Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 402160 |
| ensemblid | ENSG00000206113.12 |
| hgncid | 51180 |
| symbol | CFAP99 |
| name | cilia and flagella associated protein 99 |
| refseq_nuc | NM_001193282.4 |
| refseq_prot | NP_001180211.2 |
| ensembl_nuc | ENST00000635017.2 |
| ensembl_prot | ENSP00000488922.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 2418955 |
| end | 2463002 |
| strand | + |
| ver | v1.2 |
| region | chr4:2418955-2463002 |
| region5000 | chr4:2413955-2468002 |
| regionname0 | CFAP99_chr4_2418955_2463002 |
| regionname5000 | CFAP99_chr4_2413955_2468002 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 646 | 194 | 75 | 25 | 59 | 13 | 21 | 47 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0002 | 0/0 | 646 | 112 | 10 | 23 | 69 | 1 | 9 | 45 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0003 | 0/0 | 646 | 15 | 1 | 3 | 3 | 0 | 8 | 3 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0004 | 0/0 | 646 | 8 | 0 | 6 | 2 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0005 | 0/0 | 646 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0006 | 0/0 | 646 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0007 | 0/0 | 646 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0008 | 0/0 | 187 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(182): Show |
chr4 | 2413955 | 2468002 |
| a0009 | 0/0 | 646 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0010 | 0/0 | 646 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0011 | 0/0 | 646 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0012 | 0/0 | 646 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0013 | 0/0 | 646 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0014 | 0/0 | 646 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0015 | 0/0 | 646 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| a0016 | 0/1 | 646 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | MAYYG others(641): Show |
chr4 | 2413955 | 2468002 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1938 | 143 | 44 | 17 | 57 | 9 | 15 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0001c0003 | 0/0 | 1938 | 37 | 23 | 7 | 0 | 4 | 3 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0001c0008 | 0/0 | 1938 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0001c0009 | 0/0 | 1938 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0001c0012 | 0/0 | 1938 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0001c0014 | 0/0 | 1938 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0001c0017 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0001c0019 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0001c0020 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0001c0025 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0001c0027 | 0/0 | 1938 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0001c0029 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0002c0002 | 0/0 | 1938 | 108 | 10 | 22 | 66 | 1 | 9 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0002c0021 | 0/0 | 1938 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0002c0022 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0002c0024 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0002c0033 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0003c0004 | 0/0 | 1938 | 13 | 1 | 3 | 3 | 0 | 6 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0003c0013 | 0/0 | 1938 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0004c0005 | 0/0 | 1938 | 8 | 0 | 6 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0005c0006 | 0/0 | 1938 | 6 | 6 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0006c0011 | 0/0 | 1938 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0007c0007 | 0/0 | 1938 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0008c0026 | 0/0 | 1938 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0008c0032 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0009c0010 | 0/0 | 1938 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0010c0018 | 0/0 | 1938 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0011c0030 | 0/0 | 1938 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0012c0031 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0013c0023 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0014c0016 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0015c0015 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 | ||
| a0016c0028 | 0/1 | 1938 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | ATGGC others(1933): Show |
chr4 | 2413955 | 2468002 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2173 | 139 | 41 | 16 | 57 | 9 | 15 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0001t0002 | 0/0 | 2173 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0001t0003 | 0/0 | 2173 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0001t0005 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0003t0001 | 0/0 | 2173 | 29 | 15 | 7 | 0 | 4 | 3 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0003t0002 | 0/0 | 2173 | 8 | 8 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0008t0001 | 0/0 | 2173 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0009t0001 | 0/0 | 2173 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0012t0001 | 0/0 | 2173 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0014t0001 | 0/0 | 2173 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0017t0001 | 0/0 | 2173 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0019t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0020t0001 | 0/0 | 2173 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0025t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0027t0001 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0001c0029t0001 | 0/0 | 2173 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0002c0002t0001 | 0/0 | 2173 | 105 | 8 | 21 | 66 | 1 | 9 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0002c0002t0002 | 0/0 | 2173 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0002c0002t0004 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0002c0021t0001 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0002c0022t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0002c0024t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0002c0033t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0003c0004t0001 | 0/0 | 2173 | 13 | 1 | 3 | 3 | 0 | 6 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0003c0013t0001 | 0/0 | 2173 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0004c0005t0001 | 0/0 | 2173 | 8 | 0 | 6 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0005c0006t0001 | 0/0 | 2173 | 6 | 6 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0006c0011t0001 | 0/0 | 2173 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0007c0007t0001 | 0/0 | 2173 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0008c0026t0001 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0008c0032t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0009c0010t0001 | 0/0 | 2173 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0010c0018t0001 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0011c0030t0002 | 0/0 | 2173 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0012c0031t0001 | 0/0 | 2173 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0013c0023t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0014c0016t0001 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0015c0015t0001 | 0/0 | 2173 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| a0016c0028t0001 | 0/1 | 2173 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | GCCAA others(2168): Show |
chr4 | 2413955 | 2468002 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0003t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0008t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0008t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0009t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0009t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0012t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0012t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0014t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0014t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0017t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0019t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0020t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0025t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0027t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0001c0029t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0006 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0002t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0021t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0022t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0024t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0002c0033t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0004t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0004t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0004t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0004t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0013t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0003c0013t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0004c0005t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0004c0005t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0004c0005t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0004c0005t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0004c0005t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0004c0005t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0005c0006t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0005c0006t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0005c0006t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0005c0006t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0005c0006t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0005c0006t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0006c0011t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0006c0011t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0007c0007t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0007c0007t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0008c0026t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0008c0032t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0009c0010t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0009c0010t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0010c0018t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0011c0030t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0012c0031t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0013c0023t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0014c0016t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0015c0015t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| a0016c0028t0001g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0267 | EUR | FIN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00408 | hp2 | a0002 | c0022 | t0001 | g0279 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00438 | hp2 | a0001 | c0025 | t0001 | g0256 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0278 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00639 | hp1 | a0010 | c0018 | t0001 | g0193 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0268 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | CHS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0246 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0234 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01074 | hp1 | a0003 | c0004 | t0001 | g0057 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01074 | hp2 | a0004 | c0005 | t0001 | g0248 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01081 | hp2 | a0003 | c0004 | t0001 | g0115 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0315 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0071 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01109 | hp2 | a0011 | c0030 | t0002 | g0040 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0163 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0235 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01243 | hp1 | a0006 | c0011 | t0001 | g0169 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0013 | AMR | PUR | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0183 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0307 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0300 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01257 | hp2 | a0004 | c0005 | t0001 | g0215 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01258 | hp2 | a0004 | c0005 | t0001 | g0022 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01261 | hp1 | a0007 | c0007 | t0001 | g0106 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0199 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0217 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01358 | hp1 | a0002 | c0002 | t0004 | g0223 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0207 | EUR | IBS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0046 | EUR | IBS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01928 | hp1 | a0004 | c0005 | t0001 | g0259 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01934 | hp1 | a0004 | c0005 | t0001 | g0024 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0201 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0166 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01978 | hp1 | a0003 | c0004 | t0001 | g0121 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0276 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG01981 | hp2 | a0008 | c0026 | t0001 | g0198 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02004 | hp1 | a0002 | c0021 | t0001 | g0025 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02004 | hp2 | a0001 | c0027 | t0001 | g0185 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02055 | hp1 | a0005 | c0006 | t0001 | g0164 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02083 | hp1 | a0002 | c0024 | t0001 | g0293 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02145 | hp2 | a0001 | c0008 | t0001 | g0086 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02148 | hp1 | a0004 | c0005 | t0001 | g0022 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | CDX | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | CDX | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | CDX | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CDX | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02257 | hp2 | a0001 | c0003 | t0002 | g0047 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0042 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | PEL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02523 | hp2 | a0001 | c0019 | t0001 | g0182 | EAS | KHV | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02572 | hp2 | a0001 | c0012 | t0001 | g0012 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02602 | hp2 | a0007 | c0007 | t0001 | g0100 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02615 | hp1 | a0005 | c0006 | t0001 | g0154 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0126 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02622 | hp2 | a0005 | c0006 | t0001 | g0157 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0088 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02647 | hp2 | a0001 | c0012 | t0001 | g0284 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02683 | hp2 | a0003 | c0004 | t0001 | g0073 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02698 | hp1 | a0003 | c0004 | t0001 | g0261 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0269 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0301 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02723 | hp1 | a0005 | c0006 | t0001 | g0158 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0304 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0214 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02738 | hp1 | a0003 | c0004 | t0001 | g0249 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0281 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02895 | hp1 | a0003 | c0004 | t0001 | g0081 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0034 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0305 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0045 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0036 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0313 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0213 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03098 | hp1 | a0001 | c0003 | t0002 | g0043 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03139 | hp1 | a0001 | c0029 | t0001 | g0035 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03209 | hp1 | a0001 | c0014 | t0001 | g0160 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0048 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0233 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03453 | hp1 | a0005 | c0006 | t0001 | g0156 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0289 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0283 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03491 | hp1 | a0001 | c0009 | t0001 | g0051 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0273 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0039 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0161 | AFR | ESN | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0050 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03540 | hp2 | a0005 | c0006 | t0001 | g0155 | AFR | GWD | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0204 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0312 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03654 | hp1 | a0003 | c0004 | t0001 | g0009 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03669 | hp1 | a0003 | c0013 | t0001 | g0009 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0274 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03688 | hp1 | a0003 | c0004 | t0001 | g0255 | SAS | STU | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03704 | hp2 | a0001 | c0009 | t0001 | g0113 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0260 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03710 | hp2 | a0001 | c0020 | t0001 | g0262 | SAS | PJL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0103 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0186 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03927 | hp2 | a0012 | c0031 | t0001 | g0257 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0082 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0211 | SAS | BEB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG04199 | hp2 | a0003 | c0013 | t0001 | g0064 | SAS | STU | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG04228 | hp2 | a0003 | c0004 | t0001 | g0021 | SAS | STU | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18522 | hp1 | a0001 | c0014 | t0001 | g0128 | AFR | YRI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18522 | hp2 | a0001 | c0003 | t0002 | g0049 | AFR | YRI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0171 | AFR | YRI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18943 | hp2 | a0009 | c0010 | t0001 | g0021 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18951 | hp2 | a0004 | c0005 | t0001 | g0228 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18953 | hp2 | a0003 | c0004 | t0001 | g0296 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18975 | hp1 | a0008 | c0032 | t0001 | g0291 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18983 | hp2 | a0004 | c0005 | t0001 | g0024 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18984 | hp1 | a0003 | c0004 | t0001 | g0069 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18984 | hp2 | a0013 | c0023 | t0001 | g0147 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18995 | hp2 | a0014 | c0016 | t0001 | g0075 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18997 | hp2 | a0009 | c0010 | t0001 | g0111 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19007 | hp2 | a0002 | c0033 | t0001 | g0007 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19030 | hp2 | a0006 | c0011 | t0001 | g0168 | AFR | LWK | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | LWK | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0176 | AFR | LWK | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19074 | hp1 | a0003 | c0004 | t0001 | g0068 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA20129 | hp1 | a0015 | c0015 | t0001 | g0229 | AFR | ASW | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ASW | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0202 | EUR | TSI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | TSI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | TSI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0200 | EUR | TSI | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0302 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02486 | hp1 | a0001 | c0017 | t0001 | g0308 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0165 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG06807 | hp1 | a0001 | c0008 | t0001 | g0085 | AFR | USA | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0195 | AFR | USA | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0173 | AFR | LWK | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | LWK | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| homoSapiens | chm13v2 | a0016 | c0028 | t0001 | g0210 | REF | REF | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0194 | REF | REF | CFAP99_chr4_2413955_2468002 | CFAP99 | chr4 | 2413955 | 2468002 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2436977 | A | G | 1 | a0005 | 6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
missense_variant | MODERATE | c.215A>G | p.Asp72Gly | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/16 | 371/2173 | 215/1941 | 72/646 | chr4 | 2436977 | |||
| chr4:2436982 | C | T | 1 | a0008 | 1 | NA18975.hp1 | stop_gained | HIGH | c.220C>T | p.Arg74* | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/16 | 376/2173 | 220/1941 | 74/646 | chr4 | 2436982 | |||
| chr4:2445166 | T | C | 1 | a0015 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.500T>C | p.Leu167Pro | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/16 | 656/2173 | 500/1941 | 167/646 | chr4 | 2445166 | |||
| chr4:2445228 | A | T | 1 | a0008 | 1 | HG01981.hp2 | stop_gained | HIGH | c.562A>T | p.Lys188* | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/16 | 718/2173 | 562/1941 | 188/646 | chr4 | 2445228 | |||
| chr4:2449967 | C | T | 3 | a0003 a0008 a0012 |
17 | HG01074.hp1 HG01081.hp2 HG01978.hp1 others(14): Show |
