| geneid | 101929355 |
|---|---|
| ensemblid | ENSG00000283361.3 |
| hgncid | 53789 |
| symbol | CFAP97D2 |
| name | CFAP97 domain containing 2 |
| refseq_nuc | NM_001395229.1 |
| refseq_prot | NP_001382158.1 |
| ensembl_nuc | ENST00000636692.2 |
| ensembl_prot | ENSP00000489989.1 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 114179257 |
| end | 114223085 |
| strand | + |
| ver | v1.2 |
| region | chr13:114179257-114223085 |
| region5000 | chr13:114174257-114228085 |
| regionname0 | CFAP97D2_chr13_114179257_114223085 |
| regionname5000 | CFAP97D2_chr13_114174257_114228085 |
| 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 | 1/1 | 98 | 399 | 94 | 78 | 175 | 10 | 40 | 137 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0002 | 0/0 | 98 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| 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 | 1/1 | 297 | 396 | 92 | 77 | 175 | 10 | 40 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| c0002 | 0/0 | 297 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| c0003 | 0/0 | 297 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| c0004 | 0/0 | 297 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| 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 | 0/1 | 653 | 156 | 69 | 33 | 27 | 5 | 21 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| t0002 | 1/0 | 653 | 79 | 4 | 25 | 36 | 4 | 9 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| t0003 | 0/0 | 653 | 75 | 1 | 6 | 62 | 0 | 6 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| t0004 | 0/0 | 653 | 35 | 0 | 2 | 31 | 0 | 2 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| t0005 | 0/0 | 662 | 23 | 13 | 2 | 8 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| t0006 | 0/0 | 662 | 15 | 0 | 7 | 7 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| t0007 | 0/0 | 662 | 7 | 4 | 1 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| t0008 | 0/0 | 653 | 4 | 1 | 1 | 0 | 1 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| t0009 | 0/0 | 653 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| t0010 | 0/0 | 653 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| t0011 | 0/0 | 653 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| t0012 | 0/0 | 653 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| t0013 | 0/0 | 653 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| 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 | 5 | 0 | 0 | 5 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0004 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0009 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0031 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0313 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 297 | 396 | 92 | 77 | 175 | 10 | 40 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0002 | 0/0 | 297 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0004 | 0/0 | 297 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0002c0003 | 0/0 | 297 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 949 | 152 | 67 | 32 | 26 | 5 | 21 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0001t0002 | 1/0 | 949 | 79 | 4 | 25 | 36 | 4 | 9 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0001t0003 | 0/0 | 949 | 75 | 1 | 6 | 62 | 0 | 6 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0001t0004 | 0/0 | 949 | 35 | 0 | 2 | 31 | 0 | 2 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0001t0005 | 0/0 | 958 | 23 | 13 | 2 | 8 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0001t0006 | 0/0 | 958 | 15 | 0 | 7 | 7 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0001t0007 | 0/0 | 958 | 7 | 4 | 1 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0001t0008 | 0/0 | 949 | 4 | 1 | 1 | 0 | 1 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0001t0009 | 0/0 | 949 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0001t0010 | 0/0 | 949 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0001t0011 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0001t0012 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0001t0013 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0002t0001 | 0/0 | 949 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0001c0004t0001 | 0/0 | 949 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| a0002c0003t0001 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | copy fasta | chr13 | 114174257 | 114228085 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0004 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0031 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0313 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0006g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0006g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0006g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0006g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0006g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0006g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0006g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0006g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0006g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0006g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0006g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0006g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0007g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0007g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0007g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0008g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0008g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0008g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0009g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0009g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0010g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0011g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0012g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0001t0013g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0001c0004t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00099 | hp2 | a0001 | c0001 | t0008 | g0083 | EUR | GBR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | GBR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0281 | EUR | GBR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | FIN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0032 | EUR | FIN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0092 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0093 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0254 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0046 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | CHS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0331 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0351 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01074 | hp1 | a0001 | c0001 | t0008 | g0112 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01169 | hp2 | a0001 | c0001 | t0010 | g0325 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0098 | AMR | PUR | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0085 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0323 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0343 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0326 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0332 | EUR | IBS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0031 | EUR | IBS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | IBS | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0316 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0264 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0334 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01993 | hp1 | a0001 | c0001 | t0006 | g0348 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0346 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0347 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02040 | hp2 | a0001 | c0001 | t0006 | g0340 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02129 | hp2 | a0001 | c0001 | t0013 | g0104 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0103 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0140 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CDX | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | CDX | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | CDX | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | CDX | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02273 | hp1 | a0001 | c0001 | t0006 | g0349 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0087 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | KHV | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0312 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0094 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0268 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0088 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0337 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0116 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0089 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0053 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0327 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0336 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0130 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0320 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0256 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0248 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0097 | AFR | ESN | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0311 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0055 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0179 | SAS | PJL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0333 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03834 | hp1 | a0001 | c0001 | t0006 | g0010 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0170 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG04228 | hp1 | a0001 | c0001 | t0008 | g0099 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | STU | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | CHB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | CHB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18952 | hp1 | a0001 | c0001 | t0007 | g0183 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0344 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0350 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18963 | hp2 | a0002 | c0003 | t0001 | g0063 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0345 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19063 | hp1 | a0001 | c0001 | t0006 | g0341 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19066 | hp2 | a0001 | c0001 | t0011 | g0022 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19084 | hp2 | a0001 | c0001 | t0012 | g0328 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19086 | hp2 | a0001 | c0001 | t0006 | g0342 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19089 | hp2 | a0001 | c0001 | t0007 | g0152 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | YRI | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ASW | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ASW | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | USA | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0091 | AFR | USA | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | USA | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | USA | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0090 | AFR | LWK | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | LWK | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0243 | REF | REF | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0313 | REF | REF | CFAP97D2_chr13_114174257_114228085 | CFAP97D2 | chr13 | 114174257 | 114228085 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:114196436
|
T | C | 1 | a0002 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.131T>C | p.Leu44Pro | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/4 | 205/949 | 131/297 | 44/98 | chr13 | 114196436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:114196434
|
G | A | 1 | a0001c0002 | 2 | HG00733.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.129G>A | p.Pro43Pro | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/4 | 203/949 | 129/297 | 43/98 | chr13 | 114196434 | ||
| chr13:114196440
|
G | A | 1 | a0001c0004 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.135G>A | p.Thr45Thr | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/4 | 209/949 | 135/297 | 45/98 | chr13 | 114196440 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:114179266
|
C | T | 3 | a0001c0001t0005a0001c0001t0008a0001c0001t0013 | 28 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-65C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/4 | 65 | chr13 | 114179266 | |||||
| chr13:114179306
|
T | G | 14 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(11): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
5_prime_UTR_variant | MODIFIER | c.-25T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/4 | 25 | chr13 | 114179306 | |||||
| chr13:114179310
|
C | T | 1 | a0001c0001t0006 | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-21C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/4 | 21 | chr13 | 114179310 | |||||
| chr13:114222557
|
A | C | 1 | a0001c0001t0011 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*50A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 50 | chr13 | 114222557 | |||||
| chr13:114222561
|
A | ACAGATTC others(2): Show |
3 | a0001c0001t0005a0001c0001t0006a0001c0001t0007 | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*54_*55insCAGATTCA others(1): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 55 | chr13 | 114222561 | |||||
| chr13:114222562
|
G | A | 3 | a0001c0001t0005a0001c0001t0006a0001c0001t0007 | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*55G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 55 | chr13 | 114222562 | |||||
| chr13:114222602
|
G | A | 3 | a0001c0001t0004a0001c0001t0012a0001c0001t0013 | 37 | HG00544.hp2 HG00609.hp2 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*95G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 95 | chr13 | 114222602 | |||||
| chr13:114222619
|
A | G | 1 | a0001c0001t0009 | 2 | HG02818.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*112A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 112 | chr13 | 114222619 | |||||
| chr13:114222669
|
C | T | 2 | a0001c0001t0003a0001c0001t0011 | 76 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*162C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 162 | chr13 | 114222669 | |||||
| chr13:114222709
|
C | T | 1 | a0001c0001t0006 | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*202C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 202 | chr13 | 114222709 | |||||
| chr13:114222921
|
G | T | 1 | a0001c0001t0010 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*414G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 414 | chr13 | 114222921 | |||||
| chr13:114222922
|
T | G | 1 | a0001c0001t0010 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*415T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 4/4 | 415 | chr13 | 114222922 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:114179436
|
A | G | 2 | a0001c0001t0001g0351a0001c0001t0001g0352 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.90+16A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179436 | ||||||
| chr13:114179460
|
C | T | 1 | a0001c0001t0003g0350 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.90+40C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179460 | ||||||
| chr13:114179515
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0351others(1): Show | 4 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+95G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179515 | ||||||
| chr13:114179626
|
C | T | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+206C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179626 | ||||||
| chr13:114179626
|
CT | C | 8 | a0001c0001t0001g0039a0001c0001t0002g0042a0001c0001t0002g0043others(5): Show | 8 | HG01496.hp1 HG02895.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.90+218delT | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114179626 | |||||
| chr13:114179756
|
C | T | 2 | a0001c0001t0002g0338a0001c0001t0002g0339 | 2 | HG02165.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.90+336C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179756 | ||||||
| chr13:114179894
|
A | C | 2 | a0001c0001t0009g0336a0001c0001t0009g0337 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.90+474A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179894 | ||||||
| chr13:114179921
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(7): Show | 13 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.90+501G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179921 | ||||||
| chr13:114179941
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.90+521G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114179941 | ||||||
| chr13:114180080
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.90+660C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180080 | ||||||
| chr13:114180170
|
A | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+750A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180170 | ||||||
| chr13:114180268
|
A | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+848A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180268 | ||||||
| chr13:114180364
|
G | T | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+944G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180364 | ||||||
| chr13:114180392
|
G | A | 253 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(250): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.90+972G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180392 | ||||||
| chr13:114180445
|
C | T | 1 | a0001c0001t0007g0268 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.90+1025C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180445 | ||||||
| chr13:114180464
|
A | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+1044A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180464 | ||||||
| chr13:114180471
|
T | C | 1 | a0001c0001t0003g0012 | 2 | NA18965.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.90+1051T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180471 | ||||||
| chr13:114180497
|
T | C | 268 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(265): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.90+1077T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180497 | ||||||
| chr13:114180516
|
C | G | 278 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(275): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.90+1096C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180516 | ||||||
| chr13:114180566
|
G | A | 1 | a0001c0004t0001g0053 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.90+1146G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180566 | ||||||
| chr13:114180621
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 6 | HG01069.hp1 HG01071.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+1201C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180621 | ||||||
| chr13:114180635
|
C | T | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+1215C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180635 | ||||||
| chr13:114180671
|
T | C | 1 | a0001c0001t0003g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.90+1251T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180671 | ||||||
| chr13:114180868
|
G | A | 2 | a0001c0001t0003g0055a0001c0001t0003g0056 | 2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.90+1448G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180868 | ||||||
| chr13:114180996
|
T | C | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+1576T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114180996 | ||||||
| chr13:114181099
|
C | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0334 | 2 | HG01496.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.90+1679C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181099 | ||||||
| chr13:114181155
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.90+1735T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181155 | ||||||
| chr13:114181217
|
C | T | 54 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0220others(51): Show | 63 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.90+1797C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181217 | ||||||
| chr13:114181285
|
A | T | 1 | a0001c0001t0001g0335 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.90+1865A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181285 | ||||||
| chr13:114181383
|
A | G | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(276): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.90+1963A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181383 | ||||||
| chr13:114181418
|
C | T | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+1998C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181418 | ||||||
| chr13:114181481
|
C | T | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(276): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.90+2061C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181481 | ||||||
| chr13:114181495
|
C | A | 1 | a0001c0001t0002g0272 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.90+2075C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181495 | ||||||
| chr13:114181512
|
C | T | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+2092C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181512 | ||||||
| chr13:114181541
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(28): Show | 36 | HG00408.hp2 HG00621.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.90+2121C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181541 | ||||||
| chr13:114181717
|
T | A | 3 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194 | 3 | NA18966.hp2 NA18973.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.90+2297T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181717 | ||||||
| chr13:114181717
|
T | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(55): Show | 66 | HG00408.hp2 HG00621.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.90+2297T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181717 | ||||||
| chr13:114181839
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.90+2419C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181839 | ||||||
| chr13:114181918
|
G | A | 1 | a0001c0001t0002g0273 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.90+2498G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181918 | ||||||
| chr13:114181919
|
T | C | 1 | a0001c0001t0002g0273 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.90+2499T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181919 | ||||||
| chr13:114181963
|
C | T | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+2543C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181963 | ||||||
| chr13:114181979
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(39): Show | 47 | HG00140.hp1 HG00408.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.90+2559G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181979 | ||||||
| chr13:114181983
|
T | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0074others(3): Show | 8 | HG00738.hp2 HG01070.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.90+2563T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181983 | ||||||
| chr13:114181993
|
A | G | 2 | a0001c0001t0002g0331a0001c0001t0002g0332 | 2 | HG01069.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.90+2573A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181993 | ||||||
| chr13:114181997
|
A | G | 73 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0188others(70): Show | 83 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.90+2577A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114181997 | ||||||
| chr13:114182011
|
T | C | 117 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(114): Show | 128 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.90+2591T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182011 | ||||||
| chr13:114182032
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(5): Show | 11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.90+2612G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182032 | ||||||
| chr13:114182043
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.90+2623T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182043 | ||||||
| chr13:114182059
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.90+2639C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182059 | ||||||
| chr13:114182060
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0003g0191 | 3 | HG01243.hp1 NA18906.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.90+2640A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182060 | ||||||
| chr13:114182068
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.90+2648T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182068 | ||||||
| chr13:114182079
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.90+2659C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182079 | ||||||
| chr13:114182082
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.90+2662C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182082 | ||||||
| chr13:114182095
|
T | G | 1 | a0001c0001t0001g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.90+2675T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182095 | ||||||
| chr13:114182126
|
A | T | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(156): Show | 184 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.90+2706A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182126 | ||||||
| chr13:114182128
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.90+2708T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182128 | ||||||
| chr13:114182129
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.90+2709A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182129 | ||||||
| chr13:114182131
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.90+2711T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182131 | ||||||
| chr13:114182137
|
A | G | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+2717A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182137 | ||||||
| chr13:114182160
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0231 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.90+2740G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182160 | ||||||
| chr13:114182164
|
G | A | 1 | a0001c0001t0006g0340 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.90+2744G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182164 | ||||||
| chr13:114182168
|
A | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0109others(54): Show | 69 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.90+2748A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182168 | ||||||
| chr13:114182170
|
A | AC | 9 | a0001c0001t0001g0052a0001c0001t0001g0107a0001c0001t0001g0108others(6): Show | 9 | HG02257.hp1 HG02647.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.90+2750_90+2751ins others(1): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182170 | ||||||
| chr13:114182170
|
A | C | 1 | a0001c0001t0006g0340 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.90+2750A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182170 | ||||||
| chr13:114182172
|
C | CAT | 60 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0039others(57): Show | 72 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.90+2752_90+2753ins others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182172 | ||||||
| chr13:114182172
|
C | CGT | 7 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(4): Show | 10 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.90+2754_90+2755dup others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114182172 | |||||
| chr13:114182172
|
C | T | 11 | a0001c0001t0001g0052a0001c0001t0001g0107a0001c0001t0001g0108others(8): Show | 11 | HG01243.hp1 HG02040.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+2752C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182172 | ||||||
| chr13:114182181
|
A | T | 47 | a0001c0001t0001g0003a0001c0001t0001g0218a0001c0001t0001g0220others(44): Show | 58 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.90+2761A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182181 | ||||||
| chr13:114182185
|
G | A | 241 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(238): Show | 276 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.90+2765G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182185 | ||||||
| chr13:114182189
|
A | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(53): Show | 69 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.90+2769A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182189 | ||||||
| chr13:114182190
|
T | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0194 | 2 | HG03195.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.90+2770T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182190 | ||||||
| chr13:114182191
|
G | A | 2 | a0001c0001t0002g0274a0001c0001t0006g0340 | 2 | HG02040.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.90+2771G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182191 | ||||||
| chr13:114182194
|
G | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(82): Show | 104 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.90+2774G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182194 | ||||||
| chr13:114182196
|
A | G | 1 | a0001c0001t0006g0340 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.90+2776A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182196 | ||||||
| chr13:114182199
|
T | C | 9 | a0001c0001t0001g0027a0001c0001t0001g0034a0001c0001t0001g0078others(6): Show | 10 | HG02886.hp1 HG02886.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.90+2779T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182199 | ||||||
| chr13:114182200
|
A | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 6 | HG01243.hp1 HG01496.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+2780A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182200 | ||||||
| chr13:114182201
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(54): Show | 70 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.90+2781A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182201 | ||||||
| chr13:114182205
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0231a0001c0001t0002g0322 | 3 | HG00733.hp2 HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.90+2785C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182205 | ||||||
| chr13:114182206
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.90+2786A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182206 | ||||||
| chr13:114182211
|
A | G | 90 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0051others(87): Show | 101 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.90+2791A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182211 | ||||||
| chr13:114182213
|
G | A | 2 | a0001c0001t0002g0274a0001c0001t0006g0340 | 2 | HG02040.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.90+2793G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182213 | ||||||
| chr13:114182214
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0082a0001c0001t0001g0201 | 3 | HG01109.hp1 HG03195.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.90+2794G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182214 | ||||||
| chr13:114182216
|
AC | A | 69 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0044others(66): Show | 77 | HG00621.hp1 HG01106.hp1 HG01123.hp1 others(74): Show |
intron_variant | MODIFIER | c.90+2797delC | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182216 | ||||||
| chr13:114182222
|
C | A | 48 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0001t0001g0058others(45): Show | 49 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.90+2802C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182222 | ||||||
| chr13:114182225
|
G | A | 7 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0126others(4): Show | 7 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+2805G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182225 | ||||||
| chr13:114182226
|
G | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.90+2806G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182226 | ||||||
| chr13:114182228
|
T | C | 47 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0044others(44): Show | 49 | HG00408.hp2 HG00621.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.90+2808T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182228 | ||||||
| chr13:114182229
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0045others(6): Show | 10 | HG01346.hp2 HG01496.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+2809G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182229 | ||||||
| chr13:114182230
|
T | G | 2 | a0001c0001t0001g0017a0001c0001t0002g0274 | 3 | HG03098.hp1 HG03209.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.90+2810T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182230 | ||||||
| chr13:114182231
|
G | A | 4 | a0001c0001t0001g0137a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG01243.hp1 HG01346.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+2811G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182231 | ||||||
| chr13:114182232
|
C | T | 4 | a0001c0001t0001g0200a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01433.hp1 HG01981.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+2812C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182232 | ||||||
| chr13:114182234
|
C | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 5 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+2814C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182234 | ||||||
| chr13:114182235
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.90+2815G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182235 | ||||||
| chr13:114182235
|
G | T | 1 | a0001c0001t0006g0340 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.90+2815G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182235 | ||||||
| chr13:114182236
|
T | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0202 | 2 | HG02615.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.90+2816T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182236 | ||||||
| chr13:114182237
|
A | G | 6 | a0001c0001t0001g0137a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG01243.hp1 HG01993.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+2817A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182237 | ||||||
| chr13:114182238
|
G | A | 66 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0026others(63): Show | 72 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.90+2818G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182238 | ||||||
| chr13:114182239
|
G | T | 22 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0070others(19): Show | 25 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.90+2819G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182239 | ||||||
| chr13:114182242
|
A | G | 1 | a0001c0001t0005g0084 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.90+2822A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182242 | ||||||
