7 | 90304598 | |||||||
| chr7:90304643 | G | GTAGA | 35 | a0001c0002t0004g0161 a0001c0003t0001g0288 a0001c0003t0001g0294 others(32): Show |
37 | HG00558.hp2 HG01070.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.2189-59_2189-56dup others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr7 | 90304643 | ||||||
| chr7:90304643 | G | GTAGATAG others(1): Show |
9 | a0001c0003t0001g0306 a0002c0001t0001g0054 a0002c0001t0001g0087 others(6): Show |
9 | HG00735.hp2 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.2189-63_2189-56dup others(8): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr7 | 90304643 | ||||||
| chr7:90304643 | G | GTAGATAG others(5): Show |
1 | a0003c0005t0002g0257 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2189-67_2189-56dup others(12): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr7 | 90304643 | ||||||
| chr7:90304643 | GTAGA | G | 25 | a0001c0003t0001g0297 a0001c0003t0001g0301 a0001c0003t0001g0302 others(22): Show |
27 | HG00099.hp2 HG00140.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.2189-59_2189-56del others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr7 | 90304643 | ||||||
| chr7:90304643 | GTAGATAG others(1): Show |
G | 11 | a0002c0001t0001g0004 a0002c0001t0001g0029 a0002c0001t0001g0030 others(8): Show |
12 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.2189-63_2189-56del others(8): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr7 | 90304643 | ||||||
| chr7:90304643 | GTAGATAG others(13): Show |
G | 126 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(123): Show |
137 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.2189-75_2189-56del others(20): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr7 | 90304643 | ||||||
| chr7:90304646 | G | A | 1 | a0001c0003t0001g0289 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2189-98G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 18/22 | chr7 | 90304646 | |||||||
| chr7:90304916 | A | G | 1 | a0001c0019t0002g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2265+96A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90304916 | |||||||
| chr7:90304995 | G | C | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2265+175G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90304995 | |||||||
| chr7:90305065 | G | A | 1 | a0001c0012t0002g0198 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2265+245G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90305065 | |||||||
| chr7:90305113 | C | T | 2 | a0004c0007t0001g0266 a0004c0007t0001g0267 |
2 | HG00639.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2265+293C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90305113 | |||||||
| chr7:90305185 | A | G | 3 | a0006c0008t0002g0017 a0006c0008t0002g0242 a0006c0008t0002g0243 |
4 | HG00738.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2265+365A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90305185 | |||||||
| chr7:90305214 | G | A | 6 | a0001c0002t0002g0024 a0001c0002t0002g0133 a0001c0002t0002g0138 others(3): Show |
6 | HG00323.hp1 HG01081.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.2265+394G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90305214 | |||||||
| chr7:90305249 | G | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2265+429G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90305249 | |||||||
| chr7:90305298 | G | A | 1 | a0001c0002t0002g0193 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2265+478G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90305298 | |||||||
| chr7:90305336 | G | A | 1 | a0001c0006t0001g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2265+516G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90305336 | |||||||
| chr7:90305339 | TA | T | 7 | a0002c0001t0001g0029 a0002c0001t0001g0030 a0002c0001t0001g0032 others(4): Show |
7 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2265+532delA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr7 | 90305339 | ||||||
| chr7:90305384 | C | CAA | 110 | a0001c0006t0001g0162 a0001c0006t0001g0237 a0001c0006t0001g0239 others(107): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.2265+577_2265+578d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr7 | 90305384 | ||||||
| chr7:90305384 | C | CAAA | 12 | a0002c0001t0001g0006 a0002c0001t0001g0069 a0002c0001t0001g0088 others(9): Show |
13 | HG00438.hp1 HG02071.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2265+576_2265+578d others(5): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr7 | 90305384 | ||||||
| chr7:90305384 | CA | C | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2265+578delA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr7 | 90305384 | ||||||
| chr7:90305646 | A | G | 295 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(292): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.2265+826A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90305646 | |||||||
| chr7:90305732 | CTT | C | 124 | a0001c0006t0001g0162 a0001c0006t0001g0237 a0001c0006t0001g0239 others(121): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.2265+913_2265+914d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90305732 | |||||||
