Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 146845 |
|---|---|
| ensemblid | ENSG00000166596.15 |
| hgncid | 16053 |
| symbol | CFAP52 |
| name | cilia and flagella associated protein 52 |
| refseq_nuc | NM_145054.5 |
| refseq_prot | NP_659491.4 |
| ensembl_nuc | ENST00000352665.10 |
| ensembl_prot | ENSP00000339449.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 9576642 |
| end | 9643447 |
| strand | + |
| ver | v1.2 |
| region | chr17:9576642-9643447 |
| region5000 | chr17:9571642-9648447 |
| regionname0 | CFAP52_chr17_9576642_9643447 |
| regionname5000 | CFAP52_chr17_9571642_9648447 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 620 | 153 | 55 | 28 | 55 | 4 | 10 | 40 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0002 | 0/1 | 620 | 151 | 30 | 29 | 62 | 7 | 22 | 43 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0003 | 0/0 | 620 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0004 | 0/0 | 620 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0005 | 0/0 | 620 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0006 | 0/0 | 620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0007 | 0/0 | 620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0008 | 0/0 | 620 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0009 | 0/0 | 620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0010 | 0/0 | 620 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1863 | 149 | 29 | 29 | 61 | 7 | 22 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0002 | 1/0 | 1863 | 145 | 47 | 28 | 55 | 4 | 10 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0003 | 0/0 | 1863 | 4 | 0 | 0 | 4 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0004 | 0/0 | 1863 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0005 | 0/0 | 1863 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0006 | 0/0 | 1863 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0007 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0008 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0009 | 0/0 | 1863 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0010 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0011 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0012 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0013 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0014 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| c0015 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 304 | 249 | 80 | 31 | 109 | 7 | 22 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| t0002 | 1/1 | 304 | 55 | 3 | 27 | 8 | 5 | 10 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| t0003 | 0/0 | 304 | 7 | 0 | 0 | 7 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| t0004 | 0/0 | 304 | 5 | 5 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 1863 | 145 | 47 | 28 | 55 | 4 | 10 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0001c0004 | 0/0 | 1863 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0001c0005 | 0/0 | 1863 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0001c0012 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0002c0001 | 0/1 | 1863 | 149 | 29 | 29 | 61 | 7 | 22 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0002c0010 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0002c0011 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0003c0003 | 0/0 | 1863 | 4 | 0 | 0 | 4 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0004c0006 | 0/0 | 1863 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0005c0008 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0006c0014 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0007c0013 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0008c0009 | 0/0 | 1863 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0009c0015 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0010c0007 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 2166 | 141 | 47 | 26 | 54 | 4 | 10 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0001c0002t0002 | 1/0 | 2166 | 4 | 0 | 2 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0001c0004t0004 | 0/0 | 2166 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0001c0005t0001 | 0/0 | 2166 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0001c0005t0004 | 0/0 | 2166 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0001c0012t0001 | 0/0 | 2166 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0002c0001t0001 | 0/0 | 2166 | 91 | 26 | 4 | 47 | 2 | 12 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0002c0001t0002 | 0/1 | 2166 | 51 | 3 | 25 | 7 | 5 | 10 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0002c0001t0003 | 0/0 | 2166 | 7 | 0 | 0 | 7 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0002c0010t0001 | 0/0 | 2166 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0002c0011t0001 | 0/0 | 2166 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0003c0003t0001 | 0/0 | 2166 | 4 | 0 | 0 | 4 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0004c0006t0001 | 0/0 | 2166 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0005c0008t0001 | 0/0 | 2166 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0006c0014t0001 | 0/0 | 2166 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0007c0013t0001 | 0/0 | 2166 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0008c0009t0001 | 0/0 | 2166 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0009c0015t0001 | 0/0 | 2166 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| a0010c0007t0001 | 0/0 | 2166 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | copy fasta | chr17 | 9571642 | 9648447 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0002g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0004t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0004t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0004t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0005t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0005t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0001c0012t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0010t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0002c0011t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0004c0006t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0004c0006t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0005c0008t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0006c0014t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0007c0013t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0008c0009t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0009c0015t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| a0010c0007t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0100 | EUR | GBR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00099 | hp2 | a0002 | c0001 | t0002 | g0211 | EUR | GBR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00280 | hp1 | a0002 | c0001 | t0001 | g0172 | EUR | FIN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00280 | hp2 | a0002 | c0001 | t0002 | g0205 | EUR | FIN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0173 | EUR | FIN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | FIN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | CHS | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0113 | EAS | CHS | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | CHS | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00438 | hp2 | a0002 | c0001 | t0001 | g0266 | EAS | CHS | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | CHS | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00621 | hp2 | a0002 | c0001 | t0001 | g0110 | EAS | CHS | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0281 | EAS | CHS | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | CHS | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00735 | hp1 | a0002 | c0001 | t0002 | g0220 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00735 | hp2 | a0002 | c0001 | t0002 | g0258 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00741 | hp1 | a0002 | c0001 | t0002 | g0164 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0197 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01069 | hp1 | a0002 | c0001 | t0002 | g0285 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01069 | hp2 | a0008 | c0009 | t0001 | g0305 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0275 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01074 | hp1 | a0002 | c0001 | t0002 | g0097 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01081 | hp1 | a0002 | c0001 | t0002 | g0204 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01099 | hp1 | a0002 | c0001 | t0002 | g0225 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01106 | hp1 | a0002 | c0001 | t0001 | g0286 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01106 | hp2 | a0002 | c0001 | t0001 | g0268 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01109 | hp1 | a0002 | c0001 | t0002 | g0181 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01168 | hp2 | a0002 | c0001 | t0002 | g0191 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01169 | hp1 | a0002 | c0001 | t0002 | g0183 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01169 | hp2 | a0002 | c0001 | t0002 | g0192 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0219 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01192 | hp1 | a0002 | c0001 | t0002 | g0216 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0257 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01255 | hp1 | a0002 | c0001 | t0002 | g0098 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01257 | hp1 | a0002 | c0001 | t0002 | g0056 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01257 | hp2 | a0002 | c0001 | t0002 | g0185 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01258 | hp2 | a0002 | c0001 | t0002 | g0057 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01433 | hp2 | a0002 | c0001 | t0002 | g0087 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01515 | hp1 | a0002 | c0001 | t0002 | g0312 | EUR | IBS | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01515 | hp2 | a0002 | c0001 | t0002 | g0292 | EUR | IBS | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01884 | hp2 | a0002 | c0011 | t0001 | g0277 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01891 | hp1 | a0002 | c0001 | t0002 | g0081 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0271 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PEL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01952 | hp2 | a0002 | c0001 | t0002 | g0198 | AMR | PEL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01975 | hp2 | a0002 | c0001 | t0002 | g0201 | AMR | PEL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01978 | hp1 | a0002 | c0001 | t0002 | g0049 | AMR | PEL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01978 | hp2 | a0002 | c0001 | t0002 | g0195 | AMR | PEL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02004 | hp1 | a0002 | c0001 | t0002 | g0206 | AMR | PEL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PEL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02015 | hp1 | a0002 | c0001 | t0003 | g0228 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02015 | hp2 | a0002 | c0001 | t0001 | g0248 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02027 | hp2 | a0002 | c0001 | t0001 | g0116 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02040 | hp1 | a0002 | c0001 | t0003 | g0229 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0159 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02055 | hp1 | a0002 | c0001 | t0001 | g0053 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02055 | hp2 | a0002 | c0001 | t0001 | g0018 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02056 | hp2 | a0002 | c0001 | t0001 | g0149 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02074 | hp1 | a0002 | c0001 | t0001 | g0303 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0150 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02080 | hp2 | a0002 | c0001 | t0001 | g0089 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02083 | hp2 | a0002 | c0001 | t0001 | g0167 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0121 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0249 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02145 | hp1 | a0002 | c0001 | t0001 | g0054 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02145 | hp2 | a0001 | c0005 | t0001 | g0074 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02148 | hp1 | a0002 | c0001 | t0002 | g0060 | AMR | PEL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | CDX | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0103 | EAS | CDX | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02165 | hp1 | a0002 | c0001 | t0001 | g0272 | EAS | CDX | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | CDX | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02258 | hp1 | a0002 | c0001 | t0001 | g0200 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02258 | hp2 | a0002 | c0001 | t0001 | g0055 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02273 | hp1 | a0002 | c0001 | t0002 | g0188 | AMR | PEL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02273 | hp2 | a0002 | c0001 | t0001 | g0061 | AMR | PEL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0274 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0148 | EAS | KHV | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02602 | hp1 | a0002 | c0001 | t0001 | g0038 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02602 | hp2 | a0002 | c0001 | t0002 | g0203 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0283 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02615 | hp2 | a0001 | c0004 | t0004 | g0036 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0278 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02683 | hp1 | a0002 | c0001 | t0002 | g0091 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02723 | hp1 | a0007 | c0013 | t0001 | g0015 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0213 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0073 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02738 | hp2 | a0002 | c0001 | t0002 | g0253 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02809 | hp1 | a0002 | c0001 | t0001 | g0267 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0276 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02886 | hp1 | a0002 | c0001 | t0001 | g0269 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02895 | hp1 | a0002 | c0001 | t0001 | g0029 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02895 | hp2 | a0001 | c0004 | t0004 | g0001 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02896 | hp1 | a0002 | c0001 | t0001 | g0028 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02896 | hp2 | a0002 | c0001 | t0001 | g0279 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02897 | hp1 | a0001 | c0004 | t0004 | g0001 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02897 | hp2 | a0002 | c0001 | t0001 | g0308 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02965 | hp1 | a0001 | c0012 | t0001 | g0022 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02965 | hp2 | a0002 | c0001 | t0001 | g0051 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02970 | hp1 | a0002 | c0001 | t0001 | g0019 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02970 | hp2 | a0002 | c0001 | t0001 | g0035 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02976 | hp1 | a0002 | c0001 | t0001 | g0290 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03017 | hp1 | a0002 | c0001 | t0001 | g0313 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03041 | hp2 | a0002 | c0001 | t0001 | g0086 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03098 | hp1 | a0001 | c0005 | t0001 | g0077 | AFR | MSL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | MSL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03139 | hp2 | a0002 | c0001 | t0001 | g0047 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0078 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0284 | AFR | MSL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03209 | hp2 | a0002 | c0001 | t0002 | g0005 | AFR | MSL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | MSL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03239 | hp1 | a0002 | c0001 | t0002 | g0104 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03239 | hp2 | a0002 | c0001 | t0001 | g0259 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | MSL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03453 | hp2 | a0009 | c0015 | t0001 | g0064 | AFR | MSL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0314 | AFR | MSL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | MSL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0282 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03491 | hp2 | a0002 | c0001 | t0001 | g0071 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03516 | hp1 | a0002 | c0001 | t0001 | g0082 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | ESN | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03540 | hp1 | a0002 | c0001 | t0001 | g0013 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03688 | hp1 | a0002 | c0001 | t0002 | g0102 | SAS | STU | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0222 | SAS | STU | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03831 | hp1 | a0002 | c0001 | t0001 | g0145 | SAS | BEB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0039 | SAS | BEB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0161 | SAS | BEB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03942 | hp2 | a0002 | c0001 | t0001 | g0040 | SAS | BEB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0166 | SAS | STU | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG04115 | hp2 | a0002 | c0001 | t0002 | g0059 | SAS | STU | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0176 | SAS | BEB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG04184 | hp2 | a0002 | c0001 | t0002 | g0217 | SAS | BEB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG04199 | hp1 | a0002 | c0001 | t0002 | g0136 | SAS | STU | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG04199 | hp2 | a0002 | c0001 | t0001 | g0079 | SAS | STU | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0310 | SAS | STU | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG04204 | hp2 | a0002 | c0001 | t0002 | g0247 | SAS | STU | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0046 | SAS | STU | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG04228 | hp2 | a0002 | c0001 | t0001 | g0168 | SAS | STU | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18522 | hp1 | a0002 | c0001 | t0001 | g0017 | AFR | YRI | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | YRI | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | CHB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18747 | hp2 | a0002 | c0001 | t0003 | g0108 | EAS | CHB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | YRI | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | YRI | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18942 | hp2 | a0002 | c0010 | t0001 | g0142 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18945 | hp2 | a0002 | c0001 | t0001 | g0146 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18948 | hp2 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18949 | hp2 | a0003 | c0003 | t0001 | g0293 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18953 | hp2 | a0002 | c0001 | t0003 | g0230 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0171 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18956 | hp2 | a0002 | c0001 | t0001 | g0163 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18957 | hp2 | a0002 | c0001 | t0001 | g0264 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18959 | hp1 | a0002 | c0001 | t0001 | g0182 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18959 | hp2 | a0002 | c0001 | t0001 | g0093 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18962 | hp1 | a0002 | c0001 | t0001 | g0119 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18962 | hp2 | a0003 | c0003 | t0001 | g0294 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18966 | hp1 | a0003 | c0003 | t0001 | g0295 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0175 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0252 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18968 | hp1 | a0002 | c0001 | t0001 | g0092 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18970 | hp1 | a0002 | c0001 | t0002 | g0141 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18971 | hp1 | a0002 | c0001 | t0001 | g0270 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18971 | hp2 | a0002 | c0001 | t0001 | g0280 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18972 | hp1 | a0002 | c0001 | t0001 | g0096 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18973 | hp1 | a0002 | c0001 | t0001 | g0169 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18977 | hp1 | a0005 | c0008 | t0001 | g0261 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18978 | hp1 | a0002 | c0001 | t0001 | g0160 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18984 | hp1 | a0003 | c0003 | t0001 | g0130 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18990 | hp1 | a0002 | c0001 | t0002 | g0137 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0190 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18998 | hp2 | a0004 | c0006 | t0001 | g0315 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA18999 | hp2 | a0002 | c0001 | t0002 | g0139 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19002 | hp2 | a0002 | c0001 | t0003 | g0187 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19004 | hp1 | a0002 | c0001 | t0001 | g0114 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19005 | hp1 | a0002 | c0001 | t0001 | g0095 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19005 | hp2 | a0002 | c0001 | t0001 | g0158 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19006 | hp1 | a0002 | c0001 | t0003 | g0106 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19009 | hp1 | a0002 | c0001 | t0001 | g0174 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | LWK | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19030 | hp2 | a0002 | c0001 | t0002 | g0006 | AFR | LWK | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19054 | hp1 | a0002 | c0001 | t0002 | g0138 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19055 | hp1 | a0002 | c0001 | t0001 | g0287 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19057 | hp1 | a0002 | c0001 | t0003 | g0107 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19057 | hp2 | a0002 | c0001 | t0001 | g0297 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0254 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0128 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19068 | hp1 | a0002 | c0001 | t0002 | g0291 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19068 | hp2 | a0002 | c0001 | t0001 | g0251 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19079 | hp2 | a0004 | c0006 | t0001 | g0131 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19082 | hp1 | a0002 | c0001 | t0001 | g0233 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19084 | hp1 | a0002 | c0001 | t0001 | g0265 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19084 | hp2 | a0002 | c0001 | t0002 | g0140 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19087 | hp1 | a0002 | c0001 | t0001 | g0147 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19087 | hp2 | a0002 | c0001 | t0002 | g0109 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19091 | hp1 | a0002 | c0001 | t0001 | g0250 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19240 | hp1 | a0002 | c0001 | t0001 | g0014 | AFR | YRI | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | YRI | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0212 | EUR | TSI | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA20752 | hp2 | a0002 | c0001 | t0002 | g0037 | EUR | TSI | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA20805 | hp1 | a0010 | c0007 | t0001 | g0134 | EUR | TSI | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0262 | EUR | TSI | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0302 | SAS | GIH | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA20905 | hp2 | a0002 | c0001 | t0002 | g0058 | SAS | GIH | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0273 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG01123 | hp2 | a0002 | c0001 | t0002 | g0180 | AMR | CLM | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02109 | hp1 | a0002 | c0001 | t0001 | g0068 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02109 | hp2 | a0002 | c0001 | t0001 | g0223 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02559 | hp1 | a0006 | c0014 | t0001 | g0177 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0065 | AFR | ACB | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | MSL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG03471 | hp2 | a0001 | c0004 | t0004 | g0199 | AFR | MSL | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | USA | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0043 | AFR | USA | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0231 | AFR | USA | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA20300 | hp2 | a0002 | c0001 | t0001 | g0224 | AFR | USA | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA21309 | hp1 | a0002 | c0001 | t0001 | g0069 | AFR | LWK | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| NA21309 | hp2 | a0001 | c0005 | t0004 | g0215 | AFR | LWK | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0002 | g0050 | REF | REF | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0009 | REF | REF | CFAP52_chr17_9571642_9648447 | CFAP52 | chr17 | 9571642 | 9648447 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:9585891
|
T | A | 1 | a0010 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.189T>A | p.His63Gln | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 2/14 | 243/2166 | 189/1863 | 63/620 | chr17 | 9585891 | ||
| chr17:9585916
|
A | G | 1 | a0009 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.214A>G | p.Ile72Val | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 2/14 | 268/2166 | 214/1863 | 72/620 | chr17 | 9585916 | ||
| chr17:9598238
|
A | T | 1 | a0005 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.541A>T | p.Thr181Ser | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/14 | 595/2166 | 541/1863 | 181/620 | chr17 | 9598238 | ||
| chr17:9612395
|
T | A | 1 | a0008 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.941T>A | p.Ile314Asn | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/14 | 995/2166 | 941/1863 | 314/620 | chr17 | 9612395 | ||
| chr17:9612460
|
G | A | 5 | a0002a0003a0004others(2): Show | 159 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
missense_variant | MODERATE | c.1006G>A | p.Glu336Lys | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/14 | 1060/2166 | 1006/1863 | 336/620 | chr17 | 9612460 | ||
| chr17:9628789
|
C | A | 1 | a0003 | 4 | NA18949.hp2 NA18962.hp2 NA18966.hp1 others(1): Show |
missense_variant | MODERATE | c.1143C>A | p.Asp381Glu | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/14 | 1197/2166 | 1143/1863 | 381/620 | chr17 | 9628789 | ||
| chr17:9635504
|
G | A | 1 | a0004 | 2 | NA18998.hp2 NA19079.hp2 |
missense_variant | MODERATE | c.1420G>A | p.Glu474Lys | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/14 | 1474/2166 | 1420/1863 | 474/620 | chr17 | 9635504 | ||
| chr17:9641761
|
G | C | 1 | a0007 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1613G>C | p.Arg538Thr | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/14 | 1667/2166 | 1613/1863 | 538/620 | chr17 | 9641761 | ||
| chr17:9643107
|
C | T | 1 | a0006 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.1772C>T | p.Thr591Ile | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 14/14 | 1826/2166 | 1772/1863 | 591/620 | chr17 | 9643107 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:9598234
|
T | C | 1 | a0005c0008 | 1 | NA18977.hp1 | splice_region_variant&synonymous_variant | LOW | c.537T>C | p.Asn179Asn | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/14 | 591/2166 | 537/1863 | 179/620 | chr17 | 9598234 | ||
| chr17:9598240
|
A | C | 1 | a0005c0008 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.543A>C | p.Thr181Thr | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/14 | 597/2166 | 543/1863 | 181/620 | chr17 | 9598240 | ||
| chr17:9628711
|
T | C | 3 | a0001c0004a0001c0005a0001c0012 | 8 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(5): Show |
synonymous_variant | LOW | c.1065T>C | p.Asp355Asp | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/14 | 1119/2166 | 1065/1863 | 355/620 | chr17 | 9628711 | ||
| chr17:9628801
|
C | T | 1 | a0001c0012 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.1155C>T | p.Asp385Asp | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/14 | 1209/2166 | 1155/1863 | 385/620 | chr17 | 9628801 | ||
| chr17:9635476
|
G | T | 3 | a0001c0004a0001c0005a0002c0011 | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
synonymous_variant | LOW | c.1392G>T | p.Val464Val | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/14 | 1446/2166 | 1392/1863 | 464/620 | chr17 | 9635476 | ||
| chr17:9643027
|
A | C | 1 | a0001c0004 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.1692A>C | p.Gly564Gly | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 14/14 | 1746/2166 | 1692/1863 | 564/620 | chr17 | 9643027 | ||
| chr17:9643078
|
C | T | 1 | a0002c0010 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.1743C>T | p.His581His | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 14/14 | 1797/2166 | 1743/1863 | 581/620 | chr17 | 9643078 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:9643217
|
G | A | 1 | a0002c0001t0003 | 7 | HG02015.hp1 HG02040.hp1 NA18747.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*19G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 14/14 | 19 | chr17 | 9643217 | |||||
| chr17:9643234
|
G | A | 16 | a0001c0002t0001a0001c0004t0004a0001c0005t0001others(13): Show | 254 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*36G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 14/14 | 36 | chr17 | 9643234 | |||||
| chr17:9643320
|
C | T | 2 | a0001c0004t0004a0001c0005t0004 | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*122C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 14/14 | 122 | chr17 | 9643320 | |||||
| chr17:9643418
|
A | T | 2 | a0001c0004t0004a0001c0005t0004 | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*220A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 14/14 | 220 | chr17 | 9643418 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:9576897
|
A | C | 1 | a0004c0006t0001g0315 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.70+132A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9576897 | ||||||
| chr17:9576920
|
C | G | 1 | a0001c0002t0001g0314 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.70+155C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9576920 | ||||||
| chr17:9577239
|
A | G | 228 | a0001c0002t0001g0088a0001c0002t0001g0090a0001c0002t0001g0094others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.70+474A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9577239 | ||||||
| chr17:9577266
|
G | A | 2 | a0001c0002t0001g0003a0001c0002t0002g0002 | 2 | HG00323.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.70+501G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9577266 | ||||||
| chr17:9577268
|
A | T | 6 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.70+503A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9577268 | ||||||
| chr17:9577305
|
A | G | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.70+540A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9577305 | ||||||
| chr17:9577631
|
C | T | 1 | a0002c0001t0001g0313 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.70+866C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9577631 | ||||||
| chr17:9577797
|
A | G | 45 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0044others(42): Show | 46 | HG00639.hp1 HG01257.hp1 HG01258.hp2 others(43): Show |
intron_variant | MODIFIER | c.70+1032A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9577797 | ||||||
| chr17:9578023
|
C | A | 1 | a0002c0001t0002g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.70+1258C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578023 | ||||||
| chr17:9578048
|
C | T | 1 | a0001c0004t0004g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.70+1283C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578048 | ||||||
| chr17:9578103
|
A | G | 1 | a0001c0002t0001g0311 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.70+1338A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578103 | ||||||
| chr17:9578114
|
C | T | 11 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0030others(8): Show | 11 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+1349C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578114 | ||||||
| chr17:9578210
|
A | C | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025 | 3 | HG02886.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.70+1445A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578210 | ||||||
| chr17:9578346
|
C | T | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.70+1581C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578346 | ||||||
| chr17:9578389
|
C | G | 306 | a0001c0002t0001g0003a0001c0002t0001g0016a0001c0002t0001g0020others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.70+1624C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578389 | ||||||
| chr17:9578420
|
C | T | 1 | a0001c0002t0001g0310 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.70+1655C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578420 | ||||||
| chr17:9578430
|
A | G | 229 | a0001c0002t0001g0088a0001c0002t0001g0090a0001c0002t0001g0094others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.70+1665A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578430 | ||||||
| chr17:9578481
|
A | G | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025 | 3 | HG02886.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.70+1716A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578481 | ||||||
| chr17:9578485
|
T | A | 1 | a0002c0001t0002g0087 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.70+1720T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578485 | ||||||
| chr17:9578595
|
T | G | 306 | a0001c0002t0001g0003a0001c0002t0001g0016a0001c0002t0001g0020others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.70+1830T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578595 | ||||||
| chr17:9578596
|
T | A | 306 | a0001c0002t0001g0003a0001c0002t0001g0016a0001c0002t0001g0020others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.70+1831T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578596 | ||||||
| chr17:9578615
|
G | T | 2 | a0001c0002t0001g0003a0001c0002t0002g0002 | 2 | HG00323.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.70+1850G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578615 | ||||||
| chr17:9578703
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.70+1938G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578703 | ||||||
| chr17:9578826
|
T | G | 2 | a0002c0001t0001g0038a0002c0001t0001g0039 | 2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.70+2061T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578826 | ||||||
| chr17:9578854
|
G | A | 1 | a0002c0001t0001g0089 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.70+2089G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578854 | ||||||
| chr17:9578979
|
G | T | 2 | a0001c0002t0001g0003a0001c0002t0002g0002 | 2 | HG00323.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.70+2214G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578979 | ||||||
| chr17:9578994
|
G | T | 1 | a0001c0002t0001g0021 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.70+2229G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9578994 | ||||||
| chr17:9579067
|
G | A | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025 | 3 | HG02886.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.70+2302G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9579067 | ||||||
| chr17:9579195
|
A | G | 303 | a0001c0002t0001g0003a0001c0002t0001g0016a0001c0002t0001g0020others(300): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.70+2430A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9579195 | ||||||
| chr17:9579254
|
C | T | 137 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0184others(134): Show | 137 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.70+2489C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9579254 | ||||||
| chr17:9579332
|
G | A | 2 | a0001c0002t0001g0090a0002c0001t0002g0091 | 2 | HG01074.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.70+2567G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9579332 | ||||||
| chr17:9579389
|
G | T | 5 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025others(2): Show | 5 | HG02486.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+2624G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9579389 | ||||||
| chr17:9579426
|
G | A | 1 | a0002c0001t0001g0040 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.70+2661G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9579426 | ||||||
| chr17:9579493
|
G | A | 1 | a0001c0002t0001g0178 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.70+2728G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9579493 | ||||||
| chr17:9579586
|
G | C | 1 | a0001c0002t0001g0179 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.70+2821G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9579586 | ||||||
| chr17:9579631
|
G | A | 1 | a0002c0001t0002g0180 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.70+2866G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9579631 | ||||||
| chr17:9579648
|
A | C | 1 | a0001c0002t0001g0020 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.70+2883A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9579648 | ||||||
| chr17:9579693
|
A | G | 1 | a0001c0002t0001g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.70+2928A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9579693 | ||||||
| chr17:9579724
|
C | T | 1 | a0006c0014t0001g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.70+2959C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9579724 | ||||||
| chr17:9579859
|
C | T | 6 | a0001c0002t0001g0176a0002c0001t0001g0171a0002c0001t0001g0172others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+3094C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9579859 | ||||||