missense_variant | MODERATE | c.757C>T | p.Arg253Cys | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/16 | 913/2173 | 757/1941 | 253/646 | chr4 | 2449967 | |||
| chr4:2450973 | G | T | 1 | a0013 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.822G>T | p.Gln274His | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 9/16 | 978/2173 | 822/1941 | 274/646 | chr4 | 2450973 | |||
| chr4:2452155 | G | A | 1 | a0014 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.970G>A | p.Val324Met | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/16 | 1126/2173 | 970/1941 | 324/646 | chr4 | 2452155 | |||
| chr4:2458756 | C | T | 1 | a0011 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1195C>T | p.Arg399Trp | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/16 | 1351/2173 | 1195/1941 | 399/646 | chr4 | 2458756 | |||
| chr4:2458792 | G | C | 1 | a0007 | 2 | HG01261.hp1 HG02602.hp2 |
missense_variant | MODERATE | c.1231G>C | p.Glu411Gln | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/16 | 1387/2173 | 1231/1941 | 411/646 | chr4 | 2458792 | |||
| chr4:2458819 | G | A | 1 | a0004 | 8 | HG01074.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
missense_variant | MODERATE | c.1258G>A | p.Ala420Thr | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/16 | 1414/2173 | 1258/1941 | 420/646 | chr4 | 2458819 | |||
| chr4:2458835 | C | T | 1 | a0006 | 2 | HG01243.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.1274C>T | p.Thr425Met | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/16 | 1430/2173 | 1274/1941 | 425/646 | chr4 | 2458835 | |||
| chr4:2458844 | C | T | 4 | a0002 a0008 a0012 others(1): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
missense_variant | MODERATE | c.1283C>T | p.Ala428Val | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/16 | 1439/2173 | 1283/1941 | 428/646 | chr4 | 2458844 | |||
| chr4:2460115 | C | T | 1 | a0011 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1534C>T | p.Arg512Trp | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/16 | 1690/2173 | 1534/1941 | 512/646 | chr4 | 2460115 | |||
| chr4:2460119 | G | A | 1 | a0010 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.1538G>A | p.Arg513His | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/16 | 1694/2173 | 1538/1941 | 513/646 | chr4 | 2460119 | |||
| chr4:2462501 | G | C | 1 | a0009 | 2 | NA18943.hp2 NA18997.hp2 |
missense_variant | MODERATE | c.1720G>C | p.Val574Leu | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/16 | 1876/2173 | 1720/1941 | 574/646 | chr4 | 2462501 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2426574 | C | T | 1 | a0002c0033 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.99C>T | p.Ala33Ala | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/16 | 255/2173 | 99/1941 | 33/646 | chr4 | 2426574 | |||
| chr4:2436951 | C | T | 1 | a0001c0014 | 2 | HG03209.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.189C>T | p.Val63Val | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/16 | 345/2173 | 189/1941 | 63/646 | chr4 | 2436951 | |||
| chr4:2443204 | A | G | 9 | a0001c0003 a0001c0012 a0001c0014 others(6): Show |
60 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(57): Show |
synonymous_variant | LOW | c.426A>G | p.Pro142Pro | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/16 | 582/2173 | 426/1941 | 142/646 | chr4 | 2443204 | |||
| chr4:2445290 | C | T | 1 | a0001c0025 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.624C>T | p.Val208Val | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/16 | 780/2173 | 624/1941 | 208/646 | chr4 | 2445290 | |||
| chr4:2449963 | A | G | 1 | a0002c0024 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.753A>G | p.Glu251Glu | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/16 | 909/2173 | 753/1941 | 251/646 | chr4 | 2449963 | |||
| chr4:2452298 | G | A | 1 | a0001c0017 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1113G>A | p.Gln371Gln | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/16 | 1269/2173 | 1113/1941 | 371/646 | chr4 | 2452298 | |||
| chr4:2459120 | C | T | 2 | a0001c0020 a0001c0029 |
2 | HG03139.hp1 HG03710.hp2 |
synonymous_variant | LOW | c.1317C>T | p.Ile439Ile | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/16 | 1473/2173 | 1317/1941 | 439/646 | chr4 | 2459120 | |||
| chr4:2459222 | G | A | 1 | a0001c0008 | 2 | HG02145.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.1419G>A | p.Gln473Gln | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/16 | 1575/2173 | 1419/1941 | 473/646 | chr4 | 2459222 | |||
| chr4:2459228 | G | A | 4 | a0001c0009 a0001c0027 a0002c0021 others(1): Show |
17 | HG01074.hp1 HG01081.hp2 HG01978.hp1 others(14): Show |
synonymous_variant | LOW | c.1425G>A | p.Thr475Thr | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/16 | 1581/2173 | 1425/1941 | 475/646 | chr4 | 2459228 | |||
| chr4:2462452 | A | G | 24 | a0001c0001 a0001c0003 a0001c0008 others(21): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
synonymous_variant | LOW | c.1671A>G | p.Glu557Glu | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/16 | 1827/2173 | 1671/1941 | 557/646 | chr4 | 2462452 | |||
| chr4:2462572 | G | T | 1 | a0001c0019 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.1791G>T | p.Val597Val | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/16 | 1947/2173 | 1791/1941 | 597/646 | chr4 | 2462572 | |||
| chr4:2462818 | A | G | 1 | a0002c0022 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.1833A>G | p.Leu611Leu | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 16/16 | 1989/2173 | 1833/1941 | 611/646 | chr4 | 2462818 | |||
| chr4:2462842 | G | A | 1 | a0001c0012 | 2 | HG02572.hp2 HG02647.hp2 |
synonymous_variant | LOW | c.1857G>A | p.Leu619Leu | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 16/16 | 2013/2173 | 1857/1941 | 619/646 | chr4 | 2462842 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2418971 | G | A | 1 | a0002c0002t0004 | 1 | HG01358.hp1 | 5_prime_UTR_variant | MODIFIER | c.-140G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/16 | 7505 | chr4 | 2418971 | ||||||
| chr4:2419004 | G | A | 4 | a0001c0001t0002 a0001c0003t0002 a0002c0002t0002 others(1): Show |
12 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-107G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/16 | 7472 | chr4 | 2419004 | ||||||
| chr4:2419005 | C | A | 1 | a0001c0001t0003 | 2 | HG02896.hp1 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-106C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/16 | 7471 | chr4 | 2419005 | ||||||
| chr4:2462970 | A | C | 1 | a0001c0001t0005 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*44A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 16/16 | 44 | chr4 | 2462970 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2419112 | T | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+19T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419112 | |||||||
| chr4:2419170 | G | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+77G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419170 | |||||||
| chr4:2419195 | T | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+102T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419195 | |||||||
| chr4:2419197 | T | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0003t0001g0034 others(2): Show |
7 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+104T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419197 | |||||||
| chr4:2419240 | CT | C | 18 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0054 others(15): Show |
18 | HG01109.hp2 HG01517.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-18+160delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2419240 | ||||||
| chr4:2419262 | A | G | 1 | a0001c0003t0001g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-18+169A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419262 | |||||||
| chr4:2419264 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-18+171T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419264 | |||||||
| chr4:2419295 | C | A | 1 | a0001c0001t0001g0056 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-18+202C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419295 | |||||||
| chr4:2419314 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-18+221C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419314 | |||||||
| chr4:2419402 | G | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
91 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.-18+309G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419402 | |||||||
| chr4:2419834 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
6 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+741G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419834 | |||||||
| chr4:2419841 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(47): Show |
52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-18+748T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419841 | |||||||
| chr4:2419987 | C | G | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0054 others(10): Show |
15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+894C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2419987 | |||||||
| chr4:2420072 | A | T | 1 | a0002c0002t0001g0303 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-18+979A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420072 | |||||||
| chr4:2420184 | T | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(47): Show |
52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-18+1091T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420184 | |||||||
| chr4:2420238 | G | A | 2 | a0001c0003t0002g0039 a0001c0003t0002g0171 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+1145G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420238 | |||||||
| chr4:2420488 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(47): Show |
52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-18+1395C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420488 | |||||||
| chr4:2420546 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(81): Show |
93 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.-18+1453C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420546 | |||||||
| chr4:2420753 | C | G | 1 | a0002c0002t0001g0123 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-18+1660C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420753 | |||||||
| chr4:2420756 | TA | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0170 others(6): Show |
11 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+1666delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2420756 | ||||||
| chr4:2420817 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-18+1724C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420817 | |||||||
| chr4:2420904 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+1811T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2420904 | |||||||
| chr4:2421006 | T | A | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0054 others(10): Show |
15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+1913T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421006 | |||||||
| chr4:2421082 | A | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+1989A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421082 | |||||||
| chr4:2421099 | C | T | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-18+2006C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421099 | |||||||
| chr4:2421121 | A | C | 1 | a0002c0002t0001g0300 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-18+2028A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421121 | |||||||
| chr4:2421181 | G | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(47): Show |
52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-18+2088G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421181 | |||||||
| chr4:2421349 | C | A | 1 | a0001c0014t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18+2256C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421349 | |||||||
| chr4:2421350 | C | CT | 14 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(11): Show |
14 | HG01074.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-18+2279dupT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421350 | ||||||
| chr4:2421350 | C | CTT | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(115): Show |
129 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-18+2278_-18+2279d others(4): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421350 | ||||||
| chr4:2421350 | C | CTTT | 105 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0116 others(102): Show |
118 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-18+2277_-18+2279d others(5): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421350 | ||||||
| chr4:2421350 | C | CTTTT | 18 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(15): Show |
20 | HG00735.hp2 HG01071.hp1 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+2276_-18+2279d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421350 | ||||||
| chr4:2421377 | T | G | 1 | a0011c0030t0002g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+2284T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421377 | |||||||
| chr4:2421447 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0124 a0001c0001t0001g0125 others(3): Show |
7 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+2354C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421447 | |||||||
| chr4:2421496 | G | A | 5 | a0001c0001t0001g0216 a0002c0002t0001g0003 a0002c0002t0001g0019 others(2): Show |
8 | HG01071.hp2 HG01109.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+2403G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421496 | |||||||
| chr4:2421608 | C | T | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0054 others(10): Show |
15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+2515C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421608 | |||||||
| chr4:2421639 | G | A | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-18+2546G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421639 | |||||||
| chr4:2421725 | GA | G | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0054 others(10): Show |
15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+2639delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421725 | ||||||
| chr4:2421879 | C | CA | 24 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0033 others(21): Show |
27 | HG01081.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-18+2802dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421879 | ||||||
| chr4:2421879 | C | CAA | 31 | a0001c0001t0001g0038 a0001c0001t0001g0124 a0001c0001t0001g0129 others(28): Show |
31 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-18+2801_-18+2802d others(4): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421879 | ||||||
| chr4:2421879 | CA | C | 15 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0054 others(12): Show |
17 | HG01255.hp2 HG01256.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-18+2802delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2421879 | ||||||
| chr4:2421978 | G | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0170 others(14): Show |
19 | HG01243.hp1 HG01884.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18+2885G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2421978 | |||||||
| chr4:2422373 | C | T | 108 | a0001c0001t0001g0023 a0001c0001t0001g0216 a0001c0001t0001g0230 others(105): Show |
123 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-18+3280C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422373 | |||||||
| chr4:2422433 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0003t0001g0034 others(1): Show |
6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+3340G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422433 | |||||||
| chr4:2422470 | C | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(264): Show |
296 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.-18+3377C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422470 | |||||||
| chr4:2422648 | T | C | 113 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0029 others(110): Show |
128 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-18+3555T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422648 | |||||||
| chr4:2422711 | G | T | 6 | a0005c0006t0001g0154 a0005c0006t0001g0155 a0005c0006t0001g0156 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+3618G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422711 | |||||||
| chr4:2422755 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | NA18939.hp1 NA19079.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-18+3662G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422755 | |||||||
| chr4:2422839 | A | G | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-17-3620A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422839 | |||||||
| chr4:2422930 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-17-3529C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422930 | |||||||
| chr4:2422930 | C | T | 1 | a0002c0002t0001g0019 | 2 | HG01071.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-17-3529C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2422930 | |||||||
| chr4:2423007 | G | A | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0054 others(10): Show |
15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-3452G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423007 | |||||||
| chr4:2423257 | C | T | 2 | a0001c0003t0001g0046 a0001c0003t0001g0207 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-17-3202C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423257 | |||||||
| chr4:2423324 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-3135C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423324 | |||||||
| chr4:2423541 | T | G | 1 | a0002c0002t0001g0221 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-17-2918T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423541 | |||||||
| chr4:2423753 | C | T | 3 | a0001c0003t0002g0048 a0001c0003t0002g0049 a0001c0003t0002g0050 |
3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-2706C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423753 | |||||||
| chr4:2423754 | G | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
6 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-2705G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423754 | |||||||
| chr4:2423832 | C | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
116 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-17-2627C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423832 | |||||||
| chr4:2423841 | G | A | 1 | a0002c0002t0001g0222 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-17-2618G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423841 | |||||||
| chr4:2423842 | C | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(265): Show |
297 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.-17-2617C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423842 | |||||||
| chr4:2423907 | C | T | 3 | a0001c0001t0001g0205 a0001c0003t0001g0204 a0001c0029t0001g0035 |
3 | HG02559.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-17-2552C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423907 | |||||||
| chr4:2423967 | G | A | 2 | a0005c0006t0001g0154 a0005c0006t0001g0164 |
2 | HG02055.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-17-2492G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2423967 | |||||||
| chr4:2424013 | G | A | 1 | a0002c0002t0001g0004 | 3 | NA18967.hp1 NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-17-2446G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424013 | |||||||
| chr4:2424228 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(47): Show |
52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-17-2231G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424228 | |||||||
| chr4:2424254 | C | T | 7 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(4): Show |
7 | HG01358.hp2 HG01515.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-2205C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424254 | |||||||
| chr4:2424294 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-17-2165A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424294 | |||||||
| chr4:2424418 | A | G | 10 | a0001c0001t0002g0044 a0001c0003t0002g0039 a0001c0003t0002g0043 others(7): Show |
10 | HG01109.hp2 HG02257.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-2041A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424418 | |||||||
| chr4:2424461 | G | C | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0054 others(10): Show |
15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-1998G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424461 | |||||||
| chr4:2424480 | A | G | 108 | a0001c0001t0001g0023 a0001c0001t0001g0216 a0001c0001t0001g0230 others(105): Show |
123 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-17-1979A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424480 | |||||||
| chr4:2424503 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(47): Show |
52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-17-1956C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424503 | |||||||
| chr4:2424555 | T | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(156): Show |
173 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-17-1904T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424555 | |||||||
| chr4:2424578 | T | C | 5 | a0001c0001t0001g0216 a0002c0002t0001g0003 a0002c0002t0001g0019 others(2): Show |
8 | HG01071.hp2 HG01109.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-1881T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424578 | |||||||
| chr4:2424615 | G | T | 1 | a0002c0002t0001g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17-1844G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424615 | |||||||
| chr4:2424727 | C | T | 2 | a0002c0002t0002g0041 a0002c0002t0002g0042 |
2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-17-1732C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424727 | |||||||
| chr4:2424730 | C | T | 108 | a0001c0001t0001g0023 a0001c0001t0001g0216 a0001c0001t0001g0230 others(105): Show |
123 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-17-1729C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424730 | |||||||
| chr4:2424806 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
6 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-1653C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424806 | |||||||
| chr4:2424811 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-1648C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424811 | |||||||