| chr7:90305788 | G | C | 1 | a0001c0006t0001g0259 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2265+968G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90305788 | |||||||
| chr7:90305812 | G | T | 1 | a0001c0002t0002g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2265+992G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90305812 | |||||||
| chr7:90305908 | G | A | 1 | a0001c0019t0002g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2266-993G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90305908 | |||||||
| chr7:90305943 | C | CTT | 6 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(3): Show |
6 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2266-942_2266-941d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr7 | 90305943 | ||||||
| chr7:90305943 | CT | C | 152 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(149): Show |
166 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2266-941delT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr7 | 90305943 | ||||||
| chr7:90306114 | TG | T | 251 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(248): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.2266-778delG | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr7 | 90306114 | ||||||
| chr7:90306117 | G | C | 1 | a0001c0002t0002g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2266-784G>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90306117 | |||||||
| chr7:90306134 | T | C | 1 | a0001c0019t0002g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2266-767T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90306134 | |||||||
| chr7:90306198 | C | T | 1 | a0006c0008t0002g0242 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2266-703C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90306198 | |||||||
| chr7:90306211 | C | T | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.2266-690C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90306211 | |||||||
| chr7:90306343 | G | T | 2 | a0001c0004t0002g0206 a0001c0004t0002g0208 |
2 | HG02074.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.2266-558G>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90306343 | |||||||
| chr7:90306390 | A | G | 97 | a0002c0001t0001g0001 a0002c0001t0001g0003 a0002c0001t0001g0004 others(94): Show |
104 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2266-511A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90306390 | |||||||
| chr7:90306492 | T | C | 288 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(285): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.2266-409T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90306492 | |||||||
| chr7:90306535 | AG | A | 5 | a0001c0002t0004g0160 a0001c0002t0004g0161 a0001c0011t0003g0157 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2266-363delG | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr7 | 90306535 | ||||||
| chr7:90306574 | C | A | 143 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(140): Show |
155 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.2266-327C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 19/22 | chr7 | 90306574 | |||||||
| chr7:90307161 | C | T | 1 | a0003c0005t0002g0253 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2463+63C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 20/22 | chr7 | 90307161 | |||||||
| chr7:90307190 | A | G | 6 | a0001c0004t0002g0209 a0001c0004t0002g0222 a0001c0004t0002g0223 others(3): Show |
6 | HG02109.hp1 HG02723.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2463+92A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 20/22 | chr7 | 90307190 | |||||||
| chr7:90307332 | A | G | 3 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 |
3 | HG00140.hp2 HG00735.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.2463+234A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 20/22 | chr7 | 90307332 | |||||||
| chr7:90307629 | A | G | 1 | a0001c0002t0002g0124 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2464-139A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 20/22 | chr7 | 90307629 | |||||||
| chr7:90307713 | CA | C | 155 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(152): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.2464-43delA | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 90307713 | ||||||
| chr7:90307896 | A | G | 130 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(127): Show |
142 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.2550+42A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90307896 | |||||||
| chr7:90307937 | A | AT | 3 | a0006c0008t0002g0017 a0006c0008t0002g0242 a0006c0008t0002g0243 |
4 | HG00738.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2550+89dupT | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr7 | 90307937 | ||||||
| chr7:90307984 | T | G | 1 | a0001c0004t0002g0220 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2550+130T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90307984 | |||||||