| chr17:9580318
|
T | TA | 210 | a0001c0002t0001g0003a0001c0002t0001g0023a0001c0002t0001g0024others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.70+3570dupA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 9580318 | |||||
| chr17:9580318
|
T | TAA | 7 | a0001c0002t0002g0002a0001c0012t0001g0022a0002c0001t0001g0092others(4): Show | 7 | HG01109.hp1 HG01169.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+3569_70+3570dup others(2): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 9580318 | |||||
| chr17:9580318
|
TA | T | 7 | a0001c0002t0001g0012a0001c0002t0001g0075a0001c0002t0001g0076others(4): Show | 7 | HG02145.hp2 HG02809.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.70+3570delA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 9580318 | |||||
| chr17:9580415
|
C | T | 1 | a0002c0001t0001g0166 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.70+3650C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9580415 | ||||||
| chr17:9580582
|
G | A | 7 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025others(4): Show | 7 | HG02602.hp1 HG02886.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.70+3817G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9580582 | ||||||
| chr17:9580614
|
G | A | 2 | a0001c0002t0001g0184a0002c0001t0002g0185 | 2 | HG01168.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.70+3849G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9580614 | ||||||
| chr17:9580688
|
CA | C | 155 | a0001c0002t0001g0003a0001c0002t0001g0023a0001c0002t0001g0024others(152): Show | 156 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.70+3939delA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 9580688 | |||||
| chr17:9580688
|
CAA | C | 91 | a0001c0002t0001g0088a0001c0002t0001g0090a0001c0002t0001g0099others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.70+3938_70+3939del others(2): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 9580688 | |||||
| chr17:9580758
|
G | GA | 243 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.70+4002dupA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 9580758 | |||||
| chr17:9580853
|
T | C | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.70+4088T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9580853 | ||||||
| chr17:9580880
|
A | G | 247 | a0001c0002t0001g0003a0001c0002t0001g0023a0001c0002t0001g0024others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.70+4115A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9580880 | ||||||
| chr17:9580938
|
C | T | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025 | 3 | HG02886.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.70+4173C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9580938 | ||||||
| chr17:9581186
|
G | C | 1 | a0002c0001t0001g0014 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.70+4421G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9581186 | ||||||
| chr17:9581234
|
G | A | 5 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0101others(2): Show | 5 | HG00099.hp1 HG01074.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+4469G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9581234 | ||||||
| chr17:9581416
|
C | T | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025 | 3 | HG02886.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.71-4357C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9581416 | ||||||
| chr17:9581417
|
T | A | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025 | 3 | HG02886.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.71-4356T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9581417 | ||||||
| chr17:9581635
|
A | G | 1 | a0002c0001t0001g0286 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.71-4138A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9581635 | ||||||
| chr17:9581669
|
G | A | 1 | a0007c0013t0001g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.71-4104G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9581669 | ||||||
| chr17:9581731
|
A | T | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025 | 3 | HG02886.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.71-4042A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9581731 | ||||||
| chr17:9581741
|
A | C | 1 | a0001c0002t0001g0021 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.71-4032A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9581741 | ||||||
| chr17:9581805
|
A | G | 1 | a0002c0001t0002g0285 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.71-3968A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9581805 | ||||||
| chr17:9581809
|
A | G | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025 | 3 | HG02886.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.71-3964A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9581809 | ||||||
| chr17:9582249
|
G | A | 1 | a0001c0002t0001g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.71-3524G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9582249 | ||||||
| chr17:9582752
|
T | C | 2 | a0001c0002t0001g0034a0002c0001t0001g0035 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.71-3021T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9582752 | ||||||
| chr17:9582833
|
C | T | 4 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0033others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-2940C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9582833 | ||||||
| chr17:9582845
|
T | C | 244 | a0001c0002t0001g0003a0001c0002t0001g0023a0001c0002t0001g0024others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.71-2928T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9582845 | ||||||
| chr17:9582871
|
G | A | 3 | a0001c0002t0001g0021a0001c0002t0001g0080a0002c0001t0001g0013 | 3 | HG02572.hp2 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.71-2902G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9582871 | ||||||
| chr17:9583018
|
G | A | 1 | a0002c0001t0003g0187 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.71-2755G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9583018 | ||||||
| chr17:9583047
|
G | A | 5 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025others(2): Show | 5 | HG02486.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-2726G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9583047 | ||||||
| chr17:9583123
|
T | C | 1 | a0002c0001t0002g0188 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.71-2650T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9583123 | ||||||
| chr17:9583182
|
C | A | 244 | a0001c0002t0001g0003a0001c0002t0001g0023a0001c0002t0001g0024others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.71-2591C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9583182 | ||||||
| chr17:9583191
|
A | G | 2 | a0001c0002t0001g0034a0002c0001t0001g0035 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.71-2582A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9583191 | ||||||
| chr17:9583334
|
T | G | 2 | a0001c0002t0001g0189a0002c0001t0001g0190 | 2 | NA18945.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.71-2439T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9583334 | ||||||
| chr17:9583582
|
T | C | 241 | a0001c0002t0001g0003a0001c0002t0001g0026a0001c0002t0001g0027others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.71-2191T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9583582 | ||||||
| chr17:9583768
|
G | A | 129 | a0001c0002t0001g0088a0001c0002t0001g0090a0001c0002t0001g0094others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.71-2005G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9583768 | ||||||
| chr17:9583963
|
A | G | 1 | a0001c0002t0001g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.71-1810A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9583963 | ||||||
| chr17:9583987
|
C | T | 4 | a0001c0002t0001g0020a0001c0002t0001g0023a0001c0002t0001g0024others(1): Show | 4 | HG02886.hp2 HG02976.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-1786C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9583987 | ||||||
| chr17:9583988
|
G | A | 1 | a0007c0013t0001g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.71-1785G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9583988 | ||||||
| chr17:9584002
|
A | G | 5 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025others(2): Show | 5 | HG02486.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-1771A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584002 | ||||||
| chr17:9584047
|
CAT | C | 5 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0032others(2): Show | 5 | HG02615.hp2 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-1725_71-1724del others(2): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584047 | ||||||
| chr17:9584120
|
C | A | 40 | a0001c0002t0001g0184a0001c0002t0001g0193a0001c0002t0001g0194others(37): Show | 40 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.71-1653C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584120 | ||||||
| chr17:9584225
|
T | C | 3 | a0003c0003t0001g0293a0003c0003t0001g0294a0003c0003t0001g0295 | 3 | NA18949.hp2 NA18962.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.71-1548T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584225 | ||||||
| chr17:9584392
|
C | T | 1 | a0001c0002t0001g0282 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.71-1381C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584392 | ||||||
| chr17:9584396
|
A | C | 1 | a0001c0002t0001g0282 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.71-1377A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584396 | ||||||
| chr17:9584473
|
C | A | 1 | a0001c0005t0001g0074 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.71-1300C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584473 | ||||||
| chr17:9584539
|
C | T | 2 | a0002c0001t0001g0028a0002c0001t0001g0029 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.71-1234C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584539 | ||||||
| chr17:9584561
|
T | G | 1 | a0002c0001t0002g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.71-1212T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584561 | ||||||
| chr17:9584594
|
C | A | 1 | a0002c0001t0001g0038 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.71-1179C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584594 | ||||||
| chr17:9584599
|
T | TTCAAATA others(3): Show |
246 | a0001c0002t0001g0003a0001c0002t0001g0023a0001c0002t0001g0024others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.71-1174_71-1173ins others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584599 | ||||||
| chr17:9584608
|
AT | A | 246 | a0001c0002t0001g0003a0001c0002t0001g0023a0001c0002t0001g0024others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.71-1155delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 9584608 | |||||
| chr17:9584690
|
C | T | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.71-1083C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584690 | ||||||
| chr17:9584707
|
C | T | 2 | a0001c0002t0001g0034a0002c0001t0001g0035 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.71-1066C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584707 | ||||||
| chr17:9584717
|
G | T | 1 | a0002c0001t0001g0281 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.71-1056G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584717 | ||||||
| chr17:9584835
|
C | T | 5 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0032others(2): Show | 5 | HG02615.hp2 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-938C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584835 | ||||||
| chr17:9584866
|
G | A | 2 | a0001c0002t0001g0023a0001c0002t0001g0025 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.71-907G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9584866 | ||||||
| chr17:9585225
|
A | C | 1 | a0002c0001t0001g0280 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.71-548A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585225 | ||||||
| chr17:9585305
|
G | A | 2 | a0001c0002t0001g0221a0002c0001t0001g0103 | 2 | HG02155.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.71-468G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585305 | ||||||
| chr17:9585311
|
C | T | 1 | a0002c0001t0002g0220 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.71-462C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585311 | ||||||
| chr17:9585390
|
C | T | 41 | a0001c0002t0001g0011a0001c0002t0001g0021a0001c0002t0001g0032others(38): Show | 41 | HG01071.hp2 HG01109.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.71-383C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585390 | ||||||
| chr17:9585396
|
C | T | 1 | a0001c0002t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.71-377C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585396 | ||||||
| chr17:9585442
|
A | G | 299 | a0001c0002t0001g0003a0001c0002t0001g0010a0001c0002t0001g0011others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.71-331A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585442 | ||||||
| chr17:9585465
|
A | G | 2 | a0002c0001t0002g0164a0002c0001t0002g0211 | 2 | HG00099.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.71-308A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585465 | ||||||
| chr17:9585531
|
T | C | 1 | a0001c0002t0001g0165 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.71-242T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585531 | ||||||
| chr17:9585532
|
G | A | 1 | a0001c0002t0001g0165 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.71-241G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585532 | ||||||
| chr17:9585541
|
G | T | 1 | a0001c0002t0001g0165 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.71-232G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585541 | ||||||
| chr17:9585543
|
T | C | 127 | a0001c0002t0001g0010a0001c0002t0001g0048a0001c0002t0001g0065others(124): Show | 128 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.71-230T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585543 | ||||||
| chr17:9585564
|
G | A | 2 | a0001c0004t0004g0036a0001c0004t0004g0199 | 2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.71-209G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585564 | ||||||
| chr17:9585617
|
GC | G | 314 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0007others(311): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.71-153delC | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 9585617 | |||||
| chr17:9585711
|
A | G | 3 | a0001c0002t0001g0083a0002c0001t0001g0082a0002c0001t0001g0086 | 3 | HG03041.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.71-62A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585711 | ||||||
| chr17:9585766
|
C | T | 1 | a0002c0001t0001g0163 | 1 | NA18956.hp2 | splice_region_variant&intron_variant | LOW | c.71-7C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 1/13 | chr17 | 9585766 | ||||||
| chr17:9586162
|
C | T | 2 | a0002c0001t0001g0279a0002c0001t0001g0308 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.270+190C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 2/13 | chr17 | 9586162 | ||||||
| chr17:9586257
|
C | T | 1 | a0002c0001t0001g0254 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.270+285C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 2/13 | chr17 | 9586257 | ||||||
| chr17:9586258
|
G | A | 12 | a0001c0002t0001g0020a0001c0002t0001g0026a0001c0002t0001g0132others(9): Show | 12 | HG01175.hp1 HG01192.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.270+286G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 2/13 | chr17 | 9586258 | ||||||
| chr17:9586280
|
C | T | 2 | a0002c0001t0001g0272a0002c0001t0002g0183 | 2 | HG01169.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.270+308C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 2/13 | chr17 | 9586280 | ||||||
| chr17:9586281
|
G | A | 1 | a0002c0001t0002g0050 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.270+309G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 2/13 | chr17 | 9586281 | ||||||
| chr17:9586318
|
C | A | 25 | a0001c0002t0001g0011a0001c0002t0001g0024a0001c0002t0001g0030others(22): Show | 26 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.270+346C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 2/13 | chr17 | 9586318 | ||||||
| chr17:9586427
|
C | G | 311 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(308): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.271-271C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 2/13 | chr17 | 9586427 | ||||||
| chr17:9586455
|
C | T | 7 | a0001c0002t0001g0011a0001c0002t0001g0025a0001c0002t0001g0027others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-243C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 2/13 | chr17 | 9586455 | ||||||
| chr17:9586568
|
CA | C | 289 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(286): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.271-113delA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 9586568 | |||||
| chr17:9587014
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.407+180C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9587014 | ||||||
| chr17:9587016
|
T | TC | 314 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0007others(311): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.407+183dupC | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9587016 | |||||
| chr17:9587024
|
C | A | 87 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0048others(84): Show | 88 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.407+190C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9587024 | ||||||
| chr17:9587057
|
C | G | 1 | a0002c0001t0002g0060 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.407+223C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9587057 | ||||||
| chr17:9587133
|
T | C | 255 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.407+299T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9587133 | ||||||
| chr17:9587162
|
C | T | 307 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(304): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.407+328C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9587162 | ||||||
| chr17:9587808
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.407+974C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9587808 | ||||||
| chr17:9587809
|
G | A | 2 | a0001c0002t0001g0011a0009c0015t0001g0064 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.407+975G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9587809 | ||||||
| chr17:9587847
|
G | A | 1 | a0001c0002t0001g0083 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.407+1013G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9587847 | ||||||
| chr17:9587905
|
A | G | 3 | a0001c0002t0001g0025a0001c0002t0001g0271a0001c0002t0001g0314 | 3 | HG01891.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.407+1071A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9587905 | ||||||
| chr17:9587916
|
G | A | 2 | a0001c0002t0001g0011a0009c0015t0001g0064 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.407+1082G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9587916 | ||||||
| chr17:9587954
|
G | A | 14 | a0001c0002t0001g0020a0001c0002t0001g0026a0001c0002t0001g0065others(11): Show | 14 | HG01175.hp1 HG01192.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.407+1120G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9587954 | ||||||
| chr17:9588167
|
G | A | 2 | a0001c0002t0001g0030a0007c0013t0001g0015 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.407+1333G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588167 | ||||||
| chr17:9588268
|
G | A | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.407+1434G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588268 | ||||||
| chr17:9588271
|
A | G | 1 | a0001c0002t0001g0083 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.407+1437A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588271 | ||||||
| chr17:9588272
|
C | A | 1 | a0001c0002t0001g0296 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.407+1438C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588272 | ||||||
| chr17:9588283
|
C | T | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.407+1449C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588283 | ||||||
| chr17:9588364
|
C | T | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.407+1530C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588364 | ||||||
| chr17:9588370
|
G | A | 3 | a0001c0002t0001g0076a0001c0005t0001g0074a0001c0005t0001g0077 | 3 | HG02145.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.407+1536G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588370 | ||||||
| chr17:9588429
|
G | A | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.407+1595G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588429 | ||||||
| chr17:9588535
|
T | C | 82 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0048others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.407+1701T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588535 | ||||||
| chr17:9588597
|
G | C | 81 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0048others(78): Show | 81 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.407+1763G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588597 | ||||||
| chr17:9588746
|
A | G | 7 | a0001c0002t0001g0011a0001c0002t0001g0025a0001c0002t0001g0027others(4): Show | 7 | HG01891.hp2 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.407+1912A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588746 | ||||||
| chr17:9588774
|
A | AT | 5 | a0001c0002t0001g0111a0001c0002t0001g0231a0001c0004t0004g0001others(2): Show | 6 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.407+1955dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9588774 | |||||
| chr17:9588774
|
A | ATT | 288 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.407+1954_407+1955d others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9588774 | |||||
| chr17:9588774
|
A | ATTT | 7 | a0001c0002t0001g0063a0001c0002t0001g0070a0001c0002t0001g0083others(4): Show | 7 | HG02155.hp1 HG02155.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.407+1953_407+1955d others(5): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9588774 | |||||
| chr17:9588774
|
ATT | A | 7 | a0001c0002t0001g0011a0001c0002t0001g0025a0001c0002t0001g0027others(4): Show | 7 | HG01891.hp2 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.407+1954_407+1955d others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9588774 | |||||
| chr17:9588822
|
G | C | 4 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0257others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.407+1988G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588822 | ||||||
| chr17:9588827
|
A | G | 1 | a0002c0001t0003g0187 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.407+1993A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588827 | ||||||
| chr17:9588972
|
G | A | 3 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0284 | 3 | HG02922.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.407+2138G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9588972 | ||||||
| chr17:9589017
|
A | G | 310 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.407+2183A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589017 | ||||||
| chr17:9589024
|
C | G | 14 | a0001c0002t0001g0020a0001c0002t0001g0026a0001c0002t0001g0065others(11): Show | 14 | HG01175.hp1 HG01192.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.407+2190C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589024 | ||||||
| chr17:9589137
|
A | G | 2 | a0001c0002t0001g0010a0001c0002t0001g0078 | 2 | HG01243.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.407+2303A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589137 | ||||||
| chr17:9589240
|
A | G | 1 | a0001c0002t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.407+2406A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589240 | ||||||
| chr17:9589441
|
T | A | 14 | a0001c0002t0001g0020a0001c0002t0001g0026a0001c0002t0001g0065others(11): Show | 14 | HG01175.hp1 HG01192.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.407+2607T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589441 | ||||||
| chr17:9589452
|
G | A | 1 | a0006c0014t0001g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.407+2618G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589452 | ||||||
| chr17:9589481
|
C | A | 40 | a0001c0002t0001g0048a0001c0002t0001g0090a0001c0002t0001g0196others(37): Show | 40 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.407+2647C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589481 | ||||||
| chr17:9589481
|
C | G | 41 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0052others(38): Show | 41 | HG00621.hp2 HG00639.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.407+2647C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589481 | ||||||
| chr17:9589484
|
G | A | 2 | a0002c0001t0001g0112a0002c0010t0001g0142 | 2 | NA18942.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.407+2650G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589484 | ||||||
| chr17:9589606
|
G | A | 4 | a0001c0002t0001g0255a0001c0002t0001g0284a0002c0001t0001g0019others(1): Show | 4 | HG02109.hp2 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.407+2772G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589606 | ||||||
| chr17:9589673
|
C | T | 1 | a0001c0002t0001g0083 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.407+2839C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589673 | ||||||
| chr17:9589720
|
G | A | 2 | a0001c0002t0001g0027a0002c0001t0001g0017 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.407+2886G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589720 | ||||||
| chr17:9589727
|
C | T | 4 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0257others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.407+2893C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589727 | ||||||
| chr17:9589732
|
CA | C | 6 | a0001c0002t0001g0025a0001c0002t0001g0027a0001c0002t0001g0073others(3): Show | 6 | HG01891.hp2 HG02738.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.407+2920delA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9589732 | |||||
| chr17:9589732
|
CAA | C | 287 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(284): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.407+2919_407+2920d others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9589732 | |||||
| chr17:9589732
|
CAAA | C | 15 | a0001c0002t0001g0020a0001c0002t0001g0026a0001c0002t0001g0065others(12): Show | 15 | HG01175.hp1 HG01192.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.407+2918_407+2920d others(5): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9589732 | |||||
| chr17:9589743
|
A | T | 3 | a0001c0002t0001g0278a0002c0001t0001g0270a0002c0001t0002g0059 | 3 | HG02630.hp1 HG04115.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.407+2909A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589743 | ||||||
| chr17:9589747
|
A | T | 273 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.407+2913A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589747 | ||||||
| chr17:9589751
|
A | G | 7 | a0001c0002t0001g0048a0001c0002t0001g0075a0001c0002t0001g0084others(4): Show | 7 | HG01109.hp2 HG01433.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+2917A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589751 | ||||||
| chr17:9589751
|
A | T | 293 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.407+2917A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589751 | ||||||
| chr17:9589801
|
C | CTTTTT | 7 | a0001c0002t0001g0076a0001c0002t0001g0278a0001c0005t0001g0074others(4): Show | 7 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+2977_407+2981d others(7): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9589801 | |||||
| chr17:9589801
|
C | CTTTTTT | 18 | a0001c0002t0001g0007a0001c0002t0001g0012a0001c0002t0001g0025others(15): Show | 18 | HG01891.hp2 HG02280.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.407+2976_407+2981d others(8): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9589801 | |||||
| chr17:9589801
|
C | CTTTTTTT | 157 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0010others(154): Show | 158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.407+2975_407+2981d others(9): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9589801 | |||||
| chr17:9589801
|
C | CTTTTTTT others(1): Show |
41 | a0001c0002t0001g0011a0001c0002t0001g0020a0001c0002t0001g0026others(38): Show | 41 | HG01175.hp1 HG01192.hp2 HG01256.hp2 others(38): Show |
intron_variant | MODIFIER | c.407+2974_407+2981d others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9589801 | |||||
| chr17:9589801
|
C | CTTTTTTT others(2): Show |
74 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0048others(71): Show | 74 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.407+2973_407+2981d others(11): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9589801 | |||||
| chr17:9589801
|
C | CTTTTTTT others(3): Show |
10 | a0001c0002t0001g0084a0001c0002t0001g0085a0001c0002t0001g0176others(7): Show | 10 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.407+2972_407+2981d others(12): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9589801 | |||||
| chr17:9589830
|
C | A | 2 | a0001c0002t0001g0226a0001c0002t0001g0227 | 2 | HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.407+2996C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589830 | ||||||
| chr17:9589954
|
C | G | 1 | a0001c0005t0001g0077 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.407+3120C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9589954 | ||||||
| chr17:9590102
|
T | A | 1 | a0002c0001t0001g0270 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.407+3268T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9590102 | ||||||
| chr17:9590154
|
C | T | 2 | a0001c0002t0001g0011a0009c0015t0001g0064 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.407+3320C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9590154 | ||||||
| chr17:9590464
|
G | A | 5 | a0002c0001t0001g0039a0002c0001t0001g0040a0002c0001t0001g0046others(2): Show | 5 | HG03491.hp2 HG03831.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.407+3630G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9590464 | ||||||
| chr17:9590600
|
C | T | 8 | a0001c0002t0001g0011a0001c0002t0001g0025a0001c0002t0001g0027others(5): Show | 8 | HG01891.hp2 HG02717.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.408-3593C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9590600 | ||||||
| chr17:9590729
|
T | G | 1 | a0001c0002t0001g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.408-3464T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9590729 | ||||||
| chr17:9590751
|
C | A | 1 | a0002c0001t0001g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.408-3442C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9590751 | ||||||
| chr17:9590755
|
C | T | 2 | a0001c0002t0001g0030a0007c0013t0001g0015 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.408-3438C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9590755 | ||||||
| chr17:9590828
|
T | TA | 67 | a0001c0002t0001g0010a0001c0002t0001g0012a0001c0002t0001g0041others(64): Show | 67 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.408-3358dupA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9590828 | |||||
| chr17:9590867
|
G | T | 9 | a0001c0002t0001g0024a0001c0002t0001g0052a0001c0002t0001g0214others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.408-3326G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9590867 | ||||||
| chr17:9591030
|
C | CT | 251 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0012others(248): Show | 252 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.408-3139dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9591030 | |||||
| chr17:9591030
|
C | CTT | 27 | a0001c0002t0001g0003a0001c0002t0001g0026a0001c0002t0001g0030others(24): Show | 27 | HG00323.hp2 HG00621.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.408-3140_408-3139d others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9591030 | |||||
| chr17:9591030
|
C | CTTTTTTT others(9): Show |
1 | a0002c0001t0001g0174 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.408-3154_408-3139d others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9591030 | |||||
| chr17:9591030
|
CT | C | 6 | a0001c0002t0001g0011a0001c0002t0001g0025a0001c0002t0001g0083others(3): Show | 6 | HG02717.hp1 HG02976.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.408-3139delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9591030 | |||||
| chr17:9591073
|
T | C | 80 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0048others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.408-3120T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9591073 | ||||||
| chr17:9591163
|
A | G | 4 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0257others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.408-3030A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9591163 | ||||||
| chr17:9591183
|
A | G | 310 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.408-3010A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9591183 | ||||||
| chr17:9591210
|
C | T | 310 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.408-2983C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9591210 | ||||||
| chr17:9591225
|
CG | C | 305 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(302): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.408-2963delG | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9591225 | |||||
| chr17:9591227
|
G | A | 220 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(217): Show | 221 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.408-2966G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9591227 | ||||||
| chr17:9591258
|
G | A | 305 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(302): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.408-2935G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9591258 | ||||||
| chr17:9591289
|
C | T | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.408-2904C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9591289 | ||||||
| chr17:9591544
|
C | T | 6 | a0002c0001t0001g0313a0002c0001t0002g0164a0002c0001t0002g0181others(3): Show | 6 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.408-2649C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9591544 | ||||||
| chr17:9591554
|
T | C | 2 | a0001c0002t0001g0030a0007c0013t0001g0015 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.408-2639T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9591554 | ||||||
| chr17:9591595
|
G | T | 1 | a0002c0001t0001g0061 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.408-2598G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9591595 | ||||||
| chr17:9591663
|
G | A | 216 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(213): Show | 216 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.408-2530G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9591663 | ||||||
| chr17:9592047
|
T | C | 3 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0284 | 3 | HG02922.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.408-2146T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9592047 | ||||||
| chr17:9592075
|
G | A | 1 | a0001c0002t0001g0111 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.408-2118G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9592075 | ||||||
| chr17:9592158
|
C | A | 1 | a0001c0002t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.408-2035C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9592158 | ||||||
| chr17:9592401
|
A | AGAGGTTG others(9): Show |
2 | a0001c0002t0001g0025a0001c0002t0001g0271 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.408-1791_408-1776d others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9592401 | |||||
| chr17:9592430
|
T | C | 1 | a0001c0002t0001g0066 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.408-1763T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9592430 | ||||||
| chr17:9592464
|
C | T | 3 | a0001c0002t0001g0090a0001c0002t0001g0196a0009c0015t0001g0064 | 3 | HG01074.hp2 HG01256.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.408-1729C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9592464 | ||||||
| chr17:9592465
|
G | A | 1 | a0002c0001t0001g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.408-1728G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9592465 | ||||||
| chr17:9592522
|
A | T | 113 | a0001c0002t0001g0011a0001c0002t0001g0027a0001c0002t0001g0063others(110): Show | 114 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.408-1671A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9592522 | ||||||
| chr17:9592538
|
GC | G | 9 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0041others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.408-1651delC | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9592538 | |||||
| chr17:9592625
|
C | A | 2 | a0001c0002t0001g0179a0001c0002t0001g0306 | 2 | HG02135.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.408-1568C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9592625 | ||||||
| chr17:9592698
|
A | AT | 9 | a0001c0002t0001g0011a0001c0002t0001g0027a0001c0002t0001g0063others(6): Show | 9 | HG02630.hp2 HG02717.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.408-1489dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 9592698 | |||||
| chr17:9592795
|
T | C | 308 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.408-1398T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9592795 | ||||||
| chr17:9592869
|
C | T | 6 | a0001c0002t0001g0126a0001c0002t0001g0156a0001c0002t0001g0170others(3): Show | 6 | NA18948.hp1 NA18951.hp2 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.408-1324C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9592869 | ||||||
| chr17:9592965
|
G | C | 1 | a0009c0015t0001g0064 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408-1228G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9592965 | ||||||
| chr17:9593119
|
A | T | 1 | a0001c0002t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.408-1074A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9593119 | ||||||
| chr17:9593203
|
C | T | 4 | a0001c0002t0001g0243a0001c0002t0001g0244a0001c0002t0001g0245others(1): Show | 4 | NA18954.hp1 NA18973.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.408-990C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9593203 | ||||||
| chr17:9593279
|