| chr4:2424884 | G | A | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0054 others(10): Show |
15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-1575G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424884 | |||||||
| chr4:2424915 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-1544C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2424915 | |||||||
| chr4:2425127 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-17-1332C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425127 | |||||||
| chr4:2425167 | T | C | 1 | a0002c0002t0001g0133 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-17-1292T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425167 | |||||||
| chr4:2425193 | G | C | 1 | a0003c0013t0001g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-17-1266G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425193 | |||||||
| chr4:2425381 | T | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(278): Show |
310 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.-17-1078T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425381 | |||||||
| chr4:2425400 | C | T | 6 | a0005c0006t0001g0154 a0005c0006t0001g0155 a0005c0006t0001g0156 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-1059C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425400 | |||||||
| chr4:2425478 | T | G | 37 | a0001c0001t0001g0038 a0001c0001t0001g0129 a0001c0001t0001g0130 others(34): Show |
37 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.-17-981T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425478 | |||||||
| chr4:2425553 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(46): Show |
51 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-17-906T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425553 | |||||||
| chr4:2425663 | C | A | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0054 others(10): Show |
15 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-796C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425663 | |||||||
| chr4:2425672 | G | A | 1 | a0001c0003t0002g0043 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-17-787G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425672 | |||||||
| chr4:2425781 | C | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(43): Show |
48 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-17-678C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425781 | |||||||
| chr4:2425784 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-17-675A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425784 | |||||||
| chr4:2425917 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(35): Show |
42 | HG00673.hp1 HG01074.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.-17-542G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425917 | |||||||
| chr4:2425929 | G | C | 33 | a0001c0001t0001g0038 a0001c0001t0001g0129 a0001c0001t0001g0130 others(30): Show |
33 | HG00609.hp1 HG00621.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.-17-530G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425929 | |||||||
| chr4:2425953 | A | G | 1 | a0002c0002t0001g0290 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-17-506A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2425953 | |||||||
| chr4:2426000 | C | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(6): Show |
11 | HG01069.hp2 HG01071.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-459C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426000 | |||||||
| chr4:2426024 | C | G | 2 | a0005c0006t0001g0157 a0005c0006t0001g0158 |
2 | HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-17-435C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426024 | |||||||
| chr4:2426172 | G | A | 106 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0001g0216 others(103): Show |
121 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.-17-287G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426172 | |||||||
| chr4:2426258 | T | C | 110 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0001g0216 others(107): Show |
125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-17-201T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426258 | |||||||
| chr4:2426295 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0003t0001g0034 others(1): Show |
6 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-164C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426295 | |||||||
| chr4:2426306 | T | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(47): Show |
52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-17-153T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426306 | |||||||
| chr4:2426308 | T | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(47): Show |
52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-17-151T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426308 | |||||||
| chr4:2426309 | AGGCCC | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(47): Show |
52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-17-146_-17-142del others(5): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 2426309 | ||||||
| chr4:2426367 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(45): Show |
50 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.-17-92C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426367 | |||||||
| chr4:2426409 | G | A | 1 | a0002c0002t0004g0223 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-17-50G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 1/15 | chr4 | 2426409 | |||||||
| chr4:2426663 | A | ATGCCTTC others(8): Show |
6 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(3): Show |
8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+87_111+101dupA others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2426663 | ||||||
| chr4:2426736 | G | A | 111 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0001g0174 others(108): Show |
126 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.111+150G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2426736 | |||||||
| chr4:2426805 | G | A | 1 | a0001c0003t0001g0176 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.111+219G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2426805 | |||||||
| chr4:2426810 | C | T | 2 | a0001c0003t0001g0301 a0001c0003t0001g0302 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.111+224C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2426810 | |||||||
| chr4:2426847 | C | G | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+261C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2426847 | |||||||
| chr4:2426877 | C | T | 1 | a0005c0006t0001g0164 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.111+291C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2426877 | |||||||
| chr4:2427008 | G | A | 1 | a0002c0002t0001g0087 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.111+422G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427008 | |||||||
| chr4:2427074 | G | A | 1 | a0011c0030t0002g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.111+488G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427074 | |||||||
| chr4:2427182 | C | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.111+596C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427182 | |||||||
| chr4:2427231 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.111+645C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427231 | |||||||
| chr4:2427258 | T | G | 12 | a0001c0001t0002g0044 a0001c0003t0002g0039 a0001c0003t0002g0043 others(9): Show |
12 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.111+672T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427258 | |||||||
| chr4:2427283 | T | C | 1 | a0002c0002t0001g0224 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.111+697T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427283 | |||||||
| chr4:2427291 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+705C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427291 | |||||||
| chr4:2427295 | A | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(107): Show |
122 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.111+709A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427295 | |||||||
| chr4:2427340 | T | C | 110 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0001g0216 others(107): Show |
125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.111+754T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427340 | |||||||
| chr4:2427378 | A | G | 11 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0028 others(8): Show |
13 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.111+792A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427378 | |||||||
| chr4:2427401 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+815T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427401 | |||||||
| chr4:2427474 | A | C | 116 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(113): Show |
133 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.111+888A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427474 | |||||||
| chr4:2427559 | G | A | 1 | a0006c0011t0001g0168 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.111+973G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427559 | |||||||
| chr4:2427601 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.111+1015G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427601 | |||||||
| chr4:2427621 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0062 |
3 | HG02135.hp1 NA18948.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.111+1035C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427621 | |||||||
| chr4:2427643 | T | C | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+1057T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427643 | |||||||
| chr4:2427691 | A | G | 6 | a0005c0006t0001g0154 a0005c0006t0001g0155 a0005c0006t0001g0156 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+1105A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427691 | |||||||
| chr4:2427728 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(199): Show |
228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.111+1142G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427728 | |||||||
| chr4:2427750 | A | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0026 others(53): Show |
60 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.111+1164A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427750 | |||||||
| chr4:2427887 | C | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+1301C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427887 | |||||||
| chr4:2427907 | C | G | 6 | a0005c0006t0001g0154 a0005c0006t0001g0155 a0005c0006t0001g0156 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+1321C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427907 | |||||||
| chr4:2427927 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(3): Show |
8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+1341G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427927 | |||||||
| chr4:2427968 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+1382G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427968 | |||||||
| chr4:2427974 | G | A | 1 | a0001c0003t0001g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.111+1388G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427974 | |||||||
| chr4:2427996 | G | A | 6 | a0005c0006t0001g0154 a0005c0006t0001g0155 a0005c0006t0001g0156 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+1410G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2427996 | |||||||
| chr4:2428021 | CA | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(3): Show |
8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+1436delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428021 | |||||||
| chr4:2428155 | G | A | 9 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(6): Show |
9 | HG01255.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.111+1569G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428155 | |||||||
| chr4:2428233 | G | A | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+1647G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428233 | |||||||
| chr4:2428432 | C | A | 1 | a0001c0001t0001g0141 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.111+1846C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428432 | |||||||
| chr4:2428434 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+1848G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428434 | |||||||
| chr4:2428442 | C | G | 1 | a0001c0003t0002g0043 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.111+1856C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428442 | |||||||
| chr4:2428508 | A | G | 179 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(176): Show |
197 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.111+1922A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428508 | |||||||
| chr4:2428548 | G | A | 31 | a0001c0001t0001g0038 a0001c0001t0001g0129 a0001c0001t0001g0130 others(28): Show |
31 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.111+1962G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428548 | |||||||
| chr4:2428566 | G | A | 1 | a0002c0002t0001g0225 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.111+1980G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428566 | |||||||
| chr4:2428571 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(266): Show |
297 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.111+1985C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428571 | |||||||
| chr4:2428716 | G | A | 2 | a0001c0001t0001g0292 a0002c0002t0001g0008 |
4 | HG02257.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+2130G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428716 | |||||||
| chr4:2428819 | TCCTC | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+2239_111+2242d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2428819 | ||||||
| chr4:2428898 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.111+2312G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428898 | |||||||
| chr4:2428960 | C | G | 3 | a0001c0003t0002g0048 a0001c0003t0002g0049 a0001c0003t0002g0050 |
3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.111+2374C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428960 | |||||||
| chr4:2428971 | C | T | 1 | a0001c0003t0001g0202 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.111+2385C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428971 | |||||||
| chr4:2428977 | G | A | 2 | a0001c0001t0001g0292 a0002c0002t0001g0008 |
4 | HG02257.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+2391G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2428977 | |||||||
| chr4:2429094 | C | T | 110 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0001g0216 others(107): Show |
125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.111+2508C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429094 | |||||||
| chr4:2429131 | C | T | 1 | a0001c0003t0001g0211 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.111+2545C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429131 | |||||||
| chr4:2429160 | A | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(229): Show |
261 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.111+2574A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429160 | |||||||
| chr4:2429184 | C | A | 1 | a0002c0002t0001g0224 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.111+2598C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429184 | |||||||
| chr4:2429198 | G | A | 1 | a0002c0002t0001g0226 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.111+2612G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429198 | |||||||
| chr4:2429241 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.111+2655C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429241 | |||||||
| chr4:2429300 | C | CA | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(35): Show |
38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+2722dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2429300 | ||||||
| chr4:2429319 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.111+2733A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429319 | |||||||
| chr4:2429338 | G | C | 94 | a0001c0001t0001g0023 a0001c0001t0001g0216 a0001c0001t0001g0230 others(91): Show |
107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.111+2752G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429338 | |||||||
| chr4:2429339 | G | A | 12 | a0001c0001t0002g0044 a0001c0003t0002g0039 a0001c0003t0002g0043 others(9): Show |
12 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.111+2753G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429339 | |||||||
| chr4:2429462 | G | A | 1 | a0002c0002t0001g0227 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.111+2876G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429462 | |||||||
| chr4:2429593 | C | CT | 11 | a0001c0003t0001g0200 a0001c0003t0001g0201 a0001c0003t0002g0039 others(8): Show |
11 | HG01109.hp2 HG01934.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+3023dupT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2429593 | ||||||
| chr4:2429593 | CT | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0170 others(16): Show |
21 | HG01243.hp1 HG01256.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.111+3023delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2429593 | ||||||
| chr4:2429593 | CTT | C | 245 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(242): Show |
272 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.111+3022_111+3023d others(4): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2429593 | ||||||
| chr4:2429593 | CTTT | C | 7 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0306 others(4): Show |
7 | HG02155.hp2 HG03041.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+3021_111+3023d others(5): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2429593 | ||||||
| chr4:2429599 | T | C | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(35): Show |
38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+3013T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429599 | |||||||
| chr4:2429677 | C | T | 12 | a0001c0001t0002g0044 a0001c0003t0002g0039 a0001c0003t0002g0043 others(9): Show |
12 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.111+3091C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429677 | |||||||
| chr4:2429853 | G | A | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(279): Show |
311 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.111+3267G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429853 | |||||||
| chr4:2429917 | A | C | 2 | a0001c0003t0001g0301 a0001c0003t0001g0302 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.111+3331A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429917 | |||||||
| chr4:2429951 | TC | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(35): Show |
38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+3367delC | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2429951 | ||||||
| chr4:2429995 | G | A | 1 | a0001c0003t0002g0043 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.111+3409G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2429995 | |||||||
| chr4:2430062 | A | G | 1 | a0002c0002t0001g0112 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.111+3476A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430062 | |||||||
| chr4:2430062 | ATAAACCA others(245): Show |
A | 1 | a0015c0015t0001g0229 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.111+3495_111+3746d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430062 | ||||||
| chr4:2430081 | G | C | 110 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0001g0216 others(107): Show |
125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.111+3495G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430081 | |||||||
| chr4:2430090 | A | G | 110 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0001g0216 others(107): Show |
125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.111+3504A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430090 | |||||||
| chr4:2430108 | A | G | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(35): Show |
38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+3522A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430108 | |||||||
| chr4:2430125 | ATAAACCA others(182): Show |
A | 107 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0001g0216 others(104): Show |
120 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.111+3602_111+3790d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430125 | ||||||
| chr4:2430152 | C | T | 19 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(16): Show |
21 | HG01243.hp1 HG01884.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.111+3566C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430152 | |||||||
| chr4:2430153 | GGACTGCG others(119): Show |
G | 8 | a0001c0001t0002g0044 a0001c0003t0002g0043 a0001c0003t0002g0045 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+3602_111+3727d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430153 | ||||||
| chr4:2430188 | A | G | 37 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(34): Show |
37 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.111+3602A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430188 | |||||||
| chr4:2430188 | ATAAACCA others(119): Show |
A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(72): Show |
84 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.111+3684_111+3809d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430188 | ||||||
| chr4:2430188 | ATAAACCA others(245): Show |
A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0230 others(13): Show |
20 | HG00544.hp2 HG02055.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.111+3684_111+3935d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430188 | ||||||
| chr4:2430207 | CCGGACAG others(56): Show |
C | 1 | a0002c0002t0001g0133 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.111+3630_111+3692d others(65): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430207 | ||||||
| chr4:2430216 | GGACTGCG others(56): Show |
G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0125 a0001c0003t0001g0126 |
4 | HG02615.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+3684_111+3746d others(65): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430216 | ||||||
| chr4:2430240 | T | C | 6 | a0001c0001t0001g0063 a0001c0001t0001g0095 a0001c0003t0001g0082 others(3): Show |
6 | HG01261.hp1 HG02602.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+3654T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430240 | |||||||
| chr4:2430243 | CGCAATAC others(182): Show |