| chr13:114182256
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 7 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.90+2836C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182256 | ||||||
| chr13:114182257
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 6 | HG01069.hp1 HG01071.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+2837T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182257 | ||||||
| chr13:114182259
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0004g0230a0001c0001t0004g0264 | 3 | HG01258.hp2 HG01928.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.90+2839C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182259 | ||||||
| chr13:114182260
|
G | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(156): Show | 178 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.90+2840G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182260 | ||||||
| chr13:114182262
|
C | T | 11 | a0001c0001t0001g0109a0001c0001t0001g0198a0001c0001t0005g0015others(8): Show | 12 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.90+2842C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182262 | ||||||
| chr13:114182265
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0005g0097 | 2 | HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.90+2845A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182265 | ||||||
| chr13:114182275
|
T | C | 12 | a0001c0001t0001g0035a0001c0001t0001g0052a0001c0001t0001g0057others(9): Show | 12 | HG00735.hp2 HG01081.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.90+2855T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182275 | ||||||
| chr13:114182278
|
A | C | 7 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0107others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+2858A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182278 | ||||||
| chr13:114182279
|
G | A | 7 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0107others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+2859G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182279 | ||||||
| chr13:114182293
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0007g0268 | 3 | HG00735.hp2 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.90+2873G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182293 | ||||||
| chr13:114182298
|
C | T | 7 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0198others(4): Show | 7 | HG02129.hp2 HG02132.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.90+2878C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182298 | ||||||
| chr13:114182302
|
A | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0101a0001c0001t0002g0287 | 3 | HG01081.hp2 HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.90+2882A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182302 | ||||||
| chr13:114182306
|
C | T | 1 | a0001c0001t0002g0287 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.90+2886C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182306 | ||||||
| chr13:114182325
|
G | A | 4 | a0001c0001t0001g0115a0001c0001t0001g0324a0001c0001t0007g0116others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+2905G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182325 | ||||||
| chr13:114182331
|
G | A | 9 | a0001c0001t0001g0026a0001c0001t0001g0201a0001c0001t0001g0203others(6): Show | 10 | HG01167.hp2 HG01169.hp2 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.90+2911G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182331 | ||||||
| chr13:114182335
|
T | A | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0003g0150others(2): Show | 5 | HG00621.hp1 HG00741.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+2915T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182335 | ||||||
| chr13:114182335
|
T | G | 10 | a0001c0001t0001g0195a0001c0001t0001g0324a0001c0001t0002g0289others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+2915T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182335 | ||||||
| chr13:114182339
|
T | C | 3 | a0001c0001t0001g0195a0001c0001t0002g0289a0001c0001t0008g0099 | 3 | HG02602.hp1 HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.90+2919T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182339 | ||||||
| chr13:114182341
|
T | G | 1 | a0001c0001t0002g0290 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.90+2921T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182341 | ||||||
| chr13:114182344
|
C | A | 1 | a0001c0001t0002g0290 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.90+2924C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182344 | ||||||
| chr13:114182346
|
T | G | 3 | a0001c0001t0001g0195a0001c0001t0002g0289a0001c0001t0008g0099 | 3 | HG02602.hp1 HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.90+2926T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182346 | ||||||
| chr13:114182353
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+2933G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182353 | ||||||
| chr13:114182370
|
A | G | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+2950A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182370 | ||||||
| chr13:114182374
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.90+2954G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182374 | ||||||
| chr13:114182385
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0133 | 2 | HG02647.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.90+2965C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182385 | ||||||
| chr13:114182386
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+2966G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182386 | ||||||
| chr13:114182398
|
T | C | 1 | a0001c0001t0005g0092 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.90+2978T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182398 | ||||||
| chr13:114182412
|
A | G | 6 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+2992A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182412 | ||||||
| chr13:114182414
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+2994G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182414 | ||||||
| chr13:114182420
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+3000G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182420 | ||||||
| chr13:114182425
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.90+3005C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182425 | ||||||
| chr13:114182432
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 7 | HG01069.hp1 HG01071.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+3012T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182432 | ||||||
| chr13:114182444
|
A | T | 14 | a0001c0001t0003g0012a0001c0001t0003g0113a0001c0001t0003g0178others(11): Show | 18 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.90+3024A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182444 | ||||||
| chr13:114182450
|
C | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG01891.hp1 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.90+3030C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182450 | ||||||
| chr13:114182451
|
C | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG01891.hp1 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.90+3031C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182451 | ||||||
| chr13:114182451
|
C | T | 271 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(268): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.90+3031C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182451 | ||||||
| chr13:114182452
|
T | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG01891.hp1 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.90+3032T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182452 | ||||||
| chr13:114182454
|
C | T | 29 | a0001c0001t0001g0096a0001c0001t0005g0015a0001c0001t0005g0016others(26): Show | 31 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.90+3034C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182454 | ||||||
| chr13:114182461
|
T | G | 108 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0078others(105): Show | 123 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.90+3041T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182461 | ||||||
| chr13:114182464
|
T | C | 2 | a0001c0001t0001g0134a0001c0004t0001g0053 | 2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.90+3044T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182464 | ||||||
| chr13:114182465
|
A | C | 1 | a0001c0001t0001g0335 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.90+3045A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182465 | ||||||
| chr13:114182466
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.90+3046A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182466 | ||||||
| chr13:114182467
|
T | C | 4 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0324others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+3047T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182467 | ||||||
| chr13:114182470
|
A | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0324others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+3050A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182470 | ||||||
| chr13:114182472
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG03704.hp2 HG03831.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+3052C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182472 | ||||||
| chr13:114182475
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.90+3055A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182475 | ||||||
| chr13:114182490
|
C | T | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+3070C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182490 | ||||||
| chr13:114182491
|
C | G | 10 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0134others(7): Show | 10 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.90+3071C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182491 | ||||||
| chr13:114182494
|
T | A | 1 | a0001c0001t0002g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3074T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182494 | ||||||
| chr13:114182496
|
T | C | 11 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0341others(8): Show | 14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+3076T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182496 | ||||||
| chr13:114182498
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3078G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182498 | ||||||
| chr13:114182505
|
G | A | 11 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0341others(8): Show | 14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+3085G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182505 | ||||||
| chr13:114182507
|
T | G | 30 | a0001c0001t0001g0027a0001c0001t0001g0079a0001c0001t0001g0080others(27): Show | 34 | HG00408.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.90+3087T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182507 | ||||||
| chr13:114182510
|
A | G | 16 | a0001c0001t0001g0027a0001c0001t0001g0079a0001c0001t0001g0080others(13): Show | 17 | HG00408.hp2 HG00733.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.90+3090A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182510 | ||||||
| chr13:114182528
|
C | T | 14 | a0001c0001t0001g0027a0001c0001t0001g0079a0001c0001t0001g0080others(11): Show | 15 | HG00408.hp2 HG02280.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+3108C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182528 | ||||||
| chr13:114182531
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3111C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182531 | ||||||
| chr13:114182532
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.90+3112G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182532 | ||||||
| chr13:114182538
|
G | A | 18 | a0001c0001t0001g0027a0001c0001t0001g0078a0001c0001t0001g0079others(15): Show | 19 | HG00408.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.90+3118G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182538 | ||||||
| chr13:114182539
|
T | C | 14 | a0001c0001t0001g0027a0001c0001t0001g0079a0001c0001t0001g0080others(11): Show | 15 | HG00408.hp2 HG02280.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+3119T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182539 | ||||||
| chr13:114182542
|
T | C | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+3122T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182542 | ||||||
| chr13:114182559
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3139G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182559 | ||||||
| chr13:114182567
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3147C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182567 | ||||||
| chr13:114182581
|
C | A | 1 | a0001c0001t0002g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3161C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182581 | ||||||
| chr13:114182582
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.90+3162G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182582 | ||||||
| chr13:114182584
|
T | C | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+3164T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182584 | ||||||
| chr13:114182605
|
C | T | 12 | a0001c0001t0004g0008a0001c0001t0006g0010a0001c0001t0006g0033others(9): Show | 17 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.90+3185C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182605 | ||||||
| chr13:114182613
|
T | C | 239 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(236): Show | 273 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.90+3193T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182613 | ||||||
| chr13:114182614
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+3194G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182614 | ||||||
| chr13:114182622
|
T | C | 4 | a0001c0001t0001g0227a0001c0001t0001g0243a0001c0001t0001g0324others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+3202T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182622 | ||||||
| chr13:114182623
|
T | C | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+3203T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182623 | ||||||
| chr13:114182626
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.90+3206G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182626 | ||||||
| chr13:114182672
|
T | C | 4 | a0001c0001t0004g0040a0001c0001t0004g0226a0001c0001t0004g0240others(1): Show | 4 | NA18990.hp1 NA19009.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+3252T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182672 | ||||||
| chr13:114182688
|
G | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG01884.hp1 HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.90+3268G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182688 | ||||||
| chr13:114182705
|
C | T | 11 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0341others(8): Show | 14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+3285C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182705 | ||||||
| chr13:114182719
|
C | G | 11 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0341others(8): Show | 14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+3299C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182719 | ||||||
| chr13:114182739
|
T | C | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+3319T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182739 | ||||||
| chr13:114182752
|
G | A | 29 | a0001c0001t0001g0057a0001c0001t0001g0072a0001c0001t0005g0015others(26): Show | 31 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.90+3332G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182752 | ||||||
| chr13:114182760
|
A | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+3340A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182760 | ||||||
| chr13:114182783
|
T | G | 1 | a0001c0001t0003g0153 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.90+3363T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182783 | ||||||
| chr13:114182819
|
T | C | 73 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(70): Show | 83 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.90+3399T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182819 | ||||||
| chr13:114182936
|
A | G | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+3516A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182936 | ||||||
| chr13:114182947
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.90+3527G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114182947 | ||||||
| chr13:114183048
|
G | A | 2 | a0001c0001t0002g0300a0001c0001t0002g0301 | 2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.90+3628G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183048 | ||||||
| chr13:114183054
|
T | C | 1 | a0001c0001t0003g0144 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.90+3634T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183054 | ||||||
| chr13:114183099
|
C | T | 111 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(108): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.90+3679C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183099 | ||||||
| chr13:114183163
|
A | ATTATTTA others(5): Show |
12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+3754_90+3765dup others(12): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114183163 | |||||
| chr13:114183198
|
A | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+3778A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183198 | ||||||
| chr13:114183311
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(6): Show | 12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.90+3891C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183311 | ||||||
| chr13:114183321
|
C | T | 2 | a0001c0001t0009g0336a0001c0001t0009g0337 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.90+3901C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183321 | ||||||
| chr13:114183419
|
C | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0132 | 3 | HG02723.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.90+3999C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183419 | ||||||
| chr13:114183420
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0234 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.90+4000G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183420 | ||||||
| chr13:114183460
|
A | T | 1 | a0001c0001t0001g0014 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.90+4040A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183460 | ||||||
| chr13:114183463
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.90+4043C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183463 | ||||||
| chr13:114183570
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0004g0230a0001c0001t0004g0264 | 3 | HG01928.hp2 HG01952.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.90+4150G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183570 | ||||||
| chr13:114183596
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.90+4176T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183596 | ||||||
| chr13:114183621
|
A | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+4201A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183621 | ||||||
| chr13:114183675
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.90+4255G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183675 | ||||||
| chr13:114183765
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0351a0001c0001t0001g0352 | 3 | HG00735.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.90+4345G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183765 | ||||||
| chr13:114183771
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.90+4351C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183771 | ||||||
| chr13:114183835
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.90+4415G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183835 | ||||||
| chr13:114183839
|
C | G | 77 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(74): Show | 87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.90+4419C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183839 | ||||||
| chr13:114183907
|
G | C | 1 | a0001c0001t0002g0281 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.90+4487G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183907 | ||||||
| chr13:114183960
|
C | T | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+4540C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114183960 | ||||||
| chr13:114184001
|
G | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+4581G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184001 | ||||||
| chr13:114184164
|
G | T | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+4744G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184164 | ||||||
| chr13:114184250
|
T | A | 99 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(96): Show | 113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.90+4830T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184250 | ||||||
| chr13:114184336
|
T | C | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+4916T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184336 | ||||||
| chr13:114184352
|
G | A | 31 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0246others(28): Show | 39 | HG00544.hp2 HG00609.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.90+4932G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184352 | ||||||
| chr13:114184552
|
G | A | 46 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(43): Show | 51 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.90+5132G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184552 | ||||||
| chr13:114184595
|
G | C | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+5175G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184595 | ||||||
| chr13:114184604
|
G | A | 35 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(32): Show | 37 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.90+5184G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184604 | ||||||
| chr13:114184623
|
T | G | 1 | a0001c0001t0001g0215 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.90+5203T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184623 | ||||||
| chr13:114184638
|
T | C | 35 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(32): Show | 37 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.90+5218T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184638 | ||||||
| chr13:114184682
|
T | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(6): Show | 12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.90+5262T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184682 | ||||||
| chr13:114184719
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.90+5299T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184719 | ||||||
| chr13:114184800
|
A | G | 1 | a0001c0001t0004g0262 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.90+5380A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184800 | ||||||
| chr13:114184821
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.90+5401A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184821 | ||||||
| chr13:114184959
|
T | G | 1 | a0001c0001t0001g0082 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.90+5539T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114184959 | ||||||
| chr13:114185195
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.90+5775C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185195 | ||||||
| chr13:114185271
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0109 | 2 | HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.90+5851G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185271 | ||||||
| chr13:114185292
|
C | T | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+5872C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185292 | ||||||
| chr13:114185293
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+5873G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185293 | ||||||
| chr13:114185518
|
C | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0334 | 2 | HG01496.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.90+6098C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185518 | ||||||
| chr13:114185583
|
C | A | 21 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(18): Show | 27 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.90+6163C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185583 | ||||||
| chr13:114185597
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+6177G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185597 | ||||||
| chr13:114185656
|
C | T | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+6236C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185656 | ||||||
| chr13:114185832
|
G | GC | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+6413dupC | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114185832 | |||||
| chr13:114185854
|
C | T | 2 | a0001c0001t0002g0320a0001c0001t0002g0321 | 2 | HG01975.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.90+6434C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185854 | ||||||
| chr13:114185895
|
C | G | 1 | a0001c0001t0003g0021 | 2 | NA18986.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.90+6475C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185895 | ||||||
| chr13:114185964
|
T | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+6544T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185964 | ||||||
| chr13:114185975
|
T | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+6555T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114185975 | ||||||
| chr13:114186066
|
C | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+6646C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186066 | ||||||
| chr13:114186132
|
G | A | 1 | a0001c0001t0002g0291 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.90+6712G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186132 | ||||||
| chr13:114186143
|
T | C | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+6723T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186143 | ||||||
| chr13:114186229
|
G | C | 1 | a0001c0001t0001g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.90+6809G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186229 | ||||||
| chr13:114186229
|
G | T | 1 | a0001c0001t0002g0319 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.90+6809G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186229 | ||||||
| chr13:114186318
|
T | C | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+6898T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186318 | ||||||
| chr13:114186357
|
C | T | 37 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(34): Show | 39 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.90+6937C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186357 | ||||||
| chr13:114186420
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 5 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+7000G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186420 | ||||||
| chr13:114186441
|
C | T | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+7021C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186441 | ||||||
| chr13:114186584
|
T | G | 49 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(46): Show | 54 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.90+7164T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186584 | ||||||
| chr13:114186695
|
G | A | 2 | a0001c0001t0002g0292a0001c0001t0002g0293 | 2 | NA18945.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.90+7275G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186695 | ||||||
| chr13:114186705
|
T | C | 35 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(32): Show | 37 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.90+7285T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186705 | ||||||
| chr13:114186842
|
C | T | 7 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+7422C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186842 | ||||||
| chr13:114186875
|
T | A | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.90+7455T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186875 | ||||||
| chr13:114186893
|
C | T | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+7473C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186893 | ||||||
| chr13:114186938
|
C | T | 40 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(37): Show | 43 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.90+7518C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114186938 | ||||||
| chr13:114187098
|
G | A | 77 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(74): Show | 87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.90+7678G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114187098 | ||||||
| chr13:114187398
|
A | G | 2 | a0001c0001t0009g0336a0001c0001t0009g0337 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.90+7978A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114187398 | ||||||
| chr13:114187556
|
G | C | 77 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(74): Show | 87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.90+8136G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114187556 | ||||||
| chr13:114187556
|
G | T | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+8136G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114187556 | ||||||
| chr13:114187645
|
A | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+8225A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114187645 | ||||||
| chr13:114187724
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0111a0001c0001t0001g0117others(1): Show | 5 | HG02630.hp2 HG02647.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+8304C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114187724 | ||||||
| chr13:114188081
|
C | G | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.91-8315C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114188081 | ||||||
| chr13:114188115
|
CA | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(21): Show | 30 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.91-8268delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114188115 | |||||
| chr13:114188158
|
C | T | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 30 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.91-8238C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114188158 | ||||||
| chr13:114188271
|
C | CA | 9 | a0001c0001t0001g0120a0001c0001t0001g0137a0001c0001t0001g0208others(6): Show | 9 | HG01167.hp1 HG01243.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.91-8107dupA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114188271 | |||||
| chr13:114188271
|
CA | C | 47 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(44): Show | 53 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.91-8107delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114188271 | |||||
| chr13:114188271
|
CAA | C | 86 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(83): Show | 99 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.91-8108_91-8107del others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114188271 | |||||
| chr13:114188516
|
G | A | 53 | a0001c0001t0001g0039a0001c0001t0001g0220a0001c0001t0001g0221others(50): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.91-7880G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114188516 | ||||||
| chr13:114188634
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.91-7762G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114188634 | ||||||
| chr13:114188689
|
A | T | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-7707A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114188689 | ||||||
| chr13:114188776
|
C | CAA | 11 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(8): Show | 14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.91-7606_91-7605dup others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114188776 | |||||
| chr13:114188776
|
CA | C | 6 | a0001c0001t0001g0207a0001c0001t0001g0223a0001c0001t0002g0043others(3): Show | 6 | HG01496.hp1 HG02976.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-7605delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114188776 | |||||
| chr13:114188807
|
A | G | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-7589A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114188807 | ||||||
| chr13:114189218
|
C | T | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-7178C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189218 | ||||||
| chr13:114189250
|
A | C | 1 | a0001c0001t0008g0112 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.91-7146A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189250 | ||||||
| chr13:114189436
|
C | T | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.91-6960C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189436 | ||||||
| chr13:114189613
|
T | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-6783T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189613 | ||||||
| chr13:114189635
|
G | T | 2 | a0001c0002t0001g0197a0001c0002t0001g0199 | 2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.91-6761G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189635 | ||||||
| chr13:114189682
|
G | T | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.91-6714G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189682 | ||||||
| chr13:114189709
|
A | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-6687A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189709 | ||||||
| chr13:114189726
|
TCATATC | T | 54 | a0001c0001t0001g0039a0001c0001t0001g0220a0001c0001t0001g0221others(51): Show | 62 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.91-6669_91-6664del others(6): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189726 | ||||||
| chr13:114189855
|
T | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.91-6541T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189855 | ||||||
| chr13:114189898
|
T | C | 2 | a0001c0001t0002g0287a0001c0001t0002g0302 | 2 | HG01081.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.91-6498T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189898 | ||||||
| chr13:114189912
|
A | C | 1 | a0001c0001t0002g0319 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.91-6484A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189912 | ||||||
| chr13:114189948
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.91-6448C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189948 | ||||||
| chr13:114189959
|
T | G | 145 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(142): Show | 164 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.91-6437T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114189959 | ||||||
| chr13:114190001
|
A | G | 49 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(46): Show | 54 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.91-6395A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190001 | ||||||
| chr13:114190004
|
C | T | 77 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(74): Show | 87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.91-6392C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190004 | ||||||
| chr13:114190061