G | T | 1 | a0002c0001t0001g0019 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.408-914G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9593279 | ||||||
| chr17:9593486
|
C | T | 2 | a0001c0002t0001g0025a0001c0002t0001g0271 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.408-707C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9593486 | ||||||
| chr17:9593558
|
C | T | 1 | a0001c0002t0001g0311 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.408-635C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9593558 | ||||||
| chr17:9593826
|
A | G | 310 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.408-367A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9593826 | ||||||
| chr17:9593828
|
G | C | 13 | a0001c0002t0001g0011a0001c0002t0001g0027a0001c0002t0001g0076others(10): Show | 14 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.408-365G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9593828 | ||||||
| chr17:9593865
|
C | T | 1 | a0009c0015t0001g0064 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408-328C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9593865 | ||||||
| chr17:9593897
|
G | A | 1 | a0001c0002t0001g0027 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.408-296G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 3/13 | chr17 | 9593897 | ||||||
| chr17:9594410
|
C | T | 1 | a0002c0001t0001g0233 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.536+89C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9594410 | ||||||
| chr17:9594621
|
T | A | 1 | a0001c0002t0001g0219 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.536+300T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9594621 | ||||||
| chr17:9594754
|
C | T | 3 | a0001c0002t0001g0076a0001c0005t0001g0074a0001c0005t0001g0077 | 3 | HG02145.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.536+433C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9594754 | ||||||
| chr17:9594893
|
G | GT | 25 | a0001c0002t0001g0007a0001c0002t0001g0010a0001c0002t0001g0021others(22): Show | 25 | HG00639.hp1 HG01243.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.536+589dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9594893 | |||||
| chr17:9594893
|
G | GTT | 164 | a0001c0002t0001g0011a0001c0002t0001g0024a0001c0002t0001g0025others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.536+588_536+589dup others(2): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9594893 | |||||
| chr17:9594893
|
G | GTTT | 22 | a0001c0002t0001g0115a0001c0002t0001g0155a0001c0002t0001g0176others(19): Show | 22 | HG01255.hp1 HG01884.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.536+587_536+589dup others(3): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9594893 | |||||
| chr17:9594893
|
G | T | 1 | a0001c0002t0001g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.536+572G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9594893 | ||||||
| chr17:9594893
|
GT | G | 89 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0016others(86): Show | 89 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.536+589delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9594893 | |||||
| chr17:9595016
|
A | G | 1 | a0001c0002t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.536+695A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9595016 | ||||||
| chr17:9595052
|
G | A | 1 | a0001c0002t0001g0156 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.536+731G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9595052 | ||||||
| chr17:9595167
|
T | G | 1 | a0001c0002t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.536+846T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9595167 | ||||||
| chr17:9595490
|
G | A | 2 | a0001c0002t0001g0030a0007c0013t0001g0015 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.536+1169G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9595490 | ||||||
| chr17:9595492
|
C | T | 1 | a0002c0001t0002g0060 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.536+1171C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9595492 | ||||||
| chr17:9595493
|
A | G | 294 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0011others(291): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.536+1172A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9595493 | ||||||
| chr17:9595603
|
A | T | 303 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(300): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.536+1282A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9595603 | ||||||
| chr17:9596044
|
G | T | 2 | a0002c0001t0001g0019a0002c0001t0001g0223 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.536+1723G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596044 | ||||||
| chr17:9596051
|
A | ATG | 10 | a0001c0002t0001g0024a0001c0002t0001g0101a0001c0002t0001g0226others(7): Show | 10 | HG00639.hp2 HG01074.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.536+1738_536+1739d others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596051 | |||||
| chr17:9596051
|
A | ATGTG | 15 | a0001c0002t0001g0010a0001c0002t0001g0078a0001c0002t0001g0207others(12): Show | 15 | HG00735.hp2 HG00741.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.536+1736_536+1739d others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596051 | |||||
| chr17:9596051
|
A | ATGTGTG | 17 | a0001c0002t0001g0052a0001c0002t0001g0176a0001c0002t0001g0202others(14): Show | 17 | HG01081.hp1 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.536+1734_536+1739d others(8): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596051 | |||||
| chr17:9596051
|
A | ATGTGTGT others(1): Show |
15 | a0001c0002t0001g0090a0001c0002t0001g0196a0001c0002t0001g0222others(12): Show | 15 | HG01069.hp1 HG01069.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.536+1732_536+1739d others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596051 | |||||
| chr17:9596051
|
A | G | 6 | a0001c0002t0001g0011a0001c0002t0001g0026a0001c0002t0001g0076others(3): Show | 6 | HG00735.hp1 HG02145.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.536+1730A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596051 | ||||||
| chr17:9596051
|
ATG | A | 27 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0088others(24): Show | 28 | HG00438.hp1 HG00621.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.536+1738_536+1739d others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596051 | |||||
| chr17:9596057
|
G | GTGTA | 18 | a0001c0002t0001g0186a0001c0002t0001g0232a0001c0002t0001g0276others(15): Show | 18 | HG02055.hp2 HG02080.hp1 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.536+1738_536+1741d others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596057 | |||||
| chr17:9596057
|
GTGTA | G | 14 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0073others(11): Show | 14 | HG00423.hp1 HG00741.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.536+1738_536+1741d others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596057 | |||||
| chr17:9596057
|
GTGTATA | G | 11 | a0001c0002t0001g0016a0001c0002t0001g0045a0001c0002t0001g0094others(8): Show | 11 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.536+1738_536+1743d others(8): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596057 | |||||
| chr17:9596057
|
GTGTATAT others(1): Show |
G | 13 | a0001c0002t0001g0083a0001c0002t0001g0111a0001c0002t0001g0122others(10): Show | 13 | HG02083.hp1 HG02132.hp2 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.536+1738_536+1745d others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596057 | |||||
| chr17:9596057
|
GTGTATAT others(3): Show |
G | 10 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(7): Show | 10 | HG01175.hp2 HG01433.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.536+1738_536+1747d others(12): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596057 | |||||
| chr17:9596057
|
GTGTATAT others(5): Show |
G | 2 | a0001c0002t0001g0126a0001c0012t0001g0022 | 2 | HG02965.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.536+1738_536+1749d others(14): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596057 | |||||
| chr17:9596057
|
GTGTATAT others(21): Show |
G | 1 | a0001c0002t0001g0240 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.536+1738_536+1765d others(30): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596057 | |||||
| chr17:9596057
|
GTGTATAT others(25): Show |
G | 2 | a0001c0002t0001g0153a0001c0002t0001g0157 | 2 | HG02056.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.536+1738_536+1769d others(34): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596057 | |||||
| chr17:9596059
|
G | A | 10 | a0001c0002t0001g0003a0001c0002t0001g0031a0001c0002t0001g0062others(7): Show | 10 | HG00323.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.536+1738G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596059 | ||||||
| chr17:9596059
|
G | GTATGTA | 12 | a0001c0002t0001g0034a0001c0002t0001g0115a0001c0002t0001g0221others(9): Show | 12 | HG00621.hp2 HG00673.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.536+1741_536+1742i others(8): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
G | GTATGTAT others(1): Show |
6 | a0002c0001t0001g0038a0002c0001t0001g0095a0002c0001t0001g0112others(3): Show | 6 | HG02602.hp1 HG03831.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.536+1741_536+1742i others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
G | GTATGTAT others(7): Show |
1 | a0002c0001t0001g0190 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.536+1741_536+1742i others(16): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
G | GTGTGTGT others(1): Show |
8 | a0001c0002t0001g0100a0002c0001t0001g0053a0002c0001t0001g0055others(5): Show | 8 | HG00099.hp1 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.536+1739_536+1740i others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
G | GTGTGTGT others(3): Show |
1 | a0001c0002t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.536+1739_536+1740i others(12): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
G | GTGTGTGT others(3): Show |
2 | a0002c0001t0002g0037a0002c0001t0002g0203 | 2 | HG02602.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.536+1739_536+1740i others(12): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
GTA | G | 27 | a0001c0002t0001g0025a0001c0002t0001g0033a0001c0002t0001g0165others(24): Show | 27 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.536+1780_536+1781d others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
GTATA | G | 9 | a0001c0002t0001g0156a0001c0002t0001g0263a0001c0002t0001g0274others(6): Show | 9 | HG00438.hp2 HG02280.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.536+1778_536+1781d others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
GTATATA | G | 3 | a0001c0005t0004g0215a0002c0001t0001g0286a0005c0008t0001g0261 | 3 | HG01106.hp1 NA18977.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.536+1776_536+1781d others(8): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
GTATATAT others(1): Show |
G | 21 | a0001c0002t0001g0127a0001c0002t0001g0155a0001c0002t0001g0262others(18): Show | 21 | HG01891.hp1 HG02015.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.536+1774_536+1781d others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
GTATATAT others(3): Show |
G | 9 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0041others(6): Show | 9 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.536+1772_536+1781d others(12): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
GTATATAT others(5): Show |
G | 1 | a0001c0002t0001g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.536+1770_536+1781d others(14): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
GTATATAT others(7): Show |
G | 2 | a0001c0002t0001g0011a0001c0002t0001g0027 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.536+1768_536+1781d others(16): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
GTATATAT others(9): Show |
G | 5 | a0001c0002t0001g0063a0001c0002t0001g0070a0001c0002t0001g0076others(2): Show | 5 | HG02145.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.536+1766_536+1781d others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596059
|
GTATATAT others(17): Show |
G | 1 | a0001c0002t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.536+1758_536+1781d others(26): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596059 | |||||
| chr17:9596061
|
A | ATG | 8 | a0002c0001t0001g0040a0002c0001t0001g0046a0002c0001t0001g0068others(5): Show | 8 | HG01106.hp2 HG02109.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.536+1741_536+1742i others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596061 | |||||
| chr17:9596061
|
A | G | 38 | a0001c0002t0001g0010a0001c0002t0001g0024a0001c0002t0001g0031others(35): Show | 38 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.536+1740A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596061 | ||||||
| chr17:9596063
|
A | G | 44 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0072others(41): Show | 44 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.536+1742A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596063 | ||||||
| chr17:9596065
|
A | G | 34 | a0001c0002t0001g0025a0001c0002t0001g0031a0001c0002t0001g0165others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.536+1744A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596065 | ||||||
| chr17:9596067
|
A | G | 18 | a0001c0002t0001g0025a0001c0002t0001g0165a0001c0002t0001g0271others(15): Show | 18 | HG00280.hp2 HG00438.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.536+1746A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596067 | ||||||
| chr17:9596069
|
A | G | 3 | a0001c0005t0004g0215a0002c0001t0001g0286a0005c0008t0001g0261 | 3 | HG01106.hp1 NA18977.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.536+1748A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596069 | ||||||
| chr17:9596071
|
A | G | 26 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0041others(23): Show | 26 | HG02015.hp2 HG02080.hp2 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.536+1750A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596071 | ||||||
| chr17:9596073
|
A | G | 4 | a0001c0002t0001g0257a0001c0005t0004g0215a0002c0001t0001g0128others(1): Show | 4 | HG01243.hp1 NA19066.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.536+1752A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596073 | ||||||
| chr17:9596085
|
A | G | 1 | a0001c0002t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.536+1764A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596085 | ||||||
| chr17:9596087
|
A | G | 1 | a0001c0002t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.536+1766A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596087 | ||||||
| chr17:9596103
|
G | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0078 | 2 | HG01243.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.536+1782G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596103 | ||||||
| chr17:9596334
|
C | T | 1 | a0002c0001t0002g0195 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.537-1900C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596334 | ||||||
| chr17:9596342
|
C | T | 1 | a0002c0001t0002g0109 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.537-1892C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596342 | ||||||
| chr17:9596487
|
A | G | 2 | a0001c0002t0001g0016a0001c0002t0001g0065 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.537-1747A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596487 | ||||||
| chr17:9596707
|
T | C | 3 | a0001c0002t0001g0025a0001c0002t0001g0271a0001c0002t0001g0314 | 3 | HG01891.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.537-1527T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596707 | ||||||
| chr17:9596720
|
G | GT | 4 | a0001c0002t0001g0027a0001c0002t0001g0219a0001c0002t0001g0311others(1): Show | 4 | HG01175.hp2 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.537-1513dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9596720 | |||||
| chr17:9596722
|
G | T | 110 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0011others(107): Show | 111 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.537-1512G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9596722 | ||||||
| chr17:9597010
|
G | A | 114 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0011others(111): Show | 115 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.537-1224G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9597010 | ||||||
| chr17:9597374
|
C | G | 1 | a0001c0002t0001g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.537-860C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9597374 | ||||||
| chr17:9597650
|
G | A | 108 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0011others(105): Show | 109 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.537-584G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9597650 | ||||||
| chr17:9597664
|
G | A | 1 | a0001c0002t0001g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.537-570G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9597664 | ||||||
| chr17:9597757
|
T | C | 272 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0011others(269): Show | 273 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.537-477T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9597757 | ||||||
| chr17:9597803
|
A | AAG | 192 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0016others(189): Show | 192 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.537-405_537-404dup others(2): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9597803 | |||||
| chr17:9597803
|
A | AAGAG | 13 | a0001c0002t0001g0070a0001c0002t0001g0245a0001c0002t0001g0256others(10): Show | 13 | HG00438.hp2 HG02148.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.537-407_537-404dup others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9597803 | |||||
| chr17:9597803
|
A | AAGAGAG | 8 | a0001c0002t0001g0011a0001c0002t0001g0032a0001c0002t0001g0033others(5): Show | 8 | HG02630.hp2 HG02717.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.537-409_537-404dup others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9597803 | |||||
| chr17:9597803
|
A | AAGAGAGA others(3): Show |
1 | a0001c0002t0001g0219 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.537-413_537-404dup others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9597803 | |||||
| chr17:9597803
|
AAG | A | 3 | a0001c0002t0001g0076a0001c0005t0001g0074a0001c0005t0001g0077 | 3 | HG02145.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.537-405_537-404del others(2): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9597803 | |||||
| chr17:9597803
|
AAGAG | A | 4 | a0001c0002t0001g0027a0001c0004t0004g0001a0001c0004t0004g0036others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.537-407_537-404del others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9597803 | |||||
| chr17:9597819
|
GAGAGAGA others(5): Show |
G | 2 | a0002c0001t0001g0150a0002c0001t0001g0169 | 2 | HG02080.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.537-407_537-396del others(12): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9597819 | |||||
| chr17:9597821
|
GAGAGAGA others(11): Show |
G | 2 | a0001c0002t0001g0153a0009c0015t0001g0064 | 2 | HG02056.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.537-403_537-386del others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9597821 | |||||
| chr17:9597831
|
A | G | 59 | a0001c0002t0001g0003a0001c0002t0001g0048a0001c0002t0001g0063others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.537-403A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9597831 | ||||||
| chr17:9597831
|
AAGAGAGA others(5): Show |
A | 1 | a0001c0002t0001g0314 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.537-379_537-368del others(12): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9597831 | |||||
| chr17:9597839
|
A | G | 1 | a0001c0002t0001g0003 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.537-395A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9597839 | ||||||
| chr17:9597859
|
GAGAA | G | 6 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(3): Show | 6 | HG02559.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.537-357_537-354del others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9597859 | |||||
| chr17:9597869
|
G | T | 2 | a0001c0002t0001g0184a0001c0002t0001g0210 | 2 | HG01168.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.537-365G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9597869 | ||||||
| chr17:9597890
|
G | A | 5 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(2): Show | 5 | HG02559.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.537-344G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9597890 | ||||||
| chr17:9597898
|
T | C | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.537-336T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9597898 | ||||||
| chr17:9597996
|
A | G | 306 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.537-238A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9597996 | ||||||
| chr17:9598045
|
G | T | 1 | a0005c0008t0001g0261 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.537-189G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9598045 | ||||||
| chr17:9598048
|
A | G | 1 | a0005c0008t0001g0261 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.537-186A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9598048 | ||||||
| chr17:9598049
|
G | A | 1 | a0005c0008t0001g0261 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.537-185G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9598049 | ||||||
| chr17:9598052
|
G | A | 3 | a0001c0002t0001g0031a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG01109.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.537-182G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9598052 | ||||||
| chr17:9598078
|
G | T | 303 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(300): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.537-156G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9598078 | ||||||
| chr17:9598127
|
C | T | 2 | a0002c0001t0001g0019a0002c0001t0001g0223 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.537-107C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | chr17 | 9598127 | ||||||
| chr17:9598215
|
G | GT | 117 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0041others(114): Show | 117 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(114): Show |
splice_region_variant&intron_variant | LOW | c.537-7dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9598215 | |||||
| chr17:9598215
|
GT | G | 6 | a0001c0002t0001g0115a0001c0002t0001g0309a0001c0004t0004g0001others(3): Show | 7 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.537-7delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 9598215 | |||||
| chr17:9598417
|
T | G | 1 | a0005c0008t0001g0261 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.636+84T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9598417 | ||||||
| chr17:9598441
|
G | T | 3 | a0001c0002t0001g0076a0001c0005t0001g0074a0001c0005t0001g0077 | 3 | HG02145.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.636+108G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9598441 | ||||||
| chr17:9598519
|
T | G | 5 | a0002c0001t0001g0018a0002c0001t0001g0028a0002c0001t0001g0029others(2): Show | 5 | HG02055.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+186T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9598519 | ||||||
| chr17:9598625
|
G | A | 79 | a0001c0002t0001g0024a0001c0002t0001g0052a0001c0002t0001g0090others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.636+292G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9598625 | ||||||
| chr17:9598683
|
C | G | 2 | a0001c0002t0001g0221a0002c0001t0001g0103 | 2 | HG02155.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.636+350C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9598683 | ||||||
| chr17:9598693
|
G | A | 107 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0041others(104): Show | 107 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.636+360G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9598693 | ||||||
| chr17:9598760
|
C | CAAAAAAA | 7 | a0001c0002t0001g0003a0001c0002t0001g0083a0001c0002t0001g0210others(4): Show | 7 | HG00323.hp2 HG00639.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.636+431_636+437dup others(7): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 9598760 | |||||
| chr17:9598760
|
C | CAAAAAAA others(1): Show |
171 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0016others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.636+430_636+437dup others(8): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 9598760 | |||||
| chr17:9598760
|
C | CAAAAAAA others(2): Show |
11 | a0001c0002t0001g0011a0001c0002t0001g0073a0001c0002t0001g0076others(8): Show | 11 | HG01192.hp1 HG01978.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.636+429_636+437dup others(9): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr17 | 9598760 | |||||
| chr17:9598966
|
T | G | 109 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0041others(106): Show | 109 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.636+633T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9598966 | ||||||
| chr17:9599122
|
G | T | 1 | a0002c0001t0002g0185 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.636+789G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9599122 | ||||||
| chr17:9599442
|
G | A | 1 | a0002c0001t0001g0175 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.637-625G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9599442 | ||||||
| chr17:9599564
|
G | A | 4 | a0003c0003t0001g0130a0003c0003t0001g0293a0003c0003t0001g0294others(1): Show | 4 | NA18949.hp2 NA18962.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-503G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9599564 | ||||||
| chr17:9599672
|
A | G | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.637-395A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9599672 | ||||||
| chr17:9599747
|
T | C | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.637-320T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9599747 | ||||||
| chr17:9599954
|
T | C | 1 | a0001c0002t0001g0212 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.637-113T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9599954 | ||||||
| chr17:9600010
|
A | G | 1 | a0001c0002t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.637-57A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9600010 | ||||||
| chr17:9600011
|
T | G | 1 | a0001c0002t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.637-56T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9600011 | ||||||
| chr17:9600021
|
G | A | 1 | a0002c0001t0002g0049 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.637-46G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 5/13 | chr17 | 9600021 | ||||||
| chr17:9600327
|
T | C | 303 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(300): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.753+144T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9600327 | ||||||
| chr17:9600563
|
T | G | 3 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026 | 3 | HG02647.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.753+380T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9600563 | ||||||
| chr17:9600604
|
G | A | 1 | a0002c0001t0001g0038 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.753+421G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9600604 | ||||||
| chr17:9600621
|
G | A | 98 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0012others(95): Show | 98 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.753+438G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9600621 | ||||||
| chr17:9600693
|
T | C | 94 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0016others(91): Show | 94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.753+510T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9600693 | ||||||
| chr17:9600722
|
G | A | 2 | a0002c0001t0001g0061a0002c0001t0001g0158 | 2 | HG02273.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.753+539G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9600722 | ||||||
| chr17:9600975
|
C | T | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+792C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9600975 | ||||||
| chr17:9600981
|
T | C | 1 | a0001c0002t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.753+798T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9600981 | ||||||
| chr17:9601024
|
A | G | 3 | a0001c0002t0001g0025a0001c0002t0001g0271a0001c0002t0001g0314 | 3 | HG01891.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.753+841A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9601024 | ||||||
| chr17:9601183
|
T | G | 108 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0011others(105): Show | 109 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.753+1000T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9601183 | ||||||
| chr17:9601228
|
C | T | 92 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0016others(89): Show | 92 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.753+1045C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9601228 | ||||||
| chr17:9601336
|
C | T | 1 | a0001c0002t0001g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.753+1153C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9601336 | ||||||
| chr17:9601463
|
A | G | 5 | a0001c0002t0001g0011a0001c0002t0001g0063a0001c0002t0001g0070others(2): Show | 5 | HG02145.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+1280A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9601463 | ||||||
| chr17:9601491
|
C | T | 1 | a0002c0001t0001g0286 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.753+1308C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9601491 | ||||||
| chr17:9601614
|
A | G | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+1431A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9601614 | ||||||
| chr17:9601625
|
G | A | 107 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0011others(104): Show | 108 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.753+1442G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9601625 | ||||||
| chr17:9601792
|
G | C | 1 | a0001c0002t0002g0197 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.753+1609G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9601792 | ||||||
| chr17:9601903
|
A | G | 288 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0011others(285): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.753+1720A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9601903 | ||||||
| chr17:9602243
|
A | G | 5 | a0001c0002t0001g0011a0001c0002t0001g0063a0001c0002t0001g0070others(2): Show | 5 | HG02145.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+2060A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9602243 | ||||||
| chr17:9602370
|
C | T | 1 | a0001c0002t0001g0288 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.753+2187C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9602370 | ||||||
| chr17:9602371
|
G | A | 20 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0041others(17): Show | 20 | HG00099.hp1 HG01123.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.753+2188G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9602371 | ||||||
| chr17:9602392
|
GT | G | 171 | a0001c0002t0001g0024a0001c0002t0001g0090a0001c0002t0001g0127others(168): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.753+2213delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9602392 | |||||
| chr17:9602393
|
T | C | 20 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0041others(17): Show | 20 | HG00099.hp1 HG01123.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.753+2210T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9602393 | ||||||
| chr17:9602529
|
A | G | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+2346A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9602529 | ||||||
| chr17:9602546
|
T | C | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.753+2363T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9602546 | ||||||
| chr17:9602595
|
A | G | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+2412A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9602595 | ||||||
| chr17:9602830
|
G | A | 20 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0041others(17): Show | 20 | HG00099.hp1 HG01123.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.753+2647G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9602830 | ||||||
| chr17:9603092
|
T | C | 93 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0016others(90): Show | 93 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.753+2909T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603092 | ||||||
| chr17:9603153
|
A | AG | 196 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0024others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.753+2972dupG | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9603153 | |||||
| chr17:9603239
|
C | T | 2 | a0002c0001t0001g0150a0002c0001t0001g0169 | 2 | HG02080.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.753+3056C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603239 | ||||||
| chr17:9603247
|
C | T | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.753+3064C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603247 | ||||||
| chr17:9603248
|
G | A | 9 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0041others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.753+3065G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603248 | ||||||
| chr17:9603295
|
G | A | 1 | a0001c0002t0001g0052 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.753+3112G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603295 | ||||||
| chr17:9603328
|
T | C | 194 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0024others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.753+3145T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603328 | ||||||
| chr17:9603500
|
C | T | 6 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0002t0001g0135others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.753+3317C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603500 | ||||||
| chr17:9603509
|
C | T | 174 | a0001c0002t0001g0024a0001c0002t0001g0090a0001c0002t0001g0115others(171): Show | 175 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.753+3326C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603509 | ||||||
| chr17:9603515
|
A | G | 1 | a0010c0007t0001g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.753+3332A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603515 | ||||||
| chr17:9603520
|
T | C | 18 | a0001c0002t0001g0127a0001c0002t0001g0301a0002c0001t0001g0089others(15): Show | 18 | HG01106.hp1 HG02015.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.753+3337T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603520 | ||||||
| chr17:9603575
|
T | C | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.753+3392T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603575 | ||||||
| chr17:9603613
|
C | G | 1 | a0002c0001t0002g0164 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.753+3430C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603613 | ||||||
| chr17:9603727
|
G | C | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+3544G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603727 | ||||||
| chr17:9603741
|
C | T | 174 | a0001c0002t0001g0024a0001c0002t0001g0090a0001c0002t0001g0115others(171): Show | 175 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.753+3558C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603741 | ||||||
| chr17:9603867
|
G | A | 3 | a0001c0002t0001g0025a0001c0002t0001g0271a0001c0002t0001g0314 | 3 | HG01891.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.753+3684G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9603867 | ||||||
| chr17:9604131
|
T | G | 6 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(3): Show | 6 | HG02559.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.753+3948T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9604131 | ||||||
| chr17:9604530
|
G | A | 7 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0041others(4): Show | 7 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.754-3589G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9604530 | ||||||
| chr17:9604539
|
G | T | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.754-3580G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9604539 | ||||||
| chr17:9604593
|
C | T | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-3526C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9604593 | ||||||
| chr17:9604750
|
A | AAAAT | 27 | a0001c0002t0001g0012a0001c0002t0001g0021a0001c0002t0001g0026others(24): Show | 27 | HG00423.hp1 HG00735.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.754-3317_754-3314d others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9604750 | |||||
| chr17:9604750
|
AAAAT | A | 136 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0010others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.754-3317_754-3314d others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9604750 | |||||
| chr17:9604750
|
AAAATAAA others(1): Show |
A | 20 | a0001c0002t0001g0016a0001c0002t0001g0031a0001c0002t0001g0044others(17): Show | 20 | HG01109.hp2 HG01257.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.754-3321_754-3314d others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9604750 | |||||
| chr17:9604750
|
AAAATAAA others(5): Show |
A | 1 | a0001c0002t0001g0132 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.754-3325_754-3314d others(14): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9604750 | |||||
| chr17:9604750
|
AAAATAAA others(13): Show |
A | 1 | a0002c0001t0001g0286 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.754-3333_754-3314d others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9604750 | |||||
| chr17:9605007
|
G | A | 1 | a0001c0002t0002g0197 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.754-3112G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9605007 | ||||||
| chr17:9605011
|
G | A | 1 | a0002c0001t0002g0292 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.754-3108G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9605011 | ||||||
| chr17:9605220
|
C | T | 9 | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0002t0001g0041others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.754-2899C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9605220 | ||||||