C | 26 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0063 others(23): Show |
27 | HG00735.hp2 HG01243.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.111+3684_111+3872d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430243 | ||||||
| chr4:2430251 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0067 a0001c0001t0001g0124 others(4): Show |
8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+3665G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430251 | |||||||
| chr4:2430261 | C | T | 33 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(30): Show |
33 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.111+3675C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430261 | |||||||
| chr4:2430270 | G | C | 43 | a0001c0001t0001g0018 a0001c0001t0001g0028 a0001c0001t0001g0029 others(40): Show |
44 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.111+3684G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430270 | |||||||
| chr4:2430279 | A | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0067 a0001c0001t0001g0124 others(4): Show |
8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+3693A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430279 | |||||||
| chr4:2430303 | T | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0067 a0001c0001t0001g0124 others(3): Show |
7 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.111+3717T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430303 | |||||||
| chr4:2430314 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(4): Show |
9 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.111+3728G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430314 | |||||||
| chr4:2430333 | C | G | 8 | a0001c0001t0002g0044 a0001c0003t0002g0043 a0001c0003t0002g0045 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+3747C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430333 | |||||||
| chr4:2430342 | G | A | 8 | a0001c0001t0002g0044 a0001c0003t0002g0043 a0001c0003t0002g0045 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+3756G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430342 | |||||||
| chr4:2430342 | G | GGACTGCG others(56): Show |
1 | a0001c0003t0002g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.111+3809_111+3810i others(65): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430342 | ||||||
| chr4:2430352 | GAAATGCC others(120): Show |
G | 1 | a0001c0001t0001g0067 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.111+3769_111+3895d others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430352 | ||||||
| chr4:2430366 | T | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(3): Show |
8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+3780T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430366 | |||||||
| chr4:2430369 | CGCAATAC others(56): Show |
C | 1 | a0001c0001t0001g0140 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.111+3846_111+3908d others(65): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2430369 | ||||||
| chr4:2430377 | G | A | 253 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.111+3791G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430377 | |||||||
| chr4:2430396 | C | G | 1 | a0011c0030t0002g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.111+3810C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430396 | |||||||
| chr4:2430405 | G | A | 1 | a0011c0030t0002g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.111+3819G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430405 | |||||||
| chr4:2430429 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(179): Show |
204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.111+3843T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430429 | |||||||
| chr4:2430432 | T | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(223): Show |
250 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.111+3846T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430432 | |||||||
| chr4:2430440 | G | A | 16 | a0001c0001t0001g0027 a0001c0001t0001g0122 a0001c0001t0001g0140 others(13): Show |
17 | HG00609.hp1 HG00735.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.111+3854G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430440 | |||||||
| chr4:2430450 | C | G | 37 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(34): Show |
37 | HG00621.hp2 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.111+3864C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430450 | |||||||
| chr4:2430461 | G | A | 39 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(36): Show |
39 | HG00621.hp2 HG00738.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.111+3875G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430461 | |||||||
| chr4:2430492 | T | C | 19 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0122 others(16): Show |
22 | HG00544.hp2 HG00735.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.111+3906T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430492 | |||||||
| chr4:2430503 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(49): Show |
54 | HG00621.hp2 HG00738.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.111+3917G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430503 | |||||||
| chr4:2430576 | T | C | 5 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0002c0002t0001g0004 others(2): Show |
7 | HG00544.hp2 HG02080.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.111+3990T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430576 | |||||||
| chr4:2430594 | A | G | 4 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0002c0002t0001g0226 others(1): Show |
4 | HG00544.hp2 HG02080.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+4008A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430594 | |||||||
| chr4:2430642 | A | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(113): Show |
128 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.111+4056A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430642 | |||||||
| chr4:2430674 | G | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(35): Show |
38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+4088G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430674 | |||||||
| chr4:2430697 | C | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(35): Show |
38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.111+4111C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430697 | |||||||
| chr4:2430787 | A | T | 1 | a0001c0001t0001g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.111+4201A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430787 | |||||||
| chr4:2430828 | G | T | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(278): Show |
310 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.111+4242G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430828 | |||||||
| chr4:2430934 | A | C | 1 | a0001c0003t0002g0043 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.111+4348A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2430934 | |||||||
| chr4:2431006 | A | G | 1 | a0001c0003t0001g0204 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.111+4420A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431006 | |||||||
| chr4:2431055 | G | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(211): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.111+4469G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431055 | |||||||
| chr4:2431091 | G | A | 4 | a0002c0002t0001g0212 a0002c0002t0001g0233 a0002c0002t0001g0234 others(1): Show |
4 | HG00738.hp1 HG01069.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+4505G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431091 | |||||||
| chr4:2431134 | C | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(95): Show |
108 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.111+4548C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431134 | |||||||
| chr4:2431296 | G | C | 15 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0002c0002t0001g0005 others(12): Show |
17 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.111+4710G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431296 | |||||||
| chr4:2431316 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(266): Show |
298 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.111+4730T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431316 | |||||||
| chr4:2431331 | G | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(266): Show |
298 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.111+4745G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431331 | |||||||
| chr4:2431368 | C | CA | 203 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(200): Show |
229 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.111+4794dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2431368 | ||||||
| chr4:2431368 | C | CAAAA | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+4791_111+4794d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2431368 | ||||||
| chr4:2431472 | A | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(266): Show |
298 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.111+4886A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431472 | |||||||
| chr4:2431554 | A | G | 116 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(113): Show |
133 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.111+4968A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431554 | |||||||
| chr4:2431574 | A | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0170 others(6): Show |
11 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+4988A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431574 | |||||||
| chr4:2431676 | C | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(3): Show |
8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+5090C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431676 | |||||||
| chr4:2431699 | A | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+5113A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431699 | |||||||
| chr4:2431744 | A | AT | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-5118dupT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2431744 | ||||||
| chr4:2431744 | AT | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0028 others(162): Show |
182 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.112-5118delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2431744 | ||||||
| chr4:2431765 | C | T | 110 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0001g0216 others(107): Show |
125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.112-5109C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431765 | |||||||
| chr4:2431790 | C | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-5084C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431790 | |||||||
| chr4:2431804 | C | G | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.112-5070C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431804 | |||||||
| chr4:2431821 | A | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-5053A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431821 | |||||||
| chr4:2431848 | C | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(35): Show |
38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.112-5026C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431848 | |||||||
| chr4:2431970 | G | A | 2 | a0001c0008t0001g0085 a0001c0008t0001g0086 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.112-4904G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431970 | |||||||
| chr4:2431973 | C | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-4901C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2431973 | |||||||
| chr4:2432192 | C | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-4682C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2432192 | |||||||
| chr4:2432368 | G | A | 2 | a0002c0002t0001g0212 a0002c0002t0001g0233 |
2 | HG01069.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.112-4506G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2432368 | |||||||
| chr4:2432479 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.112-4395T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2432479 | |||||||
| chr4:2432585 | C | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-4289C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2432585 | |||||||
| chr4:2432821 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(266): Show |
298 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.112-4053T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2432821 | |||||||
| chr4:2432981 | CCCCCAGG | C | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-3881_112-3875d others(9): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2432981 | ||||||
| chr4:2433038 | C | T | 5 | a0001c0001t0001g0216 a0002c0002t0001g0003 a0002c0002t0001g0019 others(2): Show |
8 | HG01071.hp2 HG01109.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-3836C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433038 | |||||||
| chr4:2433061 | G | A | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.112-3813G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433061 | |||||||
| chr4:2433062 | G | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(35): Show |
38 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.112-3812G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433062 | |||||||
| chr4:2433079 | G | A | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-3795G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433079 | |||||||
| chr4:2433118 | CCTCA | C | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-3751_112-3748d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2433118 | ||||||
| chr4:2433176 | G | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0203 |
2 | HG01358.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.112-3698G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433176 | |||||||
| chr4:2433309 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.112-3565G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433309 | |||||||
| chr4:2433351 | C | T | 1 | a0001c0003t0002g0043 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.112-3523C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433351 | |||||||
| chr4:2433427 | C | CG | 33 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0083 others(30): Show |
34 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.112-3438dupG | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2433427 | ||||||
| chr4:2433427 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0067 |
2 | NA18986.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.112-3447C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433427 | |||||||
| chr4:2433434 | G | C | 10 | a0001c0001t0001g0063 a0001c0001t0001g0091 a0001c0001t0001g0092 others(7): Show |
11 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.112-3440G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433434 | |||||||
| chr4:2433437 | A | C | 1 | a0002c0002t0001g0162 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.112-3437A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433437 | |||||||
| chr4:2433628 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-3246C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433628 | |||||||
| chr4:2433705 | A | G | 2 | a0001c0001t0003g0305 a0001c0001t0003g0313 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.112-3169A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433705 | |||||||
| chr4:2433717 | A | G | 1 | a0002c0002t0001g0274 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.112-3157A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433717 | |||||||
| chr4:2433803 | T | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(275): Show |
305 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.112-3071T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433803 | |||||||
| chr4:2433822 | G | T | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.112-3052G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433822 | |||||||
| chr4:2433875 | G | A | 2 | a0001c0014t0001g0128 a0001c0014t0001g0160 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.112-2999G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433875 | |||||||
| chr4:2433889 | G | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(204): Show |
232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.112-2985G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433889 | |||||||
| chr4:2433904 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
290 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.112-2970T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433904 | |||||||
| chr4:2433942 | G | A | 1 | a0001c0003t0001g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.112-2932G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433942 | |||||||
| chr4:2433951 | G | A | 1 | a0001c0003t0002g0045 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.112-2923G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2433951 | |||||||
| chr4:2434099 | G | A | 1 | a0002c0002t0001g0244 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.112-2775G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434099 | |||||||
| chr4:2434254 | G | A | 37 | a0001c0001t0001g0038 a0001c0001t0001g0129 a0001c0001t0001g0130 others(34): Show |
37 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.112-2620G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434254 | |||||||
| chr4:2434315 | C | A | 110 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0001g0216 others(107): Show |
125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.112-2559C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434315 | |||||||
| chr4:2434337 | C | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0003t0001g0034 others(10): Show |
15 | HG01975.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.112-2537C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434337 | |||||||
| chr4:2434443 | G | A | 1 | a0002c0002t0001g0245 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.112-2431G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434443 | |||||||
| chr4:2434530 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(265): Show |
295 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.112-2344G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434530 | |||||||
| chr4:2434644 | G | A | 18 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(15): Show |
20 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.112-2230G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434644 | |||||||
| chr4:2434655 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.112-2219G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434655 | |||||||
| chr4:2434715 | G | A | 1 | a0001c0001t0005g0307 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.112-2159G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434715 | |||||||
| chr4:2434726 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(247): Show |
275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.112-2148T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2434726 | |||||||
| chr4:2435059 | G | A | 2 | a0006c0011t0001g0168 a0006c0011t0001g0169 |
2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.112-1815G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435059 | |||||||
| chr4:2435188 | T | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0003t0001g0034 others(10): Show |
15 | HG01975.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.112-1686T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435188 | |||||||
| chr4:2435261 | C | T | 4 | a0001c0001t0001g0170 a0001c0001t0001g0314 a0006c0011t0001g0168 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-1613C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435261 | |||||||
| chr4:2435298 | G | GA | 25 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0027 others(22): Show |
28 | HG00735.hp1 HG01255.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.112-1559dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435298 | ||||||
| chr4:2435298 | GA | G | 6 | a0001c0001t0001g0060 a0001c0003t0002g0045 a0002c0002t0001g0052 others(3): Show |
6 | HG01256.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-1559delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435298 | ||||||
| chr4:2435299 | A | G | 4 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(1): Show |
4 | HG01891.hp2 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-1575A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435299 | |||||||
| chr4:2435470 | A | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0003t0001g0034 others(10): Show |
15 | HG01975.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.112-1404A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435470 | |||||||
| chr4:2435503 | A | C | 2 | a0002c0002t0001g0273 a0015c0015t0001g0229 |
2 | HG03492.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.112-1371A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435503 | |||||||
| chr4:2435563 | G | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(192): Show |
219 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.112-1311G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435563 | |||||||
| chr4:2435661 | C | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-1213C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435661 | |||||||
| chr4:2435725 | G | T | 1 | a0001c0014t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-1149G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435725 | |||||||
| chr4:2435807 | C | CCAGCTAC others(20): Show |
1 | a0002c0002t0001g0162 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.112-1043_112-1042i others(29): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435807 | ||||||
| chr4:2435807 | CCAGCTAC others(21): Show |
C | 1 | a0002c0002t0001g0214 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.112-1013_112-986de others(29): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435807 | ||||||
| chr4:2435833 | A | AAGCAGCT others(49): Show |
1 | a0002c0002t0001g0007 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.112-1014_112-1013i others(58): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435833 | ||||||
| chr4:2435833 | A | AAGCAGCT others(77): Show |
37 | a0001c0001t0001g0270 a0001c0001t0001g0287 a0001c0001t0001g0288 others(34): Show |
38 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.112-1014_112-1013i others(86): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435833 | ||||||
| chr4:2435833 | A | AAGCAGCT others(105): Show |
3 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0083 |