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.91-6335G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190061 | ||||||
| chr13:114190106
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.91-6290C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190106 | ||||||
| chr13:114190137
|
G | A | 67 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0003g0005others(64): Show | 77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.91-6259G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190137 | ||||||
| chr13:114190137
|
G | C | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-6259G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190137 | ||||||
| chr13:114190141
|
TA | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(36): Show | 44 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.91-6245delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114190141 | |||||
| chr13:114190153
|
G | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-6243G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190153 | ||||||
| chr13:114190220
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0234 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.91-6176A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190220 | ||||||
| chr13:114190262
|
C | T | 49 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(46): Show | 54 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.91-6134C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190262 | ||||||
| chr13:114190271
|
C | T | 6 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(3): Show | 6 | HG00140.hp1 HG01109.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-6125C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190271 | ||||||
| chr13:114190357
|
G | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(6): Show | 12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-6039G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190357 | ||||||
| chr13:114190402
|
C | A | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-5994C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190402 | ||||||
| chr13:114190406
|
TAATC | T | 222 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(219): Show | 251 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.91-5986_91-5983del others(4): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114190406 | |||||
| chr13:114190455
|
A | C | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-5941A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190455 | ||||||
| chr13:114190679
|
T | A | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-5717T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190679 | ||||||
| chr13:114190993
|
A | T | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-5403A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114190993 | ||||||
| chr13:114191080
|
A | T | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-5316A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191080 | ||||||
| chr13:114191175
|
G | T | 1 | a0001c0001t0001g0014 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.91-5221G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191175 | ||||||
| chr13:114191235
|
C | G | 1 | a0001c0001t0012g0328 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.91-5161C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191235 | ||||||
| chr13:114191298
|
G | A | 99 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(96): Show | 113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.91-5098G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191298 | ||||||
| chr13:114191346
|
G | C | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-5050G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191346 | ||||||
| chr13:114191369
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91-5027C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191369 | ||||||
| chr13:114191559
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.91-4837C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191559 | ||||||
| chr13:114191827
|
A | G | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-4569A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191827 | ||||||
| chr13:114191828
|
G | A | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-4568G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191828 | ||||||
| chr13:114191829
|
A | T | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-4567A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191829 | ||||||
| chr13:114191855
|
A | T | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-4541A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191855 | ||||||
| chr13:114191856
|
T | A | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-4540T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191856 | ||||||
| chr13:114191857
|
A | T | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-4539A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191857 | ||||||
| chr13:114191858
|
A | C | 2 | a0001c0002t0001g0197a0001c0002t0001g0199 | 2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.91-4538A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191858 | ||||||
| chr13:114191895
|
T | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-4501T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191895 | ||||||
| chr13:114191910
|
G | A | 2 | a0001c0001t0002g0287a0001c0001t0002g0302 | 2 | HG01081.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.91-4486G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114191910 | ||||||
| chr13:114192057
|
C | T | 1 | a0001c0001t0002g0317 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.91-4339C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192057 | ||||||
| chr13:114192082
|
G | A | 8 | a0001c0001t0003g0144a0001c0001t0003g0156a0001c0001t0006g0010others(5): Show | 10 | HG00642.hp2 HG01993.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.91-4314G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192082 | ||||||
| chr13:114192148
|
C | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(6): Show | 12 | HG01070.hp1 HG01168.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-4248C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192148 | ||||||
| chr13:114192182
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0134 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.91-4214T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192182 | ||||||
| chr13:114192213
|
C | T | 48 | a0001c0001t0001g0039a0001c0001t0001g0114a0001c0001t0001g0202others(45): Show | 56 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.91-4183C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192213 | ||||||
| chr13:114192251
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.91-4145G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192251 | ||||||
| chr13:114192262
|
G | A | 1 | a0001c0001t0002g0287 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.91-4134G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192262 | ||||||
| chr13:114192404
|
T | C | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-3992T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192404 | ||||||
| chr13:114192406
|
T | A | 1 | a0001c0001t0003g0154 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.91-3990T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192406 | ||||||
| chr13:114192435
|
C | T | 2 | a0001c0001t0002g0279a0001c0001t0002g0280 | 2 | HG01099.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.91-3961C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192435 | ||||||
| chr13:114192529
|
A | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0246 | 2 | NA18986.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.91-3867A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192529 | ||||||
| chr13:114192636
|
C | G | 2 | a0001c0001t0002g0315a0001c0001t0002g0316 | 2 | HG01192.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.91-3760C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192636 | ||||||
| chr13:114192692
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.91-3704G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192692 | ||||||
| chr13:114192698
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.91-3698A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192698 | ||||||
| chr13:114192708
|
G | A | 1 | a0001c0001t0002g0294 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.91-3688G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192708 | ||||||
| chr13:114192806
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.91-3590T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192806 | ||||||
| chr13:114192973
|
A | G | 1 | a0001c0001t0005g0097 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.91-3423A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114192973 | ||||||
| chr13:114193218
|
A | G | 1 | a0001c0001t0002g0332 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.91-3178A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193218 | ||||||
| chr13:114193219
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.91-3177T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193219 | ||||||
| chr13:114193379
|
A | T | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-3017A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193379 | ||||||
| chr13:114193401
|
T | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-2995T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193401 | ||||||
| chr13:114193405
|
T | A | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-2991T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193405 | ||||||
| chr13:114193736
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.91-2660G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193736 | ||||||
| chr13:114193768
|
C | G | 1 | a0001c0001t0003g0146 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.91-2628C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193768 | ||||||
| chr13:114193860
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0351others(1): Show | 4 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-2536G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193860 | ||||||
| chr13:114193917
|
C | A | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-2479C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114193917 | ||||||
| chr13:114194033
|
G | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-2363G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194033 | ||||||
| chr13:114194163
|
T | A | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-2233T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194163 | ||||||
| chr13:114194389
|
A | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0058others(34): Show | 41 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.91-2007A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194389 | ||||||
| chr13:114194424
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.91-1972G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194424 | ||||||
| chr13:114194426
|
A | T | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.91-1970A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194426 | ||||||
| chr13:114194585
|
C | T | 74 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(71): Show | 84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.91-1811C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194585 | ||||||
| chr13:114194688
|
C | T | 13 | a0001c0001t0001g0120a0001c0001t0006g0010a0001c0001t0006g0033others(10): Show | 16 | HG00642.hp2 HG01361.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.91-1708C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194688 | ||||||
| chr13:114194702
|
C | G | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.91-1694C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194702 | ||||||
| chr13:114194734
|
C | CT | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(276): Show | 316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.91-1662_91-1661ins others(1): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194734 | ||||||
| chr13:114194757
|
A | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(191): Show | 218 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.91-1639A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194757 | ||||||
| chr13:114194803
|
A | G | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.91-1593A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194803 | ||||||
| chr13:114194843
|
A | G | 97 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(94): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.91-1553A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194843 | ||||||
| chr13:114194956
|
C | T | 5 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(2): Show | 5 | HG01891.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-1440C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114194956 | ||||||
| chr13:114195007
|
T | C | 1 | a0001c0001t0005g0085 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.91-1389T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195007 | ||||||
| chr13:114195014
|
A | C | 1 | a0001c0001t0006g0342 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.91-1382A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195014 | ||||||
| chr13:114195051
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.91-1345C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195051 | ||||||
| chr13:114195087
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(276): Show | 316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.91-1309T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195087 | ||||||
| chr13:114195123
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0101 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.91-1273G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195123 | ||||||
| chr13:114195207
|
G | C | 1 | a0001c0001t0001g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.91-1189G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195207 | ||||||
| chr13:114195227
|
G | A | 5 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(2): Show | 5 | NA18942.hp2 NA18962.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-1169G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195227 | ||||||
| chr13:114195255
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(276): Show | 316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.91-1141T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195255 | ||||||
| chr13:114195337
|
G | C | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-1059G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195337 | ||||||
| chr13:114195555
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.91-841A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195555 | ||||||
| chr13:114195864
|
A | G | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(276): Show | 316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.91-532A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195864 | ||||||
| chr13:114195916
|
CA | C | 128 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(125): Show | 146 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.91-463delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114195916 | |||||
| chr13:114195916
|
CAA | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(118): Show | 136 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.91-464_91-463delAA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114195916 | |||||
| chr13:114195926
|
A | G | 1 | a0001c0001t0002g0285 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.91-470A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195926 | ||||||
| chr13:114195929
|
A | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(6): Show | 12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-467A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195929 | ||||||
| chr13:114195931
|
A | C | 1 | a0001c0001t0002g0299 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.91-465A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195931 | ||||||
| chr13:114195956
|
G | A | 1 | a0001c0001t0002g0304 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.91-440G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114195956 | ||||||
| chr13:114196008
|
G | A | 134 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(131): Show | 150 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.91-388G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114196008 | ||||||
| chr13:114196076
|
C | CAAA | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-302_91-300dupAA others(1): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114196076 | |||||
| chr13:114196076
|
CA | C | 9 | a0001c0001t0001g0035a0001c0001t0001g0198a0001c0001t0001g0211others(6): Show | 9 | HG00735.hp2 HG01071.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.91-300delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114196076 | |||||
| chr13:114196076
|
CAA | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(59): Show | 71 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.91-301_91-300delAA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114196076 | |||||
| chr13:114196076
|
CAAA | C | 157 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(154): Show | 180 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.91-302_91-300delAA others(1): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114196076 | |||||
| chr13:114196076
|
CAAAA | C | 39 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(36): Show | 41 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.91-303_91-300delAA others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 114196076 | |||||
| chr13:114196099
|
C | T | 1 | a0001c0001t0003g0174 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.91-297C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114196099 | ||||||
| chr13:114196113
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.91-283G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114196113 | ||||||
| chr13:114196262
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0351a0001c0001t0001g0352 | 3 | HG00735.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.91-134G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114196262 | ||||||
| chr13:114196286
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.91-110G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 1/3 | chr13 | 114196286 | ||||||
| chr13:114196642
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.171+166G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114196642 | ||||||
| chr13:114197026
|
G | A | 10 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(7): Show | 10 | NA18954.hp2 NA18963.hp2 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.171+550G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197026 | ||||||
| chr13:114197032
|
T | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+556T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197032 | ||||||
| chr13:114197143
|
T | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(6): Show | 12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.171+667T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197143 | ||||||
| chr13:114197280
|
TA | T | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+805delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197280 | ||||||
| chr13:114197281
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0216a0001c0001t0001g0219 | 4 | HG02818.hp1 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+805A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197281 | ||||||
| chr13:114197326
|
C | T | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.171+850C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197326 | ||||||
| chr13:114197478
|
G | A | 8 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(5): Show | 8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+1002G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197478 | ||||||
| chr13:114197529
|
G | A | 74 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(71): Show | 84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.171+1053G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197529 | ||||||
| chr13:114197565
|
A | C | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+1089A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197565 | ||||||
| chr13:114197611
|
G | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+1135G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197611 | ||||||
| chr13:114197622
|
GA | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+1148delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114197622 | |||||
| chr13:114197735
|
T | TCCAGTGA others(45): Show |
8 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(5): Show | 8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+1260_171+1311d others(54): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114197735 | |||||
| chr13:114197846
|
T | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+1370T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197846 | ||||||
| chr13:114197856
|
C | T | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+1380C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197856 | ||||||
| chr13:114197961
|
A | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(66): Show | 78 | HG00408.hp2 HG00621.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.171+1485A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114197961 | ||||||
| chr13:114198147
|
C | T | 1 | a0001c0001t0002g0300 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.171+1671C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198147 | ||||||
| chr13:114198162
|
T | C | 15 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0073others(12): Show | 16 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.171+1686T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198162 | ||||||
| chr13:114198282
|
G | A | 67 | a0001c0001t0001g0115a0001c0001t0003g0005a0001c0001t0003g0006others(64): Show | 77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.171+1806G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198282 | ||||||
| chr13:114198362
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(183): Show | 210 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.171+1886C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198362 | ||||||
| chr13:114198366
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0131 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.171+1890C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198366 | ||||||
| chr13:114198384
|
A | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+1908A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198384 | ||||||
| chr13:114198429
|
A | G | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-1896A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198429 | ||||||
| chr13:114198507
|
C | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-1818C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198507 | ||||||
| chr13:114198519
|
C | G | 1 | a0001c0001t0003g0350 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.172-1806C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198519 | ||||||
| chr13:114198534
|
C | T | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.172-1791C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198534 | ||||||
| chr13:114198585
|
C | G | 1 | a0001c0001t0003g0177 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.172-1740C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198585 | ||||||
| chr13:114198605
|
G | C | 67 | a0001c0001t0001g0115a0001c0001t0003g0005a0001c0001t0003g0006others(64): Show | 77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.172-1720G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198605 | ||||||
| chr13:114198619
|
T | TGGTCCCC others(32): Show |
12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-1692_172-1691i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198619 | |||||
| chr13:114198619
|
T | TGGTCCCC others(500): Show |
3 | a0001c0001t0001g0239a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | HG01168.hp2 HG04228.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.172-1671_172-1670i others(509): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198619 | |||||
| chr13:114198619
|
T | TGGTCCCC others(461): Show |
13 | a0001c0001t0001g0039a0001c0001t0001g0114a0001c0001t0001g0220others(10): Show | 13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.172-1671_172-1670i others(470): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198619 | |||||
| chr13:114198619
|
T | TGGTCCCC others(500): Show |
1 | a0001c0001t0001g0222 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(509): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198619 | |||||
| chr13:114198619
|
TGGTCCCC others(71): Show |
T | 1 | a0001c0001t0002g0286 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.172-1670_172-1593d others(80): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198619 | |||||
| chr13:114198623
|
C | T | 74 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(71): Show | 84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.172-1702C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198623 | ||||||
| chr13:114198629
|
TGAGGGGT others(266): Show |
T | 1 | a0001c0001t0001g0018 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.172-1670_172-1398d others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198629 | |||||
| chr13:114198640
|
GGCGCGTC others(188): Show |
G | 1 | a0001c0001t0003g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-1670_172-1476d others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198640 | |||||
| chr13:114198654
|
T | TGTACGGT others(266): Show |
1 | a0001c0001t0004g0253 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(275): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
T | TGTACGGT others(384): Show |
1 | a0001c0001t0001g0221 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(393): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
T | TGTACGGT others(344): Show |
2 | a0001c0001t0001g0223a0001c0001t0004g0008 | 2 | HG02976.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.172-1671_172-1670i others(353): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
T | TGTACGGT others(383): Show |
5 | a0001c0001t0001g0267a0001c0001t0004g0001a0001c0001t0004g0235others(2): Show | 6 | HG00140.hp1 HG02083.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-1671_172-1670i others(392): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
T | TGTACGGT others(969): Show |
1 | a0001c0001t0004g0249 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(978): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
T | TGTACGGT others(969): Show |
1 | a0001c0001t0004g0250 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.172-1671_172-1670i others(978): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
T | TGTACGGT others(851): Show |
1 | a0001c0001t0012g0328 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(860): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
T | TGTACGGT others(968): Show |
3 | a0001c0001t0004g0241a0001c0001t0004g0251a0001c0001t0004g0257 | 3 | NA18947.hp1 NA18966.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.172-1671_172-1670i others(977): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
T | TGTACGGT others(1046): Show |
1 | a0001c0001t0004g0148 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(1055): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
T | TGTACGGT others(344): Show |
1 | a0001c0004t0001g0053 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(353): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
T | TGTACGGT others(968): Show |
1 | a0001c0001t0004g0245 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.172-1671_172-1670i others(977): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
T | TGTACGGT others(344): Show |
1 | a0001c0001t0004g0254 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.172-1671_172-1670i others(353): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
T | TGTACGGT others(188): Show |
1 | a0001c0001t0001g0203 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.172-1671_172-1670i others(197): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
TTTACGGT others(32): Show |
T | 1 | a0001c0001t0001g0123 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.172-1670_172-1632d others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198654
|
TTTACGGT others(656): Show |
T | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.172-1670_172-1008d others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198654 | ||||||
| chr13:114198655
|
T | G | 168 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(165): Show | 193 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.172-1670T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198655 | ||||||
| chr13:114198657
|
A | ACGGTCCC others(149): Show |
1 | a0001c0001t0002g0314 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.172-1647_172-1646i others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198657 | |||||
| chr13:114198666
|
G | A | 81 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(78): Show | 94 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.172-1659G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198666 | ||||||
| chr13:114198666
|
G | GCTGAGGG others(32): Show |
5 | a0001c0001t0001g0077a0001c0001t0001g0122a0001c0001t0001g0124others(2): Show | 5 | HG01243.hp1 HG01258.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198666 | |||||
| chr13:114198666
|
G | GCTGAGGG others(110): Show |
13 | a0001c0001t0001g0121a0001c0001t0001g0127a0001c0001t0001g0228others(10): Show | 14 | HG00733.hp2 HG02129.hp2 HG03471.hp2 others(11): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(119): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198666 | |||||
| chr13:114198668
|
T | TGAGGGGT others(151): Show |
1 | a0001c0001t0001g0128 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.172-1653_172-1652i others(160): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | |||||
| chr13:114198668
|
T | TGAGGGGT others(71): Show |
4 | a0001c0001t0001g0109a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 6 | HG00741.hp2 HG02155.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(80): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | |||||
| chr13:114198668
|
T | TGAGGGGT others(149): Show |
11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(8): Show | 14 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | |||||
| chr13:114198668
|
T | TGAGGGGT others(227): Show |
9 | a0001c0001t0001g0265a0001c0001t0004g0007a0001c0001t0004g0008others(6): Show | 10 | HG00673.hp1 HG02145.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(236): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | |||||
| chr13:114198668
|
T | TGAGGGGT others(110): Show |
1 | a0001c0001t0001g0133 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.172-1653_172-1652i others(119): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | |||||
| chr13:114198668
|
T | TGAGGGGT others(149): Show |
9 | a0001c0001t0001g0052a0001c0001t0001g0073a0001c0001t0001g0107others(6): Show | 9 | HG02145.hp2 HG02257.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | |||||
| chr13:114198668
|
T | TGAGGGGT others(188): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0111a0001c0001t0001g0117others(2): Show | 6 | HG02630.hp2 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-1653_172-1652i others(197): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | |||||
| chr13:114198668
|
T | TGAGGGGT others(188): Show |
2 | a0001c0001t0001g0028a0001c0001t0001g0234 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.172-1653_172-1652i others(197): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | |||||
| chr13:114198668
|
TGAGGCGT others(890): Show |
T | 1 | a0001c0001t0008g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.172-1646_172-750de others(1): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198668 | |||||
| chr13:114198671
|
G | A | 1 | a0001c0001t0004g0148 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.172-1654G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198671 | ||||||
| chr13:114198673
|
C | CGTGACGG others(383): Show |
1 | a0001c0001t0005g0087 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.172-1647_172-1646i others(392): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198673 | |||||
| chr13:114198673
|
C | CGTGACGG others(344): Show |
1 | a0001c0001t0001g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.172-1647_172-1646i others(353): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198673 | |||||
| chr13:114198673
|
C | CGTGACGG others(383): Show |
24 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(21): Show | 26 | HG00408.hp1 HG01891.hp1 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.172-1647_172-1646i others(392): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198673 | |||||
| chr13:114198673
|
C | CGTGACGG others(344): Show |
1 | a0001c0001t0001g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.172-1647_172-1646i others(353): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198673 | |||||
| chr13:114198673
|
C | CGTGACGG others(383): Show |
1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.172-1647_172-1646i others(392): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198673 | |||||
| chr13:114198673
|
C | G | 41 | a0001c0001t0001g0039a0001c0001t0001g0114a0001c0001t0001g0203others(38): Show | 44 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.172-1652C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198673 | ||||||
| chr13:114198679
|
A | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(267): Show | 306 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.172-1646A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198679 | ||||||
| chr13:114198681
|
T | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(272): Show | 311 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.172-1644T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198681 | ||||||
| chr13:114198683
|
G | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(272): Show | 311 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.172-1642G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198683 | ||||||
| chr13:114198693
|
C | CTTACGGT others(32): Show |
8 | a0001c0001t0001g0027a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 9 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-1632_172-1631i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198693 | ||||||
| chr13:114198693
|
C | G | 147 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(144): Show | 172 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.172-1632C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198693 | ||||||
| chr13:114198693
|
C | T | 10 | a0001c0001t0001g0115a0001c0001t0001g0324a0001c0001t0004g0241others(7): Show | 10 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-1632C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198693 | ||||||
| chr13:114198694
|
G | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-1631G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198694 | ||||||
| chr13:114198694
|
G | T | 48 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0058others(45): Show | 52 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.172-1631G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198694 | ||||||