| chr7:90308212 | C | A | 32 | a0001c0003t0001g0020 a0001c0003t0001g0021 a0001c0003t0001g0022 others(29): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2550+358C>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90308212 | |||||||
| chr7:90308253 | CTG | C | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2550+402_2550+403d others(4): Show |
CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr7 | 90308253 | ||||||
| chr7:90308358 | T | C | 4 | a0001c0004t0002g0221 a0001c0004t0002g0227 a0001c0014t0002g0211 others(1): Show |
4 | HG00639.hp1 HG01884.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2550+504T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90308358 | |||||||
| chr7:90308388 | C | T | 1 | a0001c0004t0002g0213 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2550+534C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90308388 | |||||||
| chr7:90308467 | T | A | 124 | a0001c0006t0001g0162 a0001c0006t0001g0237 a0001c0006t0001g0239 others(121): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.2550+613T>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90308467 | |||||||
| chr7:90308477 | A | T | 1 | a0001c0006t0001g0237 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2550+623A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90308477 | |||||||
| chr7:90308581 | G | A | 6 | a0004c0007t0001g0263 a0004c0007t0001g0264 a0004c0007t0001g0265 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2551-682G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90308581 | |||||||
| chr7:90308656 | A | G | 3 | a0001c0006t0001g0237 a0001c0006t0001g0239 a0001c0016t0001g0236 |
3 | HG03453.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2551-607A>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90308656 | |||||||
| chr7:90308772 | C | T | 124 | a0001c0006t0001g0162 a0001c0006t0001g0237 a0001c0006t0001g0239 others(121): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.2551-491C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90308772 | |||||||
| chr7:90308780 | G | A | 2 | a0002c0001t0001g0152 a0002c0001t0001g0153 |
2 | HG00558.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.2551-483G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90308780 | |||||||
| chr7:90308814 | C | T | 1 | a0002c0001t0001g0275 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2551-449C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90308814 | |||||||
| chr7:90308877 | G | A | 124 | a0001c0006t0001g0162 a0001c0006t0001g0237 a0001c0006t0001g0239 others(121): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.2551-386G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90308877 | |||||||
| chr7:90309022 | T | G | 4 | a0005c0009t0002g0280 a0005c0009t0002g0281 a0005c0009t0002g0282 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.2551-241T>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90309022 | |||||||
| chr7:90309250 | T | C | 1 | a0002c0001t0001g0063 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2551-13T>C | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 21/22 | chr7 | 90309250 | |||||||
| chr7:90309462 | C | G | 1 | a0002c0001t0001g0039 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2655+95C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 22/22 | chr7 | 90309462 | |||||||
| chr7:90309522 | A | T | 5 | a0001c0006t0001g0162 a0001c0006t0001g0259 a0001c0006t0001g0260 others(2): Show |
5 | HG02818.hp2 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2655+155A>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 22/22 | chr7 | 90309522 | |||||||
| chr7:90309684 | C | T | 1 | a0002c0001t0001g0097 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2655+317C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 22/22 | chr7 | 90309684 | |||||||
| chr7:90309685 | G | A | 1 | a0002c0001t0001g0061 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2655+318G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 22/22 | chr7 | 90309685 | |||||||
| chr7:90309686 | G | A | 1 | a0001c0016t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2655+319G>A | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 22/22 | chr7 | 90309686 | |||||||
| chr7:90309786 | C | T | 3 | a0001c0002t0002g0011 a0001c0002t0002g0177 a0001c0002t0002g0183 |
4 | NA18946.hp2 NA18962.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.2656-282C>T | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 22/22 | chr7 | 90309786 | |||||||
| chr7:90309842 | C | G | 2 | a0001c0002t0002g0014 a0001c0002t0002g0169 |
3 | HG02602.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2656-226C>G | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 22/22 | chr7 | 90309842 | |||||||
| chr7:90310026 | TG | T | 19 | a0002c0001t0001g0001 a0002c0001t0001g0003 a0002c0001t0001g0005 others(16): Show |
23 | HG00099.hp1 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.2656-41delG | CFAP69 | ENSG00000105792.19 | transcript | ENST00000389297.8 | protein_coding | 22/22 | chr7 | 90310026 |