3 | NA18964.hp1 NA18971.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.112-1014_112-1013i others(114): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435833 | ||||||
| chr4:2435861 | A | AAGCAGCT others(161): Show |
7 | a0001c0001t0001g0027 a0001c0001t0001g0310 a0001c0001t0001g0311 others(4): Show |
8 | HG02559.hp1 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-986_112-985ins others(168): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | ||||||
| chr4:2435861 | A | AAGCAGCT others(273): Show |
3 | a0001c0001t0001g0054 a0001c0001t0001g0309 a0001c0017t0001g0308 |
3 | HG02451.hp1 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.112-986_112-985ins others(280): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | ||||||
| chr4:2435861 | A | AAGCAGCT others(273): Show |
3 | a0001c0001t0001g0205 a0001c0001t0001g0306 a0001c0001t0005g0307 |
3 | HG01255.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.112-986_112-985ins others(280): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | ||||||
| chr4:2435861 | A | AAGCAGCT others(49): Show |
46 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(43): Show |
48 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.112-986_112-985ins others(56): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | ||||||
| chr4:2435861 | A | AAGCAGCT others(77): Show |
1 | a0001c0029t0001g0035 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.112-986_112-985ins others(84): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | ||||||
| chr4:2435861 | A | AAGCAGCT others(105): Show |
5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-986_112-985ins others(112): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | ||||||
| chr4:2435861 | A | AAGCAGCT others(21): Show |
18 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(15): Show |
20 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.112-901_112-874dup others(28): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | ||||||
| chr4:2435861 | A | AAGCAGCT others(105): Show |
28 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(25): Show |
30 | HG00099.hp1 HG00280.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.112-985_112-874dup others(112): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | ||||||
| chr4:2435861 | A | AAGCAGCT others(161): Show |
4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0003t0001g0012 others(1): Show |
4 | HG01884.hp2 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-874_112-873ins others(168): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435861 | ||||||
| chr4:2435861 | A | G | 113 | a0001c0001t0001g0023 a0001c0001t0001g0059 a0001c0001t0001g0079 others(110): Show |
128 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.112-1013A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435861 | |||||||
| chr4:2435883 | G | GGTGGGGA others(77): Show |
1 | a0001c0001t0001g0247 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.112-908_112-907ins others(84): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435883 | ||||||
| chr4:2435992 | C | CGAGGTGG others(104): Show |
1 | a0001c0001t0001g0060 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.112-874_112-873ins others(111): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | ||||||
| chr4:2435992 | C | CGAGGTGG others(161): Show |
9 | a0001c0001t0001g0063 a0001c0001t0001g0093 a0001c0001t0001g0094 others(6): Show |
9 | HG01074.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.112-874_112-873ins others(168): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | ||||||
| chr4:2435992 | C | CGAGGTGG others(105): Show |
45 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
48 | HG00408.hp1 HG00673.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.112-874_112-873ins others(112): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | ||||||
| chr4:2435992 | C | CGAGGTGG others(77): Show |
68 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0001g0216 others(65): Show |
81 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.112-874_112-873ins others(84): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | ||||||
| chr4:2435992 | C | CGAGGTGG others(179): Show |
4 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0002c0002t0001g0226 others(1): Show |
4 | HG00544.hp2 HG02080.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-874_112-873ins others(186): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | ||||||
| chr4:2435992 | C | CGAGGTGG others(49): Show |
1 | a0002c0002t0001g0263 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.112-874_112-873ins others(56): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | ||||||
| chr4:2435992 | C | CGAGGTGG others(21): Show |
1 | a0002c0002t0001g0162 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.112-874_112-873ins others(28): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2435992 | ||||||
| chr4:2435992 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(136): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.112-882C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2435992 | |||||||
| chr4:2436044 | G | A | 1 | a0001c0003t0001g0204 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.112-830G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436044 | |||||||
| chr4:2436080 | TCA | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-793_112-792del others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436080 | |||||||
| chr4:2436081 | CA | C | 14 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0089 others(11): Show |
16 | HG01516.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.112-779delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2436081 | ||||||
| chr4:2436081 | CAA | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(93): Show |
106 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.112-780_112-779del others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2436081 | ||||||
| chr4:2436116 | GAT | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0038 others(47): Show |
52 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112-750_112-749del others(2): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2436116 | ||||||
| chr4:2436124 | T | C | 1 | a0002c0002t0001g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.112-750T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436124 | |||||||
| chr4:2436165 | T | G | 4 | a0002c0002t0001g0280 a0002c0002t0001g0282 a0002c0002t0001g0285 others(1): Show |
4 | HG00673.hp2 HG02015.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-709T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436165 | |||||||
| chr4:2436251 | G | A | 1 | a0002c0002t0001g0224 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.112-623G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436251 | |||||||
| chr4:2436271 | C | T | 1 | a0002c0002t0001g0239 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.112-603C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436271 | |||||||
| chr4:2436299 | G | A | 1 | a0002c0002t0001g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.112-575G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436299 | |||||||
| chr4:2436300 | C | T | 1 | a0002c0002t0001g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.112-574C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436300 | |||||||
| chr4:2436634 | ACTGCCTC others(5): Show |
A | 1 | a0001c0001t0001g0067 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.112-237_112-226del others(12): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2436634 | ||||||
| chr4:2436639 | CTCA | C | 110 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0001g0216 others(107): Show |
125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.112-229_112-227del others(3): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 2436639 | ||||||
| chr4:2436650 | C | T | 1 | a0002c0002t0001g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.112-224C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436650 | |||||||
| chr4:2436765 | T | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(280): Show |
312 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.112-109T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436765 | |||||||
| chr4:2436856 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.112-18C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436856 | |||||||
| chr4:2436861 | G | C | 1 | a0003c0004t0001g0068 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.112-13G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 2/15 | chr4 | 2436861 | |||||||
| chr4:2437202 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0023 others(194): Show |
217 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.256+184T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437202 | |||||||
| chr4:2437550 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.257-520G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437550 | |||||||
| chr4:2437607 | C | T | 2 | a0001c0014t0001g0128 a0001c0014t0001g0160 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.257-463C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437607 | |||||||
| chr4:2437672 | C | T | 1 | a0001c0020t0001g0262 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.257-398C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437672 | |||||||
| chr4:2437696 | C | T | 1 | a0001c0001t0005g0307 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.257-374C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437696 | |||||||
| chr4:2437943 | A | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(279): Show |
311 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.257-127A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437943 | |||||||
| chr4:2437974 | G | A | 37 | a0001c0001t0001g0038 a0001c0001t0001g0129 a0001c0001t0001g0130 others(34): Show |
37 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.257-96G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437974 | |||||||
| chr4:2437999 | G | A | 1 | a0001c0029t0001g0035 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.257-71G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2437999 | |||||||
| chr4:2438011 | G | A | 128 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(125): Show |
145 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.257-59G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2438011 | |||||||
| chr4:2438018 | G | C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(15): Show |
20 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.257-52G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2438018 | |||||||
| chr4:2438029 | C | CT | 159 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0038 others(156): Show |
175 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.257-41_257-40insT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 3/15 | chr4 | 2438029 | |||||||
| chr4:2438173 | C | A | 128 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(125): Show |
144 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.351+9C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438173 | |||||||
| chr4:2438205 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(88): Show |
100 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.351+41G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438205 | |||||||
| chr4:2438226 | C | T | 6 | a0001c0001t0001g0054 a0001c0001t0001g0205 a0001c0001t0001g0306 others(3): Show |
6 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+62C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438226 | |||||||
| chr4:2438238 | G | C | 110 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0001g0216 others(107): Show |
125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.351+74G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438238 | |||||||
| chr4:2438294 | A | G | 163 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(160): Show |
180 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.351+130A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438294 | |||||||
| chr4:2438315 | G | T | 35 | a0001c0001t0001g0038 a0001c0001t0001g0129 a0001c0001t0001g0130 others(32): Show |
35 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.351+151G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438315 | |||||||
| chr4:2438324 | G | A | 31 | a0001c0001t0001g0038 a0001c0001t0001g0129 a0001c0001t0001g0130 others(28): Show |
31 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.351+160G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438324 | |||||||
| chr4:2438344 | A | G | 18 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(15): Show |
19 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.351+180A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438344 | |||||||
| chr4:2438348 | T | C | 128 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(125): Show |
144 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.351+184T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438348 | |||||||
| chr4:2438363 | T | C | 18 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(15): Show |
19 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.351+199T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438363 | |||||||
| chr4:2438364 | A | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(15): Show |
20 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.351+200A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438364 | |||||||
| chr4:2438408 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(3): Show |
8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+244G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438408 | |||||||
| chr4:2438408 | G | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(96): Show |
110 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.351+244G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438408 | |||||||
| chr4:2438420 | A | G | 18 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(15): Show |
19 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.351+256A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438420 | |||||||
| chr4:2438424 | G | A | 18 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(15): Show |
19 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.351+260G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438424 | |||||||
| chr4:2438508 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.351+344C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438508 | |||||||
| chr4:2438533 | G | A | 165 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(162): Show |
181 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.351+369G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438533 | |||||||
| chr4:2438542 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
95 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.351+378G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438542 | |||||||
| chr4:2438553 | C | T | 2 | a0002c0002t0002g0041 a0002c0002t0002g0042 |
2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.351+389C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438553 | |||||||
| chr4:2438797 | C | A | 51 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0038 others(48): Show |
53 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.351+633C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438797 | |||||||
| chr4:2438806 | C | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(10): Show |
14 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.351+642C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438806 | |||||||
| chr4:2438897 | A | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(101): Show |
115 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.351+733A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438897 | |||||||
| chr4:2438902 | G | A | 18 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(15): Show |
20 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.351+738G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438902 | |||||||
| chr4:2438943 | T | G | 1 | a0002c0002t0001g0264 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.351+779T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438943 | |||||||
| chr4:2438986 | C | T | 12 | a0001c0001t0002g0044 a0001c0003t0002g0039 a0001c0003t0002g0043 others(9): Show |
12 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.351+822C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2438986 | |||||||
| chr4:2439010 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0003t0001g0034 others(2): Show |
7 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+846C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439010 | |||||||
| chr4:2439011 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+847G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439011 | |||||||
| chr4:2439091 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0028 others(162): Show |
182 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.351+927T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439091 | |||||||
| chr4:2439194 | A | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0138 a0001c0001t0001g0140 others(1): Show |
4 | HG00609.hp1 HG00621.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+1030A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439194 | |||||||
| chr4:2439255 | G | A | 1 | a0001c0003t0001g0176 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.351+1091G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439255 | |||||||
| chr4:2439591 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.351+1427G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439591 | |||||||
| chr4:2439596 | C | T | 12 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0205 others(9): Show |
13 | HG01255.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.351+1432C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439596 | |||||||
| chr4:2439771 | C | A | 1 | a0001c0001t0001g0067 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.351+1607C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439771 | |||||||
| chr4:2439773 | A | C | 1 | a0001c0001t0001g0067 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.351+1609A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439773 | |||||||
| chr4:2439847 | AT | A | 12 | a0001c0001t0001g0091 a0001c0001t0001g0203 a0001c0001t0001g0218 others(9): Show |
12 | HG01074.hp2 HG02083.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.351+1697delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2439847 | ||||||
| chr4:2439867 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0003t0001g0034 others(10): Show |
15 | HG01975.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.351+1703G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439867 | |||||||
| chr4:2439889 | G | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(116): Show |
131 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.351+1725G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439889 | |||||||
| chr4:2439893 | G | A | 1 | a0001c0001t0001g0001 | 3 | HG02258.hp1 HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.351+1729G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439893 | |||||||
| chr4:2439912 | C | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0310 a0001c0001t0001g0311 others(4): Show |
8 | HG02559.hp1 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+1748C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439912 | |||||||
| chr4:2439975 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.351+1811C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439975 | |||||||
| chr4:2439998 | A | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0003t0001g0034 others(10): Show |
15 | HG01975.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.351+1834A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2439998 | |||||||
| chr4:2440062 | G | A | 1 | a0005c0006t0001g0157 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.351+1898G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440062 | |||||||
| chr4:2440134 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.351+1970G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440134 | |||||||
| chr4:2440149 | C | CT | 8 | a0001c0001t0001g0130 a0001c0001t0001g0137 a0002c0002t0001g0232 others(5): Show |
8 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2000dupT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | ||||||
| chr4:2440149 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0054 a0001c0001t0003g0305 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.351+1990_351+2000d others(13): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | ||||||
| chr4:2440149 | C | CTTTTTTT others(5): Show |
9 | a0001c0001t0001g0027 a0001c0001t0001g0205 a0001c0001t0001g0306 others(6): Show |
10 | HG02486.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.351+1989_351+2000d others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | ||||||
| chr4:2440149 | C | CTTTTTTT others(6): Show |
6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+1988_351+2000d others(15): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | ||||||
| chr4:2440149 | C | CTTTTTTT others(7): Show |
7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0003t0002g0039 others(4): Show |
7 | HG01109.hp2 HG01891.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+1987_351+2000d others(16): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | ||||||
| chr4:2440149 | C | CTTTTTTT others(8): Show |
10 | a0001c0001t0001g0070 a0001c0003t0001g0176 a0001c0003t0002g0043 others(7): Show |
10 | HG00673.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.351+1986_351+2000d others(17): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | ||||||
| chr4:2440149 | C | CTTTTTTT others(9): Show |
62 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(59): Show |
70 | HG00280.hp1 HG00408.hp1 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.351+2000_351+2001i others(18): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | ||||||
| chr4:2440149 | C | CTTTTTTT others(10): Show |
26 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0055 others(23): Show |
29 | HG00099.hp1 HG00735.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.351+2000_351+2001i others(19): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | ||||||
| chr4:2440149 | C | CTTTTTTT others(11): Show |
2 | a0001c0003t0001g0088 a0001c0008t0001g0086 |
2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.351+2000_351+2001i others(20): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | ||||||
| chr4:2440149 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0067 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.351+2000_351+2001i others(21): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2440149 | ||||||