| chr17:9605437
|
C | T | 1 | a0002c0001t0002g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.754-2682C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9605437 | ||||||
| chr17:9605439
|
C | T | 1 | a0002c0010t0001g0142 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.754-2680C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9605439 | ||||||
| chr17:9605465
|
A | G | 2 | a0001c0002t0001g0025a0001c0002t0001g0271 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.754-2654A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9605465 | ||||||
| chr17:9605484
|
C | T | 2 | a0002c0001t0002g0059a0002c0001t0002g0136 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.754-2635C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9605484 | ||||||
| chr17:9605694
|
G | GAAA | 6 | a0001c0002t0001g0052a0001c0002t0001g0099a0001c0002t0001g0100others(3): Show | 6 | HG00099.hp1 HG01123.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-2398_754-2396d others(5): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9605694 | |||||
| chr17:9605694
|
GAAAA | G | 26 | a0001c0002t0001g0115a0001c0002t0001g0207a0001c0002t0001g0222others(23): Show | 26 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.754-2399_754-2396d others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9605694 | |||||
| chr17:9605694
|
GAAAAA | G | 157 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0024others(154): Show | 158 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.754-2400_754-2396d others(7): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9605694 | |||||
| chr17:9605694
|
GAAAAAA | G | 86 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0016others(83): Show | 86 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.754-2401_754-2396d others(8): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9605694 | |||||
| chr17:9605944
|
T | C | 3 | a0001c0002t0001g0048a0001c0002t0001g0073a0001c0002t0001g0219 | 3 | HG01175.hp2 HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.754-2175T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9605944 | ||||||
| chr17:9606070
|
T | TA | 10 | a0001c0002t0001g0052a0001c0002t0001g0099a0001c0002t0001g0100others(7): Show | 10 | HG00099.hp1 HG01123.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.754-2041dupA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9606070 | |||||
| chr17:9606085
|
A | G | 1 | a0001c0002t0001g0242 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.754-2034A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9606085 | ||||||
| chr17:9606102
|
T | G | 106 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0011others(103): Show | 106 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.754-2017T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9606102 | ||||||
| chr17:9606134
|
G | A | 1 | a0002c0001t0001g0158 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.754-1985G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9606134 | ||||||
| chr17:9606310
|
G | A | 5 | a0001c0002t0001g0027a0001c0002t0001g0255a0001c0002t0001g0256others(2): Show | 5 | HG02922.hp2 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.754-1809G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9606310 | ||||||
| chr17:9606339
|
T | C | 8 | a0001c0002t0001g0007a0001c0002t0001g0041a0001c0002t0001g0042others(5): Show | 8 | HG01243.hp1 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.754-1780T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9606339 | ||||||
| chr17:9606384
|
TAC | T | 302 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.754-1716_754-1715d others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9606384 | |||||
| chr17:9606384
|
TACAC | T | 6 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(3): Show | 6 | HG02559.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-1718_754-1715d others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9606384 | |||||
| chr17:9606492
|
G | A | 10 | a0001c0002t0001g0052a0001c0002t0001g0099a0001c0002t0001g0100others(7): Show | 10 | HG00099.hp1 HG01123.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.754-1627G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9606492 | ||||||
| chr17:9606534
|
C | T | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.754-1585C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9606534 | ||||||
| chr17:9606576
|
T | A | 1 | a0002c0001t0001g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.754-1543T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9606576 | ||||||
| chr17:9606702
|
C | T | 10 | a0001c0002t0001g0052a0001c0002t0001g0099a0001c0002t0001g0100others(7): Show | 10 | HG00099.hp1 HG01123.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.754-1417C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9606702 | ||||||
| chr17:9606904
|
C | A | 1 | a0001c0002t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.754-1215C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9606904 | ||||||
| chr17:9607215
|
G | A | 172 | a0001c0002t0001g0024a0001c0002t0001g0063a0001c0002t0001g0070others(169): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.754-904G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9607215 | ||||||
| chr17:9607223
|
A | G | 97 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0016others(94): Show | 97 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.754-896A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9607223 | ||||||
| chr17:9607281
|
G | A | 1 | a0002c0001t0002g0137 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.754-838G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9607281 | ||||||
| chr17:9607282
|
A | G | 283 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(280): Show | 283 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.754-837A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9607282 | ||||||
| chr17:9607325
|
G | T | 1 | a0001c0002t0001g0094 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.754-794G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9607325 | ||||||
| chr17:9607486
|
G | A | 6 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(3): Show | 6 | HG02559.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-633G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9607486 | ||||||
| chr17:9607793
|
C | G | 5 | a0001c0002t0001g0027a0001c0002t0001g0255a0001c0002t0001g0256others(2): Show | 5 | HG02922.hp2 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.754-326C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | chr17 | 9607793 | ||||||
| chr17:9608001
|
AT | A | 6 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(3): Show | 6 | HG02559.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-110delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 9608001 | |||||
| chr17:9608297
|
G | T | 1 | a0002c0001t0001g0047 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.854+78G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9608297 | ||||||
| chr17:9608416
|
A | G | 1 | a0001c0002t0001g0276 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.854+197A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9608416 | ||||||
| chr17:9608445
|
G | A | 276 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0016others(273): Show | 276 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.854+226G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9608445 | ||||||
| chr17:9608452
|
C | T | 102 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0016others(99): Show | 102 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.854+233C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9608452 | ||||||
| chr17:9608458
|
T | G | 6 | a0001c0002t0001g0165a0001c0002t0001g0207a0001c0002t0001g0226others(3): Show | 6 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.854+239T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9608458 | ||||||
| chr17:9608512
|
C | T | 310 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.854+293C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9608512 | ||||||
| chr17:9608639
|
A | T | 1 | a0002c0001t0002g0137 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.854+420A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9608639 | ||||||
| chr17:9608748
|
C | T | 2 | a0002c0001t0001g0019a0002c0001t0001g0223 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.854+529C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9608748 | ||||||
| chr17:9608784
|
C | T | 91 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0016others(88): Show | 91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.854+565C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9608784 | ||||||
| chr17:9608830
|
G | A | 2 | a0001c0002t0001g0120a0001c0002t0001g0299 | 2 | NA18747.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.854+611G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9608830 | ||||||
| chr17:9609083
|
C | T | 6 | a0001c0002t0001g0027a0001c0002t0001g0255a0001c0002t0001g0256others(3): Show | 6 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.854+864C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609083 | ||||||
| chr17:9609084
|
C | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+865C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609084 | ||||||
| chr17:9609092
|
C | T | 2 | a0002c0001t0002g0180a0002c0001t0002g0292 | 2 | HG01123.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.854+873C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609092 | ||||||
| chr17:9609093
|
C | T | 1 | a0002c0001t0001g0145 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.854+874C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609093 | ||||||
| chr17:9609096
|
C | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+877C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609096 | ||||||
| chr17:9609194
|
C | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+975C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609194 | ||||||
| chr17:9609239
|
GA | G | 164 | a0001c0002t0001g0090a0001c0002t0001g0196a0001c0002t0001g0232others(161): Show | 164 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.854+1030delA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 9609239 | |||||
| chr17:9609251
|
C | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1032C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609251 | ||||||
| chr17:9609257
|
C | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1038C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609257 | ||||||
| chr17:9609293
|
C | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1074C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609293 | ||||||
| chr17:9609294
|
A | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1075A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609294 | ||||||
| chr17:9609316
|
C | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1097C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609316 | ||||||
| chr17:9609317
|
A | C | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1098A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609317 | ||||||
| chr17:9609367
|
A | C | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1148A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609367 | ||||||
| chr17:9609396
|
T | C | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1177T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609396 | ||||||
| chr17:9609398
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1179G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609398 | ||||||
| chr17:9609399
|
A | G | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1180A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609399 | ||||||
| chr17:9609430
|
C | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1211C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609430 | ||||||
| chr17:9609431
|
A | C | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1212A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609431 | ||||||
| chr17:9609432
|
C | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1213C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609432 | ||||||
| chr17:9609449
|
C | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1230C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609449 | ||||||
| chr17:9609456
|
A | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1237A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609456 | ||||||
| chr17:9609459
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1240T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609459 | ||||||
| chr17:9609673
|
A | C | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1454A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609673 | ||||||
| chr17:9609681
|
T | G | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1462T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609681 | ||||||
| chr17:9609702
|
G | A | 30 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0052others(27): Show | 30 | HG00099.hp1 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.854+1483G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609702 | ||||||
| chr17:9609711
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1492T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609711 | ||||||
| chr17:9609881
|
A | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1662A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609881 | ||||||
| chr17:9609885
|
T | C | 161 | a0001c0002t0001g0186a0001c0002t0001g0309a0002c0001t0001g0013others(158): Show | 161 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.854+1666T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609885 | ||||||
| chr17:9609979
|
A | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1760A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9609979 | ||||||
| chr17:9609990
|
G | GGA | 3 | a0001c0002t0001g0076a0001c0002t0001g0214a0006c0014t0001g0177 | 3 | HG02559.hp1 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.854+1792_854+1793d others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 9609990 | |||||
| chr17:9610007
|
G | C | 1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.854+1788G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610007 | ||||||
| chr17:9610013
|
C | G | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.854+1794C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610013 | ||||||
| chr17:9610065
|
C | G | 3 | a0001c0002t0001g0257a0001c0002t0001g0276a0001c0002t0001g0278 | 3 | HG01243.hp1 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.854+1846C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610065 | ||||||
| chr17:9610091
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1872G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610091 | ||||||
| chr17:9610092
|
T | G | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1873T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610092 | ||||||
| chr17:9610093
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1874G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610093 | ||||||
| chr17:9610106
|
G | A | 43 | a0001c0002t0001g0048a0001c0002t0001g0073a0001c0002t0001g0088others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.854+1887G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610106 | ||||||
| chr17:9610141
|
G | A | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.854+1922G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610141 | ||||||
| chr17:9610159
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1940T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610159 | ||||||
| chr17:9610171
|
C | T | 2 | a0001c0002t0001g0132a0001c0002t0001g0135 | 2 | HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.854+1952C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610171 | ||||||
| chr17:9610184
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+1965T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610184 | ||||||
| chr17:9610206
|
A | AAAAC | 4 | a0001c0002t0001g0222a0001c0005t0001g0074a0001c0005t0001g0077others(1): Show | 4 | HG02145.hp2 HG03098.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.854+1992_854+1995d others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 9610206 | |||||
| chr17:9610226
|
A | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.854+2007A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610226 | ||||||
| chr17:9610273
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-2036T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610273 | ||||||
| chr17:9610276
|
C | A | 1 | a0002c0001t0001g0290 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.855-2033C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610276 | ||||||
| chr17:9610333
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1976T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610333 | ||||||
| chr17:9610360
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1949T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610360 | ||||||
| chr17:9610363
|
C | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1946C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610363 | ||||||
| chr17:9610364
|
A | C | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1945A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610364 | ||||||
| chr17:9610466
|
A | G | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1843A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610466 | ||||||
| chr17:9610486
|
A | G | 1 | a0001c0002t0001g0278 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.855-1823A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610486 | ||||||
| chr17:9610531
|
A | AT | 102 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0010others(99): Show | 103 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.855-1766dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 9610531 | |||||
| chr17:9610544
|
G | T | 1 | a0001c0002t0001g0151 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.855-1765G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610544 | ||||||
| chr17:9610545
|
T | G | 1 | a0001c0002t0001g0151 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.855-1764T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610545 | ||||||
| chr17:9610595
|
C | T | 1 | a0002c0001t0001g0223 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.855-1714C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610595 | ||||||
| chr17:9610621
|
G | A | 3 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026 | 3 | HG02647.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.855-1688G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610621 | ||||||
| chr17:9610623
|
C | G | 1 | a0001c0002t0001g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.855-1686C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610623 | ||||||
| chr17:9610640
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1669T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610640 | ||||||
| chr17:9610684
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1625G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610684 | ||||||
| chr17:9610697
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1612G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610697 | ||||||
| chr17:9610706
|
T | C | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1603T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610706 | ||||||
| chr17:9610707
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1602T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610707 | ||||||
| chr17:9610708
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1601T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610708 | ||||||
| chr17:9610714
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1595T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610714 | ||||||
| chr17:9610716
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1593T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610716 | ||||||
| chr17:9610721
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1588T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610721 | ||||||
| chr17:9610723
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1586G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610723 | ||||||
| chr17:9610725
|
G | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1584G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610725 | ||||||
| chr17:9610726
|
A | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1583A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610726 | ||||||
| chr17:9610728
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1581G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610728 | ||||||
| chr17:9610730
|
G | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1579G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610730 | ||||||
| chr17:9610741
|
G | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1568G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610741 | ||||||
| chr17:9610776
|
T | A | 1 | a0003c0003t0001g0295 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.855-1533T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610776 | ||||||
| chr17:9610804
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1505G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610804 | ||||||
| chr17:9610816
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1493G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610816 | ||||||
| chr17:9610817
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1492G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610817 | ||||||
| chr17:9610818
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1491T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610818 | ||||||
| chr17:9610853
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1456T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610853 | ||||||
| chr17:9610892
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1417G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610892 | ||||||
| chr17:9610923
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1386G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610923 | ||||||
| chr17:9610936
|
A | G | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1373A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610936 | ||||||
| chr17:9610937
|
G | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1372G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610937 | ||||||
| chr17:9610940
|
A | G | 38 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(35): Show | 39 | HG00323.hp2 HG01123.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.855-1369A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610940 | ||||||
| chr17:9610969
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1340T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610969 | ||||||
| chr17:9610971
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1338G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610971 | ||||||
| chr17:9610983
|
T | C | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1326T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9610983 | ||||||
| chr17:9611007
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-1302G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611007 | ||||||
| chr17:9611227
|
G | C | 1 | a0001c0002t0001g0212 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.855-1082G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611227 | ||||||
| chr17:9611239
|
T | C | 1 | a0001c0002t0001g0156 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.855-1070T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611239 | ||||||
| chr17:9611245
|
CT | C | 160 | a0002c0001t0001g0013a0002c0001t0001g0014a0002c0001t0001g0017others(157): Show | 160 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.855-1053delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 9611245 | |||||
| chr17:9611356
|
C | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-953C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611356 | ||||||
| chr17:9611357
|
T | C | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-952T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611357 | ||||||
| chr17:9611409
|
C | A | 33 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(30): Show | 34 | HG00323.hp2 HG01123.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.855-900C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611409 | ||||||
| chr17:9611420
|
T | C | 1 | a0002c0001t0001g0089 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.855-889T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611420 | ||||||
| chr17:9611441
|
A | C | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-868A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611441 | ||||||
| chr17:9611447
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-862T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611447 | ||||||
| chr17:9611448
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-861G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611448 | ||||||
| chr17:9611465
|
C | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-844C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611465 | ||||||
| chr17:9611480
|
A | C | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-829A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611480 | ||||||
| chr17:9611482
|
G | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-827G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611482 | ||||||
| chr17:9611497
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-812G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611497 | ||||||
| chr17:9611522
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-787T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611522 | ||||||
| chr17:9611532
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-777T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611532 | ||||||
| chr17:9611536
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-773T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611536 | ||||||
| chr17:9611540
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-769T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611540 | ||||||
| chr17:9611542
|
A | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-767A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611542 | ||||||
| chr17:9611544
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-765T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611544 | ||||||
| chr17:9611545
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-764T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611545 | ||||||
| chr17:9611546
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-763T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611546 | ||||||
| chr17:9611558
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-751T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611558 | ||||||
| chr17:9611586
|
A | C | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-723A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611586 | ||||||
| chr17:9611619
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-690G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611619 | ||||||
| chr17:9611655
|
T | G | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.855-654T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611655 | ||||||
| chr17:9611693
|
G | T | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.855-616G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611693 | ||||||
| chr17:9611818
|
C | T | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.855-491C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611818 | ||||||
| chr17:9611838
|
T | C | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.855-471T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611838 | ||||||
| chr17:9611858
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-451T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611858 | ||||||
| chr17:9611972
|
G | T | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-337G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611972 | ||||||
| chr17:9611976
|
T | A | 1 | a0008c0009t0001g0305 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.855-333T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611976 | ||||||
| chr17:9611995
|
C | A | 3 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0045 | 3 | HG01884.hp1 HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.855-314C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9611995 | ||||||
| chr17:9612012
|
C | T | 1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.855-297C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9612012 | ||||||
| chr17:9612214
|
A | G | 1 | a0001c0002t0001g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.855-95A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 7/13 | chr17 | 9612214 | ||||||
| chr17:9612539
|
T | C | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1025+60T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9612539 | ||||||
| chr17:9612722
|
G | A | 1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1025+243G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9612722 | ||||||
| chr17:9612799
|
GA | G | 32 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(29): Show | 32 | HG00323.hp2 HG01123.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.1025+321delA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9612799 | ||||||
| chr17:9612800
|
A | T | 1 | a0001c0002t0001g0314 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1025+321A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9612800 | ||||||
| chr17:9613061
|
C | T | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1025+582C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9613061 | ||||||
| chr17:9613110
|
A | G | 3 | a0001c0002t0001g0076a0001c0002t0001g0214a0006c0014t0001g0177 | 3 | HG02559.hp1 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1025+631A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9613110 | ||||||
| chr17:9613162
|
A | C | 1 | a0001c0002t0001g0125 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1025+683A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9613162 | ||||||
| chr17:9613192
|
A | G | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1025+713A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9613192 | ||||||
| chr17:9613316
|
A | G | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1025+837A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9613316 | ||||||
| chr17:9613494
|
T | G | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1025+1015T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9613494 | ||||||
| chr17:9613502
|
T | TTTTG | 4 | a0002c0001t0001g0150a0002c0001t0001g0169a0002c0001t0001g0268others(1): Show | 4 | HG00673.hp1 HG01106.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+1051_1025+105 others(8): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9613502 | |||||
| chr17:9613502
|
TTTTG | T | 31 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0010others(28): Show | 31 | HG00323.hp2 HG01123.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1025+1051_1025+105 others(8): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9613502 | |||||
| chr17:9613502
|
TTTTGTTT others(1): Show |
T | 6 | a0001c0002t0001g0008a0001c0002t0001g0066a0001c0002t0001g0184others(3): Show | 6 | HG01168.hp1 HG01255.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1025+1047_1025+105 others(12): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9613502 | |||||
| chr17:9613540
|
C | T | 1 | a0002c0001t0001g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1025+1061C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9613540 | ||||||
| chr17:9613607
|
T | C | 2 | a0002c0001t0002g0180a0002c0001t0002g0292 | 2 | HG01123.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1025+1128T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9613607 | ||||||
| chr17:9613620
|
C | T | 1 | a0002c0001t0002g0109 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1025+1141C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9613620 | ||||||
| chr17:9613665
|
G | A | 2 | a0002c0001t0001g0039a0002c0001t0001g0046 | 2 | HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1025+1186G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9613665 | ||||||
| chr17:9613747
|
G | A | 1 | a0002c0011t0001g0277 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1025+1268G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9613747 | ||||||
| chr17:9613799
|
G | A | 1 | a0001c0002t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1025+1320G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9613799 | ||||||
| chr17:9613903
|
G | C | 68 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0031others(65): Show | 68 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1025+1424G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9613903 | ||||||
| chr17:9613903
|
G | GT | 162 | a0001c0002t0001g0186a0001c0002t0001g0309a0001c0002t0002g0002others(159): Show | 162 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1025+1425dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9613903 | |||||
| chr17:9613984
|
C | CT | 11 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0045others(8): Show | 11 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1025+1514dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9613984 | |||||
| chr17:9614021
|
C | T | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1025+1542C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9614021 | ||||||
| chr17:9614082
|
T | G | 1 | a0001c0002t0001g0012 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1025+1603T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9614082 | ||||||
| chr17:9614132
|
CCTTTTCT others(4): Show |
C | 1 | a0001c0002t0001g0012 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1025+1663_1025+167 others(15): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9614132 | |||||
| chr17:9614157
|
CT | C | 188 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(185): Show | 188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1025+1695delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9614157 | |||||
| chr17:9614157
|
CTT | C | 84 | a0001c0002t0001g0010a0001c0002t0001g0016a0001c0002t0001g0021others(81): Show | 85 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.1025+1694_1025+169 others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9614157 | |||||
| chr17:9614162
|
T | C | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1025+1683T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9614162 | ||||||
| chr17:9614254
|
C | A | 1 | a0002c0001t0001g0223 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1025+1775C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9614254 | ||||||
| chr17:9614403
|
G | A | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1025+1924G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9614403 | ||||||
| chr17:9614578
|
G | A | 7 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0002t0001g0135others(4): Show | 7 | HG01175.hp1 HG01192.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1025+2099G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9614578 | ||||||
| chr17:9614606
|
A | G | 264 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(261): Show | 264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.1025+2127A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9614606 | ||||||
| chr17:9614672
|
A | G | 3 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026 | 3 | HG02647.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1025+2193A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9614672 | ||||||
| chr17:9614674
|
C | A | 33 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0052others(30): Show | 33 | HG00099.hp1 HG00438.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1025+2195C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9614674 | ||||||
| chr17:9614748
|
G | A | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1025+2269G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9614748 | ||||||
| chr17:9614770
|
ATCAGACG others(11): Show |
A | 1 | a0001c0002t0001g0031 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1025+2294_1025+231 others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9614770 | |||||
| chr17:9614778
|
C | T | 1 | a0002c0001t0001g0159 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1025+2299C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9614778 | ||||||
| chr17:9614916
|
G | A | 1 | a0002c0001t0001g0182 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1025+2437G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9614916 | ||||||
| chr17:9615057
|
A | C | 5 | a0001c0002t0001g0007a0001c0002t0001g0041a0001c0002t0001g0042others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025+2578A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615057 | ||||||
| chr17:9615271
|
T | C | 5 | a0002c0001t0002g0137a0002c0001t0002g0138a0002c0001t0002g0139others(2): Show | 5 | NA18970.hp1 NA18990.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025+2792T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615271 | ||||||
| chr17:9615400
|
T | C | 1 | a0002c0001t0001g0158 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1025+2921T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615400 | ||||||
| chr17:9615455
|
A | C | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1025+2976A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615455 | ||||||
| chr17:9615546
|
C | T | 279 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(276): Show | 280 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.1025+3067C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615546 | ||||||
| chr17:9615621
|
GT | G | 33 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0052others(30): Show | 33 | HG00099.hp1 HG00438.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1025+3151delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9615621 | |||||
| chr17:9615638
|
G | C | 1 | a0002c0001t0002g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1025+3159G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615638 | ||||||
| chr17:9615651
|
C | T | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1025+3172C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615651 | ||||||
| chr17:9615752
|
G | T | 101 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(98): Show | 101 | HG00323.hp2 HG00423.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.1025+3273G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615752 | ||||||
| chr17:9615791
|