| chr13:114198698
|
G | A | 1 | a0001c0001t0003g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.172-1627G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198698 | ||||||
| chr13:114198705
|
G | A | 9 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0134others(6): Show | 11 | HG00741.hp2 HG01169.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-1620G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198705 | ||||||
| chr13:114198707
|
T | C | 127 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(124): Show | 146 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.172-1618T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198707 | ||||||
| chr13:114198712
|
G | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(162): Show | 189 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.172-1613G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198712 | ||||||
| chr13:114198718
|
G | A | 3 | a0001c0001t0001g0238a0001c0001t0004g0230a0001c0001t0004g0264 | 3 | HG01169.hp1 HG01928.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.172-1607G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198718 | ||||||
| chr13:114198732
|
T | C | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(81): Show | 91 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.172-1593T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198732 | ||||||
| chr13:114198732
|
T | G | 126 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0017others(123): Show | 144 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.172-1593T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198732 | ||||||
| chr13:114198732
|
T | TGTACGGT others(305): Show |
1 | a0001c0001t0001g0194 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.172-1589_172-1588i others(314): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198732 | |||||
| chr13:114198733
|
G | GTACGGTC others(149): Show |
21 | a0001c0001t0001g0026a0001c0001t0001g0058a0001c0001t0001g0059others(18): Show | 22 | HG02602.hp1 HG02698.hp2 HG03486.hp2 others(19): Show |
intron_variant | MODIFIER | c.172-1589_172-1588i others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198733 | |||||
| chr13:114198733
|
G | GTACGGTC others(188): Show |
2 | a0001c0001t0001g0196a0001c0001t0001g0209 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.172-1589_172-1588i others(197): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198733 | |||||
| chr13:114198733
|
G | GTACGGTC others(227): Show |
1 | a0001c0001t0001g0200 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.172-1589_172-1588i others(236): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198733 | |||||
| chr13:114198733
|
G | GTACGGTC others(500): Show |
1 | a0001c0001t0005g0098 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.172-1589_172-1588i others(509): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198733 | |||||
| chr13:114198733
|
G | GTACGGTC others(149): Show |
8 | a0001c0001t0001g0072a0001c0001t0001g0208a0001c0001t0001g0211others(5): Show | 8 | HG00408.hp2 HG00621.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.172-1589_172-1588i others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198733 | |||||
| chr13:114198733
|
G | T | 30 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(27): Show | 34 | HG00609.hp2 HG00673.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.172-1592G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198733 | ||||||
| chr13:114198737
|
A | G | 277 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(274): Show | 313 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.172-1588A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198737 | ||||||
| chr13:114198744
|
G | A | 10 | a0001c0001t0001g0077a0001c0001t0001g0122a0001c0001t0001g0123others(7): Show | 10 | HG00558.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-1581G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198744 | ||||||
| chr13:114198746
|
T | C | 105 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(102): Show | 121 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.172-1579T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198746 | ||||||
| chr13:114198749
|
G | A | 6 | a0001c0001t0004g0241a0001c0001t0004g0245a0001c0001t0004g0249others(3): Show | 6 | NA18940.hp1 NA18947.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1576G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198749 | ||||||
| chr13:114198751
|
G | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(134): Show | 160 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.172-1574G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198751 | ||||||
| chr13:114198757
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.172-1568G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198757 | ||||||
| chr13:114198771
|
C | G | 110 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(107): Show | 126 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.172-1554C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198771 | ||||||
| chr13:114198771
|
C | T | 18 | a0001c0001t0001g0324a0001c0001t0002g0318a0001c0001t0004g0008others(15): Show | 21 | HG00544.hp2 HG00558.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.172-1554C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198771 | ||||||
| chr13:114198772
|
T | G | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(149): Show | 173 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.172-1553T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198772 | ||||||
| chr13:114198782
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(276): Show | 315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.172-1543T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198782 | ||||||
| chr13:114198783
|
G | A | 94 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(91): Show | 110 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.172-1542G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198783 | ||||||
| chr13:114198785
|
T | C | 27 | a0001c0001t0001g0077a0001c0001t0001g0109a0001c0001t0001g0115others(24): Show | 30 | HG00733.hp2 HG00741.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.172-1540T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198785 | ||||||
| chr13:114198788
|
G | A | 1 | a0001c0001t0004g0148 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.172-1537G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198788 | ||||||
| chr13:114198790
|
C | G | 80 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 91 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.172-1535C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198790 | ||||||
| chr13:114198790
|
C | T | 1 | a0001c0001t0002g0318 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.172-1535C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198790 | ||||||
| chr13:114198796
|
A | G | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(276): Show | 315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.172-1529A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198796 | ||||||
| chr13:114198798
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(276): Show | 315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.172-1527T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198798 | ||||||
| chr13:114198800
|
G | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(276): Show | 315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.172-1525G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198800 | ||||||
| chr13:114198801
|
G | T | 71 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(68): Show | 84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.172-1524G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198801 | ||||||
| chr13:114198806
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.172-1519C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198806 | ||||||
| chr13:114198808
|
T | TGCTTACG others(186): Show |
1 | a0001c0001t0001g0202 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.172-1516_172-1515i others(195): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198808 | |||||
| chr13:114198810
|
T | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(146): Show | 164 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.172-1515T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198810 | ||||||
| chr13:114198810
|
T | G | 108 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(105): Show | 124 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.172-1515T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198810 | ||||||
| chr13:114198810
|
T | TGTACGGT others(110): Show |
2 | a0001c0001t0009g0336a0001c0001t0009g0337 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.172-1502_172-1501i others(119): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198810 | |||||
| chr13:114198811
|
G | GTACGGTC others(344): Show |
1 | a0001c0001t0005g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.172-1497_172-1496i others(353): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198811 | |||||
| chr13:114198811
|
G | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0026others(79): Show | 89 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.172-1514G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198811 | ||||||
| chr13:114198817
|
T | TCCCCGCT others(73): Show |
1 | a0001c0001t0001g0221 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.172-1497_172-1496i others(82): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198817 | |||||
| chr13:114198822
|
G | A | 4 | a0001c0001t0001g0123a0001c0001t0001g0188a0001c0001t0002g0318others(1): Show | 4 | HG00558.hp2 HG01123.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-1503G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198822 | ||||||
| chr13:114198824
|
T | C | 90 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(87): Show | 105 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.172-1501T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198824 | ||||||
| chr13:114198829
|
C | G | 72 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0052others(69): Show | 79 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.172-1496C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198829 | ||||||
| chr13:114198835
|
A | G | 277 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(274): Show | 313 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.172-1490A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198835 | ||||||
| chr13:114198840
|
G | T | 1 | a0001c0001t0003g0149 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.172-1485G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198840 | ||||||
| chr13:114198847
|
T | TGCTTACG others(264): Show |
1 | a0001c0001t0012g0328 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.172-1477_172-1476i others(273): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198847 | |||||
| chr13:114198847
|
T | TGCTTACG others(420): Show |
1 | a0001c0001t0005g0085 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.172-1477_172-1476i others(429): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198847 | |||||
| chr13:114198847
|
T | TGCTTACG others(537): Show |
1 | a0001c0001t0005g0093 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.172-1477_172-1476i others(546): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198847 | |||||
| chr13:114198849
|
T | C | 150 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0026others(147): Show | 160 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.172-1476T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198849 | ||||||
| chr13:114198849
|
T | G | 113 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(110): Show | 133 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.172-1476T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198849 | ||||||
| chr13:114198850
|
G | GCT | 3 | a0001c0001t0005g0085a0001c0001t0005g0093a0001c0001t0012g0328 | 3 | HG00423.hp2 HG01257.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.172-1475_172-1474i others(4): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198850 | ||||||
| chr13:114198850
|
G | T | 112 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0034others(109): Show | 120 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(117): Show |
intron_variant | MODIFIER | c.172-1475G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198850 | ||||||
| chr13:114198853
|
C | T | 1 | a0001c0001t0003g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.172-1472C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198853 | ||||||
| chr13:114198861
|
G | A | 88 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(85): Show | 104 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.172-1464G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198861 | ||||||
| chr13:114198863
|
T | C | 13 | a0001c0001t0001g0115a0001c0001t0001g0123a0001c0001t0001g0188others(10): Show | 13 | HG00558.hp2 HG01123.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.172-1462T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198863 | ||||||
| chr13:114198866
|
G | A | 6 | a0001c0001t0004g0241a0001c0001t0004g0245a0001c0001t0004g0249others(3): Show | 6 | NA18940.hp1 NA18947.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1459G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198866 | ||||||
| chr13:114198868
|
G | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(117): Show | 142 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.172-1457G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198868 | ||||||
| chr13:114198888
|
T | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(138): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.172-1437T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198888 | ||||||
| chr13:114198888
|
T | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0017others(100): Show | 117 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.172-1437T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198888 | ||||||
| chr13:114198889
|
G | GTACGGTC others(384): Show |
1 | a0001c0001t0007g0152 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.172-1426_172-1425i others(393): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198889 | |||||
| chr13:114198889
|
G | GTACGGTC others(384): Show |
1 | a0001c0001t0008g0099 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.172-1426_172-1425i others(393): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198889 | |||||
| chr13:114198889
|
G | GTACGGTC others(266): Show |
1 | a0001c0001t0001g0082 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.172-1426_172-1425i others(275): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198889 | |||||
| chr13:114198889
|
G | T | 85 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0034others(82): Show | 94 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.172-1436G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198889 | ||||||
| chr13:114198900
|
A | ACTGAGGC others(32): Show |
1 | a0001c0001t0006g0347 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.172-1424_172-1423i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198900 | |||||
| chr13:114198900
|
A | G | 266 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(263): Show | 299 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.172-1425A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198900 | ||||||
| chr13:114198902
|
C | T | 194 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(191): Show | 217 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.172-1423C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198902 | ||||||
| chr13:114198907
|
G | C | 115 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0027others(112): Show | 133 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.172-1418G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198907 | ||||||
| chr13:114198916
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-1409G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198916 | ||||||
| chr13:114198917
|
C | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-1408C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198917 | ||||||
| chr13:114198923
|
C | T | 5 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG03491.hp1 HG03831.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-1402C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198923 | ||||||
| chr13:114198927
|
T | C | 164 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(161): Show | 183 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.172-1398T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198927 | ||||||
| chr13:114198927
|
T | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(81): Show | 97 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.172-1398T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198927 | ||||||
| chr13:114198928
|
G | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(50): Show | 60 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.172-1397G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198928 | ||||||
| chr13:114198939
|
G | A | 69 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(66): Show | 80 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.172-1386G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198939 | ||||||
| chr13:114198941
|
T | C | 17 | a0001c0001t0001g0115a0001c0001t0001g0188a0001c0001t0001g0238others(14): Show | 19 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.172-1384T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198941 | ||||||
| chr13:114198944
|
G | A | 1 | a0001c0001t0004g0148 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.172-1381G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198944 | ||||||
| chr13:114198946
|
T | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(144): Show | 172 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.172-1379T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198946 | ||||||
| chr13:114198946
|
T | G | 132 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0026others(129): Show | 144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.172-1379T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198946 | ||||||
| chr13:114198951
|
T | C | 350 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(347): Show | 397 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(394): Show |
intron_variant | MODIFIER | c.172-1374T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198951 | ||||||
| chr13:114198966
|
G | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(152): Show | 173 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.172-1359G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198966 | ||||||
| chr13:114198966
|
G | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(84): Show | 101 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.172-1359G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198966 | ||||||
| chr13:114198967
|
G | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(54): Show | 63 | HG00140.hp1 HG00408.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.172-1358G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198967 | ||||||
| chr13:114198978
|
A | G | 269 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(266): Show | 303 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.172-1347A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198978 | ||||||
| chr13:114198980
|
T | C | 75 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(72): Show | 86 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.172-1345T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198980 | ||||||
| chr13:114198980
|
T | TGAGGCGT others(32): Show |
1 | a0001c0001t0002g0318 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.172-1335_172-1334i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114198980 | |||||
| chr13:114198985
|
C | G | 137 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(134): Show | 152 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.172-1340C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198985 | ||||||
| chr13:114198991
|
A | G | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(277): Show | 316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.172-1334A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198991 | ||||||
| chr13:114198993
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-1332C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198993 | ||||||
| chr13:114198994
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-1331G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198994 | ||||||
| chr13:114198995
|
C | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-1330C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198995 | ||||||
| chr13:114198995
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-1330C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198995 | ||||||
| chr13:114198996
|
G | T | 1 | a0001c0001t0003g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-1329G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114198996 | ||||||
| chr13:114199001
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-1324C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199001 | ||||||
| chr13:114199003
|
T | TGCTTACG others(30): Show |
11 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(8): Show | 14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-1321_172-1320i others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199003 | |||||
| chr13:114199003
|
T | TGCTTACG others(537): Show |
1 | a0001c0001t0007g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.172-1321_172-1320i others(546): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199003 | |||||
| chr13:114199003
|
T | TGCTTACG others(225): Show |
1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.172-1321_172-1320i others(234): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199003 | |||||
| chr13:114199005
|
T | C | 163 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(160): Show | 178 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.172-1320T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199005 | ||||||
| chr13:114199005
|
T | CTTACGGT others(32): Show |
1 | a0001c0001t0006g0347 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.172-1321_172-1320i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199005 | ||||||
| chr13:114199005
|
T | G | 78 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0018others(75): Show | 92 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.172-1320T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199005 | ||||||
| chr13:114199006
|
G | GCTTACGG others(34): Show |
11 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(8): Show | 14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-1319_172-1318i others(43): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199006 | ||||||
| chr13:114199006
|
G | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0057others(79): Show | 88 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.172-1319G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199006 | ||||||
| chr13:114199008
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-1317A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199008 | ||||||
| chr13:114199009
|
C | T | 38 | a0001c0001t0003g0006a0001c0001t0003g0012a0001c0001t0003g0022others(35): Show | 42 | HG00558.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.172-1316C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199009 | ||||||
| chr13:114199019
|
C | T | 195 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(192): Show | 218 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.172-1306C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199019 | ||||||
| chr13:114199022
|
G | A | 6 | a0001c0001t0004g0241a0001c0001t0004g0245a0001c0001t0004g0249others(3): Show | 6 | NA18940.hp1 NA18947.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1303G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199022 | ||||||
| chr13:114199024
|
G | C | 90 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0018others(87): Show | 104 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.172-1301G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199024 | ||||||
| chr13:114199034
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-1291C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199034 | ||||||
| chr13:114199044
|
G | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(150): Show | 171 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.172-1281G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199044 | ||||||
| chr13:114199044
|
G | T | 42 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(39): Show | 46 | HG00408.hp1 HG00639.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.172-1281G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199044 | ||||||
| chr13:114199045
|
G | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-1280G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199045 | ||||||
| chr13:114199045
|
G | T | 66 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0034others(63): Show | 68 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.172-1280G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199045 | ||||||
| chr13:114199048
|
C | T | 7 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0145others(4): Show | 9 | HG00544.hp1 HG02135.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-1277C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199048 | ||||||
| chr13:114199056
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0002g0318a0001c0001t0003g0170 | 4 | HG00558.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1269G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199056 | ||||||
| chr13:114199058
|
T | C | 85 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(82): Show | 99 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.172-1267T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199058 | ||||||
| chr13:114199063
|
C | CGTGACGG others(188): Show |
1 | a0001c0001t0001g0265 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.172-1243_172-1242i others(197): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199063 | |||||
| chr13:114199063
|
C | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0026others(114): Show | 130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.172-1262C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199063 | ||||||
| chr13:114199071
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.172-1254C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199071 | ||||||
| chr13:114199074
|
G | T | 1 | a0001c0001t0002g0318 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.172-1251G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199074 | ||||||
| chr13:114199083
|
T | C | 157 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(154): Show | 178 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.172-1242T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199083 | ||||||
| chr13:114199083
|
T | G | 90 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0018others(87): Show | 105 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.172-1242T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199083 | ||||||
| chr13:114199084
|
G | GTACGGTC others(188): Show |
8 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0248others(5): Show | 9 | HG00673.hp1 HG03490.hp2 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.172-1224_172-1223i others(197): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199084 | |||||
| chr13:114199084
|
G | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(47): Show | 56 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.172-1241G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199084 | ||||||
| chr13:114199095
|
G | A | 3 | a0001c0001t0002g0032a0001c0001t0002g0273a0001c0001t0003g0159 | 4 | HG00323.hp2 HG01074.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1230G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199095 | ||||||
| chr13:114199097
|
T | C | 84 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0018others(81): Show | 98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.172-1228T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199097 | ||||||
| chr13:114199102
|
C | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(115): Show | 131 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.172-1223C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199102 | ||||||
| chr13:114199113
|
G | T | 2 | a0001c0001t0002g0032a0001c0001t0002g0273 | 3 | HG00323.hp2 HG01074.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.172-1212G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199113 | ||||||
| chr13:114199122
|
G | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(114): Show | 135 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.172-1203G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199122 | ||||||
| chr13:114199122
|
G | T | 43 | a0001c0001t0001g0039a0001c0001t0001g0082a0001c0001t0001g0114others(40): Show | 46 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.172-1203G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199122 | ||||||
| chr13:114199122
|
GGTACGGT others(71): Show |
G | 1 | a0001c0001t0002g0273 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.172-1191_172-1114d others(80): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199122 | |||||
| chr13:114199123
|
G | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(34): Show | 47 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.172-1202G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199123 | ||||||
| chr13:114199134
|
A | G | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(262): Show | 300 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.172-1191A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199134 | ||||||
| chr13:114199136
|
T | C | 44 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0018others(41): Show | 54 | HG00323.hp2 HG00544.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.172-1189T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199136 | ||||||
| chr13:114199136
|
T | TGAGGCGT others(32): Show |
1 | a0001c0001t0002g0312 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.172-1125_172-1087d others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199136 | |||||
| chr13:114199141
|
C | CGTGACGG others(110): Show |
2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.172-1165_172-1164i others(119): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199141 | |||||
| chr13:114199141
|
C | G | 171 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(168): Show | 188 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.172-1184C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199141 | ||||||
| chr13:114199152
|
G | T | 1 | a0001c0001t0001g0202 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.172-1173G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199152 | ||||||
| chr13:114199159
|
T | TGCTTACG others(69): Show |
2 | a0001c0001t0001g0003a0001c0001t0001g0218 | 5 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-1165_172-1164i others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199159 | |||||
| chr13:114199161
|
T | C | 127 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(124): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.172-1164T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199161 | ||||||
| chr13:114199161
|
T | G | 85 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(82): Show | 99 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.172-1164T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199161 | ||||||
| chr13:114199162
|
G | GCT | 2 | a0001c0001t0001g0003a0001c0001t0001g0218 | 5 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-1163_172-1162i others(4): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199162 | ||||||
| chr13:114199162
|
G | T | 81 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0026others(78): Show | 85 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.172-1163G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199162 | ||||||
| chr13:114199173
|
G | A | 1 | a0001c0001t0002g0032 | 2 | HG00323.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.172-1152G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199173 | ||||||
| chr13:114199175
|
C | T | 204 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(201): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.172-1150C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199175 | ||||||
| chr13:114199180
|
C | G | 81 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(78): Show | 99 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.172-1145C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199180 | ||||||
| chr13:114199186
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.172-1139G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199186 | ||||||
| chr13:114199200
|
T | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(120): Show | 142 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.172-1125T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199200 | ||||||
| chr13:114199200
|
T | G | 121 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(118): Show | 137 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-1125T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199200 | ||||||
| chr13:114199201
|
G | T | 25 | a0001c0001t0001g0018a0001c0001t0001g0196a0001c0001t0001g0209others(22): Show | 28 | HG00609.hp2 HG00673.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.172-1124G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199201 | ||||||
| chr13:114199204
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-1121C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199204 | ||||||
| chr13:114199212
|
G | A | 4 | a0001c0001t0001g0115a0001c0001t0002g0304a0001c0001t0003g0158others(1): Show | 4 | HG03225.hp1 NA18965.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1113G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199212 | ||||||
| chr13:114199214
|
C | T | 203 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(200): Show | 228 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.172-1111C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199214 | ||||||
| chr13:114199219
|
C | G | 147 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(144): Show | 162 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.172-1106C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199219 | ||||||
| chr13:114199225
|
G | A | 2 | a0001c0001t0003g0159a0001c0001t0003g0161 | 2 | HG02109.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.172-1100G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199225 | ||||||
| chr13:114199227
|
C | T | 2 | a0001c0001t0003g0159a0001c0001t0003g0161 | 2 | HG02109.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.172-1098C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199227 | ||||||
| chr13:114199229
|
C | G | 2 | a0001c0001t0003g0159a0001c0001t0003g0161 | 2 | HG02109.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.172-1096C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199229 | ||||||
| chr13:114199230
|
G | T | 1 | a0001c0001t0002g0304 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.172-1095G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199230 | ||||||
| chr13:114199235
|
C | CGTGCTTA others(32): Show |