| chr4:2440177 | C | T | 1 | a0002c0002t0001g0234 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.351+2013C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440177 | |||||||
| chr4:2440178 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(117): Show |
132 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.351+2014G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440178 | |||||||
| chr4:2440208 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(117): Show |
132 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.351+2044A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440208 | |||||||
| chr4:2440239 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0108 |
2 | HG00673.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.351+2075C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440239 | |||||||
| chr4:2440247 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(115): Show |
130 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.351+2083C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440247 | |||||||
| chr4:2440290 | G | A | 5 | a0001c0001t0001g0216 a0002c0002t0001g0003 a0002c0002t0001g0019 others(2): Show |
8 | HG01071.hp2 HG01109.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+2126G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440290 | |||||||
| chr4:2440307 | C | T | 1 | a0001c0003t0001g0202 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.351+2143C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440307 | |||||||
| chr4:2440336 | C | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(118): Show |
133 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.351+2172C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440336 | |||||||
| chr4:2440438 | G | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0003t0001g0034 others(2): Show |
7 | HG02258.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+2274G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440438 | |||||||
| chr4:2440565 | G | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(117): Show |
132 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.351+2401G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440565 | |||||||
| chr4:2440627 | C | T | 1 | a0002c0002t0001g0264 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.351+2463C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2440627 | |||||||
| chr4:2441011 | T | C | 3 | a0001c0001t0002g0044 a0001c0003t0002g0045 a0001c0003t0002g0047 |
3 | HG02257.hp2 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.352-2119T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441011 | |||||||
| chr4:2441196 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0124 a0001c0001t0001g0127 |
4 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-1934C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441196 | |||||||
| chr4:2441243 | C | T | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.352-1887C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441243 | |||||||
| chr4:2441273 | T | C | 2 | a0001c0014t0001g0128 a0001c0014t0001g0160 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.352-1857T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441273 | |||||||
| chr4:2441330 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.352-1800G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441330 | |||||||
| chr4:2441359 | C | T | 2 | a0001c0014t0001g0128 a0001c0014t0001g0160 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.352-1771C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441359 | |||||||
| chr4:2441372 | C | CA | 149 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0026 others(146): Show |
168 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.352-1739dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2441372 | ||||||
| chr4:2441372 | CA | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
111 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.352-1739delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2441372 | ||||||
| chr4:2441477 | C | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0037 others(7): Show |
13 | HG02135.hp1 HG02155.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.352-1653C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441477 | |||||||
| chr4:2441478 | C | G | 5 | a0001c0001t0001g0216 a0002c0002t0001g0003 a0002c0002t0001g0019 others(2): Show |
8 | HG01071.hp2 HG01109.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-1652C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441478 | |||||||
| chr4:2441520 | G | A | 1 | a0001c0003t0001g0176 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.352-1610G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441520 | |||||||
| chr4:2441558 | C | T | 2 | a0001c0001t0002g0044 a0001c0003t0002g0045 |
2 | HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.352-1572C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441558 | |||||||
| chr4:2441644 | C | T | 6 | a0001c0001t0002g0044 a0001c0003t0002g0039 a0001c0003t0002g0045 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.352-1486C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441644 | |||||||
| chr4:2441862 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.352-1268C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441862 | |||||||
| chr4:2441894 | G | T | 1 | a0002c0002t0001g0298 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.352-1236G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441894 | |||||||
| chr4:2441916 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.352-1214G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2441916 | |||||||
| chr4:2442002 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.352-1128G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442002 | |||||||
| chr4:2442374 | G | A | 1 | a0001c0027t0001g0185 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.352-756G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442374 | |||||||
| chr4:2442425 | G | A | 1 | a0003c0004t0001g0249 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.352-705G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442425 | |||||||
| chr4:2442453 | A | T | 1 | a0001c0003t0002g0043 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.352-677A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442453 | |||||||
| chr4:2442459 | G | A | 2 | a0002c0002t0001g0250 a0002c0002t0001g0303 |
2 | NA18944.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.352-671G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442459 | |||||||
| chr4:2442467 | G | A | 1 | a0001c0003t0001g0186 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.352-663G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442467 | |||||||
| chr4:2442639 | G | A | 1 | a0007c0007t0001g0100 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.352-491G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442639 | |||||||
| chr4:2442670 | G | T | 1 | a0014c0016t0001g0075 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.352-460G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442670 | |||||||
| chr4:2442682 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0172 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.352-448G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442682 | |||||||
| chr4:2442861 | TGGCCTTG others(161): Show |
T | 2 | a0001c0003t0001g0301 a0001c0003t0001g0302 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.352-231_352-64del | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442861 | ||||||
| chr4:2442881 | TCACTGGG others(59): Show |
T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(217): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.352-138_352-73delT others(65): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442881 | ||||||
| chr4:2442881 | TCACTGGG others(125): Show |
T | 8 | a0001c0001t0001g0063 a0001c0001t0001g0091 a0001c0001t0001g0092 others(5): Show |
8 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-204_352-73del | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442881 | ||||||
| chr4:2442908 | G | A | 1 | a0001c0003t0001g0071 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.352-222G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442908 | |||||||
| chr4:2442917 | TCACTGGG others(23): Show |
T | 2 | a0001c0003t0001g0176 a0001c0029t0001g0035 |
2 | HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.352-204_352-175del others(30): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442917 | ||||||
| chr4:2442922 | GGGGTGCT others(58): Show |
G | 16 | a0001c0003t0001g0046 a0001c0003t0001g0071 a0001c0003t0001g0082 others(13): Show |
16 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.352-204_352-140del others(65): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442922 | ||||||
| chr4:2442934 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.352-196G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442934 | |||||||
| chr4:2442947 | C | CCACTGGG others(334): Show |
1 | a0002c0002t0001g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.352-66_352-65insTG others(339): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442947 | ||||||
| chr4:2442954 | G | A | 1 | a0001c0012t0001g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.352-176G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442954 | |||||||
| chr4:2442962 | G | A | 1 | a0001c0003t0002g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.352-168G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2442962 | |||||||
| chr4:2442983 | TCACTGGG others(23): Show |
T | 1 | a0001c0003t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-138_352-109del others(30): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2442983 | ||||||
| chr4:2443007 | G | GGGCAGGG others(176): Show |
1 | a0001c0001t0001g0031 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.352-121_352-120ins others(183): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2443007 | ||||||
| chr4:2443013 | C | CT | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.352-117_352-116ins others(1): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | chr4 | 2443013 | |||||||
| chr4:2443018 | G | GGGGGTGC others(64): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0032 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.352-64_352-63insGC others(69): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 2443018 | ||||||
| chr4:2443259 | G | A | 1 | a0001c0003t0001g0202 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.464+17G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443259 | |||||||
| chr4:2443291 | A | G | 7 | a0002c0002t0001g0225 a0002c0002t0001g0238 a0002c0002t0001g0258 others(4): Show |
7 | HG00438.hp1 HG00597.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.464+49A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443291 | |||||||
| chr4:2443308 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.464+66G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443308 | |||||||
| chr4:2443440 | A | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(120): Show |
135 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.464+198A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443440 | |||||||
| chr4:2443505 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
74 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.464+263C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443505 | |||||||
| chr4:2443555 | G | A | 1 | a0002c0024t0001g0293 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.464+313G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443555 | |||||||
| chr4:2443661 | G | A | 15 | a0001c0001t0001g0001 a0001c0003t0001g0034 a0001c0003t0001g0036 others(12): Show |
17 | HG02257.hp2 HG02258.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.464+419G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443661 | |||||||
| chr4:2443676 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0124 a0001c0001t0001g0127 |
4 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+434G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443676 | |||||||
| chr4:2443848 | A | G | 22 | a0001c0001t0001g0033 a0001c0001t0001g0172 a0001c0003t0001g0046 others(19): Show |
22 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.464+606A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443848 | |||||||
| chr4:2443902 | G | A | 2 | a0001c0008t0001g0085 a0001c0008t0001g0086 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.464+660G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2443902 | |||||||
| chr4:2444180 | C | A | 2 | a0006c0011t0001g0168 a0006c0011t0001g0169 |
2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.464+938C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444180 | |||||||
| chr4:2444385 | A | G | 1 | a0001c0012t0001g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.465-746A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444385 | |||||||
| chr4:2444388 | G | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0124 a0001c0001t0001g0127 |
4 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.465-743G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444388 | |||||||
| chr4:2444403 | C | T | 3 | a0001c0001t0001g0096 a0001c0003t0001g0204 a0001c0012t0001g0284 |
3 | HG02647.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.465-728C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444403 | |||||||
| chr4:2444413 | A | G | 3 | a0001c0001t0001g0096 a0001c0003t0001g0204 a0001c0012t0001g0284 |
3 | HG02647.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.465-718A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444413 | |||||||
| chr4:2444447 | C | T | 3 | a0002c0002t0001g0105 a0002c0002t0001g0109 a0002c0002t0001g0120 |
3 | NA18950.hp1 NA18986.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.465-684C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444447 | |||||||
| chr4:2444498 | C | G | 1 | a0001c0003t0001g0204 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.465-633C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444498 | |||||||
| chr4:2444805 | G | A | 226 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(223): Show |
243 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.465-326G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444805 | |||||||
| chr4:2444833 | C | T | 227 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(224): Show |
244 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.465-298C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444833 | |||||||
| chr4:2444895 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.465-236C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444895 | |||||||
| chr4:2444917 | G | A | 227 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(224): Show |
244 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.465-214G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444917 | |||||||
| chr4:2444986 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.465-145G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444986 | |||||||
| chr4:2444993 | G | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(88): Show |
103 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.465-138G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444993 | |||||||
| chr4:2444998 | C | G | 48 | a0001c0001t0001g0027 a0001c0001t0001g0038 a0001c0001t0001g0054 others(45): Show |
49 | HG00609.hp1 HG00621.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.465-133C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2444998 | |||||||
| chr4:2445092 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.465-39G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 5/15 | chr4 | 2445092 | |||||||
| chr4:2445554 | T | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0117 |
2 | NA18961.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.642+246T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445554 | |||||||
| chr4:2445626 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.642+318C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445626 | |||||||
| chr4:2445627 | G | A | 1 | a0001c0017t0001g0308 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.642+319G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445627 | |||||||
| chr4:2445676 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.642+368A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445676 | |||||||
| chr4:2445875 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.642+567G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445875 | |||||||
| chr4:2445960 | A | G | 13 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0184 others(10): Show |
13 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.642+652A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445960 | |||||||
| chr4:2445980 | A | C | 1 | a0011c0030t0002g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.642+672A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2445980 | |||||||
| chr4:2446001 | C | T | 1 | a0010c0018t0001g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.642+693C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446001 | |||||||
| chr4:2446050 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0172 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.642+742G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446050 | |||||||
| chr4:2446249 | C | G | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.642+941C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446249 | |||||||
| chr4:2446249 | C | T | 25 | a0001c0001t0001g0033 a0001c0001t0001g0096 a0001c0001t0001g0172 others(22): Show |
25 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.642+941C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446249 | |||||||
| chr4:2446285 | CCTGCCTA others(4): Show |
C | 3 | a0001c0003t0001g0088 a0001c0003t0001g0304 a0001c0003t0001g0312 |
3 | HG02647.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.642+987_642+997del others(11): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446285 | ||||||
| chr4:2446368 | G | GTTA | 8 | a0001c0001t0001g0016 a0001c0001t0001g0083 a0001c0003t0002g0048 others(5): Show |
8 | HG02683.hp2 HG02698.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.642+1099_642+1101d others(5): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | ||||||
| chr4:2446368 | G | GTTATTA | 8 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0060 others(5): Show |
8 | HG02257.hp2 NA18948.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+1096_642+1101d others(8): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | ||||||
| chr4:2446368 | G | GTTATTAT others(2): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(4): Show |
10 | HG02135.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.642+1093_642+1101d others(11): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | ||||||
| chr4:2446368 | GTTA | G | 22 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0017 others(19): Show |
24 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.642+1099_642+1101d others(5): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | ||||||
| chr4:2446368 | GTTATTA | G | 4 | a0001c0014t0001g0128 a0001c0014t0001g0160 a0001c0029t0001g0035 others(1): Show |
4 | HG01109.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.642+1096_642+1101d others(8): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | ||||||
| chr4:2446368 | GTTATTAT others(5): Show |
G | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.642+1090_642+1101d others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | ||||||
| chr4:2446368 | GTTATTAT others(8): Show |
G | 6 | a0001c0001t0001g0170 a0001c0001t0001g0314 a0001c0003t0001g0012 others(3): Show |
7 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.642+1087_642+1101d others(17): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | ||||||
| chr4:2446368 | GTTATTAT others(11): Show |
G | 219 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(216): Show |
236 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.642+1084_642+1101d others(20): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | ||||||
| chr4:2446368 | GTTATTAT others(17): Show |
G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(2): Show |
5 | HG01192.hp1 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+1078_642+1101d others(26): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446368 | ||||||
| chr4:2446371 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.642+1063A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446371 | |||||||
| chr4:2446374 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.642+1066A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446374 | |||||||
| chr4:2446420 | T | A | 5 | a0002c0002t0001g0222 a0002c0002t0001g0263 a0002c0002t0001g0265 others(2): Show |
5 | NA18944.hp2 NA18952.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+1112T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446420 | |||||||
| chr4:2446424 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(4): Show |
9 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.642+1116G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446424 | |||||||
| chr4:2446449 | G | A | 1 | a0001c0029t0001g0035 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.642+1141G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446449 | |||||||
| chr4:2446517 | C | T | 1 | a0006c0011t0001g0168 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.642+1209C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446517 | |||||||
| chr4:2446518 | G | A | 1 | a0002c0002t0001g0227 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.642+1210G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446518 | |||||||
| chr4:2446593 | A | T | 1 | a0002c0002t0001g0263 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.642+1285A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446593 | |||||||
| chr4:2446662 | T | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.642+1354T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446662 | |||||||
| chr4:2446726 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.642+1418A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446726 | |||||||
| chr4:2446808 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.642+1500G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446808 | |||||||
| chr4:2446812 | G | GATGA | 7 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(4): Show |
9 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.642+1508_642+1511d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446812 | ||||||
| chr4:2446816 | A | AATGG | 104 | a0001c0001t0001g0023 a0001c0001t0001g0089 a0001c0001t0001g0102 others(101): Show |
118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.642+1528_642+1531d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2446816 | ||||||