A | C | 1 | a0001c0002t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1025+3312A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615791 | ||||||
| chr17:9615793
|
TTC | T | 22 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0052others(19): Show | 22 | HG00099.hp1 HG01074.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1025+3316_1025+331 others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9615793 | |||||
| chr17:9615794
|
TC | T | 9 | a0001c0002t0001g0118a0001c0002t0001g0132a0001c0002t0001g0135others(6): Show | 9 | HG00438.hp1 HG01175.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1025+3316delC | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615794 | ||||||
| chr17:9615795
|
C | CT | 66 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0012others(63): Show | 66 | HG00323.hp1 HG00438.hp2 HG01109.hp2 others(63): Show |
intron_variant | MODIFIER | c.1025+3340dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9615795 | |||||
| chr17:9615795
|
C | CTT | 75 | a0001c0002t0001g0021a0001c0002t0001g0026a0001c0002t0001g0033others(72): Show | 75 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1025+3339_1025+334 others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9615795 | |||||
| chr17:9615795
|
C | CTTT | 27 | a0001c0002t0001g0016a0001c0002t0001g0032a0001c0002t0001g0034others(24): Show | 27 | HG00423.hp1 HG00621.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1025+3338_1025+334 others(7): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9615795 | |||||
| chr17:9615795
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1025+3316C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615795 | ||||||
| chr17:9615795
|
CTTTTT | C | 12 | a0001c0002t0001g0063a0001c0002t0001g0070a0001c0002t0001g0271others(9): Show | 13 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1025+3336_1025+334 others(9): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9615795 | |||||
| chr17:9615795
|
CTTTTTT | C | 28 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(25): Show | 28 | HG00323.hp2 HG01123.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.1025+3335_1025+334 others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9615795 | |||||
| chr17:9615819
|
T | C | 9 | a0001c0002t0001g0176a0001c0005t0001g0074a0001c0005t0001g0077others(6): Show | 9 | HG01074.hp1 HG01255.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1025+3340T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615819 | ||||||
| chr17:9615819
|
T | TTC | 31 | a0002c0001t0001g0092a0002c0001t0001g0313a0002c0001t0002g0037others(28): Show | 31 | HG00099.hp2 HG00280.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.1025+3340_1025+334 others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615819 | ||||||
| chr17:9615819
|
T | TTTC | 23 | a0001c0002t0001g0125a0002c0001t0001g0259a0002c0001t0002g0049others(20): Show | 23 | HG00735.hp2 HG00741.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.1025+3340_1025+334 others(7): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615819 | ||||||
| chr17:9615990
|
G | C | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1025+3511G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9615990 | ||||||
| chr17:9616023
|
G | T | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1025+3544G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616023 | ||||||
| chr17:9616031
|
G | T | 1 | a0001c0002t0001g0296 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1025+3552G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616031 | ||||||
| chr17:9616100
|
A | C | 1 | a0001c0002t0001g0179 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1025+3621A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616100 | ||||||
| chr17:9616123
|
C | T | 2 | a0002c0001t0001g0096a0002c0001t0001g0160 | 2 | NA18972.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1025+3644C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616123 | ||||||
| chr17:9616143
|
CACCGTGC others(4): Show |
C | 15 | a0002c0001t0001g0013a0002c0001t0001g0035a0002c0001t0001g0043others(12): Show | 15 | HG01071.hp2 HG01106.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1025+3665_1025+367 others(15): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616143 | ||||||
| chr17:9616147
|
G | A | 1 | a0001c0002t0001g0027 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1025+3668G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616147 | ||||||
| chr17:9616192
|
G | A | 1 | a0001c0002t0001g0189 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1025+3713G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616192 | ||||||
| chr17:9616218
|
C | A | 11 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(8): Show | 12 | HG02559.hp1 HG02615.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1025+3739C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616218 | ||||||
| chr17:9616218
|
C | G | 4 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+3739C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616218 | ||||||
| chr17:9616255
|
C | T | 2 | a0002c0001t0001g0019a0002c0001t0001g0223 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1025+3776C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616255 | ||||||
| chr17:9616269
|
C | A | 1 | a0002c0001t0001g0166 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1025+3790C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616269 | ||||||
| chr17:9616337
|
C | T | 1 | a0001c0002t0001g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1025+3858C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616337 | ||||||
| chr17:9616338
|
A | G | 2 | a0001c0002t0001g0124a0001c0002t0001g0257 | 2 | HG01243.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1025+3859A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616338 | ||||||
| chr17:9616359
|
A | G | 34 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0052others(31): Show | 34 | HG00099.hp1 HG00438.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1025+3880A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616359 | ||||||
| chr17:9616362
|
T | G | 1 | a0001c0002t0001g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1025+3883T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616362 | ||||||
| chr17:9616368
|
A | G | 1 | a0002c0001t0001g0116 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1025+3889A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616368 | ||||||
| chr17:9616448
|
G | C | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1025+3969G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616448 | ||||||
| chr17:9616449
|
C | A | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1025+3970C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616449 | ||||||
| chr17:9616468
|
C | T | 3 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026 | 3 | HG02647.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1025+3989C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616468 | ||||||
| chr17:9616500
|
A | G | 1 | a0002c0001t0002g0203 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1025+4021A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616500 | ||||||
| chr17:9616511
|
C | A | 2 | a0002c0001t0001g0096a0002c0001t0001g0160 | 2 | NA18972.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1025+4032C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616511 | ||||||
| chr17:9616590
|
C | A | 16 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(13): Show | 17 | HG02145.hp2 HG02559.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1025+4111C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616590 | ||||||
| chr17:9616638
|
T | G | 3 | a0002c0001t0002g0005a0002c0001t0002g0006a0002c0001t0002g0081 | 3 | HG01891.hp1 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1025+4159T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616638 | ||||||
| chr17:9616654
|
G | T | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1025+4175G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616654 | ||||||
| chr17:9616657
|
C | A | 3 | a0002c0001t0002g0005a0002c0001t0002g0006a0002c0001t0002g0081 | 3 | HG01891.hp1 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1025+4178C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616657 | ||||||
| chr17:9616684
|
C | T | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1025+4205C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616684 | ||||||
| chr17:9616700
|
C | T | 1 | a0001c0002t0001g0307 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1025+4221C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616700 | ||||||
| chr17:9616774
|
C | T | 3 | a0001c0002t0001g0076a0001c0002t0001g0214a0006c0014t0001g0177 | 3 | HG02559.hp1 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1025+4295C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616774 | ||||||
| chr17:9616879
|
T | C | 1 | a0001c0002t0001g0032 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1025+4400T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616879 | ||||||
| chr17:9616932
|
C | T | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1025+4453C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616932 | ||||||
| chr17:9616933
|
G | A | 33 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0052others(30): Show | 33 | HG00099.hp1 HG00438.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1025+4454G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9616933 | ||||||
| chr17:9617005
|
T | C | 1 | a0001c0002t0001g0314 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1025+4526T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617005 | ||||||
| chr17:9617020
|
A | G | 1 | a0001c0002t0001g0314 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1025+4541A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617020 | ||||||
| chr17:9617022
|
A | G | 1 | a0001c0002t0001g0314 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1025+4543A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617022 | ||||||
| chr17:9617043
|
G | A | 140 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(137): Show | 141 | HG00323.hp2 HG00423.hp1 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.1025+4564G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617043 | ||||||
| chr17:9617114
|
G | A | 1 | a0001c0002t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1025+4635G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617114 | ||||||
| chr17:9617148
|
A | G | 141 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(138): Show | 142 | HG00323.hp2 HG00423.hp1 HG00621.hp1 others(139): Show |
intron_variant | MODIFIER | c.1025+4669A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617148 | ||||||
| chr17:9617163
|
T | C | 2 | a0001c0002t0001g0027a0007c0013t0001g0015 | 2 | HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1025+4684T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617163 | ||||||
| chr17:9617224
|
C | T | 23 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(20): Show | 23 | HG00323.hp2 HG01123.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1025+4745C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617224 | ||||||
| chr17:9617325
|
G | C | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1025+4846G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617325 | ||||||
| chr17:9617517
|
T | C | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1025+5038T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617517 | ||||||
| chr17:9617539
|
C | T | 1 | a0001c0002t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1025+5060C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617539 | ||||||
| chr17:9617631
|
T | C | 1 | a0002c0001t0001g0259 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1025+5152T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617631 | ||||||
| chr17:9617652
|
C | T | 4 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(1): Show | 4 | HG02647.hp2 HG02809.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+5173C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617652 | ||||||
| chr17:9617768
|
G | T | 3 | a0001c0002t0001g0076a0001c0002t0001g0214a0006c0014t0001g0177 | 3 | HG02559.hp1 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1025+5289G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617768 | ||||||
| chr17:9617784
|
C | T | 4 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+5305C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617784 | ||||||
| chr17:9617873
|
C | T | 11 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(8): Show | 12 | HG02559.hp1 HG02615.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1025+5394C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617873 | ||||||
| chr17:9617883
|
T | C | 313 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(310): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.1025+5404T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9617883 | ||||||
| chr17:9618062
|
A | G | 1 | a0002c0001t0001g0174 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1025+5583A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9618062 | ||||||
| chr17:9618177
|
A | G | 29 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(26): Show | 29 | HG00323.hp2 HG01123.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.1025+5698A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9618177 | ||||||
| chr17:9618196
|
A | G | 125 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(122): Show | 125 | HG00323.hp2 HG00423.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.1025+5717A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9618196 | ||||||
| chr17:9618215
|
A | C | 1 | a0002c0001t0001g0251 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1025+5736A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9618215 | ||||||
| chr17:9618522
|
C | T | 4 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+6043C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9618522 | ||||||
| chr17:9618526
|
C | T | 1 | a0001c0002t0002g0121 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1025+6047C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9618526 | ||||||
| chr17:9618764
|
G | A | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1025+6285G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9618764 | ||||||
| chr17:9618837
|
A | T | 2 | a0002c0001t0001g0028a0002c0001t0001g0029 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1025+6358A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9618837 | ||||||
| chr17:9618838
|
C | G | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+6359C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9618838 | ||||||
| chr17:9618838
|
C | T | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1025+6359C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9618838 | ||||||
| chr17:9619026
|
C | T | 1 | a0001c0002t0001g0003 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1025+6547C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619026 | ||||||
| chr17:9619104
|
CAAGACTA others(3): Show |
C | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1025+6630_1025+663 others(14): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9619104 | |||||
| chr17:9619132
|
G | A | 2 | a0001c0002t0001g0025a0001c0002t0001g0271 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1025+6653G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619132 | ||||||
| chr17:9619157
|
G | GC | 3 | a0001c0002t0001g0257a0001c0002t0001g0276a0001c0002t0001g0278 | 3 | HG01243.hp1 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1025+6678_1025+667 others(5): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619157 | ||||||
| chr17:9619158
|
A | C | 3 | a0001c0002t0001g0257a0001c0002t0001g0276a0001c0002t0001g0278 | 3 | HG01243.hp1 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1025+6679A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619158 | ||||||
| chr17:9619204
|
C | T | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1025+6725C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619204 | ||||||
| chr17:9619228
|
C | T | 4 | a0002c0001t0003g0106a0002c0001t0003g0107a0002c0001t0003g0187others(1): Show | 4 | HG02040.hp1 NA19002.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+6749C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619228 | ||||||
| chr17:9619229
|
G | A | 1 | a0002c0001t0002g0164 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1025+6750G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619229 | ||||||
| chr17:9619384
|
G | A | 313 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(310): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.1025+6905G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619384 | ||||||
| chr17:9619386
|
G | A | 2 | a0002c0001t0001g0019a0002c0001t0001g0223 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1025+6907G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619386 | ||||||
| chr17:9619531
|
G | A | 3 | a0001c0002t0001g0076a0001c0002t0001g0214a0006c0014t0001g0177 | 3 | HG02559.hp1 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1025+7052G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619531 | ||||||
| chr17:9619573
|
C | T | 3 | a0002c0001t0001g0014a0002c0001t0001g0200a0009c0015t0001g0064 | 3 | HG02258.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1025+7094C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619573 | ||||||
| chr17:9619679
|
A | T | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+7200A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619679 | ||||||
| chr17:9619700
|
T | C | 310 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1025+7221T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619700 | ||||||
| chr17:9619780
|
A | G | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1025+7301A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619780 | ||||||
| chr17:9619966
|
G | A | 1 | a0002c0001t0001g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1025+7487G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619966 | ||||||
| chr17:9619988
|
G | A | 2 | a0002c0001t0002g0180a0002c0001t0002g0292 | 2 | HG01123.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1025+7509G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9619988 | ||||||
| chr17:9620078
|
G | A | 2 | a0001c0002t0001g0186a0001c0005t0004g0215 | 2 | NA19060.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1025+7599G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9620078 | ||||||
| chr17:9620108
|
G | A | 11 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(8): Show | 12 | HG02559.hp1 HG02615.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1025+7629G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9620108 | ||||||
| chr17:9620165
|
A | C | 1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1025+7686A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9620165 | ||||||
| chr17:9620205
|
G | A | 4 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+7726G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9620205 | ||||||
| chr17:9620338
|
C | T | 136 | a0001c0002t0001g0309a0001c0002t0002g0197a0002c0001t0001g0013others(133): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1025+7859C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9620338 | ||||||
| chr17:9620386
|
A | G | 125 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(122): Show | 125 | HG00323.hp2 HG00423.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.1025+7907A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9620386 | ||||||
| chr17:9620407
|
T | C | 4 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+7928T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9620407 | ||||||
| chr17:9620535
|
G | A | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1025+8056G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9620535 | ||||||
| chr17:9620539
|
C | T | 7 | a0002c0001t0003g0106a0002c0001t0003g0107a0002c0001t0003g0108others(4): Show | 7 | HG02015.hp1 HG02040.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.1025+8060C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9620539 | ||||||
| chr17:9620590
|
T | C | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1026-8082T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9620590 | ||||||
| chr17:9620593
|
C | T | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1026-8079C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9620593 | ||||||
| chr17:9620924
|
G | A | 18 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(15): Show | 19 | HG01106.hp1 HG02145.hp2 HG02273.hp2 others(16): Show |
intron_variant | MODIFIER | c.1026-7748G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9620924 | ||||||
| chr17:9620939
|
A | G | 4 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-7733A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9620939 | ||||||
| chr17:9621075
|
C | CA | 124 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(121): Show | 124 | HG00323.hp2 HG00423.hp1 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.1026-7596dupA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9621075 | |||||
| chr17:9621091
|
C | T | 84 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0031others(81): Show | 84 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1026-7581C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621091 | ||||||
| chr17:9621095
|
G | A | 84 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0031others(81): Show | 84 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1026-7577G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621095 | ||||||
| chr17:9621189
|
C | T | 1 | a0002c0001t0002g0087 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1026-7483C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621189 | ||||||
| chr17:9621193
|
G | C | 1 | a0001c0002t0002g0121 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1026-7479G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621193 | ||||||
| chr17:9621366
|
G | C | 1 | a0002c0001t0001g0014 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1026-7306G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621366 | ||||||
| chr17:9621517
|
G | T | 2 | a0002c0001t0001g0175a0002c0001t0001g0251 | 2 | NA18966.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1026-7155G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621517 | ||||||
| chr17:9621549
|
G | A | 1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1026-7123G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621549 | ||||||
| chr17:9621616
|
A | C | 138 | a0001c0002t0001g0186a0001c0002t0001g0309a0001c0002t0002g0002others(135): Show | 138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1026-7056A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621616 | ||||||
| chr17:9621635
|
A | C | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1026-7037A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621635 | ||||||
| chr17:9621748
|
A | G | 4 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-6924A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621748 | ||||||
| chr17:9621870
|
G | A | 1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1026-6802G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621870 | ||||||
| chr17:9621871
|
A | G | 4 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-6801A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621871 | ||||||
| chr17:9621876
|
G | T | 1 | a0001c0002t0001g0151 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1026-6796G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621876 | ||||||
| chr17:9621885
|
G | A | 1 | a0001c0002t0001g0162 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1026-6787G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621885 | ||||||
| chr17:9621903
|
T | G | 1 | a0002c0001t0001g0061 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1026-6769T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621903 | ||||||
| chr17:9621964
|
C | A | 84 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0031others(81): Show | 84 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1026-6708C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9621964 | ||||||
| chr17:9622065
|
T | C | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1026-6607T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9622065 | ||||||
| chr17:9622112
|
C | A | 33 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0052others(30): Show | 33 | HG00099.hp1 HG00438.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1026-6560C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9622112 | ||||||
| chr17:9622374
|
C | A | 1 | a0002c0001t0001g0019 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1026-6298C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9622374 | ||||||
| chr17:9622549
|
A | AAGAAGAA others(40): Show |
1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1026-6122_1026-612 others(51): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9622549 | |||||
| chr17:9622552
|
A | AAAG | 4 | a0001c0002t0001g0186a0001c0004t0004g0001a0001c0004t0004g0036others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-6100_1026-609 others(7): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9622552 | |||||
| chr17:9622552
|
A | AAGAAGAA others(4): Show |
2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1026-6119_1026-611 others(15): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9622552 | |||||
| chr17:9622552
|
A | G | 3 | a0001c0002t0002g0197a0001c0005t0004g0215a0002c0001t0001g0119 | 3 | HG00741.hp2 NA18962.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1026-6120A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9622552 | ||||||
| chr17:9622572
|
AGAT | A | 5 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0084others(2): Show | 5 | HG01109.hp2 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026-6085_1026-608 others(7): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9622572 | |||||
| chr17:9622575
|
T | A | 172 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0007others(169): Show | 173 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1026-6097T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9622575 | ||||||
| chr17:9622663
|
T | TA | 16 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(13): Show | 17 | HG02145.hp2 HG02559.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1026-6008dupA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9622663 | |||||
| chr17:9622725
|
C | G | 3 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026 | 3 | HG02647.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1026-5947C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9622725 | ||||||
| chr17:9622731
|
A | G | 3 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026 | 3 | HG02647.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1026-5941A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9622731 | ||||||
| chr17:9622852
|
C | T | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-5820C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9622852 | ||||||
| chr17:9622927
|
A | G | 1 | a0001c0002t0001g0004 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1026-5745A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9622927 | ||||||
| chr17:9622978
|
G | T | 1 | a0001c0002t0001g0065 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1026-5694G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9622978 | ||||||
| chr17:9623086
|
T | G | 1 | a0001c0002t0001g0162 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1026-5586T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9623086 | ||||||
| chr17:9623114
|
A | T | 1 | a0001c0002t0001g0072 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1026-5558A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9623114 | ||||||
| chr17:9623188
|
C | T | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1026-5484C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9623188 | ||||||
| chr17:9623432
|
C | G | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1026-5240C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9623432 | ||||||
| chr17:9623445
|
G | T | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1026-5227G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9623445 | ||||||
| chr17:9623488
|
A | G | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1026-5184A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9623488 | ||||||
| chr17:9623515
|
A | G | 1 | a0001c0002t0001g0307 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1026-5157A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9623515 | ||||||
| chr17:9623566
|
G | A | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1026-5106G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9623566 | ||||||
| chr17:9623670
|
T | TTTTG | 9 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(6): Show | 10 | HG02559.hp1 HG02615.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1026-4974_1026-497 others(8): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9623670 | |||||
| chr17:9623670
|
TTTTG | T | 123 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(120): Show | 123 | HG00323.hp2 HG00423.hp1 HG00621.hp1 others(120): Show |
intron_variant | MODIFIER | c.1026-4974_1026-497 others(8): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9623670 | |||||
| chr17:9623691
|
T | C | 33 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0052others(30): Show | 33 | HG00099.hp1 HG00438.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1026-4981T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9623691 | ||||||
| chr17:9623694
|
G | A | 1 | a0001c0002t0001g0021 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1026-4978G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9623694 | ||||||
| chr17:9623908
|
C | G | 1 | a0002c0001t0001g0223 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1026-4764C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9623908 | ||||||
| chr17:9624090
|
C | A | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1026-4582C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9624090 | ||||||
| chr17:9624107
|
T | C | 16 | a0002c0001t0001g0013a0002c0001t0001g0017a0002c0001t0001g0035others(13): Show | 16 | HG01071.hp2 HG01106.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1026-4565T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9624107 | ||||||
| chr17:9624202
|
A | G | 1 | a0001c0002t0001g0123 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1026-4470A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9624202 | ||||||
| chr17:9624363
|
T | A | 1 | a0001c0002t0001g0083 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1026-4309T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9624363 | ||||||
| chr17:9624626
|
G | T | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1026-4046G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9624626 | ||||||
| chr17:9624656
|
GTACCTGG others(17): Show |
G | 1 | a0001c0002t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1026-4014_1026-399 others(28): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9624656 | |||||
| chr17:9624842
|
A | G | 1 | a0001c0002t0001g0027 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1026-3830A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9624842 | ||||||
| chr17:9625082
|
G | A | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1026-3590G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9625082 | ||||||
| chr17:9625129
|
G | C | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1026-3543G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9625129 | ||||||
| chr17:9625203
|
TA | T | 8 | a0001c0002t0001g0048a0001c0002t0001g0073a0001c0002t0001g0219others(5): Show | 9 | HG01175.hp2 HG01433.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1026-3459delA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9625203 | |||||
| chr17:9625306
|
GGCAGTGT others(153): Show |
G | 4 | a0001c0002t0001g0222a0001c0004t0004g0001a0001c0004t0004g0036others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-3245_1026-308 others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9625306 | |||||
| chr17:9625491
|
A | G | 2 | a0001c0004t0004g0036a0001c0004t0004g0199 | 2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1026-3181A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9625491 | ||||||
| chr17:9625995
|
G | A | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1026-2677G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9625995 | ||||||
| chr17:9626087
|
A | G | 1 | a0002c0001t0001g0174 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1026-2585A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626087 | ||||||
| chr17:9626214
|
T | C | 178 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0007others(175): Show | 179 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1026-2458T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626214 | ||||||
| chr17:9626288
|
G | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0078 | 2 | HG01243.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1026-2384G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626288 | ||||||
| chr17:9626375
|
G | A | 23 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(20): Show | 23 | HG00323.hp2 HG01123.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1026-2297G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626375 | ||||||
| chr17:9626421
|
C | G | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1026-2251C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626421 | ||||||
| chr17:9626426
|
T | A | 3 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026 | 3 | HG02647.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1026-2246T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626426 | ||||||
| chr17:9626634
|
C | T | 3 | a0001c0002t0001g0257a0001c0002t0001g0276a0001c0002t0001g0278 | 3 | HG01243.hp1 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1026-2038C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626634 | ||||||
| chr17:9626709
|
A | G | 1 | a0002c0011t0001g0277 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1026-1963A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626709 | ||||||
| chr17:9626741
|
C | T | 8 | a0002c0001t0001g0116a0002c0001t0001g0146a0002c0001t0001g0147others(5): Show | 8 | HG02027.hp2 HG02040.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026-1931C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626741 | ||||||
| chr17:9626765
|
C | T | 4 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0179others(1): Show | 4 | HG02135.hp1 HG02809.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1907C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626765 | ||||||
| chr17:9626786
|
G | C | 1 | a0001c0002t0001g0004 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1026-1886G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626786 | ||||||
| chr17:9626840
|
T | A | 1 | a0001c0002t0001g0162 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1026-1832T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626840 | ||||||
| chr17:9626861
|
T | C | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1026-1811T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626861 | ||||||
| chr17:9626907
|
G | T | 1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1026-1765G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626907 | ||||||
| chr17:9626933
|
C | T | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215 | 3 | HG02145.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1026-1739C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626933 | ||||||
| chr17:9626995
|
T | C | 1 | a0001c0002t0001g0314 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1026-1677T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9626995 | ||||||
| chr17:9627006
|
C | A | 2 | a0001c0002t0001g0021a0001c0002t0001g0218 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1026-1666C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9627006 | ||||||
| chr17:9627044
|
A | C | 4 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1628A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9627044 | ||||||
| chr17:9627111
|
C | A | 1 | a0002c0001t0001g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1026-1561C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9627111 | ||||||
| chr17:9627112
|
C | CT | 92 | a0001c0002t0001g0003a0001c0002t0001g0016a0001c0002t0001g0021others(89): Show | 92 | HG00323.hp2 HG00423.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1026-1545dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9627112 | |||||
| chr17:9627247
|
C | T | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1026-1425C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9627247 | ||||||
| chr17:9627249
|
C | T | 7 | a0001c0002t0001g0004a0001c0002t0001g0030a0001c0002t0001g0076others(4): Show | 7 | HG02109.hp2 HG02559.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1026-1423C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9627249 | ||||||
| chr17:9627375
|
G | A | 3 | a0001c0002t0001g0030a0002c0001t0001g0019a0002c0001t0001g0223 | 3 | HG02109.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1026-1297G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9627375 | ||||||
| chr17:9627489
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1026-1183G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9627489 | ||||||
| chr17:9627641
|
A | G | 1 | a0001c0005t0001g0077 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1026-1031A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9627641 | ||||||
| chr17:9628093
|
T | G | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1026-579T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9628093 | ||||||
| chr17:9628204
|
G | A | 3 | a0001c0002t0001g0076a0001c0002t0001g0214a0006c0014t0001g0177 | 3 | HG02559.hp1 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1026-468G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9628204 | ||||||
| chr17:9628282
|
C | CT | 8 | a0001c0002t0001g0076a0001c0002t0001g0176a0001c0002t0001g0214others(5): Show | 8 | HG02559.hp1 HG02717.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026-375dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9628282 | |||||
| chr17:9628282
|
CT | C | 15 | a0001c0002t0001g0004a0001c0002t0001g0044a0001c0002t0001g0062others(12): Show | 16 | HG01168.hp2 HG01496.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1026-375delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 9628282 | |||||
| chr17:9628306
|
G | T | 1 | a0002c0001t0002g0109 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1026-366G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9628306 | ||||||
| chr17:9628375
|