2 | a0001c0001t0001g0188a0001c0001t0003g0175 | 2 | HG02080.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.172-1087_172-1086i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199235 | |||||
| chr13:114199235
|
C | CGTGCTTA others(266): Show |
4 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 6 | HG01069.hp1 HG01071.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-1087_172-1086i others(275): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199235 | |||||
| chr13:114199235
|
C | T | 2 | a0001c0001t0003g0159a0001c0001t0003g0161 | 2 | HG02109.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.172-1090C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199235 | ||||||
| chr13:114199239
|
G | C | 140 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(137): Show | 157 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.172-1086G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199239 | ||||||
| chr13:114199239
|
G | T | 69 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(66): Show | 77 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.172-1086G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199239 | ||||||
| chr13:114199240
|
G | A | 11 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(8): Show | 14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-1085G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199240 | ||||||
| chr13:114199240
|
G | T | 85 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(82): Show | 91 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.172-1085G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199240 | ||||||
| chr13:114199242
|
A | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(5): Show | 10 | HG01069.hp1 HG01071.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-1083A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199242 | ||||||
| chr13:114199251
|
A | G | 227 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(224): Show | 257 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.172-1074A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199251 | ||||||
| chr13:114199253
|
T | C | 18 | a0001c0001t0001g0047a0001c0001t0001g0079a0001c0001t0001g0324others(15): Show | 21 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.172-1072T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199253 | ||||||
| chr13:114199256
|
G | A | 19 | a0001c0001t0001g0039a0001c0001t0001g0114a0001c0001t0001g0220others(16): Show | 19 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.172-1069G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199256 | ||||||
| chr13:114199258
|
C | G | 152 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(149): Show | 170 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.172-1067C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199258 | ||||||
| chr13:114199264
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-1061G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199264 | ||||||
| chr13:114199266
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.172-1059C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199266 | ||||||
| chr13:114199268
|
C | T | 4 | a0001c0001t0001g0188a0001c0001t0003g0159a0001c0001t0003g0161others(1): Show | 4 | HG02080.hp2 HG02109.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-1057C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199268 | ||||||
| chr13:114199269
|
T | G | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(279): Show | 320 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.172-1056T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199269 | ||||||
| chr13:114199278
|
G | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(118): Show | 144 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.172-1047G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199278 | ||||||
| chr13:114199278
|
G | T | 134 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0034others(131): Show | 144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.172-1047G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199278 | ||||||
| chr13:114199279
|
G | T | 42 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(39): Show | 55 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.172-1046G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199279 | ||||||
| chr13:114199290
|
G | A | 11 | a0001c0001t0001g0079a0001c0001t0002g0032a0001c0001t0002g0304others(8): Show | 14 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-1035G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199290 | ||||||
| chr13:114199292
|
C | T | 269 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(266): Show | 306 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.172-1033C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199292 | ||||||
| chr13:114199295
|
G | A | 12 | a0001c0001t0001g0223a0001c0001t0004g0001a0001c0001t0004g0007others(9): Show | 14 | HG00673.hp1 HG02083.hp2 HG02976.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-1030G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199295 | ||||||
| chr13:114199297
|
C | G | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(147): Show | 173 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.172-1028C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199297 | ||||||
| chr13:114199303
|
G | A | 9 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(6): Show | 9 | HG02080.hp2 HG02109.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-1022G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199303 | ||||||
| chr13:114199305
|
C | G | 4 | a0001c0001t0001g0196a0001c0001t0001g0209a0001c0001t0001g0271others(1): Show | 4 | HG01243.hp2 HG02280.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1020C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199305 | ||||||
| chr13:114199307
|
C | T | 4 | a0001c0001t0001g0188a0001c0001t0003g0159a0001c0001t0003g0161others(1): Show | 4 | HG02080.hp2 HG02109.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-1018C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199307 | ||||||
| chr13:114199308
|
G | T | 2 | a0001c0001t0002g0032a0001c0001t0007g0041 | 3 | HG00323.hp2 HG02148.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.172-1017G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199308 | ||||||
| chr13:114199313
|
C | CGTGCTTA others(32): Show |
2 | a0001c0001t0003g0158a0001c0001t0003g0162 | 2 | NA18977.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.172-1009_172-1008i others(41): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199313 | |||||
| chr13:114199313
|
C | CGTGCTTA others(266): Show |
3 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0048 | 4 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1009_172-1008i others(275): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199313 | |||||
| chr13:114199317
|
G | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(99): Show | 117 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.172-1008G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199317 | ||||||
| chr13:114199317
|
G | T | 110 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0027others(107): Show | 122 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.172-1008G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199317 | ||||||
| chr13:114199318
|
G | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0039others(49): Show | 59 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.172-1007G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199318 | ||||||
| chr13:114199320
|
A | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0048others(2): Show | 6 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1005A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199320 | ||||||
| chr13:114199329
|
A | G | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(279): Show | 320 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.172-996A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199329 | ||||||
| chr13:114199331
|
T | C | 64 | a0001c0001t0001g0047a0001c0001t0001g0078a0001c0001t0001g0080others(61): Show | 73 | HG00323.hp2 HG00423.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.172-994T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199331 | ||||||
| chr13:114199334
|
G | A | 2 | a0001c0001t0001g0267a0001c0001t0004g0244 | 2 | HG00140.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.172-991G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199334 | ||||||
| chr13:114199336
|
C | CGTGACGG others(501): Show |
1 | a0001c0001t0001g0238 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.172-970_172-969ins others(508): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199336 | |||||
| chr13:114199336
|
C | G | 153 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(150): Show | 175 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.172-989C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199336 | ||||||
| chr13:114199342
|
G | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0115a0001c0001t0001g0188others(3): Show | 6 | HG02080.hp2 HG02109.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-983G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199342 | ||||||
| chr13:114199344
|
C | G | 41 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0034others(38): Show | 43 | HG00408.hp2 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.172-981C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199344 | ||||||
| chr13:114199344
|
C | T | 5 | a0001c0001t0001g0115a0001c0001t0001g0188a0001c0001t0003g0159others(2): Show | 5 | HG02080.hp2 HG02109.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-981C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199344 | ||||||
| chr13:114199346
|
C | CGTCCCCG others(71): Show |
2 | a0001c0001t0003g0167a0001c0001t0003g0168 | 2 | NA19058.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.172-970_172-969ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199346 | |||||
| chr13:114199346
|
C | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0188a0001c0001t0003g0159others(2): Show | 5 | HG02080.hp2 HG02109.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-979C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199346 | ||||||
| chr13:114199346
|
C | T | 2 | a0001c0001t0003g0158a0001c0001t0003g0162 | 2 | NA18977.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.172-979C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199346 | ||||||
| chr13:114199352
|
C | CGTGCTTA others(151): Show |
1 | a0001c0001t0003g0169 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.172-970_172-969ins others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199352 | |||||
| chr13:114199352
|
C | CGTGCTTA others(150): Show |
1 | a0001c0001t0003g0182 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.172-970_172-969ins others(157): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199352 | |||||
| chr13:114199352
|
C | CGTGCTTA others(149): Show |
47 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0012others(44): Show | 55 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.172-970_172-969ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199352 | |||||
| chr13:114199352
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(6): Show | 11 | HG01069.hp1 HG01071.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-973C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199352 | ||||||
| chr13:114199356
|
G | C | 95 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0017others(92): Show | 111 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.172-969G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199356 | ||||||
| chr13:114199356
|
G | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(125): Show | 145 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.172-969G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199356 | ||||||
| chr13:114199357
|
G | A | 11 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(8): Show | 14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-968G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199357 | ||||||
| chr13:114199357
|
G | GTACGGTC others(461): Show |
2 | a0001c0001t0004g0230a0001c0001t0004g0264 | 2 | HG01928.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.172-956_172-955ins others(468): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199357 | |||||
| chr13:114199357
|
G | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(20): Show | 28 | HG00544.hp2 HG00673.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.172-968G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199357 | ||||||
| chr13:114199359
|
A | T | 54 | a0001c0001t0001g0115a0001c0001t0001g0188a0001c0001t0003g0005others(51): Show | 62 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.172-966A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199359 | ||||||
| chr13:114199368
|
G | A | 2 | a0001c0001t0002g0032a0001c0001t0002g0273 | 3 | HG00323.hp2 HG01074.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.172-957G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199368 | ||||||
| chr13:114199368
|
G | C | 7 | a0001c0001t0001g0027a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 8 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-957G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199368 | ||||||
| chr13:114199370
|
C | T | 268 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(265): Show | 304 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.172-955C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199370 | ||||||
| chr13:114199373
|
G | A | 2 | a0001c0001t0004g0008a0001c0001t0004g0254 | 2 | HG00544.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.172-952G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199373 | ||||||
| chr13:114199375
|
C | G | 160 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(157): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.172-950C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199375 | ||||||
| chr13:114199381
|
G | A | 62 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(59): Show | 70 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(67): Show |
intron_variant | MODIFIER | c.172-944G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199381 | ||||||
| chr13:114199383
|
C | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.172-942C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199383 | ||||||
| chr13:114199383
|
C | T | 5 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG03491.hp1 HG03831.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-942C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199383 | ||||||
| chr13:114199385
|
C | CGTCCCCG others(188): Show |
8 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(5): Show | 10 | HG00544.hp1 HG00558.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-931_172-930ins others(195): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199385 | |||||
| chr13:114199385
|
C | G | 5 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG03491.hp1 HG03831.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-940C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199385 | ||||||
| chr13:114199385
|
C | T | 58 | a0001c0001t0001g0115a0001c0001t0001g0188a0001c0001t0003g0005others(55): Show | 66 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.172-940C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199385 | ||||||
| chr13:114199386
|
G | T | 1 | a0001c0001t0002g0273 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.172-939G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199386 | ||||||
| chr13:114199391
|
C | CGTGCTTA others(32): Show |
1 | a0001c0001t0001g0079 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.172-931_172-930ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199391 | |||||
| chr13:114199391
|
C | T | 5 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG03491.hp1 HG03831.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-934C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199391 | ||||||
| chr13:114199395
|
G | C | 130 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(127): Show | 149 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.172-930G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199395 | ||||||
| chr13:114199395
|
G | T | 72 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0045others(69): Show | 79 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.172-930G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199395 | ||||||
| chr13:114199396
|
G | T | 44 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(41): Show | 51 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.172-929G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199396 | ||||||
| chr13:114199398
|
A | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-927A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199398 | ||||||
| chr13:114199401
|
G | T | 1 | a0001c0001t0002g0300 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.172-924G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199401 | ||||||
| chr13:114199408
|
CCGAGGCG others(539): Show |
C | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.172-916_172-371del | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199408 | ||||||
| chr13:114199409
|
C | CGAGGCGT others(305): Show |
1 | a0001c0001t0001g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.172-892_172-891ins others(312): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199409 | |||||
| chr13:114199409
|
C | T | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(210): Show | 240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.172-916C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199409 | ||||||
| chr13:114199412
|
G | A | 1 | a0001c0001t0004g0253 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.172-913G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199412 | ||||||
| chr13:114199414
|
C | G | 125 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0039others(122): Show | 137 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-911C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199414 | ||||||
| chr13:114199420
|
G | A | 4 | a0001c0001t0003g0158a0001c0001t0003g0162a0001c0001t0003g0167others(1): Show | 4 | NA18977.hp1 NA19000.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-905G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199420 | ||||||
| chr13:114199422
|
C | G | 36 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0001g0067others(33): Show | 41 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.172-903C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199422 | ||||||
| chr13:114199422
|
C | T | 4 | a0001c0001t0003g0158a0001c0001t0003g0162a0001c0001t0003g0167others(1): Show | 4 | NA18977.hp1 NA19000.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-903C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199422 | ||||||
| chr13:114199424
|
C | G | 4 | a0001c0001t0003g0158a0001c0001t0003g0162a0001c0001t0003g0167others(1): Show | 4 | NA18977.hp1 NA19000.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-901C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199424 | ||||||
| chr13:114199424
|
C | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-901C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199424 | ||||||
| chr13:114199425
|
G | GTCCCCGT others(71): Show |
1 | a0001c0001t0002g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.172-880_172-879ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199425 | |||||
| chr13:114199430
|
C | CGTGCTTA others(149): Show |
1 | a0001c0001t0003g0191 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.172-892_172-891ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199430 | |||||
| chr13:114199430
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(8): Show | 14 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.172-895C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199430 | ||||||
| chr13:114199434
|
G | C | 149 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0017others(146): Show | 173 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.172-891G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199434 | ||||||
| chr13:114199434
|
G | T | 87 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(84): Show | 96 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.172-891G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199434 | ||||||
| chr13:114199435
|
G | T | 104 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0017others(101): Show | 122 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.172-890G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199435 | ||||||
| chr13:114199437
|
A | T | 5 | a0001c0001t0003g0158a0001c0001t0003g0162a0001c0001t0003g0167others(2): Show | 5 | NA18955.hp1 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-888A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199437 | ||||||
| chr13:114199446
|
A | G | 268 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(265): Show | 303 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.172-879A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199446 | ||||||
| chr13:114199448
|
T | C | 3 | a0001c0001t0001g0324a0001c0001t0002g0318a0001c0001t0010g0325 | 3 | HG00558.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-877T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199448 | ||||||
| chr13:114199453
|
C | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(174): Show | 208 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.172-872C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199453 | ||||||
| chr13:114199459
|
G | A | 77 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(74): Show | 89 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.172-866G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199459 | ||||||
| chr13:114199461
|
C | G | 22 | a0001c0001t0001g0039a0001c0001t0001g0082a0001c0001t0001g0114others(19): Show | 22 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.172-864C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199461 | ||||||
| chr13:114199461
|
C | T | 66 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(63): Show | 78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.172-864C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199461 | ||||||
| chr13:114199463
|
C | G | 66 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(63): Show | 78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.172-862C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199463 | ||||||
| chr13:114199463
|
C | T | 11 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(8): Show | 11 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-862C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199463 | ||||||
| chr13:114199464
|
T | G | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(280): Show | 321 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.172-861T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199464 | ||||||
| chr13:114199469
|
C | T | 66 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(63): Show | 78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.172-856C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199469 | ||||||
| chr13:114199473
|
G | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(52): Show | 68 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.172-852G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199473 | ||||||
| chr13:114199473
|
G | T | 137 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0039others(134): Show | 156 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.172-852G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199473 | ||||||
| chr13:114199474
|
G | T | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(18): Show | 25 | HG00558.hp2 HG00733.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.172-851G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199474 | ||||||
| chr13:114199476
|
A | T | 66 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(63): Show | 78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.172-849A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199476 | ||||||
| chr13:114199487
|
C | T | 267 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(264): Show | 302 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.172-838C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199487 | ||||||
| chr13:114199490
|
G | A | 19 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(16): Show | 23 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.172-835G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199490 | ||||||
| chr13:114199492
|
C | G | 118 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(115): Show | 128 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.172-833C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199492 | ||||||
| chr13:114199498
|
G | A | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-827G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199498 | ||||||
| chr13:114199500
|
C | G | 15 | a0001c0001t0001g0223a0001c0001t0004g0001a0001c0001t0004g0007others(12): Show | 17 | HG00673.hp1 HG01928.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.172-825C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199500 | ||||||
| chr13:114199500
|
C | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-825C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199500 | ||||||
| chr13:114199502
|
C | G | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-823C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199502 | ||||||
| chr13:114199508
|
C | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0047others(7): Show | 11 | HG01496.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-817C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199508 | ||||||
| chr13:114199512
|
G | C | 137 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(134): Show | 159 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.172-813G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199512 | ||||||
| chr13:114199512
|
G | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0039others(62): Show | 74 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.172-813G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199512 | ||||||
| chr13:114199513
|
G | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0017others(50): Show | 61 | HG00323.hp2 HG00733.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.172-812G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199513 | ||||||
| chr13:114199515
|
A | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-810A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199515 | ||||||
| chr13:114199524
|
A | G | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(279): Show | 320 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.172-801A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199524 | ||||||
| chr13:114199526
|
T | C | 4 | a0001c0001t0001g0115a0001c0001t0001g0324a0001c0001t0003g0170others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-799T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199526 | ||||||
| chr13:114199529
|
G | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0073others(11): Show | 15 | HG01258.hp2 HG01516.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-796G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199529 | ||||||
| chr13:114199531
|
C | G | 219 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(216): Show | 242 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.172-794C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199531 | ||||||
| chr13:114199537
|
G | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(15): Show | 21 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.172-788G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199537 | ||||||
| chr13:114199539
|
C | G | 2 | a0001c0001t0001g0267a0001c0001t0004g0244 | 2 | HG00140.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.172-786C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199539 | ||||||
| chr13:114199539
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(9): Show | 15 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.172-786C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199539 | ||||||
| chr13:114199541
|
C | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(9): Show | 15 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.172-784C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199541 | ||||||
| chr13:114199541
|
C | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-784C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199541 | ||||||
| chr13:114199547
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(9): Show | 15 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.172-778C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199547 | ||||||
| chr13:114199551
|
T | C | 104 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(101): Show | 120 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.172-774T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199551 | ||||||
| chr13:114199551
|
T | G | 47 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0001g0067others(44): Show | 52 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.172-774T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199551 | ||||||
| chr13:114199552
|
G | T | 126 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(123): Show | 143 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.172-773G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199552 | ||||||
| chr13:114199554
|
A | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(9): Show | 15 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.172-771A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199554 | ||||||
| chr13:114199563
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-762G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199563 | ||||||
| chr13:114199563
|
G | T | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.172-762G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199563 | ||||||
| chr13:114199565
|
C | T | 269 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(266): Show | 306 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.172-760C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199565 | ||||||
| chr13:114199570
|
C | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(152): Show | 176 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.172-755C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199570 | ||||||
| chr13:114199576
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-749G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199576 | ||||||
| chr13:114199578
|
C | G | 29 | a0001c0001t0001g0039a0001c0001t0001g0114a0001c0001t0001g0220others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.172-747C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199578 | ||||||
| chr13:114199578
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-747C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199578 | ||||||
| chr13:114199580
|
C | G | 1 | a0001c0001t0003g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-745C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199580 | ||||||
| chr13:114199586
|
C | T | 61 | a0001c0001t0001g0047a0001c0001t0001g0188a0001c0001t0003g0005others(58): Show | 71 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.172-739C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199586 | ||||||
| chr13:114199590
|
C | CT | 11 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(8): Show | 14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-733dupT | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199590 | |||||
| chr13:114199590
|
C | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0218others(3): Show | 9 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-735C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199590 | ||||||
| chr13:114199590
|
C | T | 65 | a0001c0001t0001g0028a0001c0001t0001g0057a0001c0001t0001g0067others(62): Show | 71 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.172-735C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199590 | ||||||
| chr13:114199591
|
T | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(81): Show | 97 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.172-734T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199591 | ||||||
| chr13:114199593
|
A | ACGGTCCC others(32): Show |
3 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0048 | 4 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-717_172-716ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199593 | |||||
| chr13:114199593
|
A | ACGGTCCC others(110): Show |
1 | a0001c0001t0001g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.172-717_172-716ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199593 | |||||
| chr13:114199593
|
A | T | 1 | a0001c0001t0003g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-732A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199593 | ||||||
| chr13:114199604
|
T | C | 5 | a0001c0001t0001g0324a0001c0001t0002g0279a0001c0001t0002g0291others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-721T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199604 | ||||||
| chr13:114199607
|
G | A | 20 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0123others(17): Show | 23 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.172-718G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199607 | ||||||
| chr13:114199609
|
C | CGTGACGG others(71): Show |
2 | a0001c0001t0002g0289a0001c0001t0002g0329 | 2 | HG00673.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.172-683_172-682ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199609 | |||||
| chr13:114199609
|
C | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(177): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.172-716C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199609 | ||||||
| chr13:114199615
|
G | A | 7 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(4): Show | 7 | HG03225.hp1 HG03491.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.172-710G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199615 | ||||||
| chr13:114199617
|
C | G | 16 | a0001c0001t0001g0223a0001c0001t0004g0001a0001c0001t0004g0007others(13): Show | 18 | HG00673.hp1 HG01928.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.172-708C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199617 | ||||||
| chr13:114199617
|
C | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-708C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199617 | ||||||
| chr13:114199619
|
C | G | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-706C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199619 | ||||||
| chr13:114199619
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-706C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199619 | ||||||
| chr13:114199625
|
C | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-700C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199625 | ||||||
| chr13:114199629
|
C | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0324a0001c0001t0010g0325 | 3 | HG01167.hp2 HG01169.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.172-696C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199629 | ||||||
| chr13:114199629
|
C | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0034others(61): Show | 71 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(68): Show |