| chr4:2446836 | G | C | 1 | a0005c0006t0001g0154 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.642+1528G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446836 | |||||||
| chr4:2446931 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.642+1623G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2446931 | |||||||
| chr4:2447095 | GATGGATG others(19): Show |
G | 1 | a0008c0032t0001g0291 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.642+1802_642+1827d others(28): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447095 | ||||||
| chr4:2447105 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | NA18946.hp1 NA18992.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.642+1797T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447105 | |||||||
| chr4:2447145 | G | T | 1 | a0001c0001t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.642+1837G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447145 | |||||||
| chr4:2447146 | A | G | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.642+1838A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447146 | |||||||
| chr4:2447195 | T | A | 22 | a0001c0001t0001g0033 a0001c0001t0001g0172 a0001c0003t0001g0046 others(19): Show |
22 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.642+1887T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447195 | |||||||
| chr4:2447215 | T | C | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.642+1907T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447215 | |||||||
| chr4:2447224 | GCATGGAA others(53): Show |
G | 1 | a0001c0003t0002g0043 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.642+1933_642+1992d others(62): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447224 | ||||||
| chr4:2447258 | C | CTGGA | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.642+1971_642+1974d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447258 | ||||||
| chr4:2447279 | T | C | 5 | a0001c0014t0001g0128 a0001c0014t0001g0160 a0001c0029t0001g0035 others(2): Show |
5 | HG01243.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+1971T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447279 | |||||||
| chr4:2447442 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.642+2134T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447442 | |||||||
| chr4:2447474 | G | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(93): Show |
108 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.642+2166G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447474 | |||||||
| chr4:2447503 | G | A | 3 | a0001c0003t0001g0088 a0001c0003t0001g0304 a0001c0003t0001g0312 |
3 | HG02647.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.643-2167G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447503 | |||||||
| chr4:2447614 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.643-2056T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447614 | |||||||
| chr4:2447645 | G | GTGGA | 3 | a0001c0003t0001g0012 a0001c0003t0001g0013 a0001c0012t0001g0012 |
4 | HG01243.hp2 HG01884.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-2004_643-2001d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447645 | ||||||
| chr4:2447645 | GTGGATGG others(5): Show |
G | 1 | a0003c0004t0001g0057 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.643-2012_643-2001d others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447645 | ||||||
| chr4:2447809 | AATGG | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(90): Show |
105 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.643-1852_643-1849d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447809 | ||||||
| chr4:2447818 | A | G | 141 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(138): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.643-1852A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447818 | |||||||
| chr4:2447834 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0172 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.643-1836A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447834 | |||||||
| chr4:2447913 | GTGAA | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0079 others(24): Show |
31 | HG01074.hp1 HG01074.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.643-1750_643-1747d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447913 | ||||||
| chr4:2447916 | AATGAATG others(21): Show |
A | 3 | a0001c0014t0001g0128 a0001c0014t0001g0160 a0001c0029t0001g0035 |
3 | HG03139.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.643-1750_643-1723d others(30): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447916 | ||||||
| chr4:2447917 | ATGAATGG others(5): Show |
A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(58): Show |
69 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.643-1750_643-1739d others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447917 | ||||||
| chr4:2447929 | G | GTGGA | 10 | a0001c0001t0001g0033 a0001c0001t0001g0092 a0001c0001t0001g0172 others(7): Show |
10 | HG01891.hp1 HG02015.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.643-1693_643-1690d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447929 | ||||||
| chr4:2447929 | GTGGA | G | 162 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(159): Show |
177 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.643-1693_643-1690d others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447929 | ||||||
| chr4:2447929 | GTGGATGG others(1): Show |
G | 30 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(27): Show |
30 | HG00099.hp2 HG00597.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.643-1697_643-1690d others(10): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447929 | ||||||
| chr4:2447929 | GTGGATGG others(5): Show |
G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(6): Show |
11 | HG00609.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.643-1701_643-1690d others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447929 | ||||||
| chr4:2447929 | GTGGATGG others(9): Show |
G | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.643-1705_643-1690d others(18): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2447929 | ||||||
| chr4:2447937 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
70 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.643-1733A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447937 | |||||||
| chr4:2447953 | A | G | 3 | a0001c0014t0001g0128 a0001c0014t0001g0160 a0001c0029t0001g0035 |
3 | HG03139.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.643-1717A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2447953 | |||||||
| chr4:2448004 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(4): Show |
9 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.643-1666G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448004 | |||||||
| chr4:2448020 | A | AATGGATG others(1): Show |
85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(82): Show |
96 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.643-1634_643-1627d others(10): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2448020 | ||||||
| chr4:2448020 | A | AATGGATG others(5): Show |
9 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(6): Show |
10 | HG01243.hp2 HG01884.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.643-1638_643-1627d others(14): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2448020 | ||||||
| chr4:2448077 | A | T | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.643-1593A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448077 | |||||||
| chr4:2448184 | C | A | 3 | a0001c0003t0001g0012 a0001c0003t0001g0013 a0001c0012t0001g0012 |
4 | HG01243.hp2 HG01884.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-1486C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448184 | |||||||
| chr4:2448255 | C | T | 1 | a0001c0019t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.643-1415C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448255 | |||||||
| chr4:2448332 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.643-1338A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448332 | |||||||
| chr4:2448403 | G | A | 2 | a0001c0003t0001g0034 a0001c0003t0001g0036 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.643-1267G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448403 | |||||||
| chr4:2448614 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.643-1056G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448614 | |||||||
| chr4:2448710 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.643-960T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448710 | |||||||
| chr4:2448746 | G | A | 6 | a0005c0006t0001g0154 a0005c0006t0001g0155 a0005c0006t0001g0156 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-924G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448746 | |||||||
| chr4:2448755 | C | CG | 5 | a0001c0001t0001g0134 a0001c0001t0001g0153 a0002c0002t0001g0224 others(2): Show |
5 | HG00735.hp1 HG02135.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-911dupG | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 2448755 | ||||||
| chr4:2448957 | T | C | 1 | a0002c0002t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.643-713T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2448957 | |||||||
| chr4:2449165 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.643-505G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2449165 | |||||||
| chr4:2449207 | G | C | 1 | a0002c0002t0001g0264 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.643-463G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2449207 | |||||||
| chr4:2449307 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.643-363C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2449307 | |||||||
| chr4:2449308 | G | A | 1 | a0001c0003t0001g0186 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.643-362G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 6/15 | chr4 | 2449308 | |||||||
| chr4:2449884 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.724-50G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 7/15 | chr4 | 2449884 | |||||||
| chr4:2449911 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.724-23G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 7/15 | chr4 | 2449911 | |||||||
| chr4:2450085 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.795+80C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450085 | |||||||
| chr4:2450196 | G | A | 3 | a0001c0003t0002g0048 a0001c0003t0002g0049 a0001c0003t0002g0050 |
3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.795+191G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450196 | |||||||
| chr4:2450222 | A | G | 228 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(225): Show |
245 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.795+217A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450222 | |||||||
| chr4:2450360 | C | T | 85 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(82): Show |
86 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.795+355C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450360 | |||||||
| chr4:2450474 | G | A | 1 | a0001c0014t0001g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.795+469G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450474 | |||||||
| chr4:2450489 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.796-458G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450489 | |||||||
| chr4:2450601 | G | A | 13 | a0001c0001t0001g0001 a0001c0003t0001g0034 a0001c0003t0001g0036 others(10): Show |
15 | HG01109.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.796-346G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450601 | |||||||
| chr4:2450870 | G | A | 2 | a0002c0002t0001g0104 a0002c0002t0001g0266 |
2 | HG02155.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.796-77G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 8/15 | chr4 | 2450870 | |||||||
| chr4:2451064 | AC | A | 83 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(80): Show |
84 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.867+50delC | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 2451064 | ||||||
| chr4:2451086 | C | T | 1 | a0001c0003t0001g0186 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.867+68C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 9/15 | chr4 | 2451086 | |||||||
| chr4:2451206 | T | C | 228 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(225): Show |
245 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.868-58T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 9/15 | chr4 | 2451206 | |||||||
| chr4:2451452 | G | A | 1 | a0015c0015t0001g0229 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.956+100G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451452 | |||||||
| chr4:2451497 | G | A | 18 | a0001c0003t0001g0046 a0001c0003t0001g0071 a0001c0003t0001g0082 others(15): Show |
18 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.956+145G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451497 | |||||||
| chr4:2451519 | T | A | 1 | a0002c0002t0001g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.956+167T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451519 | |||||||
| chr4:2451548 | G | A | 218 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(215): Show |
235 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.956+196G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451548 | |||||||
| chr4:2451630 | C | G | 224 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(221): Show |
241 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.956+278C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451630 | |||||||
| chr4:2451698 | T | C | 227 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(224): Show |
244 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.956+346T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451698 | |||||||
| chr4:2451724 | C | T | 7 | a0001c0001t0001g0063 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.956+372C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451724 | |||||||
| chr4:2451733 | AGGCTGTG others(3): Show |
A | 224 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0026 others(221): Show |
241 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.956+384_956+393del others(10): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr4 | 2451733 | ||||||
| chr4:2451744 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.956+392G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451744 | |||||||
| chr4:2451869 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.957-273T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451869 | |||||||
| chr4:2451949 | C | T | 46 | a0001c0001t0001g0027 a0001c0001t0001g0038 a0001c0001t0001g0054 others(43): Show |
47 | HG00609.hp1 HG00621.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.957-193C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451949 | |||||||
| chr4:2451989 | C | T | 4 | a0002c0002t0001g0222 a0002c0002t0001g0263 a0002c0002t0001g0275 others(1): Show |
4 | NA18944.hp2 NA18977.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-153C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2451989 | |||||||
| chr4:2452056 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(2): Show |
7 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.957-86A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 10/15 | chr4 | 2452056 | |||||||
| chr4:2452362 | G | C | 3 | a0001c0003t0002g0048 a0001c0003t0002g0049 a0001c0003t0002g0050 |
3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1161+16G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452362 | |||||||
| chr4:2452408 | G | A | 3 | a0001c0003t0002g0048 a0001c0003t0002g0049 a0001c0003t0002g0050 |
3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1161+62G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452408 | |||||||
| chr4:2452456 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1161+110G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452456 | |||||||
| chr4:2452468 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1161+122G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452468 | |||||||
| chr4:2452605 | C | T | 3 | a0001c0003t0002g0048 a0001c0003t0002g0049 a0001c0003t0002g0050 |
3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1161+259C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452605 | |||||||
| chr4:2452682 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(2): Show |
7 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1161+336C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452682 | |||||||
| chr4:2452687 | A | C | 1 | a0002c0002t0001g0239 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1161+341A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452687 | |||||||
| chr4:2452693 | T | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0110 |
2 | NA18947.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1161+347T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452693 | |||||||
| chr4:2452893 | T | A | 1 | a0001c0001t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1161+547T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452893 | |||||||
| chr4:2452920 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1161+574G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452920 | |||||||
| chr4:2452924 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1161+578A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452924 | |||||||
| chr4:2452979 | C | T | 108 | a0001c0001t0001g0023 a0001c0001t0001g0038 a0001c0001t0001g0089 others(105): Show |
122 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1161+633C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452979 | |||||||
| chr4:2452988 | G | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1161+642G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2452988 | |||||||
| chr4:2453007 | G | A | 1 | a0001c0003t0002g0045 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1161+661G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453007 | |||||||
| chr4:2453038 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(2): Show |
7 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1161+692G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453038 | |||||||
| chr4:2453050 | G | A | 1 | a0011c0030t0002g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1161+704G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453050 | |||||||
| chr4:2453347 | G | C | 1 | a0012c0031t0001g0257 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1161+1001G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453347 | |||||||
| chr4:2453353 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(85): Show |
100 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1161+1007C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453353 | |||||||
| chr4:2453391 | G | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(85): Show |
100 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1161+1045G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453391 | |||||||
| chr4:2453456 | G | A | 2 | a0002c0002t0001g0236 a0002c0002t0001g0241 |
2 | HG02056.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1161+1110G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453456 | |||||||
| chr4:2453636 | A | G | 24 | a0001c0001t0001g0033 a0001c0001t0001g0098 a0001c0001t0001g0099 others(21): Show |
24 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1161+1290A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453636 | |||||||
| chr4:2453664 | T | TTC | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(315): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1161+1319_1161+132 others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2453664 | ||||||
| chr4:2453741 | C | CT | 24 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0099 others(21): Show |
24 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1161+1410dupT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2453741 | ||||||
| chr4:2453741 | CT | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(16): Show |
21 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1161+1410delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2453741 | ||||||
| chr4:2453741 | CTT | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(80): Show |
93 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1161+1409_1161+141 others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2453741 | ||||||
| chr4:2453816 | AT | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(91): Show |
108 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1161+1485delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2453816 | ||||||
| chr4:2453880 | C | T | 3 | a0002c0002t0001g0221 a0002c0002t0001g0246 a0002c0002t0001g0268 |
3 | HG00642.hp2 HG00735.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1161+1534C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453880 | |||||||
| chr4:2453903 | TC | T | 3 | a0001c0014t0001g0128 a0001c0014t0001g0160 a0001c0029t0001g0035 |
3 | HG03139.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1161+1560delC | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2453903 | ||||||
| chr4:2453915 | G | A | 1 | a0002c0002t0001g0104 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1161+1569G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453915 | |||||||
| chr4:2453935 | T | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(85): Show |
100 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1161+1589T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2453935 | |||||||
| chr4:2454087 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1161+1741C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454087 | |||||||
| chr4:2454237 | G | A | 1 | a0001c0003t0001g0126 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1161+1891G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454237 | |||||||
| chr4:2454335 | CTG | C | 3 | a0001c0014t0001g0128 a0001c0014t0001g0160 a0001c0029t0001g0035 |
3 | HG03139.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1161+1993_1161+199 others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2454335 | ||||||
| chr4:2454528 | GA | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(69): Show |
81 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1161+2184delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2454528 | ||||||
| chr4:2454531 | C | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(69): Show |
81 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1161+2185C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454531 | |||||||