G | T | 3 | a0001c0002t0001g0076a0001c0002t0001g0214a0006c0014t0001g0177 | 3 | HG02559.hp1 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1026-297G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9628375 | ||||||
| chr17:9628383
|
G | A | 3 | a0001c0002t0001g0076a0001c0002t0001g0214a0006c0014t0001g0177 | 3 | HG02559.hp1 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1026-289G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9628383 | ||||||
| chr17:9628514
|
G | A | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1026-158G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9628514 | ||||||
| chr17:9628565
|
C | T | 1 | a0003c0003t0001g0130 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1026-107C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9628565 | ||||||
| chr17:9628567
|
G | A | 3 | a0001c0002t0001g0030a0002c0001t0001g0019a0002c0001t0001g0223 | 3 | HG02109.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1026-105G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9628567 | ||||||
| chr17:9628669
|
C | T | 3 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026 | 3 | HG02647.hp2 HG02809.hp2 NA19240.hp2 |
splice_region_variant&intron_variant | LOW | c.1026-3C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 8/13 | chr17 | 9628669 | ||||||
| chr17:9628941
|
C | G | 5 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(2): Show | 6 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174+121C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9628941 | ||||||
| chr17:9629101
|
G | A | 14 | a0002c0001t0001g0089a0002c0001t0001g0128a0002c0001t0001g0175others(11): Show | 14 | HG01106.hp1 HG02015.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1174+281G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629101 | ||||||
| chr17:9629145
|
T | C | 3 | a0001c0002t0001g0025a0001c0002t0001g0271a0001c0002t0001g0314 | 3 | HG01891.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1174+325T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629145 | ||||||
| chr17:9629249
|
C | T | 1 | a0002c0001t0002g0216 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1174+429C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629249 | ||||||
| chr17:9629310
|
G | A | 1 | a0001c0002t0001g0276 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1174+490G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629310 | ||||||
| chr17:9629329
|
T | A | 2 | a0001c0002t0001g0184a0001c0002t0001g0210 | 2 | HG01168.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1174+509T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629329 | ||||||
| chr17:9629375
|
C | T | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174+555C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629375 | ||||||
| chr17:9629387
|
C | T | 2 | a0002c0001t0001g0019a0002c0001t0001g0223 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1174+567C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629387 | ||||||
| chr17:9629399
|
G | T | 1 | a0002c0001t0002g0192 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1174+579G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629399 | ||||||
| chr17:9629439
|
CCAGGAAA others(48): Show |
C | 1 | a0001c0002t0001g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1174+621_1174+675d others(57): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9629439 | |||||
| chr17:9629474
|
C | CCTTTCTT others(9): Show |
1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1174+663_1174+678d others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9629474 | |||||
| chr17:9629474
|
CCTTT | C | 33 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0052others(30): Show | 33 | HG00099.hp1 HG00438.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1174+675_1174+678d others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9629474 | |||||
| chr17:9629475
|
C | T | 4 | a0002c0001t0001g0113a0002c0001t0001g0148a0002c0001t0001g0149others(1): Show | 4 | HG00423.hp2 HG02056.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+655C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629475 | ||||||
| chr17:9629491
|
CTTTCT | C | 14 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(11): Show | 14 | HG02015.hp2 HG02080.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1174+684_1174+688d others(7): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9629491 | |||||
| chr17:9629495
|
CT | C | 80 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0031others(77): Show | 80 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1174+679delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9629495 | |||||
| chr17:9629496
|
T | TTTC | 28 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0011others(25): Show | 28 | HG00323.hp2 HG01123.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.1174+678_1174+679i others(5): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9629496 | |||||
| chr17:9629496
|
T | TTTCTTTC | 3 | a0001c0002t0001g0010a0001c0002t0001g0025a0001c0002t0001g0066 | 3 | HG01243.hp2 HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1174+678_1174+679i others(9): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9629496 | |||||
| chr17:9629496
|
T | TTTCTTTC others(4): Show |
1 | a0001c0002t0001g0143 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1174+678_1174+679i others(13): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9629496 | |||||
| chr17:9629496
|
T | TTTCTTTC others(12): Show |
2 | a0001c0002t0001g0008a0001c0002t0001g0274 | 2 | HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1174+678_1174+679i others(21): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9629496 | |||||
| chr17:9629499
|
TC | T | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174+680delC | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629499 | ||||||
| chr17:9629500
|
C | T | 10 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(7): Show | 10 | HG02145.hp2 HG02559.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1174+680C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629500 | ||||||
| chr17:9629547
|
C | CT | 13 | a0001c0002t0001g0063a0001c0002t0001g0070a0001c0002t0001g0222others(10): Show | 14 | HG00280.hp1 HG00323.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1174+742dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9629547 | |||||
| chr17:9629562
|
T | C | 1 | a0001c0002t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1174+742T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629562 | ||||||
| chr17:9629646
|
C | T | 2 | a0001c0002t0001g0226a0001c0002t0001g0227 | 2 | HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1174+826C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629646 | ||||||
| chr17:9629660
|
G | A | 1 | a0002c0001t0002g0049 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1174+840G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629660 | ||||||
| chr17:9629685
|
TTACAGGC others(34): Show |
T | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+873_1174+913d others(43): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9629685 | |||||
| chr17:9629784
|
T | C | 1 | a0002c0001t0001g0270 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1174+964T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629784 | ||||||
| chr17:9629837
|
G | A | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174+1017G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629837 | ||||||
| chr17:9629872
|
G | A | 1 | a0001c0002t0001g0004 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1174+1052G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629872 | ||||||
| chr17:9629951
|
G | C | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1174+1131G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629951 | ||||||
| chr17:9629976
|
C | A | 1 | a0001c0002t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1174+1156C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9629976 | ||||||
| chr17:9630029
|
T | C | 1 | a0001c0002t0001g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1174+1209T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630029 | ||||||
| chr17:9630041
|
C | T | 2 | a0002c0001t0001g0028a0002c0001t0001g0029 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1174+1221C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630041 | ||||||
| chr17:9630043
|
C | G | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+1223C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630043 | ||||||
| chr17:9630082
|
C | A | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1174+1262C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630082 | ||||||
| chr17:9630218
|
A | G | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+1398A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630218 | ||||||
| chr17:9630296
|
G | A | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1174+1476G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630296 | ||||||
| chr17:9630312
|
C | T | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174+1492C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630312 | ||||||
| chr17:9630359
|
G | A | 4 | a0001c0002t0001g0063a0001c0002t0001g0257a0001c0002t0001g0276others(1): Show | 4 | HG01243.hp1 HG02630.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+1539G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630359 | ||||||
| chr17:9630379
|
T | C | 83 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0031others(80): Show | 83 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1174+1559T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630379 | ||||||
| chr17:9630426
|
A | AT | 93 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0027others(90): Show | 93 | HG00423.hp1 HG00621.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.1174+1625dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9630426 | |||||
| chr17:9630426
|
A | ATT | 9 | a0001c0002t0001g0031a0001c0002t0001g0115a0001c0002t0001g0162others(6): Show | 9 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174+1624_1174+162 others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9630426 | |||||
| chr17:9630426
|
A | ATTTTTTT others(9): Show |
2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174+1610_1174+162 others(20): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9630426 | |||||
| chr17:9630426
|
AT | A | 17 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0025others(14): Show | 17 | HG00323.hp1 HG01099.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.1174+1625delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9630426 | |||||
| chr17:9630453
|
G | A | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174+1633G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630453 | ||||||
| chr17:9630460
|
T | C | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+1640T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630460 | ||||||
| chr17:9630461
|
T | G | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+1641T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630461 | ||||||
| chr17:9630462
|
T | C | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+1642T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630462 | ||||||
| chr17:9630468
|
C | T | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+1648C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630468 | ||||||
| chr17:9630469
|
T | C | 1 | a0001c0002t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1174+1649T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630469 | ||||||
| chr17:9630469
|
T | G | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+1649T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630469 | ||||||
| chr17:9630470
|
C | T | 1 | a0001c0002t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1174+1650C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630470 | ||||||
| chr17:9630474
|
G | A | 1 | a0001c0002t0001g0307 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1174+1654G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630474 | ||||||
| chr17:9630485
|
G | A | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+1665G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630485 | ||||||
| chr17:9630493
|
G | A | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+1673G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630493 | ||||||
| chr17:9630543
|
C | T | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1174+1723C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630543 | ||||||
| chr17:9630554
|
C | T | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1174+1734C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630554 | ||||||
| chr17:9630562
|
T | C | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1174+1742T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630562 | ||||||
| chr17:9630574
|
C | T | 3 | a0001c0002t0001g0076a0001c0002t0001g0214a0006c0014t0001g0177 | 3 | HG02559.hp1 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1174+1754C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630574 | ||||||
| chr17:9630581
|
T | C | 130 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(127): Show | 131 | HG00323.hp2 HG00423.hp1 HG00621.hp1 others(128): Show |
intron_variant | MODIFIER | c.1174+1761T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630581 | ||||||
| chr17:9630646
|
G | A | 2 | a0001c0002t0001g0063a0001c0002t0001g0070 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1174+1826G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630646 | ||||||
| chr17:9630651
|
G | C | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+1831G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630651 | ||||||
| chr17:9630677
|
G | A | 1 | a0002c0001t0003g0230 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1174+1857G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630677 | ||||||
| chr17:9630681
|
C | T | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174+1861C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630681 | ||||||
| chr17:9630682
|
G | A | 2 | a0002c0001t0002g0097a0002c0001t0002g0098 | 2 | HG01074.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1174+1862G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630682 | ||||||
| chr17:9630714
|
G | A | 1 | a0002c0001t0001g0166 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1174+1894G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630714 | ||||||
| chr17:9630768
|
C | T | 3 | a0001c0002t0001g0025a0001c0002t0001g0271a0001c0002t0001g0314 | 3 | HG01891.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1174+1948C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630768 | ||||||
| chr17:9630781
|
T | G | 1 | a0001c0002t0001g0310 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1174+1961T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630781 | ||||||
| chr17:9630792
|
C | A | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1174+1972C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630792 | ||||||
| chr17:9630878
|
C | T | 1 | a0001c0002t0001g0120 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1175-2010C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630878 | ||||||
| chr17:9630988
|
A | AAGAAGAA others(240): Show |
1 | a0001c0002t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1175-1899_1175-189 others(251): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9630988 | |||||
| chr17:9630990
|
A | AAAAGAAA others(189): Show |
1 | a0001c0002t0001g0170 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(200): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9630990 | |||||
| chr17:9630990
|
A | AAAAGAAA others(193): Show |
1 | a0001c0002t0001g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(204): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9630990 | |||||
| chr17:9630990
|
A | AAAAGAAA others(213): Show |
1 | a0001c0002t0001g0094 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(224): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9630990 | |||||
| chr17:9630990
|
A | AAAG | 6 | a0001c0002t0001g0052a0001c0002t0001g0115a0001c0002t0001g0132others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1175-1896_1175-189 others(7): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9630990 | |||||
| chr17:9630990
|
A | G | 5 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0101others(2): Show | 5 | HG00099.hp1 HG02683.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1175-1898A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630990 | ||||||
| chr17:9630990
|
AAAAGAAA others(9): Show |
A | 1 | a0002c0001t0001g0268 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1175-1872_1175-185 others(20): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9630990 | |||||
| chr17:9630994
|
G | A | 2 | a0001c0002t0001g0152a0001c0005t0004g0215 | 2 | NA18956.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1175-1894G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630994 | ||||||
| chr17:9630996
|
A | AAGAAAGA others(141): Show |
1 | a0001c0002t0001g0196 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(152): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9630996 | |||||
| chr17:9630997
|
A | AGAAAGAA others(53): Show |
1 | a0001c0002t0001g0118 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(64): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9630997 | |||||
| chr17:9630998
|
G | A | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1890G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9630998 | ||||||
| chr17:9631000
|
A | C | 1 | a0001c0002t0001g0262 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1175-1888A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631000 | ||||||
| chr17:9631004
|
A | AAGAAAGA others(273): Show |
1 | a0001c0002t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1175-1875_1175-187 others(284): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631004 | |||||
| chr17:9631012
|
A | AAGAGAGA others(5): Show |
1 | a0001c0002t0001g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1175-1873_1175-187 others(16): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631012 | |||||
| chr17:9631016
|
A | G | 9 | a0001c0002t0001g0020a0001c0002t0001g0026a0001c0002t0001g0076others(6): Show | 9 | HG02273.hp2 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1175-1872A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631016 | ||||||
| chr17:9631016
|
AAGAAAGA others(17): Show |
A | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1175-1868_1175-184 others(28): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631016 | |||||
| chr17:9631020
|
A | AAGAGAGA others(19): Show |
1 | a0001c0002t0001g0202 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1175-1865_1175-186 others(30): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631020 | |||||
| chr17:9631020
|
A | AG | 4 | a0002c0001t0001g0145a0002c0001t0001g0266a0002c0001t0001g0281others(1): Show | 4 | HG00438.hp2 HG00673.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1868_1175-186 others(5): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631020 | ||||||
| chr17:9631020
|
A | G | 16 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(13): Show | 16 | HG02080.hp1 HG02273.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1175-1868A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631020 | ||||||
| chr17:9631020
|
A | T | 1 | a0001c0002t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1175-1868A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631020 | ||||||
| chr17:9631024
|
A | AAGAGAGA others(3): Show |
1 | a0001c0002t0001g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1175-1861_1175-186 others(14): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631024 | |||||
| chr17:9631024
|
A | AAGAGAGA others(7): Show |
1 | a0002c0001t0001g0128 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1175-1861_1175-186 others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631024 | |||||
| chr17:9631024
|
A | AAGAGAGA others(9): Show |
1 | a0002c0001t0001g0302 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1175-1861_1175-186 others(20): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631024 | |||||
| chr17:9631024
|
A | AAGAGAGA others(11): Show |
1 | a0007c0013t0001g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1175-1861_1175-186 others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631024 | |||||
| chr17:9631024
|
A | AAGAGAGA others(15): Show |
1 | a0002c0001t0001g0175 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1175-1861_1175-186 others(26): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631024 | |||||
| chr17:9631024
|
A | AAGAGAGA others(25): Show |
1 | a0001c0002t0001g0244 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1175-1861_1175-186 others(36): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631024 | |||||
| chr17:9631024
|
A | AAGAGAGA others(31): Show |
1 | a0001c0002t0001g0288 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1175-1861_1175-186 others(42): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631024 | |||||
| chr17:9631024
|
A | AGAGAGAG others(48): Show |
1 | a0001c0002t0001g0123 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1175-1864_1175-186 others(59): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631024 | ||||||
| chr17:9631024
|
A | G | 66 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(63): Show | 66 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1175-1864A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631024 | ||||||
| chr17:9631025
|
A | G | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1175-1863A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631025 | ||||||
| chr17:9631028
|
A | AAGAAAGA others(132): Show |
1 | a0001c0002t0001g0263 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(143): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(211): Show |
1 | a0001c0002t0001g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(222): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(218): Show |
1 | a0001c0002t0001g0310 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(229): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(109): Show |
1 | a0001c0002t0001g0179 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(120): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(83): Show |
1 | a0001c0002t0001g0314 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(94): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(75): Show |
1 | a0001c0002t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(86): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(59): Show |
1 | a0001c0002t0001g0306 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(70): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(65): Show |
1 | a0001c0002t0001g0271 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(76): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(47): Show |
1 | a0001c0002t0001g0052 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(58): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(47): Show |
1 | a0001c0002t0001g0193 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(58): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(49): Show |
1 | a0001c0002t0001g0194 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(60): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(72): Show |
1 | a0001c0002t0001g0221 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(83): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(41): Show |
1 | a0001c0002t0001g0135 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(52): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(43): Show |
1 | a0001c0002t0001g0133 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(54): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(39): Show |
1 | a0001c0002t0001g0132 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(50): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(35): Show |
1 | a0010c0007t0001g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(46): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(11): Show |
1 | a0001c0002t0001g0207 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(15): Show |
2 | a0001c0002t0001g0067a0001c0002t0001g0242 | 2 | HG02027.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1175-1857_1175-185 others(26): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(19): Show |
1 | a0001c0002t0001g0273 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(30): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(47): Show |
1 | a0001c0002t0001g0241 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(58): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(18): Show |
1 | a0002c0001t0001g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(29): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(36): Show |
1 | a0001c0002t0001g0115 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(47): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(7): Show |
3 | a0001c0002t0001g0075a0001c0002t0001g0143a0001c0002t0001g0231 | 3 | HG03710.hp2 NA18984.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1175-1857_1175-185 others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(13): Show |
1 | a0001c0002t0001g0178 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(24): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(21): Show |
1 | a0001c0002t0001g0184 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(32): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAAAGA others(31): Show |
1 | a0001c0002t0001g0282 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(42): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAGAGA others(3): Show |
1 | a0001c0005t0001g0074 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1175-1842_1175-183 others(14): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAGAGA others(7): Show |
1 | a0001c0002t0001g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1175-1846_1175-183 others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAGAGA others(9): Show |
2 | a0001c0002t0001g0010a0003c0003t0001g0293 | 2 | HG01243.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1175-1848_1175-183 others(20): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAGAGA others(13): Show |
1 | a0002c0001t0001g0286 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1175-1852_1175-183 others(24): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAGAGA others(21): Show |
1 | a0001c0002t0001g0246 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(32): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAGAGA others(23): Show |
2 | a0001c0002t0001g0048a0001c0002t0001g0127 | 2 | HG01433.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(34): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAGAGA others(31): Show |
1 | a0002c0001t0001g0040 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(42): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAGAGA others(37): Show |
2 | a0001c0002t0001g0243a0001c0002t0001g0262 | 2 | NA18973.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(48): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAGAGA others(47): Show |
1 | a0001c0002t0001g0245 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(58): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AAGAGAGA others(63): Show |
1 | a0001c0002t0001g0162 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(74): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631028 | |||||
| chr17:9631028
|
A | AGAGAGAG others(12): Show |
1 | a0003c0003t0001g0295 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1175-1860_1175-185 others(23): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631028 | ||||||
| chr17:9631028
|
A | AGAGAGAG others(20): Show |
1 | a0003c0003t0001g0294 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1175-1860_1175-185 others(31): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631028 | ||||||
| chr17:9631028
|
A | G | 96 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0026others(93): Show | 96 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1175-1860A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631028 | ||||||
| chr17:9631029
|
A | G | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1859A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631029 | ||||||
| chr17:9631030
|
G | GAAAGAAA others(63): Show |
1 | a0001c0002t0001g0105 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(74): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631030 | |||||
| chr17:9631030
|
G | GAAAGAAA others(151): Show |
1 | a0001c0002t0001g0300 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(162): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631030 | |||||
| chr17:9631030
|
G | GAAAGAAA others(231): Show |
1 | a0001c0002t0001g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(242): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631030 | |||||
| chr17:9631030
|
G | GAAAGAAA others(251): Show |
1 | a0001c0002t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(262): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631030 | |||||
| chr17:9631030
|
G | GAAAGAAA others(195): Show |
1 | a0001c0002t0001g0208 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(206): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631030 | |||||
| chr17:9631030
|
G | GAAAGAAA others(125): Show |
1 | a0001c0002t0001g0090 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(136): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631030 | |||||
| chr17:9631030
|
G | GAAAGAAA others(47): Show |
1 | a0001c0002t0001g0236 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1175-1857_1175-185 others(58): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631030 | |||||
| chr17:9631031
|
AGAGAGAG others(6): Show |
A | 2 | a0001c0004t0004g0036a0001c0004t0004g0199 | 2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1175-1856_1175-184 others(17): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631031 | ||||||
| chr17:9631031
|
AGAGAGAG others(14): Show |
A | 1 | a0001c0004t0004g0001 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1175-1856_1175-183 others(25): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631031 | ||||||
| chr17:9631032
|
G | A | 45 | a0001c0002t0001g0004a0001c0002t0001g0016a0001c0002t0001g0020others(42): Show | 45 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1175-1856G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631032 | ||||||
| chr17:9631032
|
G | GAGAA | 4 | a0001c0002t0001g0026a0002c0001t0001g0279a0002c0001t0001g0308others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1853_1175-185 others(8): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631032 | |||||
| chr17:9631034
|
G | A | 8 | a0001c0002t0001g0094a0001c0002t0001g0099a0001c0002t0001g0100others(5): Show | 8 | HG00099.hp1 HG00438.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-1854G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631034 | ||||||
| chr17:9631036
|
G | A | 24 | a0001c0002t0001g0020a0001c0002t0001g0023a0001c0002t0001g0024others(21): Show | 24 | HG01074.hp2 HG01975.hp1 HG02165.hp2 others(21): Show |
intron_variant | MODIFIER | c.1175-1852G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631036 | ||||||
| chr17:9631036
|
G | GAGAAAGA others(5): Show |
1 | a0002c0001t0001g0061 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1175-1849_1175-184 others(16): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631036 | |||||
| chr17:9631038
|
G | A | 2 | a0001c0002t0001g0161a0001c0002t0001g0170 | 2 | HG03942.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1175-1850G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631038 | ||||||
| chr17:9631038
|
G | GAAAGAAA others(132): Show |
1 | a0001c0002t0001g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1175-1849_1175-184 others(143): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631038 | |||||
| chr17:9631040
|
G | A | 21 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0023others(18): Show | 21 | HG00099.hp1 HG02273.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.1175-1848G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631040 | ||||||
| chr17:9631040
|
G | GAAAGAAA others(7): Show |
2 | a0002c0001t0001g0171a0002c0001t0001g0182 | 2 | NA18954.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1175-1847_1175-184 others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631040 | |||||
| chr17:9631040
|
G | GAAAGAAA others(11): Show |
1 | a0002c0001t0001g0119 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1175-1847_1175-184 others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631040 | |||||
| chr17:9631040
|
G | GAAAGAAG others(14): Show |
1 | a0002c0001t0001g0145 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1175-1847_1175-184 others(25): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631040 | |||||
| chr17:9631040
|
G | GAGAAAGA others(1): Show |
4 | a0002c0001t0001g0113a0002c0001t0001g0116a0002c0001t0001g0148others(1): Show | 4 | HG00423.hp2 HG02027.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1845_1175-184 others(12): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631040 | |||||
| chr17:9631040
|
G | GAGAAAGA others(5): Show |
4 | a0002c0001t0001g0103a0002c0001t0001g0147a0002c0001t0001g0149others(1): Show | 4 | HG02056.hp2 HG02155.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1845_1175-184 others(16): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631040 | |||||
| chr17:9631040
|
G | GAGAAAGA others(9): Show |
4 | a0002c0001t0001g0159a0002c0001t0001g0167a0002c0001t0001g0233others(1): Show | 4 | HG02040.hp2 HG02074.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1845_1175-184 others(20): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631040 | |||||
| chr17:9631040
|
G | GAGAAAGA others(13): Show |
1 | a0002c0001t0001g0071 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1175-1845_1175-184 others(24): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631040 | |||||
| chr17:9631040
|
G | GAGAAAGA others(21): Show |
1 | a0004c0006t0001g0131 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1175-1845_1175-184 others(32): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631040 | |||||
| chr17:9631044
|
G | A | 45 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0023others(42): Show | 45 | HG00423.hp2 HG00438.hp2 HG02027.hp2 others(42): Show |
intron_variant | MODIFIER | c.1175-1844G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631044 | ||||||
| chr17:9631044
|
G | GAAAGAAA others(3): Show |
1 | a0002c0001t0001g0275 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1175-1843_1175-184 others(14): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631044 | |||||
| chr17:9631044
|
G | GAAAGAAA others(7): Show |
3 | a0002c0001t0001g0038a0002c0001t0001g0095a0002c0001t0001g0281 | 3 | HG00673.hp1 HG02602.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1175-1843_1175-184 others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631044 | |||||
| chr17:9631044
|
G | GAAAGAAA others(11): Show |
1 | a0002c0001t0001g0146 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1175-1843_1175-184 others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631044 | |||||
| chr17:9631044
|
G | GAAAGAAA others(19): Show |
1 | a0004c0006t0001g0315 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1175-1843_1175-184 others(30): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631044 | |||||
| chr17:9631044
|
G | GAAAGAAA others(23): Show |
1 | a0002c0001t0001g0254 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1175-1843_1175-184 others(34): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631044 | |||||
| chr17:9631044
|
G | GAAGAAAG others(6): Show |
2 | a0002c0001t0001g0150a0002c0001t0001g0166 | 2 | HG02080.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1175-1843_1175-184 others(17): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631044 | |||||
| chr17:9631044
|
G | GAAGAAAG others(10): Show |
1 | a0002c0001t0001g0169 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1175-1843_1175-184 others(21): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631044 | |||||
| chr17:9631044
|
G | GAAGAAAG others(14): Show |
1 | a0002c0001t0001g0039 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1175-1843_1175-184 others(25): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631044 | |||||
| chr17:9631044
|
G | GAGAAAGA others(5): Show |
2 | a0002c0001t0001g0158a0002c0001t0001g0173 | 2 | HG00323.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1175-1841_1175-184 others(16): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631044 | |||||
| chr17:9631044
|
G | GAGAAAGA others(9): Show |
2 | a0002c0001t0001g0267a0002c0001t0001g0280 | 2 | HG02809.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1175-1841_1175-184 others(20): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631044 | |||||
| chr17:9631044
|
G | GAGAAAGA others(13): Show |
3 | a0002c0001t0001g0013a0002c0001t0001g0017a0002c0001t0001g0051 | 3 | HG02965.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1175-1841_1175-184 others(24): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631044 | |||||
| chr17:9631047
|
A | G | 2 | a0001c0004t0004g0036a0001c0004t0004g0199 | 2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1175-1841A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631047 | ||||||
| chr17:9631048
|
G | A | 72 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0023others(69): Show | 72 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1175-1840G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631048 | ||||||
| chr17:9631048
|
G | GAAAGAAA others(7): Show |
9 | a0002c0001t0001g0053a0002c0001t0001g0110a0002c0001t0001g0168others(6): Show | 9 | HG00280.hp1 HG00621.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1175-1839_1175-183 others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631048 | |||||
| chr17:9631048
|
G | GAAAGAAA others(11): Show |
2 | a0001c0002t0001g0154a0002c0001t0003g0187 | 2 | HG00673.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1175-1839_1175-183 others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631048 | |||||
| chr17:9631048
|
G | GAAAGAAA others(15): Show |
2 | a0001c0002t0001g0186a0002c0001t0001g0259 | 2 | HG03239.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1175-1839_1175-183 others(26): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631048 | |||||
| chr17:9631048
|
G | GAAAGAAA others(19): Show |
1 | a0002c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1175-1839_1175-183 others(30): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631048 | |||||
| chr17:9631048
|
G | GAGAAAGA others(5): Show |
2 | a0002c0001t0003g0228a0002c0001t0003g0229 | 2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1175-1837_1175-183 others(16): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631048 | |||||