intron_variant | MODIFIER | c.172-696C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199629 | ||||||
| chr13:114199630
|
G | T | 54 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0001g0067others(51): Show | 62 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.172-695G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199630 | ||||||
| chr13:114199632
|
A | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-693A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199632 | ||||||
| chr13:114199643
|
C | CGAGGCGT others(149): Show |
1 | a0001c0001t0002g0287 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.172-657_172-656ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199643 | |||||
| chr13:114199643
|
C | CGAGGCGT others(188): Show |
1 | a0001c0001t0002g0319 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.172-658_172-657ins others(195): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199643 | |||||
| chr13:114199643
|
C | T | 281 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(278): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.172-682C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199643 | ||||||
| chr13:114199645
|
A | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 9 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-680A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199645 | ||||||
| chr13:114199647
|
G | T | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.172-678G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199647 | ||||||
| chr13:114199648
|
C | CGTGACAG others(71): Show |
6 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0343others(3): Show | 9 | HG00642.hp2 HG01361.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-672_172-671ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199648 | |||||
| chr13:114199648
|
C | CGTGACAG others(149): Show |
5 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0347others(2): Show | 5 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-672_172-671ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199648 | |||||
| chr13:114199648
|
C | G | 187 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(184): Show | 209 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.172-677C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199648 | ||||||
| chr13:114199649
|
G | A | 1 | a0001c0001t0008g0091 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.172-676G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199649 | ||||||
| chr13:114199654
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-671G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199654 | ||||||
| chr13:114199656
|
C | G | 2 | a0001c0001t0001g0267a0001c0001t0004g0244 | 2 | HG00140.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.172-669C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199656 | ||||||
| chr13:114199658
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-667C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199658 | ||||||
| chr13:114199660
|
T | TCCCCGTG others(151): Show |
1 | a0001c0001t0002g0302 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.172-657_172-656ins others(158): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199660 | |||||
| chr13:114199664
|
C | T | 6 | a0001c0001t0001g0188a0001c0001t0003g0158a0001c0001t0003g0162others(3): Show | 6 | HG04115.hp2 NA18955.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-661C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199664 | ||||||
| chr13:114199668
|
C | G | 1 | a0001c0001t0003g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-657C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199668 | ||||||
| chr13:114199668
|
C | T | 20 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(17): Show | 20 | HG00544.hp2 HG00609.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.172-657C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199668 | ||||||
| chr13:114199669
|
T | G | 230 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0017others(227): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.172-656T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199669 | ||||||
| chr13:114199669
|
T | TTACGGTC others(149): Show |
1 | a0001c0001t0002g0292 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.172-644_172-643ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199669 | |||||
| chr13:114199669
|
T | TTACGGTC others(110): Show |
1 | a0001c0001t0002g0327 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.172-561_172-560ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199669 | |||||
| chr13:114199669
|
T | TTACGGTC others(110): Show |
1 | a0001c0001t0002g0311 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.172-579_172-578ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199669 | |||||
| chr13:114199669
|
T | TTACGGTC others(150): Show |
1 | a0001c0001t0002g0315 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.172-579_172-578ins others(157): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199669 | |||||
| chr13:114199669
|
T | TTACGGTC others(149): Show |
45 | a0001c0001t0001g0106a0001c0001t0002g0002a0001c0001t0002g0009others(42): Show | 54 | HG00609.hp1 HG00642.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.172-579_172-578ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199669 | |||||
| chr13:114199669
|
T | TTACGGTC others(32): Show |
1 | a0001c0001t0002g0318 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.172-639_172-638ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199669 | |||||
| chr13:114199671
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.172-654A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199671 | ||||||
| chr13:114199675
|
T | TCCCCGCT others(150): Show |
2 | a0001c0001t0002g0275a0001c0001t0002g0295 | 2 | HG02056.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.172-579_172-578ins others(157): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199675 | |||||
| chr13:114199681
|
CTGAGGCG others(188): Show |
C | 3 | a0001c0001t0001g0126a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | HG00140.hp2 HG01255.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.172-617_172-423del | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199681 | |||||
| chr13:114199682
|
T | C | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-643T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199682 | ||||||
| chr13:114199687
|
C | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(193): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.172-638C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199687 | ||||||
| chr13:114199693
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0003g0170a0001c0001t0006g0342 | 3 | HG03225.hp1 HG03942.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.172-632G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199693 | ||||||
| chr13:114199695
|
C | G | 9 | a0001c0001t0004g0008a0001c0001t0004g0241a0001c0001t0004g0245others(6): Show | 9 | HG00544.hp2 HG00609.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-630C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199695 | ||||||
| chr13:114199695
|
C | T | 3 | a0001c0001t0001g0115a0001c0001t0003g0170a0001c0001t0006g0342 | 3 | HG03225.hp1 HG03942.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.172-630C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199695 | ||||||
| chr13:114199697
|
C | G | 3 | a0001c0001t0001g0115a0001c0001t0003g0170a0001c0001t0006g0342 | 3 | HG03225.hp1 HG03942.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.172-628C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199697 | ||||||
| chr13:114199703
|
C | T | 63 | a0001c0001t0001g0115a0001c0001t0003g0005a0001c0001t0003g0006others(60): Show | 73 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.172-622C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199703 | ||||||
| chr13:114199707
|
C | T | 12 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(9): Show | 12 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.172-618C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199707 | ||||||
| chr13:114199708
|
G | T | 75 | a0001c0001t0001g0018a0001c0001t0001g0077a0001c0001t0001g0125others(72): Show | 89 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.172-617G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199708 | ||||||
| chr13:114199710
|
A | T | 3 | a0001c0001t0001g0115a0001c0001t0003g0170a0001c0001t0006g0342 | 3 | HG03225.hp1 HG03942.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.172-615A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199710 | ||||||
| chr13:114199721
|
T | C | 3 | a0001c0001t0001g0115a0001c0001t0001g0324a0001c0001t0010g0325 | 3 | HG01167.hp2 HG01169.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.172-604T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199721 | ||||||
| chr13:114199726
|
G | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0039others(52): Show | 60 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.172-599G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199726 | ||||||
| chr13:114199732
|
G | A | 61 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0012others(58): Show | 71 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.172-593G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199732 | ||||||
| chr13:114199734
|
C | G | 35 | a0001c0001t0001g0039a0001c0001t0001g0114a0001c0001t0001g0220others(32): Show | 37 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.172-591C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199734 | ||||||
| chr13:114199734
|
C | T | 60 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0012others(57): Show | 70 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.172-591C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199734 | ||||||
| chr13:114199736
|
C | G | 60 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0012others(57): Show | 70 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.172-589C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199736 | ||||||
| chr13:114199736
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.172-589C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199736 | ||||||
| chr13:114199742
|
C | T | 66 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(63): Show | 76 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.172-583C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199742 | ||||||
| chr13:114199743
|
G | GTGCTTAC others(1012): Show |
1 | a0001c0001t0002g0305 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.172-579_172-578ins others(1019): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199743 | |||||
| chr13:114199743
|
G | GTGCTTAC others(1008): Show |
1 | a0001c0001t0002g0306 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.172-579_172-578ins others(1015): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199743 | |||||
| chr13:114199743
|
G | GTGCTTAC others(1007): Show |
2 | a0001c0001t0002g0312a0001c0001t0002g0316 | 2 | HG01884.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.172-579_172-578ins others(1014): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199743 | |||||
| chr13:114199743
|
G | T | 1 | a0001c0001t0008g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.172-582G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199743 | ||||||
| chr13:114199746
|
C | G | 4 | a0001c0001t0001g0115a0001c0001t0001g0324a0001c0001t0003g0170others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-579C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199746 | ||||||
| chr13:114199746
|
C | T | 60 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0012others(57): Show | 70 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.172-579C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199746 | ||||||
| chr13:114199747
|
G | T | 28 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(25): Show | 31 | HG00642.hp2 HG01361.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.172-578G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199747 | ||||||
| chr13:114199749
|
A | ACGGTCCC others(71): Show |
3 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0345 | 6 | HG00642.hp2 HG02273.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-540_172-539ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199749 | |||||
| chr13:114199749
|
A | T | 60 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0012others(57): Show | 70 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.172-576A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199749 | ||||||
| chr13:114199760
|
T | C | 64 | a0001c0001t0001g0115a0001c0001t0001g0324a0001c0001t0003g0005others(61): Show | 74 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.172-565T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199760 | ||||||
| chr13:114199760
|
T | TGAGGCGT others(71): Show |
1 | a0001c0001t0003g0191 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.172-561_172-560ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199760 | |||||
| chr13:114199765
|
G | C | 139 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(136): Show | 159 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.172-560G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199765 | ||||||
| chr13:114199765
|
G | GGTGACGG others(32): Show |
2 | a0001c0001t0002g0278a0001c0001t0002g0339 | 2 | HG01928.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.172-527_172-489dup others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199765 | |||||
| chr13:114199771
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0128 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.172-554G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199771 | ||||||
| chr13:114199773
|
C | G | 25 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(22): Show | 30 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.172-552C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199773 | ||||||
| chr13:114199775
|
C | T | 5 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0347others(2): Show | 5 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-550C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199775 | ||||||
| chr13:114199781
|
C | T | 5 | a0001c0001t0001g0188a0001c0001t0003g0158a0001c0001t0003g0162others(2): Show | 5 | HG04115.hp2 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-544C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199781 | ||||||
| chr13:114199785
|
C | CTTACGGT others(149): Show |
3 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0137 | 3 | HG01243.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.172-540_172-539ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199785 | ||||||
| chr13:114199785
|
C | G | 63 | a0001c0001t0001g0324a0001c0001t0003g0005a0001c0001t0003g0006others(60): Show | 73 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.172-540C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199785 | ||||||
| chr13:114199785
|
C | T | 14 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0118others(11): Show | 16 | HG00733.hp1 HG00741.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.172-540C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199785 | ||||||
| chr13:114199786
|
G | T | 20 | a0001c0001t0001g0115a0001c0001t0001g0188a0001c0001t0003g0158others(17): Show | 23 | HG00099.hp2 HG00642.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.172-539G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199786 | ||||||
| chr13:114199798
|
CTGAGGCG others(149): Show |
C | 1 | a0001c0001t0002g0042 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.172-500_172-345del | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199798 | |||||
| chr13:114199799
|
T | C | 63 | a0001c0001t0001g0324a0001c0001t0003g0005a0001c0001t0003g0006others(60): Show | 73 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.172-526T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199799 | ||||||
| chr13:114199804
|
C | CGTGACGG others(110): Show |
1 | a0001c0001t0002g0326 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.172-489_172-488ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199804 | |||||
| chr13:114199804
|
C | CGTGACGG others(71): Show |
11 | a0001c0001t0001g0073a0001c0001t0001g0267a0001c0001t0004g0008others(8): Show | 11 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-514_172-513ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199804 | |||||
| chr13:114199804
|
C | CGTGACGG others(305): Show |
3 | a0001c0001t0004g0040a0001c0001t0004g0226a0001c0001t0004g0242 | 3 | NA18990.hp1 NA19075.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.172-514_172-513ins others(312): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199804 | |||||
| chr13:114199804
|
C | CGTGACGG others(305): Show |
3 | a0001c0001t0004g0001a0001c0001t0004g0007a0001c0001t0013g0104 | 6 | HG02129.hp2 HG02155.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-514_172-513ins others(312): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199804 | |||||
| chr13:114199804
|
C | CGTGACGG others(344): Show |
5 | a0001c0001t0001g0228a0001c0001t0001g0233a0001c0001t0001g0243others(2): Show | 5 | HG00733.hp2 HG03471.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-514_172-513ins others(351): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199804 | |||||
| chr13:114199804
|
C | CGTGACGG others(305): Show |
1 | a0001c0001t0004g0240 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.172-514_172-513ins others(312): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199804 | |||||
| chr13:114199804
|
C | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(141): Show | 156 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.172-521C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199804 | ||||||
| chr13:114199810
|
G | A | 6 | a0001c0001t0001g0115a0001c0001t0001g0188a0001c0001t0003g0170others(3): Show | 6 | HG01361.hp2 HG01993.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-515G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199810 | ||||||
| chr13:114199812
|
C | G | 11 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0077others(8): Show | 12 | HG01258.hp2 HG01516.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-513C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199812 | ||||||
| chr13:114199812
|
C | T | 6 | a0001c0001t0001g0115a0001c0001t0001g0188a0001c0001t0003g0170others(3): Show | 6 | HG01361.hp2 HG01993.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-513C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199812 | ||||||
| chr13:114199814
|
C | G | 6 | a0001c0001t0001g0115a0001c0001t0001g0188a0001c0001t0003g0170others(3): Show | 6 | HG01361.hp2 HG01993.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-511C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199814 | ||||||
| chr13:114199814
|
C | T | 5 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0347others(2): Show | 5 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-511C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199814 | ||||||
| chr13:114199820
|
C | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(13): Show | 18 | HG01069.hp1 HG01071.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.172-505C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199820 | ||||||
| chr13:114199824
|
C | G | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-501C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199824 | ||||||
| chr13:114199824
|
C | T | 38 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(35): Show | 42 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.172-501C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199824 | ||||||
| chr13:114199825
|
G | T | 74 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(71): Show | 89 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.172-500G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199825 | ||||||
| chr13:114199827
|
A | T | 12 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(9): Show | 12 | HG01361.hp2 HG01993.hp2 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-498A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199827 | ||||||
| chr13:114199837
|
A | C | 347 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(344): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.172-488A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199837 | ||||||
| chr13:114199838
|
T | C | 4 | a0001c0001t0001g0188a0001c0001t0001g0324a0001c0001t0008g0083others(1): Show | 4 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-487T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199838 | ||||||
| chr13:114199843
|
G | C | 33 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0044others(30): Show | 35 | HG00099.hp2 HG00558.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.172-482G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199843 | ||||||
| chr13:114199843
|
G | GGTGACAG others(71): Show |
4 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 6 | HG01069.hp1 HG01071.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-477_172-476ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199843 | |||||
| chr13:114199843
|
GGTGACGG others(32): Show |
G | 1 | a0001c0001t0002g0032 | 2 | HG00323.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.172-349_172-311del others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199843 | |||||
| chr13:114199849
|
G | A | 65 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(62): Show | 77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.172-476G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199849 | ||||||
| chr13:114199851
|
C | CGCGTCCC others(32): Show |
1 | a0001c0001t0001g0133 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.172-462_172-461ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199851 | |||||
| chr13:114199851
|
C | T | 65 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(62): Show | 77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.172-474C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199851 | ||||||
| chr13:114199853
|
C | CGTCCCTG others(110): Show |
4 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0047others(1): Show | 5 | HG01496.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-467_172-466ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199853 | |||||
| chr13:114199853
|
C | G | 65 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0050others(62): Show | 77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.172-472C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199853 | ||||||
| chr13:114199853
|
C | T | 1 | a0001c0001t0006g0342 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.172-472C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199853 | ||||||
| chr13:114199859
|
C | T | 59 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0012others(56): Show | 69 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.172-466C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199859 | ||||||
| chr13:114199860
|
G | T | 41 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0058others(38): Show | 45 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.172-465G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199860 | ||||||
| chr13:114199863
|
C | CGTACGGT others(32): Show |
1 | a0001c0001t0001g0109 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.172-462_172-461ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199863 | ||||||
| chr13:114199863
|
C | CGTACGGT others(32): Show |
1 | a0001c0001t0001g0223 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.172-462_172-461ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199863 | ||||||
| chr13:114199863
|
C | G | 3 | a0001c0001t0001g0188a0001c0001t0001g0324a0001c0001t0010g0325 | 3 | HG01167.hp2 HG01169.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.172-462C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199863 | ||||||
| chr13:114199863
|
C | T | 63 | a0001c0001t0001g0077a0001c0001t0001g0125a0001c0001t0003g0005others(60): Show | 73 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.172-462C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199863 | ||||||
| chr13:114199864
|
T | G | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(272): Show | 309 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.172-461T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199864 | ||||||
| chr13:114199866
|
A | T | 61 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0012others(58): Show | 71 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.172-459A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199866 | ||||||
| chr13:114199876
|
A | C | 346 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(343): Show | 392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.172-449A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199876 | ||||||
| chr13:114199877
|
T | C | 3 | a0001c0001t0001g0188a0001c0001t0001g0324a0001c0001t0010g0325 | 3 | HG01167.hp2 HG01169.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.172-448T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199877 | ||||||
| chr13:114199882
|
C | CGTGACGG others(855): Show |
1 | a0001c0001t0002g0315 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.172-411_172-410ins others(862): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199882 | |||||
| chr13:114199882
|
C | CGTGACGG others(71): Show |
1 | a0001c0001t0001g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.172-436_172-435ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199882 | |||||
| chr13:114199882
|
C | CGTGACGG others(110): Show |
1 | a0001c0004t0001g0053 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.172-436_172-435ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199882 | |||||
| chr13:114199882
|
C | CGTGACGG others(149): Show |
1 | a0001c0001t0001g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.172-436_172-435ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199882 | |||||
| chr13:114199882
|
C | G | 199 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(196): Show | 223 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.172-443C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199882 | ||||||
| chr13:114199892
|
C | T | 4 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0342others(1): Show | 7 | HG00642.hp2 HG02273.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-433C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199892 | ||||||
| chr13:114199898
|
C | T | 4 | a0001c0001t0003g0158a0001c0001t0003g0162a0001c0001t0003g0167others(1): Show | 4 | NA18977.hp1 NA19000.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-427C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199898 | ||||||
| chr13:114199902
|
C | G | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-423C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199902 | ||||||
| chr13:114199902
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(5): Show | 11 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-423C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199902 | ||||||
| chr13:114199903
|
T | G | 216 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(213): Show | 245 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.172-422T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199903 | ||||||
| chr13:114199905
|
A | ACGGTCCC others(1046): Show |
2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-411_172-410ins others(1053): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199905 | |||||
| chr13:114199915
|
A | C | 350 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(347): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.172-410A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199915 | ||||||
| chr13:114199916
|
T | C | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-409T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199916 | ||||||
| chr13:114199921
|
C | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(120): Show | 142 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.172-404C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199921 | ||||||
| chr13:114199927
|
G | A | 5 | a0001c0001t0001g0188a0001c0001t0003g0158a0001c0001t0003g0162others(2): Show | 5 | HG04115.hp2 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-398G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199927 | ||||||
| chr13:114199929
|
C | T | 5 | a0001c0001t0001g0188a0001c0001t0003g0158a0001c0001t0003g0162others(2): Show | 5 | HG04115.hp2 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-396C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199929 | ||||||
| chr13:114199931
|
C | G | 5 | a0001c0001t0001g0188a0001c0001t0003g0158a0001c0001t0003g0162others(2): Show | 5 | HG04115.hp2 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-394C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199931 | ||||||
| chr13:114199931
|
C | T | 8 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(5): Show | 11 | HG00642.hp2 HG01993.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-394C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199931 | ||||||
| chr13:114199937
|
C | T | 11 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(8): Show | 11 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-388C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199937 | ||||||
| chr13:114199941
|
C | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(16): Show | 22 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.172-384C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199941 | ||||||
| chr13:114199942
|
T | G | 264 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(261): Show | 298 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.172-383T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199942 | ||||||
| chr13:114199942
|
T | TTACGGTC others(149): Show |
1 | a0001c0001t0006g0342 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.172-372_172-371ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199942 | |||||
| chr13:114199942
|
T | TTACGGTC others(71): Show |
4 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0347others(1): Show | 4 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-372_172-371ins others(78): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199942 | |||||
| chr13:114199944
|
A | T | 5 | a0001c0001t0001g0188a0001c0001t0003g0158a0001c0001t0003g0162others(2): Show | 5 | HG04115.hp2 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-381A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199944 | ||||||
| chr13:114199954
|
A | C | 350 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(347): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.172-371A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199954 | ||||||
| chr13:114199955
|
T | C | 4 | a0001c0001t0003g0158a0001c0001t0003g0162a0001c0001t0003g0167others(1): Show | 4 | NA18977.hp1 NA19000.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-370T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199955 | ||||||
| chr13:114199955
|
T | TGAGGGGT others(32): Show |
6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 6 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-366_172-365ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199955 | |||||
| chr13:114199960
|
C | CGTGACGG others(32): Show |
1 | a0001c0001t0002g0330 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.172-346_172-345ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199960 | |||||
| chr13:114199960
|
C | G | 8 | a0001c0001t0001g0115a0001c0001t0006g0010a0001c0001t0006g0033others(5): Show | 11 | HG00642.hp2 HG01361.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-365C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199960 | ||||||
| chr13:114199966
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-359G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199966 | ||||||
| chr13:114199968
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-357C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199968 | ||||||
| chr13:114199969
|
G | T | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG02280.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.172-356G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199969 | ||||||
| chr13:114199970
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-355C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199970 | ||||||
| chr13:114199970
|
C | T | 3 | a0001c0001t0006g0343a0001c0001t0006g0344a0001c0001t0006g0349 | 3 | HG01361.hp2 HG02273.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.172-355C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199970 | ||||||
| chr13:114199976
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-349C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199976 | ||||||
| chr13:114199980
|
C | CT | 9 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(6): Show | 12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.172-343dupT | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199980 | |||||
| chr13:114199980
|
C | G | 10 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(7): Show | 10 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-345C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199980 | ||||||
| chr13:114199980
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-345C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199980 | ||||||
| chr13:114199981
|
T | G | 78 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(75): Show | 88 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.172-344T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199981 | ||||||
| chr13:114199981
|
T | TTACGGTC others(149): Show |
1 | a0001c0001t0006g0343 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.172-333_172-332ins others(156): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199981 | |||||
| chr13:114199981
|
T | TTATGGTC others(32): Show |
5 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342others(2): Show | 5 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-342_172-341ins others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199981 | |||||
| chr13:114199983
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.172-342A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199983 | ||||||
| chr13:114199993
|
A | C | 352 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(349): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.172-332A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199993 | ||||||
| chr13:114199994
|
T | C | 10 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(7): Show | 10 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-331T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199994 | ||||||
| chr13:114199999
|
C | CGTAACAG others(110): Show |
1 | a0001c0001t0006g0349 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.172-324_172-323ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114199999 | |||||
| chr13:114199999
|
C | G | 11 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(8): Show | 14 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-326C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114199999 | ||||||
| chr13:114200004
|
C | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(6): Show | 12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.172-321C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200004 | ||||||
| chr13:114200009
|
C | T | 2 | a0001c0001t0006g0344a0001c0001t0006g0346 | 2 | HG01993.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.172-316C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200009 | ||||||