| chr4:2454581 | C | T | 1 | a0002c0002t0001g0246 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1161+2235C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454581 | |||||||
| chr4:2454581 | CT | C | 110 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0061 others(107): Show |
124 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1161+2247delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2454581 | ||||||
| chr4:2454582 | T | C | 1 | a0002c0002t0001g0246 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1161+2236T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454582 | |||||||
| chr4:2454593 | T | G | 19 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0003t0001g0046 others(16): Show |
19 | HG00609.hp2 HG01106.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.1161+2247T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454593 | |||||||
| chr4:2454593 | T | TG | 6 | a0001c0014t0001g0128 a0001c0014t0001g0160 a0001c0029t0001g0035 others(3): Show |
6 | HG01074.hp1 HG01243.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+2248dupG | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2454593 | ||||||
| chr4:2454594 | G | T | 27 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(24): Show |
27 | HG00609.hp2 HG01106.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1161+2248G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454594 | |||||||
| chr4:2454594 | GT | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0096 others(16): Show |
22 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1161+2263delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2454594 | ||||||
| chr4:2454595 | T | C | 7 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(4): Show |
7 | HG01358.hp2 HG01515.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+2249T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454595 | |||||||
| chr4:2454595 | T | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(66): Show |
78 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1161+2249T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454595 | |||||||
| chr4:2454596 | T | G | 15 | a0001c0001t0001g0001 a0001c0003t0001g0012 a0001c0003t0001g0013 others(12): Show |
18 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1161+2250T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454596 | |||||||
| chr4:2454701 | A | G | 1 | a0001c0003t0001g0176 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1161+2355A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454701 | |||||||
| chr4:2454845 | C | G | 9 | a0001c0001t0001g0001 a0001c0003t0001g0034 a0001c0003t0001g0036 others(6): Show |
11 | HG02257.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1161+2499C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2454845 | |||||||
| chr4:2455075 | T | G | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1161+2729T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455075 | |||||||
| chr4:2455081 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1161+2735G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455081 | |||||||
| chr4:2455184 | G | A | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1161+2838G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455184 | |||||||
| chr4:2455228 | A | C | 1 | a0003c0004t0001g0081 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1161+2882A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455228 | |||||||
| chr4:2455262 | T | G | 1 | a0001c0001t0001g0187 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1161+2916T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455262 | |||||||
| chr4:2455410 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0117 |
2 | NA18961.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1161+3064C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455410 | |||||||
| chr4:2455510 | TA | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(89): Show |
104 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1161+3171delA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2455510 | ||||||
| chr4:2455795 | T | A | 2 | a0001c0003t0001g0034 a0001c0003t0001g0036 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1162-2928T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455795 | |||||||
| chr4:2455964 | G | C | 17 | a0001c0001t0001g0001 a0001c0003t0001g0012 a0001c0003t0001g0013 others(14): Show |
20 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-2759G>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2455964 | |||||||
| chr4:2456223 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1162-2500C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456223 | |||||||
| chr4:2456351 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(90): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1162-2372A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456351 | |||||||
| chr4:2456372 | G | GA | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(90): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1162-2348dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2456372 | ||||||
| chr4:2456408 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1162-2315G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456408 | |||||||
| chr4:2456508 | G | A | 1 | a0001c0003t0001g0082 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1162-2215G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456508 | |||||||
| chr4:2456607 | C | T | 5 | a0001c0014t0001g0128 a0001c0014t0001g0160 a0001c0029t0001g0035 others(2): Show |
5 | HG01243.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-2116C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456607 | |||||||
| chr4:2456666 | T | G | 1 | a0002c0002t0001g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1162-2057T>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456666 | |||||||
| chr4:2456763 | C | T | 2 | a0001c0008t0001g0085 a0001c0008t0001g0086 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1162-1960C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456763 | |||||||
| chr4:2456808 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1162-1915C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456808 | |||||||
| chr4:2456810 | C | T | 2 | a0002c0002t0001g0209 a0002c0002t0001g0298 |
2 | NA18961.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1162-1913C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456810 | |||||||
| chr4:2456813 | C | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(70): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1162-1910C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456813 | |||||||
| chr4:2456846 | C | T | 1 | a0001c0001t0001g0001 | 3 | HG02258.hp1 HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1162-1877C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456846 | |||||||
| chr4:2456878 | G | A | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(315): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1162-1845G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456878 | |||||||
| chr4:2456923 | A | T | 17 | a0001c0001t0001g0001 a0001c0003t0001g0012 a0001c0003t0001g0013 others(14): Show |
20 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-1800A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456923 | |||||||
| chr4:2456950 | C | CT | 63 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1162-1753dupT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2456950 | ||||||
| chr4:2456950 | CT | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0033 others(142): Show |
161 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1162-1753delT | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2456950 | ||||||
| chr4:2456950 | CTT | C | 9 | a0001c0001t0001g0098 a0002c0002t0001g0020 a0002c0002t0001g0105 others(6): Show |
10 | HG00609.hp2 HG01975.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.1162-1754_1162-175 others(6): Show |
CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 2456950 | ||||||
| chr4:2456957 | T | C | 1 | a0001c0003t0001g0161 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1162-1766T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2456957 | |||||||
| chr4:2457001 | G | A | 17 | a0001c0001t0001g0001 a0001c0003t0001g0012 a0001c0003t0001g0013 others(14): Show |
20 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-1722G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457001 | |||||||
| chr4:2457141 | G | A | 1 | a0003c0004t0001g0296 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1162-1582G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457141 | |||||||
| chr4:2457206 | G | A | 1 | a0002c0002t0001g0245 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1162-1517G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457206 | |||||||
| chr4:2457395 | G | A | 17 | a0001c0001t0001g0001 a0001c0003t0001g0012 a0001c0003t0001g0013 others(14): Show |
20 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-1328G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457395 | |||||||
| chr4:2457423 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(90): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1162-1300A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457423 | |||||||
| chr4:2457426 | G | A | 17 | a0001c0001t0001g0001 a0001c0003t0001g0012 a0001c0003t0001g0013 others(14): Show |
20 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-1297G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457426 | |||||||
| chr4:2457473 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0003t0001g0186 |
3 | HG03491.hp2 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1162-1250C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457473 | |||||||
| chr4:2457635 | G | T | 1 | a0002c0002t0001g0227 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1162-1088G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457635 | |||||||
| chr4:2457654 | AC | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(2): Show |
7 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1162-1068delC | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457654 | |||||||
| chr4:2457708 | T | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(70): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1162-1015T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457708 | |||||||
| chr4:2457731 | C | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(17): Show |
23 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1162-992C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457731 | |||||||
| chr4:2457768 | C | T | 5 | a0001c0001t0001g0096 a0001c0003t0001g0204 a0001c0008t0001g0085 others(2): Show |
5 | HG02145.hp2 HG02647.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-955C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457768 | |||||||
| chr4:2457781 | C | T | 1 | a0002c0002t0001g0238 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1162-942C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457781 | |||||||
| chr4:2457782 | G | A | 2 | a0001c0008t0001g0085 a0001c0008t0001g0086 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1162-941G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457782 | |||||||
| chr4:2457839 | G | T | 1 | a0001c0001t0001g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1162-884G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457839 | |||||||
| chr4:2457875 | G | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0124 others(6): Show |
11 | HG01884.hp1 HG01975.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1162-848G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2457875 | |||||||
| chr4:2458017 | C | A | 3 | a0001c0003t0001g0012 a0001c0003t0001g0013 a0001c0012t0001g0012 |
4 | HG01243.hp2 HG01884.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1162-706C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458017 | |||||||
| chr4:2458083 | C | G | 2 | a0001c0008t0001g0085 a0001c0008t0001g0086 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1162-640C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458083 | |||||||
| chr4:2458127 | G | A | 3 | a0001c0003t0002g0048 a0001c0003t0002g0049 a0001c0003t0002g0050 |
3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1162-596G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458127 | |||||||
| chr4:2458171 | T | C | 48 | a0001c0001t0001g0027 a0001c0001t0001g0038 a0001c0001t0001g0054 others(45): Show |
49 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1162-552T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458171 | |||||||
| chr4:2458200 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1162-523G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458200 | |||||||
| chr4:2458295 | T | A | 1 | a0001c0012t0001g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1162-428T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458295 | |||||||
| chr4:2458316 | A | G | 1 | a0001c0003t0001g0161 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1162-407A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458316 | |||||||
| chr4:2458450 | A | G | 3 | a0001c0001t0001g0096 a0001c0003t0001g0204 a0001c0012t0001g0284 |
3 | HG02647.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1162-273A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458450 | |||||||
| chr4:2458464 | T | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0098 a0001c0001t0001g0099 others(19): Show |
22 | HG01106.hp1 HG01106.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1162-259T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458464 | |||||||
| chr4:2458475 | A | G | 1 | a0002c0002t0001g0242 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1162-248A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458475 | |||||||
| chr4:2458542 | C | T | 2 | a0001c0001t0001g0138 a0001c0003t0001g0176 |
2 | HG00621.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1162-181C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458542 | |||||||
| chr4:2458565 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.1162-158C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458565 | |||||||
| chr4:2458574 | T | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1162-149T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458574 | |||||||
| chr4:2458636 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1162-87C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 11/15 | chr4 | 2458636 | |||||||
| chr4:2458913 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1303+49G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/15 | chr4 | 2458913 | |||||||
| chr4:2459037 | G | T | 1 | a0001c0001t0001g0314 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1304-70G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/15 | chr4 | 2459037 | |||||||
| chr4:2459076 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(214): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1304-31A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/15 | chr4 | 2459076 | |||||||
| chr4:2459098 | G | A | 1 | a0001c0012t0001g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1304-9G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 12/15 | chr4 | 2459098 | |||||||
| chr4:2459408 | A | C | 2 | a0001c0001t0001g0094 a0001c0003t0001g0088 |
2 | HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1455+150A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459408 | |||||||
| chr4:2459417 | G | A | 1 | a0002c0002t0001g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1455+159G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459417 | |||||||
| chr4:2459452 | C | T | 1 | a0001c0003t0001g0200 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1455+194C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459452 | |||||||
| chr4:2459482 | A | C | 3 | a0001c0001t0001g0124 a0001c0008t0001g0085 a0001c0008t0001g0086 |
3 | HG02055.hp2 HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1455+224A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459482 | |||||||
| chr4:2459614 | A | G | 2 | a0001c0001t0001g0074 a0014c0016t0001g0075 |
2 | NA18946.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1455+356A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459614 | |||||||
| chr4:2459664 | T | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0172 others(2): Show |
6 | HG02723.hp1 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1456-373T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459664 | |||||||
| chr4:2459759 | A | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(298): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1456-278A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459759 | |||||||
| chr4:2459780 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1456-257G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 13/15 | chr4 | 2459780 | |||||||
| chr4:2460268 | C | A | 5 | a0001c0001t0001g0031 a0001c0003t0001g0195 a0001c0003t0001g0202 others(2): Show |
5 | HG00639.hp1 HG02004.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661+26C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460268 | |||||||
| chr4:2460422 | A | G | 1 | a0001c0025t0001g0256 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1661+180A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460422 | |||||||
| chr4:2460522 | C | T | 2 | a0001c0029t0001g0035 a0011c0030t0002g0040 |
2 | HG01109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1661+280C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460522 | |||||||
| chr4:2460899 | C | T | 1 | a0002c0002t0001g0142 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1661+657C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460899 | |||||||
| chr4:2460900 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1661+658G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460900 | |||||||
| chr4:2460921 | C | G | 1 | a0001c0003t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1661+679C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460921 | |||||||
| chr4:2460973 | G | A | 5 | a0001c0001t0001g0197 a0001c0001t0001g0203 a0003c0004t0001g0081 others(2): Show |
5 | HG02055.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1661+731G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2460973 | |||||||
| chr4:2461054 | G | A | 9 | a0001c0001t0001g0027 a0001c0001t0001g0139 a0001c0001t0001g0286 others(6): Show |
10 | HG01891.hp2 HG02559.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1661+812G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461054 | |||||||
| chr4:2461137 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0172 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1661+895C>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461137 | |||||||
| chr4:2461233 | G | A | 8 | a0001c0001t0001g0031 a0001c0003t0001g0195 a0001c0003t0001g0202 others(5): Show |
8 | HG00639.hp1 HG02004.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1661+991G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461233 | |||||||
| chr4:2461337 | G | A | 266 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0015 others(263): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1661+1095G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461337 | |||||||
| chr4:2461361 | G | A | 1 | a0001c0003t0001g0161 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1662-1082G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461361 | |||||||
| chr4:2461526 | A | G | 4 | a0005c0006t0001g0154 a0005c0006t0001g0156 a0005c0006t0001g0157 others(1): Show |
4 | HG02615.hp1 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662-917A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461526 | |||||||
| chr4:2461594 | A | T | 15 | a0001c0001t0001g0033 a0001c0001t0001g0172 a0001c0003t0001g0088 others(12): Show |
15 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1662-849A>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461594 | |||||||
| chr4:2461909 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1662-534G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461909 | |||||||
| chr4:2461942 | G | A | 12 | a0001c0001t0001g0033 a0001c0001t0001g0172 a0001c0003t0001g0088 others(9): Show |
12 | HG01243.hp1 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1662-501G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461942 | |||||||
| chr4:2461978 | T | TA | 22 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0172 others(19): Show |
22 | HG00639.hp1 HG01243.hp1 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.1662-458dupA | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr4 | 2461978 | ||||||
| chr4:2461982 | A | C | 5 | a0001c0001t0001g0063 a0001c0001t0001g0094 a0001c0001t0001g0095 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662-461A>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2461982 | |||||||
| chr4:2462088 | T | A | 1 | a0001c0019t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1662-355T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2462088 | |||||||
| chr4:2462117 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1662-326A>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2462117 | |||||||
| chr4:2462248 | T | C | 2 | a0002c0002t0001g0087 a0002c0002t0001g0272 |
2 | HG02083.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1662-195T>C | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2462248 | |||||||
| chr4:2462295 | G | A | 3 | a0001c0003t0002g0048 a0001c0003t0002g0049 a0001c0003t0002g0050 |
3 | HG03225.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1662-148G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2462295 | |||||||
| chr4:2462368 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0172 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1662-75G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 14/15 | chr4 | 2462368 | |||||||
| chr4:2462657 | T | A | 8 | a0003c0004t0001g0009 a0003c0004t0001g0069 a0003c0004t0001g0249 others(5): Show |
8 | HG02698.hp1 HG02738.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.1824+52T>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/15 | chr4 | 2462657 | |||||||
| chr4:2462673 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1824+68G>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/15 | chr4 | 2462673 | |||||||
| chr4:2462689 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1824+84C>A | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/15 | chr4 | 2462689 | |||||||
| chr4:2462689 | C | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0288 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1824+84C>G | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/15 | chr4 | 2462689 | |||||||
| chr4:2462718 | G | T | 1 | a0001c0001t0001g0110 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1825-92G>T | CFAP99 | ENSG00000206113.12 | transcript | ENST00000635017.2 | protein_coding | 15/15 | chr4 | 2462718 |