| chr17:9631048
|
G | GAGAAAGA others(9): Show |
3 | a0001c0002t0001g0004a0002c0001t0002g0141a0002c0001t0003g0106 | 3 | HG03130.hp1 NA18970.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1175-1837_1175-183 others(20): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631048 | |||||
| chr17:9631048
|
G | GAGAAAGA others(13): Show |
1 | a0002c0001t0001g0144 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1175-1837_1175-183 others(24): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631048 | |||||
| chr17:9631048
|
G | GAGAAGAA others(12): Show |
1 | a0002c0001t0001g0160 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1175-1837_1175-183 others(23): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631048 | |||||
| chr17:9631051
|
A | G | 2 | a0001c0004t0004g0036a0001c0004t0004g0199 | 2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1175-1837A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631051 | ||||||
| chr17:9631052
|
G | A | 102 | a0001c0002t0001g0004a0001c0002t0001g0012a0001c0002t0001g0020others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1175-1836G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631052 | ||||||
| chr17:9631052
|
G | GAAAGAAA others(3): Show |
7 | a0002c0001t0002g0005a0002c0001t0002g0188a0002c0001t0002g0201others(4): Show | 7 | HG00099.hp2 HG00280.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175-1835_1175-183 others(14): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAAAGAAA others(7): Show |
3 | a0002c0001t0002g0060a0002c0001t0002g0087a0002c0001t0002g0204 | 3 | HG01081.hp1 HG01433.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1175-1835_1175-183 others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAAAGAAA others(11): Show |
1 | a0001c0002t0001g0309 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1175-1835_1175-183 others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAAAGAAA others(15): Show |
2 | a0001c0002t0001g0276a0002c0001t0001g0054 | 2 | HG02145.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1175-1835_1175-183 others(26): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAAGAAAG others(10): Show |
1 | a0002c0001t0001g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1175-1835_1175-183 others(21): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAAGAAAG others(18): Show |
1 | a0002c0001t0001g0252 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1175-1835_1175-183 others(29): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAAAGA others(5): Show |
8 | a0001c0002t0002g0121a0002c0001t0002g0006a0002c0001t0002g0097others(5): Show | 8 | HG01069.hp1 HG01074.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-1816_1175-180 others(16): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAAAGA others(9): Show |
4 | a0001c0002t0002g0197a0002c0001t0001g0313a0002c0001t0002g0104others(1): Show | 4 | HG00741.hp2 HG01168.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1820_1175-180 others(20): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAAAGA others(13): Show |
3 | a0002c0001t0002g0058a0002c0001t0002g0220a0002c0001t0003g0107 | 3 | HG00735.hp1 NA19057.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1175-1824_1175-180 others(24): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAAAGA others(17): Show |
1 | a0002c0001t0002g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1175-1828_1175-180 others(28): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAAGAA others(4): Show |
1 | a0002c0001t0002g0057 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1175-1832_1175-183 others(15): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAAA others(3): Show |
3 | a0002c0001t0002g0056a0002c0001t0002g0185a0002c0001t0002g0312 | 3 | HG01257.hp1 HG01257.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(14): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAAA others(7): Show |
5 | a0002c0001t0002g0059a0002c0001t0002g0109a0002c0001t0002g0192others(2): Show | 5 | HG00735.hp2 HG01169.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAAA others(11): Show |
3 | a0001c0002t0001g0255a0002c0001t0002g0183a0002c0001t0002g0198 | 3 | HG01169.hp1 HG01952.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAAG others(6): Show |
2 | a0002c0001t0002g0049a0002c0001t0002g0180 | 2 | HG01123.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(17): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAAG others(10): Show |
1 | a0002c0001t0002g0203 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(21): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAAG others(14): Show |
2 | a0002c0001t0002g0140a0002c0001t0003g0230 | 2 | NA18953.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(25): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(5): Show |
1 | a0001c0002t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(16): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(9): Show |
3 | a0002c0001t0002g0164a0002c0001t0002g0181a0002c0001t0002g0291 | 3 | HG00741.hp1 HG01109.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(20): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(13): Show |
5 | a0002c0001t0002g0050a0002c0001t0002g0136a0002c0001t0002g0138others(2): Show | 5 | HG01192.hp1 HG04199.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(24): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(17): Show |
1 | a0002c0001t0002g0137 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(28): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(21): Show |
1 | a0001c0002t0001g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(32): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(7): Show |
1 | a0001c0002t0001g0007 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(15): Show |
1 | a0001c0002t0001g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(26): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(19): Show |
1 | a0001c0002t0001g0278 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(30): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(23): Show |
2 | a0002c0001t0001g0223a0002c0011t0001g0277 | 2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(34): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(9): Show |
2 | a0001c0002t0001g0041a0002c0001t0002g0102 | 2 | HG02818.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(20): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(25): Show |
1 | a0001c0002t0002g0002 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(36): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(20): Show |
1 | a0002c0001t0002g0225 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(31): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(24): Show |
1 | a0001c0002t0001g0284 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(35): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(11): Show |
1 | a0001c0002t0001g0042 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(27): Show |
1 | a0001c0002t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(38): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(9): Show |
1 | a0001c0002t0001g0066 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(20): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(17): Show |
1 | a0001c0002t0001g0153 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(28): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(25): Show |
2 | a0001c0002t0001g0032a0002c0001t0001g0082 | 2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(36): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(10): Show |
1 | a0001c0002t0001g0062 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(21): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(11): Show |
1 | a0002c0001t0001g0290 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(31): Show |
1 | a0001c0002t0001g0151 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(42): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(12): Show |
1 | a0001c0002t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(23): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(19): Show |
3 | a0001c0002t0001g0124a0001c0002t0001g0226a0001c0002t0001g0227 | 3 | HG00639.hp2 HG01081.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(30): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(27): Show |
1 | a0002c0001t0001g0086 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(38): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(31): Show |
1 | a0002c0001t0001g0019 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(42): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(17): Show |
2 | a0001c0002t0001g0003a0001c0002t0001g0008 | 2 | HG00323.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(28): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(25): Show |
3 | a0001c0002t0001g0083a0001c0002t0001g0189a0008c0009t0001g0305 | 3 | HG01069.hp2 HG06807.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(36): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(23): Show |
4 | a0001c0002t0001g0238a0001c0002t0001g0296a0001c0002t0001g0301others(1): Show | 4 | NA18977.hp2 NA18998.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(34): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(27): Show |
2 | a0001c0002t0001g0157a0001c0002t0001g0239 | 2 | NA18951.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(38): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(21): Show |
1 | a0002c0001t0001g0029 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(32): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(25): Show |
3 | a0001c0002t0001g0031a0001c0002t0001g0122a0002c0001t0001g0093 | 3 | HG02083.hp1 HG03130.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(36): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(29): Show |
2 | a0001c0002t0001g0085a0001c0002t0001g0117 | 2 | HG03453.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(40): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(33): Show |
1 | a0001c0002t0001g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(44): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(24): Show |
1 | a0001c0002t0001g0165 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(35): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(23): Show |
4 | a0001c0002t0001g0021a0001c0002t0001g0045a0001c0002t0001g0073others(1): Show | 4 | HG02572.hp1 HG02572.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(34): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(27): Show |
2 | a0001c0002t0001g0209a0001c0002t0001g0298 | 2 | NA18522.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(38): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(31): Show |
1 | a0001c0002t0001g0260 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(42): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(26): Show |
1 | a0001c0002t0001g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(37): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(25): Show |
2 | a0001c0002t0001g0210a0001c0002t0001g0299 | 2 | HG01255.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(36): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(29): Show |
2 | a0001c0002t0001g0027a0002c0001t0001g0047 | 2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(40): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(33): Show |
3 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0084 | 3 | HG01109.hp2 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(44): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(32): Show |
1 | a0001c0002t0001g0289 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(43): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(31): Show |
2 | a0001c0002t0001g0218a0001c0002t0001g0307 | 2 | HG02280.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(42): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(35): Show |
4 | a0001c0002t0001g0034a0001c0002t0001g0111a0001c0002t0001g0219others(1): Show | 4 | HG01175.hp2 HG02486.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1833_1175-183 others(46): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(43): Show |
1 | a0001c0002t0001g0232 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(54): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(34): Show |
1 | a0002c0001t0001g0092 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(45): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(29): Show |
1 | a0001c0002t0001g0129 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(40): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(31): Show |
1 | a0001c0002t0001g0235 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(42): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(35): Show |
1 | a0001c0002t0001g0234 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(46): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(47): Show |
1 | a0001c0002t0001g0212 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(58): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(33): Show |
1 | a0001c0002t0001g0120 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(44): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(35): Show |
1 | a0001c0002t0001g0125 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(46): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631052
|
G | GAGAGAGA others(61): Show |
1 | a0001c0002t0001g0240 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(72): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631052 | |||||
| chr17:9631055
|
A | AGAGAGAG others(8): Show |
1 | a0001c0002t0001g0283 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(19): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631055 | ||||||
| chr17:9631055
|
A | AGAGAGAG others(16): Show |
1 | a0001c0002t0001g0072 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(27): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631055 | ||||||
| chr17:9631055
|
A | AGAGAGAG others(26): Show |
1 | a0001c0002t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1175-1833_1175-183 others(37): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631055 | ||||||
| chr17:9631055
|
A | G | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1833A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631055 | ||||||
| chr17:9631056
|
A | G | 55 | a0001c0002t0001g0011a0001c0002t0001g0024a0001c0002t0001g0025others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1175-1832A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631056 | ||||||
| chr17:9631059
|
A | G | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1829A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631059 | ||||||
| chr17:9631060
|
A | G | 45 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0052others(42): Show | 45 | HG00099.hp1 HG00438.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.1175-1828A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631060 | ||||||
| chr17:9631063
|
A | G | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1825A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631063 | ||||||
| chr17:9631064
|
A | G | 43 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0052others(40): Show | 43 | HG00099.hp1 HG00438.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1175-1824A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631064 | ||||||
| chr17:9631067
|
A | AAGAAGAA others(18): Show |
1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-1820_1175-181 others(29): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631067 | |||||
| chr17:9631067
|
A | AGAGAGAG others(14): Show |
1 | a0003c0003t0001g0130 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1175-1821_1175-182 others(25): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631067 | ||||||
| chr17:9631067
|
A | AGAGAGAG others(20): Show |
1 | a0002c0001t0001g0270 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1175-1821_1175-182 others(31): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631067 | ||||||
| chr17:9631067
|
A | G | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1821A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631067 | ||||||
| chr17:9631068
|
A | AAGAAAGA others(193): Show |
1 | a0001c0002t0001g0065 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1175-1805_1175-180 others(204): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631068 | |||||
| chr17:9631068
|
A | AAGAAAGA others(181): Show |
1 | a0001c0002t0001g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1175-1805_1175-180 others(192): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631068 | |||||
| chr17:9631068
|
A | AAGAAAGA others(153): Show |
1 | a0001c0002t0001g0126 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1175-1805_1175-180 others(164): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631068 | |||||
| chr17:9631068
|
A | AAGAAAGA others(125): Show |
1 | a0001c0002t0001g0156 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1175-1805_1175-180 others(136): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631068 | |||||
| chr17:9631068
|
A | AAGAAAGA others(92): Show |
1 | a0001c0002t0001g0152 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1175-1805_1175-180 others(103): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631068 | |||||
| chr17:9631068
|
A | AAGAAAGA others(67): Show |
1 | a0001c0002t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1175-1805_1175-180 others(78): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631068 | |||||
| chr17:9631068
|
A | AAGAAAGA others(33): Show |
1 | a0001c0002t0001g0263 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1175-1809_1175-180 others(44): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631068 | |||||
| chr17:9631068
|
A | G | 36 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0052others(33): Show | 36 | HG00099.hp1 HG00438.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.1175-1820A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631068 | ||||||
| chr17:9631071
|
A | AGAGAGAG others(4): Show |
1 | a0002c0001t0001g0249 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1175-1817_1175-181 others(15): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631071 | ||||||
| chr17:9631071
|
A | G | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1817A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631071 | ||||||
| chr17:9631072
|
A | G | 10 | a0001c0002t0001g0052a0001c0002t0001g0105a0001c0002t0001g0132others(7): Show | 10 | HG01099.hp2 HG01175.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1175-1816A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631072 | ||||||
| chr17:9631075
|
A | G | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1813A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631075 | ||||||
| chr17:9631077
|
A | G | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1175-1811A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631077 | ||||||
| chr17:9631079
|
A | G | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1809A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631079 | ||||||
| chr17:9631080
|
A | G | 1 | a0002c0001t0001g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1175-1808A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631080 | ||||||
| chr17:9631081
|
A | G | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1175-1807A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631081 | ||||||
| chr17:9631082
|
G | A | 1 | a0002c0001t0001g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1175-1806G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631082 | ||||||
| chr17:9631082
|
G | GAA | 81 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0030others(78): Show | 81 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.1175-1805_1175-180 others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631082 | |||||
| chr17:9631082
|
G | GAAAGAA | 3 | a0001c0002t0001g0067a0002c0001t0001g0089a0002c0001t0001g0251 | 3 | HG02080.hp2 HG03041.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1175-1805_1175-180 others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631082 | |||||
| chr17:9631082
|
G | GAAAGAAA others(3): Show |
1 | a0001c0002t0001g0207 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1175-1805_1175-180 others(14): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631082 | |||||
| chr17:9631082
|
G | GAAAGAAA others(7): Show |
4 | a0002c0001t0001g0112a0002c0001t0001g0264a0002c0001t0001g0266others(1): Show | 4 | HG00438.hp2 NA18953.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1805_1175-180 others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631082 | |||||
| chr17:9631082
|
G | GAAAGAAA others(11): Show |
1 | a0002c0010t0001g0142 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1175-1805_1175-180 others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631082 | |||||
| chr17:9631082
|
G | GAAAGAAA others(15): Show |
1 | a0002c0001t0001g0114 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1175-1805_1175-180 others(26): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631082 | |||||
| chr17:9631082
|
G | GAAAGAAA others(19): Show |
1 | a0002c0001t0001g0163 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1175-1805_1175-180 others(30): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631082 | |||||
| chr17:9631082
|
GA | G | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1805delA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631082 | ||||||
| chr17:9631083
|
A | AAGGAAGG others(15): Show |
1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1175-1805_1175-180 others(26): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631083 | ||||||
| chr17:9631084
|
G | A | 2 | a0002c0001t0001g0171a0002c0001t0001g0254 | 2 | NA18954.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1175-1804G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631084 | ||||||
| chr17:9631086
|
A | AAG | 7 | a0002c0001t0001g0112a0002c0001t0001g0114a0002c0001t0001g0163others(4): Show | 7 | HG00438.hp2 NA18942.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1175-1800_1175-179 others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631086 | |||||
| chr17:9631086
|
A | G | 2 | a0002c0001t0001g0171a0002c0001t0001g0254 | 2 | NA18954.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1175-1802A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631086 | ||||||
| chr17:9631087
|
A | G | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175-1801A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631087 | ||||||
| chr17:9631091
|
A | G | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175-1797A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631091 | ||||||
| chr17:9631095
|
A | G | 2 | a0001c0004t0004g0001a0001c0005t0004g0215 | 3 | HG02895.hp2 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1175-1793A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631095 | ||||||
| chr17:9631099
|
A | G | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1789A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631099 | ||||||
| chr17:9631101
|
A | G | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1175-1787A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631101 | ||||||
| chr17:9631103
|
A | G | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1785A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631103 | ||||||
| chr17:9631105
|
A | G | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1175-1783A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631105 | ||||||
| chr17:9631105
|
AG | A | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1782delG | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631105 | ||||||
| chr17:9631124
|
G | A | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1175-1764G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631124 | ||||||
| chr17:9631182
|
C | T | 1 | a0001c0002t0001g0299 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1175-1706C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631182 | ||||||
| chr17:9631214
|
C | T | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1175-1674C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631214 | ||||||
| chr17:9631232
|
C | T | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175-1656C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631232 | ||||||
| chr17:9631333
|
T | G | 1 | a0002c0001t0001g0082 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1175-1555T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631333 | ||||||
| chr17:9631395
|
C | T | 2 | a0001c0005t0001g0074a0001c0005t0001g0077 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1175-1493C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631395 | ||||||
| chr17:9631416
|
G | A | 1 | a0001c0002t0001g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1175-1472G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631416 | ||||||
| chr17:9631490
|
C | A | 1 | a0001c0002t0001g0072 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1175-1398C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631490 | ||||||
| chr17:9631534
|
G | C | 1 | a0002c0001t0002g0312 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1175-1354G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631534 | ||||||
| chr17:9631580
|
G | A | 6 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(3): Show | 6 | HG01243.hp1 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1175-1308G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631580 | ||||||
| chr17:9631623
|
G | C | 1 | a0001c0002t0001g0083 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1175-1265G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631623 | ||||||
| chr17:9631677
|
T | C | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175-1211T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631677 | ||||||
| chr17:9631683
|
T | G | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175-1205T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631683 | ||||||
| chr17:9631769
|
G | GT | 14 | a0001c0002t0001g0152a0001c0002t0001g0161a0001c0002t0001g0162others(11): Show | 14 | HG01071.hp2 HG01978.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1175-1104dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9631769 | |||||
| chr17:9631770
|
T | A | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-1118T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631770 | ||||||
| chr17:9631827
|
C | G | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175-1061C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631827 | ||||||
| chr17:9631904
|
A | G | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-984A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631904 | ||||||
| chr17:9631905
|
T | A | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-983T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9631905 | ||||||
| chr17:9632037
|
C | T | 4 | a0001c0002t0001g0122a0001c0002t0001g0239a0001c0002t0001g0296others(1): Show | 4 | HG02083.hp1 NA18951.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-851C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632037 | ||||||
| chr17:9632064
|
C | T | 1 | a0001c0012t0001g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1175-824C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632064 | ||||||
| chr17:9632077
|
C | CT | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175-801dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9632077 | |||||
| chr17:9632077
|
CT | C | 117 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(114): Show | 117 | HG00323.hp2 HG00423.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.1175-801delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9632077 | |||||
| chr17:9632087
|
T | C | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-801T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632087 | ||||||
| chr17:9632088
|
C | T | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-800C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632088 | ||||||
| chr17:9632089
|
T | C | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-799T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632089 | ||||||
| chr17:9632110
|
C | T | 6 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(3): Show | 7 | HG02145.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175-778C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632110 | ||||||
| chr17:9632199
|
T | C | 1 | a0001c0002t0001g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1175-689T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632199 | ||||||
| chr17:9632200
|
C | T | 1 | a0001c0002t0001g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1175-688C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632200 | ||||||
| chr17:9632221
|
G | T | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-667G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632221 | ||||||
| chr17:9632234
|
T | C | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-654T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632234 | ||||||
| chr17:9632239
|
G | T | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-649G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632239 | ||||||
| chr17:9632242
|
A | T | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-646A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632242 | ||||||
| chr17:9632243
|
A | T | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-645A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632243 | ||||||
| chr17:9632244
|
G | A | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175-644G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632244 | ||||||
| chr17:9632244
|
G | T | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-644G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632244 | ||||||
| chr17:9632245
|
T | G | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-643T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632245 | ||||||
| chr17:9632248
|
T | A | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-640T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632248 | ||||||
| chr17:9632250
|
T | G | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-638T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632250 | ||||||
| chr17:9632254
|
G | GT | 17 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(14): Show | 17 | HG00621.hp2 HG01106.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1175-623dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9632254 | |||||
| chr17:9632254
|
G | T | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-634G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632254 | ||||||
| chr17:9632254
|
GT | G | 5 | a0001c0002t0001g0099a0001c0004t0004g0001a0001c0004t0004g0036others(2): Show | 6 | HG02615.hp2 HG02683.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1175-623delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9632254 | |||||
| chr17:9632256
|
T | G | 1 | a0002c0001t0001g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1175-632T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632256 | ||||||
| chr17:9632264
|
T | C | 1 | a0001c0002t0001g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1175-624T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632264 | ||||||
| chr17:9632267
|
A | G | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1175-621A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632267 | ||||||
| chr17:9632299
|
T | C | 1 | a0001c0002t0001g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1175-589T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632299 | ||||||
| chr17:9632307
|
T | C | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1175-581T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632307 | ||||||
| chr17:9632338
|
C | T | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0002c0011t0001g0277 | 3 | HG01884.hp2 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1175-550C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632338 | ||||||
| chr17:9632396
|
T | A | 5 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215others(2): Show | 5 | HG00735.hp1 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1175-492T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632396 | ||||||
| chr17:9632533
|
G | A | 1 | a0001c0002t0001g0152 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1175-355G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632533 | ||||||
| chr17:9632584
|
T | C | 1 | a0002c0001t0003g0187 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1175-304T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632584 | ||||||
| chr17:9632638
|
G | A | 1 | a0002c0001t0002g0291 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1175-250G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632638 | ||||||
| chr17:9632639
|
A | T | 1 | a0002c0001t0002g0291 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1175-249A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632639 | ||||||
| chr17:9632641
|
T | G | 1 | a0002c0001t0002g0291 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1175-247T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632641 | ||||||
| chr17:9632670
|
C | T | 1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1175-218C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632670 | ||||||
| chr17:9632671
|
A | G | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1175-217A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632671 | ||||||
| chr17:9632715
|
G | T | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1175-173G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632715 | ||||||
| chr17:9632717
|
A | AACTTTAC others(218): Show |
3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-169_1175-168i others(227): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9632717 | |||||
| chr17:9632717
|
A | AACTTTAC others(218): Show |
4 | a0001c0005t0001g0074a0001c0005t0001g0077a0001c0005t0004g0215others(1): Show | 4 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-169_1175-168i others(227): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 9632717 | |||||
| chr17:9632788
|
A | G | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1175-100A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632788 | ||||||
| chr17:9632792
|
C | T | 56 | a0001c0002t0001g0154a0001c0002t0001g0186a0001c0002t0001g0309others(53): Show | 56 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1175-96C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632792 | ||||||
| chr17:9632859
|
G | T | 12 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(9): Show | 12 | HG01106.hp2 HG02559.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1175-29G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 9/13 | chr17 | 9632859 | ||||||
| chr17:9633051
|
T | C | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0002c0011t0001g0277 | 3 | HG01884.hp2 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1320+18T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633051 | ||||||
| chr17:9633141
|
A | T | 1 | a0002c0001t0001g0287 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1320+108A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633141 | ||||||
| chr17:9633212
|
A | G | 7 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(4): Show | 7 | HG01106.hp2 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1320+179A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633212 | ||||||
| chr17:9633229
|
G | A | 1 | a0002c0001t0001g0128 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1320+196G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633229 | ||||||
| chr17:9633321
|
C | T | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1320+288C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633321 | ||||||
| chr17:9633356
|
C | A | 1 | a0001c0002t0001g0132 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1320+323C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633356 | ||||||
| chr17:9633357
|
G | A | 10 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0045others(7): Show | 11 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1320+324G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633357 | ||||||
| chr17:9633361
|
T | C | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1320+328T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633361 | ||||||
| chr17:9633361
|
T | G | 1 | a0002c0001t0001g0287 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1320+328T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633361 | ||||||
| chr17:9633407
|
G | A | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1320+374G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633407 | ||||||
| chr17:9633467
|
A | G | 1 | a0001c0002t0002g0002 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1320+434A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633467 | ||||||
| chr17:9633487
|
G | A | 1 | a0001c0002t0001g0241 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1320+454G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633487 | ||||||
| chr17:9633601
|
G | A | 6 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257others(3): Show | 6 | HG01243.hp1 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1320+568G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633601 | ||||||
| chr17:9633659
|
C | T | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1320+626C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633659 | ||||||
| chr17:9633660
|
G | A | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1320+627G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633660 | ||||||
| chr17:9633673
|
A | G | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1320+640A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633673 | ||||||
| chr17:9633675
|
C | CT | 9 | a0001c0002t0001g0016a0001c0002t0001g0151a0001c0002t0001g0306others(6): Show | 9 | HG01884.hp1 HG01978.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1320+658dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 9633675 | |||||
| chr17:9633825
|
T | C | 1 | a0001c0002t0001g0307 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1320+792T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633825 | ||||||
| chr17:9633843
|
AT | A | 14 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(11): Show | 15 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1320+819delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 9633843 | |||||
| chr17:9633883
|
G | A | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0002c0011t0001g0277 | 3 | HG01884.hp2 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1320+850G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633883 | ||||||
| chr17:9633903
|
G | A | 1 | a0002c0001t0001g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1320+870G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633903 | ||||||