| chr13:114200015
|
T | C | 85 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(82): Show | 98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.172-310T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200015 | ||||||
| chr13:114200020
|
T | G | 62 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(59): Show | 72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-305T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200020 | ||||||
| chr13:114200023
|
C | T | 7 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342others(4): Show | 7 | HG01361.hp2 HG01993.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.172-302C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200023 | ||||||
| chr13:114200032
|
A | C | 352 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(349): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.172-293A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200032 | ||||||
| chr13:114200038
|
G | C | 62 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(59): Show | 72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-287G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200038 | ||||||
| chr13:114200044
|
A | G | 74 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(71): Show | 87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.172-281A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200044 | ||||||
| chr13:114200046
|
T | C | 74 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(71): Show | 87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.172-279T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200046 | ||||||
| chr13:114200048
|
G | C | 71 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(68): Show | 81 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.172-277G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200048 | ||||||
| chr13:114200048
|
G | T | 3 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0345 | 6 | HG00642.hp2 HG02273.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-277G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200048 | ||||||
| chr13:114200054
|
T | C | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-271T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200054 | ||||||
| chr13:114200056
|
T | TGCTTACG others(304): Show |
1 | a0001c0001t0006g0344 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.172-268_172-267ins others(311): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200056 | |||||
| chr13:114200056
|
T | TGCTTACG others(303): Show |
1 | a0001c0001t0006g0346 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.172-268_172-267ins others(310): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200056 | |||||
| chr13:114200058
|
T | C | 72 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(69): Show | 85 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.172-267T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200058 | ||||||
| chr13:114200059
|
G | T | 72 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(69): Show | 85 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.172-266G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200059 | ||||||
| chr13:114200061
|
T | A | 74 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(71): Show | 87 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.172-264T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200061 | ||||||
| chr13:114200061
|
TCGGTCCC others(32): Show |
T | 2 | a0001c0001t0001g0115a0001c0001t0003g0170 | 2 | HG03225.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.172-252_172-214del others(39): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200061 | |||||
| chr13:114200072
|
T | C | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-253T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200072 | ||||||
| chr13:114200073
|
T | G | 193 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(190): Show | 223 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.172-252T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200073 | ||||||
| chr13:114200077
|
G | C | 12 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG03491.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-248G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200077 | ||||||
| chr13:114200083
|
G | A | 62 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(59): Show | 72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-242G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200083 | ||||||
| chr13:114200085
|
C | T | 62 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(59): Show | 72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-240C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200085 | ||||||
| chr13:114200087
|
T | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(27): Show | 33 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.172-238T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200087 | ||||||
| chr13:114200087
|
T | G | 62 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(59): Show | 72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-238T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200087 | ||||||
| chr13:114200087
|
T | TGTCCCCG others(227): Show |
2 | a0001c0001t0006g0010a0001c0001t0006g0345 | 2 | HG02273.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.172-179_172-178ins others(234): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200087 | |||||
| chr13:114200093
|
C | T | 62 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(59): Show | 72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-232C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200093 | ||||||
| chr13:114200097
|
C | T | 62 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(59): Show | 72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-228C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200097 | ||||||
| chr13:114200098
|
T | G | 72 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(69): Show | 82 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.172-227T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200098 | ||||||
| chr13:114200100
|
A | ACGGTCCC others(111): Show |
1 | a0001c0001t0001g0101 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.172-217_172-216ins others(118): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200100 | |||||
| chr13:114200100
|
A | ACGGTCCC others(110): Show |
4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0081others(1): Show | 4 | HG03491.hp1 HG03704.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-207_172-206ins others(117): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200100 | |||||
| chr13:114200100
|
A | ACGGTCCC others(266): Show |
2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-210_172-209ins others(273): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200100 | |||||
| chr13:114200100
|
A | ACGGTCCC others(188): Show |
3 | a0001c0001t0003g0158a0001c0001t0003g0162a0001c0001t0003g0168 | 3 | NA18977.hp1 NA19000.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.172-210_172-209ins others(195): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200100 | |||||
| chr13:114200100
|
A | T | 62 | a0001c0001t0001g0188a0001c0001t0003g0005a0001c0001t0003g0006others(59): Show | 72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.172-225A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200100 | ||||||
| chr13:114200104
|
T | TCCCCGCT others(112): Show |
1 | a0001c0001t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.172-207_172-206ins others(119): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200104 | |||||
| chr13:114200104
|
T | TCCCCGCT others(189): Show |
1 | a0001c0001t0003g0167 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.172-210_172-209ins others(196): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200104 | |||||
| chr13:114200141
|
G | C | 19 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(16): Show | 22 | HG01069.hp1 HG01071.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.172-184G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200141 | ||||||
| chr13:114200141
|
G | GGTCCCCG others(227): Show |
2 | a0001c0001t0006g0010a0001c0001t0006g0033 | 4 | HG00642.hp2 HG03834.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-179_172-178ins others(234): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 114200141 | |||||
| chr13:114200199
|
T | C | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.172-126T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 2/3 | chr13 | 114200199 | ||||||
| chr13:114200502
|
G | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.290+59G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114200502 | ||||||
| chr13:114200503
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.290+60G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114200503 | ||||||
| chr13:114200570
|
CA | C | 85 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(82): Show | 98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.290+128delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114200570 | ||||||
| chr13:114200588
|
G | T | 1 | a0001c0001t0002g0310 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.290+145G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114200588 | ||||||
| chr13:114200794
|
G | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.290+351G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114200794 | ||||||
| chr13:114200965
|
A | G | 41 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0058others(38): Show | 45 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+522A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114200965 | ||||||
| chr13:114201027
|
G | A | 1 | a0001c0001t0002g0276 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.290+584G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114201027 | ||||||
| chr13:114201117
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.290+674C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114201117 | ||||||
| chr13:114201621
|
T | C | 7 | a0001c0001t0001g0027a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 8 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+1178T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114201621 | ||||||
| chr13:114201753
|
C | T | 1 | a0001c0001t0007g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.290+1310C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114201753 | ||||||
| chr13:114202020
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.290+1577C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202020 | ||||||
| chr13:114202021
|
G | A | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG02280.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.290+1578G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202021 | ||||||
| chr13:114202051
|
G | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.290+1608G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202051 | ||||||
| chr13:114202117
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.290+1674G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202117 | ||||||
| chr13:114202145
|
G | A | 1 | a0001c0001t0005g0085 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.290+1702G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202145 | ||||||
| chr13:114202160
|
A | G | 27 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(24): Show | 29 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.290+1717A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202160 | ||||||
| chr13:114202166
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.290+1723C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202166 | ||||||
| chr13:114202227
|
T | C | 1 | a0001c0001t0003g0180 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.290+1784T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202227 | ||||||
| chr13:114202229
|
T | G | 8 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(5): Show | 8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+1786T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202229 | ||||||
| chr13:114202365
|
G | A | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.290+1922G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202365 | ||||||
| chr13:114202414
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.290+1971T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202414 | ||||||
| chr13:114202577
|
G | A | 12 | a0001c0001t0001g0027a0001c0001t0001g0034a0001c0001t0001g0035others(9): Show | 13 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.290+2134G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202577 | ||||||
| chr13:114202623
|
C | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0077a0001c0001t0001g0124others(7): Show | 11 | HG01243.hp1 HG01258.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.290+2180C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202623 | ||||||
| chr13:114202635
|
T | C | 13 | a0001c0001t0002g0291a0001c0001t0006g0010a0001c0001t0006g0033others(10): Show | 16 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.290+2192T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202635 | ||||||
| chr13:114202704
|
A | T | 1 | a0001c0001t0003g0151 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.290+2261A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202704 | ||||||
| chr13:114202747
|
T | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(174): Show | 201 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.290+2304T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202747 | ||||||
| chr13:114202771
|
T | C | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(180): Show | 209 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(206): Show |
intron_variant | MODIFIER | c.290+2328T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202771 | ||||||
| chr13:114202823
|
C | T | 1 | a0001c0001t0002g0309 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.290+2380C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202823 | ||||||
| chr13:114202866
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.290+2423C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202866 | ||||||
| chr13:114202930
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.290+2487A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114202930 | ||||||
| chr13:114203439
|
G | T | 1 | a0001c0001t0002g0302 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.290+2996G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203439 | ||||||
| chr13:114203677
|
A | G | 1 | a0001c0001t0005g0097 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.290+3234A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203677 | ||||||
| chr13:114203732
|
C | T | 7 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0069others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+3289C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203732 | ||||||
| chr13:114203757
|
C | G | 52 | a0001c0001t0001g0039a0001c0001t0001g0220a0001c0001t0001g0221others(49): Show | 60 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.290+3314C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203757 | ||||||
| chr13:114203820
|
T | C | 87 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0028others(84): Show | 101 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.290+3377T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203820 | ||||||
| chr13:114203892
|
C | A | 7 | a0001c0001t0003g0006a0001c0001t0003g0012a0001c0001t0003g0113others(4): Show | 10 | HG01123.hp1 HG01975.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+3449C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203892 | ||||||
| chr13:114203992
|
A | G | 1 | a0001c0001t0006g0345 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.290+3549A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114203992 | ||||||
| chr13:114204158
|
A | G | 30 | a0001c0001t0001g0068a0001c0001t0001g0223a0001c0001t0005g0015others(27): Show | 32 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.290+3715A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204158 | ||||||
| chr13:114204206
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.290+3763A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204206 | ||||||
| chr13:114204244
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.290+3801C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204244 | ||||||
| chr13:114204358
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0335 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.290+3915G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204358 | ||||||
| chr13:114204422
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.290+3979T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204422 | ||||||
| chr13:114204499
|
T | A | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(179): Show | 205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+4056T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204499 | ||||||
| chr13:114204529
|
A | G | 1 | a0001c0001t0003g0021 | 2 | NA18986.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.290+4086A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204529 | ||||||
| chr13:114204622
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 5 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+4179G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204622 | ||||||
| chr13:114204685
|
C | T | 2 | a0001c0001t0002g0032a0001c0004t0001g0053 | 3 | HG00323.hp2 HG02148.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.290+4242C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204685 | ||||||
| chr13:114204776
|
G | C | 2 | a0001c0001t0009g0336a0001c0001t0009g0337 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.290+4333G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204776 | ||||||
| chr13:114204805
|
G | T | 7 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(4): Show | 7 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+4362G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204805 | ||||||
| chr13:114204811
|
CAAG | C | 9 | a0001c0001t0005g0015a0001c0001t0005g0036a0001c0001t0005g0086others(6): Show | 10 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.290+4373_290+4375d others(5): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114204811 | |||||
| chr13:114204871
|
T | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.290+4428T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204871 | ||||||
| chr13:114204961
|
C | T | 2 | a0001c0001t0003g0180a0001c0001t0003g0190 | 2 | NA18972.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.290+4518C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114204961 | ||||||
| chr13:114205187
|
C | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+4744C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114205187 | ||||||
| chr13:114205254
|
A | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(179): Show | 205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+4811A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114205254 | ||||||
| chr13:114205381
|
CA | C | 2 | a0001c0001t0003g0024a0001c0001t0003g0165 | 3 | NA18997.hp2 NA19007.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.290+4940delA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114205381 | |||||
| chr13:114205584
|
T | G | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG02280.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.290+5141T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114205584 | ||||||
| chr13:114205648
|
C | A | 1 | a0001c0001t0002g0307 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.290+5205C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114205648 | ||||||
| chr13:114205770
|
G | A | 1 | a0001c0001t0003g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.290+5327G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114205770 | ||||||
| chr13:114205980
|
G | T | 9 | a0001c0001t0003g0022a0001c0001t0003g0140a0001c0001t0003g0143others(6): Show | 9 | HG00558.hp1 HG02148.hp2 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.290+5537G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114205980 | ||||||
| chr13:114206104
|
CT | C | 151 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(148): Show | 172 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.290+5678delT | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114206104 | |||||
| chr13:114206208
|
T | G | 7 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(4): Show | 7 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+5765T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206208 | ||||||
| chr13:114206247
|
C | T | 1 | a0001c0001t0004g0148 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.290+5804C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206247 | ||||||
| chr13:114206248
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0003g0140 | 2 | HG02148.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.290+5805G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206248 | ||||||
| chr13:114206446
|
C | T | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+6003C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206446 | ||||||
| chr13:114206585
|
A | G | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.290+6142A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206585 | ||||||
| chr13:114206690
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0048 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.290+6247C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206690 | ||||||
| chr13:114206708
|
T | C | 1 | a0001c0001t0007g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.290+6265T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206708 | ||||||
| chr13:114206869
|
C | T | 5 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(2): Show | 5 | HG01891.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+6426C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206869 | ||||||
| chr13:114206870
|
T | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(139): Show | 160 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.290+6427T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114206870 | ||||||
| chr13:114207021
|
G | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+6578G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207021 | ||||||
| chr13:114207052
|
C | G | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+6609C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207052 | ||||||
| chr13:114207075
|
A | G | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+6632A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207075 | ||||||
| chr13:114207106
|
C | T | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.290+6663C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207106 | ||||||
| chr13:114207184
|
T | C | 7 | a0001c0001t0003g0006a0001c0001t0003g0012a0001c0001t0003g0113others(4): Show | 10 | HG01123.hp1 HG01975.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+6741T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207184 | ||||||
| chr13:114207207
|
A | G | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+6764A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207207 | ||||||
| chr13:114207318
|
C | T | 3 | a0001c0001t0002g0306a0001c0001t0002g0320a0001c0001t0002g0321 | 3 | HG01099.hp1 HG01975.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.290+6875C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207318 | ||||||
| chr13:114207453
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.290+7010C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207453 | ||||||
| chr13:114207493
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0003g0138 | 2 | HG02698.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.290+7050C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207493 | ||||||
| chr13:114207513
|
C | T | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(179): Show | 205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+7070C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207513 | ||||||
| chr13:114207590
|
C | T | 7 | a0001c0001t0003g0006a0001c0001t0003g0012a0001c0001t0003g0113others(4): Show | 10 | HG01123.hp1 HG01975.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+7147C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207590 | ||||||
| chr13:114207644
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.290+7201C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207644 | ||||||
| chr13:114207814
|
C | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(139): Show | 160 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.290+7371C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207814 | ||||||
| chr13:114207833
|
G | T | 53 | a0001c0001t0001g0039a0001c0001t0001g0114a0001c0001t0001g0220others(50): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.290+7390G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114207833 | ||||||
| chr13:114208053
|
C | T | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.290+7610C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208053 | ||||||
| chr13:114208064
|
G | A | 2 | a0001c0001t0009g0336a0001c0001t0009g0337 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.290+7621G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208064 | ||||||
| chr13:114208066
|
C | T | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.290+7623C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208066 | ||||||
| chr13:114208297
|
C | T | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(179): Show | 205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+7854C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208297 | ||||||
| chr13:114208298
|
G | A | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.290+7855G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208298 | ||||||
| chr13:114208382
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 5 | HG01496.hp2 HG02109.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+7939A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208382 | ||||||
| chr13:114208447
|
C | T | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+8004C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208447 | ||||||
| chr13:114208625
|
G | A | 7 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(4): Show | 7 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+8182G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208625 | ||||||
| chr13:114208761
|
A | G | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(179): Show | 205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+8318A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208761 | ||||||
| chr13:114208822
|
T | TA | 2 | a0001c0001t0001g0019a0001c0001t0001g0128 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.290+8380dupA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114208822 | |||||
| chr13:114208848
|
C | T | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.290+8405C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208848 | ||||||
| chr13:114208885
|
C | A | 16 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0073others(13): Show | 17 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.290+8442C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208885 | ||||||
| chr13:114208982
|
G | T | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.290+8539G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114208982 | ||||||
| chr13:114209077
|
G | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+8634G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209077 | ||||||
| chr13:114209174
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.290+8731C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209174 | ||||||
| chr13:114209220
|
G | T | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(179): Show | 205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+8777G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209220 | ||||||
| chr13:114209236
|
A | G | 8 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(5): Show | 8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+8793A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209236 | ||||||
| chr13:114209326
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0234 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.290+8883A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209326 | ||||||
| chr13:114209396
|
T | C | 2 | a0001c0001t0009g0336a0001c0001t0009g0337 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.290+8953T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209396 | ||||||
| chr13:114209450
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.290+9007C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209450 | ||||||
| chr13:114209499
|
G | A | 1 | a0001c0001t0003g0140 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.290+9056G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209499 | ||||||
| chr13:114209550
|
G | T | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+9107G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209550 | ||||||
| chr13:114209619
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.290+9176G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209619 | ||||||
| chr13:114209633
|
C | T | 1 | a0001c0001t0003g0191 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.290+9190C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209633 | ||||||
| chr13:114209646
|
C | T | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.290+9203C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209646 | ||||||
| chr13:114209648
|
G | A | 5 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(2): Show | 5 | HG01891.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+9205G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209648 | ||||||
| chr13:114209682
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.290+9239T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209682 | ||||||
| chr13:114209723
|
A | G | 1 | a0001c0001t0002g0308 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.290+9280A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209723 | ||||||
| chr13:114209739
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0234 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.290+9296C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209739 | ||||||
| chr13:114209751
|
C | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(139): Show | 160 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.290+9308C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114209751 | ||||||
| chr13:114210529
|
T | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0351others(1): Show | 4 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+10086T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210529 | ||||||
| chr13:114210543
|
A | G | 7 | a0001c0001t0001g0026a0001c0001t0001g0201a0001c0001t0001g0203others(4): Show | 8 | NA18940.hp2 NA18942.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+10100A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210543 | ||||||
| chr13:114210577
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0234 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.290+10134G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210577 | ||||||
| chr13:114210618
|
A | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(179): Show | 205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.290+10175A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210618 | ||||||
| chr13:114210695
|
C | T | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.290+10252C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210695 | ||||||
| chr13:114210703
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.290+10260C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210703 | ||||||
| chr13:114210841
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0128 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.290+10398G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210841 | ||||||
| chr13:114210855
|
T | TAC | 69 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0035others(66): Show | 79 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.290+10447_290+1044 others(6): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | |||||
| chr13:114210855
|
T | TACAC | 31 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(28): Show | 32 | HG00140.hp1 HG00408.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.290+10445_290+1044 others(8): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | |||||
| chr13:114210855
|
T | TACACAC | 40 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0044others(37): Show | 45 | HG00099.hp1 HG00423.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.290+10443_290+1044 others(10): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | |||||
| chr13:114210855
|
T | TACACACA others(1): Show |
48 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0001g0129others(45): Show | 54 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.290+10441_290+1044 others(12): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | |||||
| chr13:114210855
|
T | TACACACA others(3): Show |
32 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0048others(29): Show | 39 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.290+10439_290+1044 others(14): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | |||||
| chr13:114210855
|
T | TACACACA others(5): Show |
7 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0050others(4): Show | 8 | HG02257.hp2 HG02258.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+10437_290+1044 others(16): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | |||||
| chr13:114210855
|
T | TACACACA others(7): Show |
3 | a0001c0001t0001g0216a0001c0001t0003g0139a0001c0001t0003g0160 | 3 | HG02165.hp1 HG02523.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.290+10435_290+1044 others(18): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | |||||
| chr13:114210855
|
TAC | T | 23 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0060others(20): Show | 24 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.290+10447_290+1044 others(6): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114210855 | |||||
| chr13:114210941
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.290+10498G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210941 | ||||||
| chr13:114210981
|
T | C | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(180): Show | 206 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.290+10538T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114210981 | ||||||
| chr13:114211058
|
A | G | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.290+10615A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211058 | ||||||
| chr13:114211090
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.290+10647G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211090 | ||||||
| chr13:114211198
|
C | T | 1 | a0001c0001t0002g0309 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.290+10755C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211198 | ||||||
| chr13:114211293
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0125 | 2 | HG01516.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.290+10850G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211293 | ||||||
| chr13:114211404
|