| chr17:9633923
|
C | T | 6 | a0001c0002t0001g0165a0001c0002t0001g0207a0001c0002t0001g0226others(3): Show | 6 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1320+890C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633923 | ||||||
| chr17:9633960
|
C | T | 1 | a0001c0002t0001g0282 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1320+927C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9633960 | ||||||
| chr17:9634029
|
A | G | 1 | a0002c0001t0001g0095 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1320+996A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634029 | ||||||
| chr17:9634031
|
A | G | 1 | a0001c0002t0001g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1320+998A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634031 | ||||||
| chr17:9634152
|
C | A | 1 | a0002c0001t0001g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1320+1119C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634152 | ||||||
| chr17:9634259
|
A | T | 1 | a0001c0002t0001g0176 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1321-1146A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634259 | ||||||
| chr17:9634260
|
T | A | 1 | a0002c0001t0002g0291 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1321-1145T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634260 | ||||||
| chr17:9634295
|
C | T | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1321-1110C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634295 | ||||||
| chr17:9634478
|
C | G | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1321-927C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634478 | ||||||
| chr17:9634506
|
C | T | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1321-899C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634506 | ||||||
| chr17:9634507
|
G | A | 1 | a0002c0001t0001g0047 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1321-898G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634507 | ||||||
| chr17:9634529
|
G | T | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0002c0011t0001g0277 | 3 | HG01884.hp2 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1321-876G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634529 | ||||||
| chr17:9634533
|
C | T | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0002c0011t0001g0277 | 3 | HG01884.hp2 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1321-872C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634533 | ||||||
| chr17:9634543
|
CCATTG | C | 20 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(17): Show | 21 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1321-854_1321-850d others(7): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 9634543 | |||||
| chr17:9634576
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1321-829C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634576 | ||||||
| chr17:9634597
|
G | GA | 5 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(2): Show | 6 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1321-799dupA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 9634597 | |||||
| chr17:9634689
|
A | G | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1321-716A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634689 | ||||||
| chr17:9634718
|
C | T | 7 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(4): Show | 7 | HG01106.hp2 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1321-687C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634718 | ||||||
| chr17:9634721
|
G | A | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1321-684G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634721 | ||||||
| chr17:9634751
|
A | G | 1 | a0002c0001t0001g0163 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1321-654A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9634751 | ||||||
| chr17:9635009
|
A | G | 1 | a0002c0011t0001g0277 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1321-396A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9635009 | ||||||
| chr17:9635027
|
G | A | 3 | a0002c0001t0001g0014a0002c0001t0001g0200a0009c0015t0001g0064 | 3 | HG02258.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1321-378G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9635027 | ||||||
| chr17:9635139
|
T | A | 29 | a0001c0002t0001g0024a0001c0002t0001g0090a0001c0002t0001g0094others(26): Show | 29 | HG00099.hp1 HG00438.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1321-266T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9635139 | ||||||
| chr17:9635258
|
A | G | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1321-147A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9635258 | ||||||
| chr17:9635295
|
TA | T | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1321-103delA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 9635295 | |||||
| chr17:9635325
|
G | A | 1 | a0002c0001t0001g0251 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1321-80G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9635325 | ||||||
| chr17:9635332
|
G | T | 83 | a0001c0002t0001g0004a0001c0002t0001g0016a0001c0002t0001g0021others(80): Show | 83 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1321-73G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 10/13 | chr17 | 9635332 | ||||||
| chr17:9635682
|
G | GAT | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1472+127_1472+128d others(4): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9635682 | |||||
| chr17:9635699
|
G | A | 1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1472+143G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9635699 | ||||||
| chr17:9635735
|
G | A | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1472+179G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9635735 | ||||||
| chr17:9635753
|
G | A | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1472+197G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9635753 | ||||||
| chr17:9635883
|
G | A | 1 | a0001c0002t0001g0123 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1472+327G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9635883 | ||||||
| chr17:9635894
|
C | T | 31 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(28): Show | 31 | HG00323.hp2 HG01123.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1472+338C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9635894 | ||||||
| chr17:9635899
|
G | A | 1 | a0001c0002t0001g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1472+343G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9635899 | ||||||
| chr17:9635908
|
T | C | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1472+352T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9635908 | ||||||
| chr17:9635971
|
G | A | 1 | a0002c0001t0001g0254 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1472+415G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9635971 | ||||||
| chr17:9635993
|
T | C | 1 | a0002c0001t0002g0109 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1472+437T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9635993 | ||||||
| chr17:9635999
|
C | T | 120 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0007others(117): Show | 120 | HG00323.hp2 HG00423.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.1472+443C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9635999 | ||||||
| chr17:9636103
|
T | C | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1472+547T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636103 | ||||||
| chr17:9636174
|
C | A | 1 | a0002c0001t0002g0198 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1472+618C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636174 | ||||||
| chr17:9636176
|
AAAAAAAG others(8): Show |
A | 1 | a0002c0001t0002g0217 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1472+624_1472+638d others(17): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636176 | |||||
| chr17:9636178
|
A | AAAAAGAA others(6): Show |
2 | a0001c0002t0001g0178a0001c0002t0001g0282 | 2 | HG01361.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1472+626_1472+638d others(15): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636178 | |||||
| chr17:9636179
|
A | AAAAG | 16 | a0001c0002t0001g0300a0001c0002t0002g0002a0001c0002t0002g0121others(13): Show | 16 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1472+693_1472+696d others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636179 | |||||
| chr17:9636179
|
A | AAAAGAAA others(1): Show |
10 | a0001c0002t0001g0024a0001c0002t0001g0052a0001c0002t0001g0094others(7): Show | 10 | HG02015.hp1 HG02258.hp1 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.1472+689_1472+696d others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636179 | |||||
| chr17:9636179
|
A | AAAAGAAA others(5): Show |
2 | a0001c0002t0001g0161a0002c0001t0002g0180 | 2 | HG01123.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1472+685_1472+696d others(14): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636179 | |||||
| chr17:9636179
|
AAAAG | A | 15 | a0002c0001t0002g0049a0002c0001t0002g0056a0002c0001t0002g0098others(12): Show | 15 | HG01069.hp1 HG01099.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.1472+693_1472+696d others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636179 | |||||
| chr17:9636179
|
AAAAGAAA others(1): Show |
A | 11 | a0002c0001t0002g0005a0002c0001t0002g0057a0002c0001t0002g0060others(8): Show | 11 | HG00280.hp2 HG01109.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1472+689_1472+696d others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636179 | |||||
| chr17:9636179
|
AAAAGAAA others(13): Show |
A | 1 | a0002c0001t0002g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1472+677_1472+696d others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636179 | |||||
| chr17:9636181
|
AAGAAAGA others(23): Show |
A | 2 | a0001c0004t0004g0001a0001c0004t0004g0199 | 3 | HG02895.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1472+627_1472+656d others(32): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636181 | |||||
| chr17:9636182
|
AGAAAGAA others(22): Show |
A | 2 | a0001c0004t0004g0036a0001c0005t0004g0215 | 2 | HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1472+627_1472+655d others(31): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636182 | ||||||
| chr17:9636183
|
G | A | 1 | a0001c0005t0001g0077 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1472+627G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636183 | ||||||
| chr17:9636183
|
G | GAAAGAAA others(2): Show |
7 | a0001c0002t0001g0007a0001c0002t0001g0034a0001c0002t0001g0044others(4): Show | 7 | HG02027.hp1 HG02486.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1472+630_1472+638d others(11): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636183 | |||||
| chr17:9636187
|
G | GAAAGA | 22 | a0001c0002t0001g0004a0001c0002t0001g0010a0001c0002t0001g0016others(19): Show | 22 | HG01243.hp2 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1472+634_1472+638d others(7): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636187 | |||||
| chr17:9636191
|
G | GA | 25 | a0001c0002t0001g0025a0001c0002t0001g0062a0001c0002t0001g0072others(22): Show | 25 | HG00639.hp1 HG01106.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1472+638dupA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636191 | |||||
| chr17:9636192
|
AAAG | A | 23 | a0001c0002t0001g0021a0001c0002t0001g0073a0001c0002t0001g0115others(20): Show | 23 | HG00423.hp1 HG00639.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.1472+639_1472+641d others(5): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636192 | |||||
| chr17:9636192
|
AAAGAAAG | A | 13 | a0001c0002t0001g0011a0001c0002t0001g0032a0001c0002t0001g0033others(10): Show | 13 | HG01433.hp1 HG02056.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1472+639_1472+645d others(9): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636192 | |||||
| chr17:9636192
|
AAAGAAAG others(4): Show |
A | 7 | a0001c0002t0001g0075a0001c0002t0001g0088a0001c0002t0001g0117others(4): Show | 7 | HG02523.hp1 HG03710.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.1472+639_1472+649d others(13): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636192 | |||||
| chr17:9636192
|
AAAGAAAG others(8): Show |
A | 7 | a0001c0002t0001g0008a0001c0002t0001g0078a0001c0002t0001g0083others(4): Show | 7 | HG02280.hp1 HG02647.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1472+639_1472+653d others(17): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636192 | |||||
| chr17:9636192
|
AAAGAAAG others(12): Show |
A | 10 | a0001c0002t0001g0003a0001c0002t0001g0111a0001c0002t0001g0120others(7): Show | 10 | HG00323.hp2 HG00621.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1472+639_1472+657d others(21): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636192 | |||||
| chr17:9636192
|
AAAGAAAG others(16): Show |
A | 1 | a0001c0002t0001g0066 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1472+639_1472+661d others(25): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636192 | |||||
| chr17:9636192
|
AAAGAAAG others(20): Show |
A | 2 | a0001c0002t0001g0289a0001c0002t0001g0304 | 2 | NA18978.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1472+639_1472+665d others(29): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636192 | |||||
| chr17:9636215
|
G | A | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1472+659G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636215 | ||||||
| chr17:9636219
|
G | A | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1472+663G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636219 | ||||||
| chr17:9636223
|
G | A | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1472+667G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636223 | ||||||
| chr17:9636227
|
G | A | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1472+671G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636227 | ||||||
| chr17:9636229
|
AAGAAAGA others(7): Show |
A | 2 | a0001c0002t0001g0041a0001c0002t0001g0042 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1472+675_1472+688d others(16): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636229 | |||||
| chr17:9636229
|
AAGAAAGA others(17): Show |
A | 2 | a0002c0001t0001g0144a0002c0001t0001g0280 | 2 | NA18948.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1472+675_1472+698d others(26): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636229 | |||||
| chr17:9636233
|
AAGAAAGA others(13): Show |
A | 1 | a0001c0002t0001g0030 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1472+679_1472+698d others(22): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636233 | |||||
| chr17:9636237
|
AAGAAAGA others(7): Show |
A | 2 | a0002c0001t0001g0281a0002c0001t0002g0059 | 2 | HG00673.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1472+691_1472+704d others(16): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636237 | |||||
| chr17:9636237
|
AAGAAAGA others(9): Show |
A | 5 | a0002c0001t0001g0046a0002c0001t0001g0071a0002c0001t0001g0079others(2): Show | 5 | HG03017.hp1 HG03491.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1472+683_1472+698d others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636237 | |||||
| chr17:9636239
|
GAAAGAAA others(9): Show |
G | 1 | a0006c0014t0001g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1472+685_1472+700d others(18): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636239 | |||||
| chr17:9636240
|
AAAGAAAG others(4): Show |
A | 1 | a0002c0001t0002g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1472+686_1472+696d others(13): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636240 | |||||
| chr17:9636241
|
AAGAAAGA others(3): Show |
A | 1 | a0002c0001t0001g0095 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1472+695_1472+704d others(12): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636241 | |||||
| chr17:9636241
|
AAGAAAGA others(5): Show |
A | 20 | a0001c0002t0001g0213a0002c0001t0001g0061a0002c0001t0001g0068others(17): Show | 20 | HG00323.hp1 HG00423.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1472+687_1472+698d others(14): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636241 | |||||
| chr17:9636245
|
AAGAAAGA others(1): Show |
A | 25 | a0001c0002t0001g0063a0001c0002t0001g0070a0001c0002t0001g0105others(22): Show | 25 | HG00438.hp2 HG00673.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1472+691_1472+698d others(10): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636245 | |||||
| chr17:9636249
|
A | G | 2 | a0002c0001t0002g0136a0002c0001t0003g0187 | 2 | HG04199.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1472+693A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636249 | ||||||
| chr17:9636249
|
AAGAG | A | 24 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0065others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1472+695_1472+698d others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9636249 | |||||
| chr17:9636253
|
G | A | 170 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0007others(167): Show | 171 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.1472+697G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636253 | ||||||
| chr17:9636260
|
A | G | 1 | a0002c0001t0001g0281 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1472+704A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636260 | ||||||
| chr17:9636331
|
G | A | 1 | a0001c0002t0001g0310 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1472+775G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636331 | ||||||
| chr17:9636407
|
C | T | 26 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0008others(23): Show | 26 | HG00323.hp2 HG01123.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1472+851C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636407 | ||||||
| chr17:9636412
|
G | A | 1 | a0002c0001t0003g0187 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1472+856G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636412 | ||||||
| chr17:9636430
|
A | G | 2 | a0004c0006t0001g0131a0004c0006t0001g0315 | 2 | NA18998.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1472+874A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636430 | ||||||
| chr17:9636563
|
T | C | 9 | a0001c0002t0001g0076a0001c0002t0001g0214a0001c0004t0004g0001others(6): Show | 10 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1472+1007T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636563 | ||||||
| chr17:9636585
|
C | T | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1472+1029C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636585 | ||||||
| chr17:9636644
|
C | G | 1 | a0001c0002t0001g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1472+1088C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636644 | ||||||
| chr17:9636901
|
T | C | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1472+1345T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636901 | ||||||
| chr17:9636916
|
G | A | 3 | a0001c0002t0001g0016a0001c0002t0001g0044a0001c0002t0001g0045 | 3 | HG01884.hp1 HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1472+1360G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636916 | ||||||
| chr17:9636916
|
G | T | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1472+1360G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636916 | ||||||
| chr17:9636970
|
G | A | 2 | a0001c0002t0001g0007a0001c0002t0001g0080 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1472+1414G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9636970 | ||||||
| chr17:9637000
|
G | A | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1472+1444G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637000 | ||||||
| chr17:9637013
|
C | T | 7 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(4): Show | 7 | HG01106.hp2 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1472+1457C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637013 | ||||||
| chr17:9637071
|
G | A | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0002c0011t0001g0277 | 3 | HG01884.hp2 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1472+1515G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637071 | ||||||
| chr17:9637072
|
C | CA | 37 | a0001c0002t0001g0021a0001c0002t0001g0044a0001c0002t0001g0075others(34): Show | 37 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.1472+1525dupA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9637072 | |||||
| chr17:9637072
|
CA | C | 7 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(4): Show | 8 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1472+1525delA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 9637072 | |||||
| chr17:9637202
|
G | C | 20 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(17): Show | 21 | HG01106.hp2 HG01884.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1473-1407G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637202 | ||||||
| chr17:9637276
|
A | C | 1 | a0001c0002t0001g0236 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1473-1333A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637276 | ||||||
| chr17:9637299
|
C | T | 2 | a0001c0002t0001g0076a0001c0002t0001g0214 | 2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1473-1310C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637299 | ||||||
| chr17:9637320
|
C | G | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0002c0011t0001g0277 | 3 | HG01884.hp2 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1473-1289C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637320 | ||||||
| chr17:9637354
|
G | A | 84 | a0001c0002t0001g0004a0001c0002t0001g0016a0001c0002t0001g0021others(81): Show | 84 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1473-1255G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637354 | ||||||
| chr17:9637424
|
C | A | 6 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0002t0001g0135others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473-1185C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637424 | ||||||
| chr17:9637583
|
C | A | 2 | a0001c0002t0001g0222a0002c0001t0002g0087 | 2 | HG01433.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1473-1026C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637583 | ||||||
| chr17:9637593
|
G | C | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0002c0011t0001g0277 | 3 | HG01884.hp2 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1473-1016G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637593 | ||||||
| chr17:9637651
|
T | A | 1 | a0001c0002t0001g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1473-958T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637651 | ||||||
| chr17:9637724
|
G | A | 1 | a0001c0002t0001g0090 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1473-885G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637724 | ||||||
| chr17:9637883
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1473-726C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637883 | ||||||
| chr17:9637949
|
G | T | 1 | a0001c0002t0001g0162 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1473-660G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9637949 | ||||||
| chr17:9638090
|
C | A | 1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1473-519C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9638090 | ||||||
| chr17:9638099
|
G | C | 1 | a0001c0002t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1473-510G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9638099 | ||||||
| chr17:9638113
|
A | G | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1473-496A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9638113 | ||||||
| chr17:9638127
|
C | T | 2 | a0002c0001t0001g0014a0002c0001t0001g0200 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1473-482C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9638127 | ||||||
| chr17:9638187
|
C | T | 3 | a0001c0002t0001g0115a0001c0002t0001g0117a0001c0002t0001g0298 | 3 | NA18949.hp1 NA18999.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1473-422C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9638187 | ||||||
| chr17:9638404
|
C | T | 2 | a0001c0002t0001g0007a0001c0002t0001g0080 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1473-205C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9638404 | ||||||
| chr17:9638512
|
C | A | 1 | a0002c0001t0002g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1473-97C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9638512 | ||||||
| chr17:9638577
|
C | T | 1 | a0006c0014t0001g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1473-32C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9638577 | ||||||
| chr17:9638598
|
C | A | 1 | a0002c0001t0001g0038 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1473-11C>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 11/13 | chr17 | 9638598 | ||||||
| chr17:9638768
|
C | T | 1 | a0002c0001t0001g0167 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1575+57C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9638768 | ||||||
| chr17:9638850
|
G | T | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+139G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9638850 | ||||||
| chr17:9638945
|
T | C | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+234T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9638945 | ||||||
| chr17:9638948
|
T | C | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+237T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9638948 | ||||||
| chr17:9639040
|
G | C | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0002c0011t0001g0277 | 3 | HG01884.hp2 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1575+329G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9639040 | ||||||
| chr17:9639212
|
C | T | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1575+501C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9639212 | ||||||
| chr17:9639227
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1575+516C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9639227 | ||||||
| chr17:9639355
|
T | C | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+644T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9639355 | ||||||
| chr17:9639403
|
T | A | 3 | a0002c0001t0001g0172a0002c0001t0001g0173a0002c0001t0001g0297 | 3 | HG00280.hp1 HG00323.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1575+692T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9639403 | ||||||
| chr17:9639430
|
T | TA | 6 | a0001c0002t0001g0162a0001c0005t0001g0074a0001c0005t0001g0077others(3): Show | 6 | HG00735.hp1 HG00735.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1575+734dupA | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr17 | 9639430 | |||||
| chr17:9639712
|
C | T | 1 | a0001c0002t0001g0133 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1575+1001C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9639712 | ||||||
| chr17:9639773
|
G | A | 14 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0026others(11): Show | 14 | HG01106.hp2 HG02559.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1575+1062G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9639773 | ||||||
| chr17:9639843
|
A | C | 1 | a0002c0001t0003g0106 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1575+1132A>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9639843 | ||||||
| chr17:9639877
|
A | G | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+1166A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9639877 | ||||||
| chr17:9639889
|
A | G | 8 | a0001c0002t0001g0222a0001c0004t0004g0001a0001c0004t0004g0036others(5): Show | 9 | HG01884.hp2 HG02145.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1575+1178A>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9639889 | ||||||
| chr17:9639995
|
G | A | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+1284G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9639995 | ||||||
| chr17:9640019
|
T | C | 32 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0052others(29): Show | 32 | HG00099.hp1 HG01074.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.1575+1308T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640019 | ||||||
| chr17:9640224
|
CT | C | 23 | a0001c0002t0001g0025a0001c0002t0001g0030a0001c0002t0001g0067others(20): Show | 24 | HG01071.hp1 HG01891.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1576-1481delT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr17 | 9640224 | |||||
| chr17:9640228
|
T | A | 32 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0052others(29): Show | 32 | HG00099.hp1 HG01074.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.1576-1496T>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640228 | ||||||
| chr17:9640241
|
T | C | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-1483T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640241 | ||||||
| chr17:9640262
|
T | C | 4 | a0001c0002t0001g0063a0001c0002t0001g0070a0001c0002t0001g0076others(1): Show | 4 | HG02630.hp2 HG02717.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1576-1462T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640262 | ||||||
| chr17:9640289
|
C | G | 3 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199 | 4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1576-1435C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640289 | ||||||
| chr17:9640292
|
T | C | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-1432T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640292 | ||||||
| chr17:9640308
|
G | A | 3 | a0001c0002t0001g0063a0001c0002t0001g0070a0002c0001t0001g0259 | 3 | HG02630.hp2 HG02922.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1576-1416G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640308 | ||||||
| chr17:9640359
|
T | G | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-1365T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640359 | ||||||
| chr17:9640380
|
T | C | 1 | a0002c0001t0001g0303 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1576-1344T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640380 | ||||||
| chr17:9640389
|
T | C | 2 | a0001c0002t0001g0260a0008c0009t0001g0305 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1576-1335T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640389 | ||||||
| chr17:9640441
|
C | CAT | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-1283_1576-128 others(6): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640441 | ||||||
| chr17:9640442
|
G | T | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-1282G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640442 | ||||||
| chr17:9640481
|
TGAGAACA others(36): Show |
T | 1 | a0002c0001t0003g0106 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1576-1242_1576-120 others(47): Show |
CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640481 | ||||||
| chr17:9640517
|
T | C | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0002c0011t0001g0277 | 3 | HG01884.hp2 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1576-1207T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640517 | ||||||
| chr17:9640553
|
T | G | 1 | a0006c0014t0001g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1576-1171T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640553 | ||||||
| chr17:9640558
|
C | T | 7 | a0001c0005t0001g0074a0001c0005t0001g0077a0002c0011t0001g0277others(4): Show | 7 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576-1166C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640558 | ||||||
| chr17:9640566
|
G | A | 1 | a0001c0002t0001g0083 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1576-1158G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640566 | ||||||
| chr17:9640605
|
G | A | 1 | a0001c0002t0001g0273 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1576-1119G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640605 | ||||||
| chr17:9640664
|
C | T | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1576-1060C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640664 | ||||||
| chr17:9640696
|
T | C | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-1028T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640696 | ||||||
| chr17:9640726
|
T | G | 1 | a0001c0002t0001g0307 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1576-998T>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640726 | ||||||
| chr17:9640825
|
G | T | 1 | a0001c0002t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1576-899G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640825 | ||||||
| chr17:9640848
|
T | C | 5 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(2): Show | 6 | HG02109.hp2 HG02615.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1576-876T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640848 | ||||||
| chr17:9640926
|
G | A | 1 | a0001c0002t0001g0132 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1576-798G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640926 | ||||||
| chr17:9640930
|
C | T | 1 | a0002c0001t0002g0192 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1576-794C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640930 | ||||||
| chr17:9640953
|
G | C | 1 | a0006c0014t0001g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1576-771G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640953 | ||||||
| chr17:9640983
|
G | A | 32 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0052others(29): Show | 32 | HG00099.hp1 HG01074.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.1576-741G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9640983 | ||||||
| chr17:9641039
|
G | A | 1 | a0002c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1576-685G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9641039 | ||||||
| chr17:9641333
|
G | C | 2 | a0001c0002t0001g0153a0001c0002t0001g0157 | 2 | HG02056.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1576-391G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9641333 | ||||||
| chr17:9641511
|
G | C | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-213G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9641511 | ||||||
| chr17:9641592
|
A | T | 1 | a0002c0001t0003g0106 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1576-132A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9641592 | ||||||
| chr17:9641702
|
A | AT | 6 | a0001c0002t0001g0165a0001c0002t0001g0207a0001c0002t0001g0226others(3): Show | 6 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1576-21dupT | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr17 | 9641702 | |||||
| chr17:9641703
|
T | C | 1 | a0002c0001t0002g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1576-21T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 12/13 | chr17 | 9641703 | ||||||
| chr17:9641909
|
G | A | 1 | a0001c0002t0001g0262 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1687+74G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9641909 | ||||||
| chr17:9641910
|
G | A | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1687+75G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9641910 | ||||||
| chr17:9641934
|
G | C | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0002c0011t0001g0277 | 3 | HG01884.hp2 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1687+99G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9641934 | ||||||
| chr17:9641988
|
G | T | 1 | a0001c0005t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1687+153G>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9641988 | ||||||
| chr17:9642045
|
G | A | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1687+210G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642045 | ||||||
| chr17:9642082
|
C | G | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1687+247C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642082 | ||||||
| chr17:9642107
|
T | C | 3 | a0001c0005t0001g0074a0001c0005t0001g0077a0002c0011t0001g0277 | 3 | HG01884.hp2 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1687+272T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642107 | ||||||
| chr17:9642113
|
A | T | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1687+278A>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642113 | ||||||
| chr17:9642207
|
C | T | 1 | a0001c0002t0001g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1687+372C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642207 | ||||||
| chr17:9642275
|
C | T | 1 | a0002c0001t0001g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1687+440C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642275 | ||||||
| chr17:9642350
|
G | A | 1 | a0001c0002t0001g0299 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1687+515G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642350 | ||||||
| chr17:9642481
|
G | A | 1 | a0002c0001t0001g0252 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1688-542G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642481 | ||||||
| chr17:9642496
|
C | T | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1688-527C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642496 | ||||||
| chr17:9642510
|
G | C | 1 | a0002c0001t0001g0287 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1688-513G>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642510 | ||||||
| chr17:9642515
|
T | C | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1688-508T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642515 | ||||||
| chr17:9642614
|
C | T | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1688-409C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642614 | ||||||
| chr17:9642633
|
G | A | 1 | a0002c0001t0001g0233 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1688-390G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642633 | ||||||
| chr17:9642687
|
C | T | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1688-336C>T | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642687 | ||||||
| chr17:9642743
|
G | A | 1 | a0001c0002t0001g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1688-280G>A | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642743 | ||||||
| chr17:9642748
|
C | G | 4 | a0001c0004t0004g0001a0001c0004t0004g0036a0001c0004t0004g0199others(1): Show | 5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1688-275C>G | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642748 | ||||||
| chr17:9642846
|
T | C | 18 | a0001c0002t0001g0090a0001c0002t0001g0094a0001c0002t0001g0105others(15): Show | 18 | HG01074.hp2 HG01099.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1688-177T>C | CFAP52 | ENSG00000166596.15 | transcript | ENST00000352665.10 | protein_coding | 13/13 | chr17 | 9642846 |