G | A | 15 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.290+10961G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211404 | ||||||
| chr13:114211504
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.291-10997C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211504 | ||||||
| chr13:114211526
|
C | G | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291-10975C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211526 | ||||||
| chr13:114211526
|
C | T | 7 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(4): Show | 7 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-10975C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211526 | ||||||
| chr13:114211563
|
T | TG | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-10935dupG | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114211563 | |||||
| chr13:114211685
|
G | A | 1 | a0001c0001t0004g0235 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.291-10816G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211685 | ||||||
| chr13:114211722
|
G | T | 1 | a0001c0001t0002g0043 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.291-10779G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211722 | ||||||
| chr13:114211810
|
C | T | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-10691C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211810 | ||||||
| chr13:114211820
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.291-10681C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211820 | ||||||
| chr13:114211953
|
G | A | 2 | a0001c0001t0004g0254a0001c0001t0013g0104 | 2 | HG00544.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.291-10548G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211953 | ||||||
| chr13:114211964
|
C | T | 1 | a0001c0001t0008g0091 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.291-10537C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114211964 | ||||||
| chr13:114212107
|
C | T | 85 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(82): Show | 98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.291-10394C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212107 | ||||||
| chr13:114212214
|
T | C | 1 | a0001c0001t0008g0099 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.291-10287T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212214 | ||||||
| chr13:114212223
|
A | G | 47 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(44): Show | 52 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.291-10278A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212223 | ||||||
| chr13:114212283
|
T | C | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG02280.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.291-10218T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212283 | ||||||
| chr13:114212307
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.291-10194G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212307 | ||||||
| chr13:114212552
|
T | TA | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9942dupA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114212552 | |||||
| chr13:114212695
|
A | G | 1 | a0001c0004t0001g0053 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.291-9806A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212695 | ||||||
| chr13:114212829
|
G | A | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291-9672G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212829 | ||||||
| chr13:114212839
|
G | A | 6 | a0001c0001t0005g0015a0001c0001t0005g0036a0001c0001t0005g0087others(3): Show | 7 | HG02451.hp1 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-9662G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212839 | ||||||
| chr13:114212847
|
G | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9654G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212847 | ||||||
| chr13:114212852
|
A | AAAAT | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9641_291-9638d others(6): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114212852 | |||||
| chr13:114212985
|
T | C | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9516T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212985 | ||||||
| chr13:114212998
|
T | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9503T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114212998 | ||||||
| chr13:114213080
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.291-9421A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213080 | ||||||
| chr13:114213133
|
C | T | 8 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(5): Show | 8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-9368C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213133 | ||||||
| chr13:114213313
|
AG | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9187delG | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213313 | ||||||
| chr13:114213387
|
T | C | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-9114T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213387 | ||||||
| chr13:114213446
|
C | T | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-9055C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213446 | ||||||
| chr13:114213516
|
A | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(179): Show | 205 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.291-8985A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213516 | ||||||
| chr13:114213547
|
C | G | 1 | a0001c0001t0003g0151 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.291-8954C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213547 | ||||||
| chr13:114213557
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.291-8944C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213557 | ||||||
| chr13:114213562
|
C | G | 1 | a0001c0001t0003g0163 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.291-8939C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213562 | ||||||
| chr13:114213571
|
C | G | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8930C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213571 | ||||||
| chr13:114213621
|
TACCCCTG others(154): Show |
T | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-8863_291-8703d others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114213621 | |||||
| chr13:114213675
|
A | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(52): Show | 60 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.291-8826A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213675 | ||||||
| chr13:114213734
|
C | G | 1 | a0001c0001t0005g0037 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.291-8767C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213734 | ||||||
| chr13:114213752
|
T | C | 1 | a0001c0001t0004g0226 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.291-8749T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213752 | ||||||
| chr13:114213767
|
C | T | 39 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(36): Show | 43 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.291-8734C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213767 | ||||||
| chr13:114213778
|
A | C | 6 | a0001c0001t0006g0010a0001c0001t0006g0342a0001c0001t0006g0343others(3): Show | 8 | HG00642.hp2 HG01361.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-8723A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213778 | ||||||
| chr13:114213799
|
C | T | 39 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(36): Show | 43 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.291-8702C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213799 | ||||||
| chr13:114213821
|
GTGGAAGC others(57): Show |
G | 11 | a0001c0001t0006g0010a0001c0001t0006g0340a0001c0001t0006g0341others(8): Show | 13 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.291-8661_291-8598d others(66): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114213821 | |||||
| chr13:114213840
|
G | A | 29 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(26): Show | 32 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.291-8661G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213840 | ||||||
| chr13:114213844
|
C | T | 66 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0012others(63): Show | 76 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.291-8657C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213844 | ||||||
| chr13:114213863
|
C | T | 1 | a0001c0001t0006g0033 | 2 | NA18999.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.291-8638C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213863 | ||||||
| chr13:114213873
|
A | G | 29 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(26): Show | 32 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.291-8628A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213873 | ||||||
| chr13:114213875
|
CCCCACCC others(89): Show |
C | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8622_291-8527d others(98): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114213875 | |||||
| chr13:114213885
|
A | G | 1 | a0001c0001t0006g0033 | 2 | NA18999.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.291-8616A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213885 | ||||||
| chr13:114213889
|
AAGCTCCA others(56): Show |
A | 1 | a0001c0001t0002g0321 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.291-8611_291-8549d others(65): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213889 | ||||||
| chr13:114213953
|
G | C | 1 | a0001c0001t0002g0321 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.291-8548G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213953 | ||||||
| chr13:114213977
|
T | C | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8524T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213977 | ||||||
| chr13:114213982
|
G | A | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8519G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114213982 | ||||||
| chr13:114214012
|
G | C | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8489G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214012 | ||||||
| chr13:114214078
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0234 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.291-8423C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214078 | ||||||
| chr13:114214082
|
G | A | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8419G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214082 | ||||||
| chr13:114214085
|
C | A | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8416C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214085 | ||||||
| chr13:114214101
|
A | T | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-8400A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214101 | ||||||
| chr13:114214115
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.291-8386C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214115 | ||||||
| chr13:114214137
|
T | C | 1 | a0001c0001t0002g0318 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.291-8364T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214137 | ||||||
| chr13:114214243
|
G | C | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8258G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214243 | ||||||
| chr13:114214244
|
C | T | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8257C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214244 | ||||||
| chr13:114214246
|
G | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8255G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214246 | ||||||
| chr13:114214247
|
G | T | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8254G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214247 | ||||||
| chr13:114214249
|
C | G | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8252C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214249 | ||||||
| chr13:114214250
|
A | AT | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8250dupT | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114214250 | |||||
| chr13:114214267
|
G | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8234G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214267 | ||||||
| chr13:114214328
|
T | G | 85 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(82): Show | 98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.291-8173T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214328 | ||||||
| chr13:114214372
|
A | T | 85 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(82): Show | 98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.291-8129A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214372 | ||||||
| chr13:114214439
|
C | T | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-8062C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214439 | ||||||
| chr13:114214582
|
T | TTTTG | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(184): Show | 211 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.291-7900_291-7897d others(6): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114214582 | |||||
| chr13:114214582
|
T | TTTTGTTT others(5): Show |
11 | a0001c0001t0005g0015a0001c0001t0005g0036a0001c0001t0005g0084others(8): Show | 12 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.291-7908_291-7897d others(14): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114214582 | |||||
| chr13:114214582
|
T | TTTTGTTT others(9): Show |
16 | a0001c0001t0005g0016a0001c0001t0005g0037a0001c0001t0005g0085others(13): Show | 17 | HG00408.hp1 HG00423.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.291-7912_291-7897d others(18): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114214582 | |||||
| chr13:114214647
|
C | T | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.291-7854C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214647 | ||||||
| chr13:114214728
|
A | T | 3 | a0001c0001t0005g0016a0001c0001t0005g0094a0001c0001t0007g0116 | 4 | HG02572.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.291-7773A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214728 | ||||||
| chr13:114214729
|
G | A | 8 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(5): Show | 8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-7772G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214729 | ||||||
| chr13:114214821
|
A | C | 1 | a0001c0001t0003g0172 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.291-7680A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214821 | ||||||
| chr13:114214912
|
CTTAAT | C | 85 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(82): Show | 98 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.291-7585_291-7581d others(7): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114214912 | |||||
| chr13:114214976
|
C | T | 67 | a0001c0001t0001g0115a0001c0001t0003g0005a0001c0001t0003g0006others(64): Show | 77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.291-7525C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114214976 | ||||||
| chr13:114215144
|
G | T | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-7357G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215144 | ||||||
| chr13:114215145
|
C | T | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG02280.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.291-7356C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215145 | ||||||
| chr13:114215214
|
A | T | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-7287A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215214 | ||||||
| chr13:114215228
|
G | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0298 | 3 | NA18957.hp2 NA18993.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.291-7273G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215228 | ||||||
| chr13:114215317
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.291-7184T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215317 | ||||||
| chr13:114215518
|
T | C | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-6983T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215518 | ||||||
| chr13:114215632
|
A | G | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-6869A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215632 | ||||||
| chr13:114215751
|
C | T | 19 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(16): Show | 22 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.291-6750C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215751 | ||||||
| chr13:114215752
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.291-6749C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215752 | ||||||
| chr13:114215831
|
C | T | 2 | a0001c0001t0009g0336a0001c0001t0009g0337 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.291-6670C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215831 | ||||||
| chr13:114215881
|
G | A | 223 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(220): Show | 251 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.291-6620G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215881 | ||||||
| chr13:114215908
|
C | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0234 | 3 | HG02258.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.291-6593C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215908 | ||||||
| chr13:114215985
|
A | T | 1 | a0001c0001t0001g0064 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.291-6516A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215985 | ||||||
| chr13:114215997
|
A | T | 1 | a0001c0001t0001g0064 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.291-6504A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114215997 | ||||||
| chr13:114216215
|
C | T | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-6286C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216215 | ||||||
| chr13:114216282
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.291-6219A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216282 | ||||||
| chr13:114216332
|
G | A | 18 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0052others(15): Show | 20 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.291-6169G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216332 | ||||||
| chr13:114216478
|
A | C | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-6023A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216478 | ||||||
| chr13:114216592
|
C | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-5909C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216592 | ||||||
| chr13:114216656
|
C | T | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-5845C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216656 | ||||||
| chr13:114216670
|
T | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-5831T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216670 | ||||||
| chr13:114216753
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(6): Show | 12 | HG00738.hp2 HG01070.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.291-5748G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216753 | ||||||
| chr13:114216821
|
G | C | 1 | a0001c0001t0002g0311 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.291-5680G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216821 | ||||||
| chr13:114216911
|
T | C | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.291-5590T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216911 | ||||||
| chr13:114216939
|
T | C | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(180): Show | 206 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.291-5562T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114216939 | ||||||
| chr13:114217027
|
T | G | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291-5474T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217027 | ||||||
| chr13:114217047
|
G | A | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291-5454G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217047 | ||||||
| chr13:114217132
|
G | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-5369G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217132 | ||||||
| chr13:114217249
|
A | T | 1 | a0001c0001t0001g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.291-5252A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217249 | ||||||
| chr13:114217383
|
A | G | 47 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(44): Show | 52 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.291-5118A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217383 | ||||||
| chr13:114217446
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.291-5055G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217446 | ||||||
| chr13:114217601
|
G | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.291-4900G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217601 | ||||||
| chr13:114217643
|
C | T | 2 | a0001c0002t0001g0197a0001c0002t0001g0199 | 2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.291-4858C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217643 | ||||||
| chr13:114217709
|
G | C | 7 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(4): Show | 7 | HG03491.hp1 HG03704.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-4792G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217709 | ||||||
| chr13:114217801
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0121 | 3 | HG01257.hp2 HG01258.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.291-4700A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217801 | ||||||
| chr13:114217939
|
G | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-4562G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217939 | ||||||
| chr13:114217944
|
C | T | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-4557C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217944 | ||||||
| chr13:114217969
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(139): Show | 160 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.291-4532A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114217969 | ||||||
| chr13:114218035
|
G | A | 1 | a0001c0001t0002g0296 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.291-4466G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218035 | ||||||
| chr13:114218105
|
G | A | 8 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(5): Show | 8 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-4396G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218105 | ||||||
| chr13:114218283
|
C | T | 1 | a0001c0001t0002g0294 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.291-4218C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218283 | ||||||
| chr13:114218294
|
AAATACCT others(3): Show |
A | 1 | a0001c0001t0003g0038 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.291-4203_291-4194d others(12): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114218294 | |||||
| chr13:114218316
|
C | A | 1 | a0001c0001t0003g0186 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.291-4185C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218316 | ||||||
| chr13:114218360
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.291-4141C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218360 | ||||||
| chr13:114218405
|
C | T | 2 | a0001c0001t0009g0336a0001c0001t0009g0337 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.291-4096C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218405 | ||||||
| chr13:114218406
|
G | T | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-4095G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218406 | ||||||
| chr13:114218530
|
G | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-3971G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218530 | ||||||
| chr13:114218541
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-3960G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218541 | ||||||
| chr13:114218609
|
T | C | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-3892T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218609 | ||||||
| chr13:114218701
|
A | G | 1 | a0001c0001t0002g0282 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.291-3800A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218701 | ||||||
| chr13:114218884
|
G | A | 74 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(71): Show | 84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.291-3617G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218884 | ||||||
| chr13:114218898
|
A | G | 1 | a0001c0001t0003g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.291-3603A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218898 | ||||||
| chr13:114218922
|
G | C | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-3579G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114218922 | ||||||
| chr13:114219011
|
G | A | 1 | a0001c0001t0003g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.291-3490G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219011 | ||||||
| chr13:114219057
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0111a0001c0001t0001g0117others(1): Show | 5 | HG02630.hp2 HG02647.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-3444C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219057 | ||||||
| chr13:114219097
|
G | A | 1 | a0001c0001t0003g0154 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.291-3404G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219097 | ||||||
| chr13:114219130
|
TGACAAAG others(44): Show |
T | 1 | a0001c0001t0004g0241 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.291-3370_291-3320d others(53): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219130 | ||||||
| chr13:114219221
|
T | C | 1 | a0001c0001t0002g0288 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.291-3280T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219221 | ||||||
| chr13:114219223
|
T | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(52): Show | 60 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.291-3278T>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219223 | ||||||
| chr13:114219272
|
C | G | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-3229C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219272 | ||||||
| chr13:114219321
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(52): Show | 60 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.291-3180G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219321 | ||||||
| chr13:114219408
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(52): Show | 60 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.291-3093A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219408 | ||||||
| chr13:114219593
|
A | T | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-2908A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219593 | ||||||
| chr13:114219615
|
A | C | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.291-2886A>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219615 | ||||||
| chr13:114219713
|
C | T | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-2788C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219713 | ||||||
| chr13:114219755
|
G | T | 1 | a0001c0001t0001g0064 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.291-2746G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114219755 | ||||||
| chr13:114220140
|
A | G | 67 | a0001c0001t0001g0115a0001c0001t0003g0005a0001c0001t0003g0006others(64): Show | 77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.291-2361A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220140 | ||||||
| chr13:114220162
|
C | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-2339C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220162 | ||||||
| chr13:114220163
|
C | A | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-2338C>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220163 | ||||||
| chr13:114220173
|
C | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0132 | 3 | HG02723.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291-2328C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220173 | ||||||
| chr13:114220239
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(6): Show | 12 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.291-2262C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220239 | ||||||
| chr13:114220272
|
G | A | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG02280.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.291-2229G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220272 | ||||||
| chr13:114220381
|
G | T | 28 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(25): Show | 33 | HG00639.hp1 HG00642.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.291-2120G>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220381 | ||||||
| chr13:114220392
|
C | T | 1 | a0001c0001t0005g0102 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.291-2109C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220392 | ||||||
| chr13:114220400
|
G | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(51): Show | 59 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.291-2101G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220400 | ||||||
| chr13:114220427
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.291-2074T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220427 | ||||||
| chr13:114220511
|
C | T | 1 | a0001c0001t0002g0290 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.291-1990C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220511 | ||||||
| chr13:114220756
|
C | T | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0145others(1): Show | 6 | HG00544.hp1 NA18986.hp2 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.291-1745C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220756 | ||||||
| chr13:114220773
|
G | A | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0145others(1): Show | 6 | HG00544.hp1 NA18986.hp2 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.291-1728G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220773 | ||||||
| chr13:114220818
|
T | C | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-1683T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114220818 | ||||||
| chr13:114221014
|
C | G | 2 | a0001c0001t0001g0324a0001c0001t0010g0325 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.291-1487C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221014 | ||||||
| chr13:114221023
|
C | T | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291-1478C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221023 | ||||||
| chr13:114221134
|
C | T | 53 | a0001c0001t0001g0039a0001c0001t0001g0114a0001c0001t0001g0220others(50): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.291-1367C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221134 | ||||||
| chr13:114221158
|
G | A | 1 | a0001c0001t0007g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291-1343G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221158 | ||||||
| chr13:114221179
|
G | A | 1 | a0001c0001t0005g0085 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.291-1322G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221179 | ||||||
| chr13:114221198
|
C | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0027others(99): Show | 112 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.291-1303C>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221198 | ||||||
| chr13:114221223
|
G | A | 15 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0068others(12): Show | 15 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.291-1278G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221223 | ||||||
| chr13:114221242
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.291-1259G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221242 | ||||||
| chr13:114221379
|
G | A | 1 | a0001c0001t0003g0266 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.291-1122G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221379 | ||||||
| chr13:114221419
|
A | G | 44 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(41): Show | 50 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.291-1082A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221419 | ||||||
| chr13:114221580
|
A | G | 43 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(40): Show | 48 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.291-921A>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221580 | ||||||
| chr13:114221714
|
A | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0058others(26): Show | 33 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.291-787A>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221714 | ||||||
| chr13:114221762
|
G | GA | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(211): Show | 240 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.291-730dupA | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114221762 | |||||
| chr13:114221762
|
G | GAA | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.291-731_291-730dup others(2): Show |
CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 114221762 | |||||
| chr13:114221858
|
G | A | 12 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(9): Show | 15 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.291-643G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221858 | ||||||
| chr13:114221860
|
C | T | 2 | a0001c0001t0009g0336a0001c0001t0009g0337 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.291-641C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221860 | ||||||
| chr13:114221877
|
G | C | 129 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(126): Show | 148 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.291-624G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221877 | ||||||
| chr13:114221886
|
C | T | 7 | a0001c0001t0002g0029a0001c0001t0002g0274a0001c0001t0002g0275others(4): Show | 8 | HG00609.hp1 HG01099.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.291-615C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221886 | ||||||
| chr13:114221909
|
T | C | 13 | a0001c0001t0006g0010a0001c0001t0006g0033a0001c0001t0006g0340others(10): Show | 16 | HG00642.hp2 HG01361.hp2 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.291-592T>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221909 | ||||||
| chr13:114221989
|
C | T | 129 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(126): Show | 148 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.291-512C>T | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221989 | ||||||
| chr13:114221993
|
G | C | 40 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(37): Show | 45 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.291-508G>C | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114221993 | ||||||
| chr13:114222083
|
G | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0044others(83): Show | 99 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.291-418G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114222083 | ||||||
| chr13:114222251
|
T | G | 1 | a0001c0001t0001g0208 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.291-250T>G | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114222251 | ||||||
| chr13:114222276
|
G | A | 129 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(126): Show | 148 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.291-225G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114222276 | ||||||
| chr13:114222468
|
G | A | 27 | a0001c0001t0005g0015a0001c0001t0005g0016a0001c0001t0005g0036others(24): Show | 29 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.291-33G>A | CFAP97D2 | ENSG00000283361.3 | transcript | ENST00000636692.2 | protein_coding | 3/3 | chr13 | 114222468 |